CN108698379B

CN108698379B - Interlayers having enhanced optical properties

Info

Publication number: CN108698379B
Application number: CN201780013000.7A
Authority: CN
Inventors: L.L.斯庞勒; J.B.赫尔巴特; 吕军
Original assignee: Solutia Inc
Current assignee: Solutia Inc
Priority date: 2016-02-23
Filing date: 2017-02-08
Publication date: 2021-05-25
Anticipated expiration: 2037-02-08
Also published as: WO2017146901A1; MX2018008766A; JP2019513162A; KR20180116283A; JP6960932B2; EP3419824A1; CN108698379A

Abstract

A tapered interlayer is provided that includes at least one polymer layer and has a tapered zone with an overall wedge angle of no greater than 0.85 mrad. The polymer layer has a refractive index of 1.480 or higher. Multilayer sheets formed from such interlayers can exhibit desirable optical properties, including lower "ghosting" when used as part of a head-up display (HUD) display panel for automotive and aircraft applications, for example.

Description

Interlayers having enhanced optical properties

Cross reference to related applications

This application is a partial continuation of U.S. patent application serial No. 14/563,011, currently filed 2014, 8/12, pending, the disclosure of which is hereby incorporated by reference in its entirety.

Background

1. Field of the invention

The present disclosure relates to polymer resins, particularly to polymer resins suitable for use in polymer interlayers, including those used in multilayer panels.

2. Description of the related Art

Poly (vinyl butyral) (PVB) is commonly used in the manufacture of polymer sheets that can be used as interlayers in multilayer sheets, including, for example, light transmitting laminates such as safety glass or polymer laminates. PVB is also used in photovoltaic solar panels to encapsulate panels used to generate and supply electricity for commercial and residential applications.

Safety glass generally refers to a transparent laminate comprising at least one polymer sheet or interlayer disposed between two sheets of glass. Safety glass is commonly used as a transparent barrier in architectural and automotive applications, and one of its primary functions is to absorb energy from an impact or blow without allowing an object to penetrate the glass and to keep the glass bonded even when the applied force is sufficient to break the glass. This prevents the spreading of sharp glass fragments to minimize injury and damage to people or objects within the enclosed area. Safety glass can also provide other benefits, such as reduced Ultraviolet (UV) and/or Infrared (IR) radiation, which can also enhance the aesthetic appearance of the window by adding color, texture, and the like. In addition, safety glass has also been manufactured with desirable acoustic properties, which results in a quieter interior space.

Laminated safety glass has been used in vehicles equipped with head-up display (HUD) systems that project images of the instrument cluster or other important information to the vehicle driver at the windshield location at line of sight. Such a display enables the driver to concentrate on the forward travel path while visually acquiring dashboard information. When projected onto a flat windshield having a uniform and consistent thickness, disturbing ghosting or "ghosting" of reflections occurs due to differences in the position of the projected image when reflected from the inner and outer surfaces of the glass.

One approach to addressing these ghosting images is to include a coating, such as a dielectric coating, between the glass and the polymer interlayer on one of the surfaces of the windshield. The coating is designed to produce a third ghost image very close to the primary image while significantly reducing the brightness of the secondary image so that the secondary image appears to blend into the background. Unfortunately, sometimes, the effectiveness of such coatings is limited and the coatings themselves may interfere with the adhesion of the polymer interlayer to the glass substrate, causing optical distortion and other problems.

At the same time, due in part to the desire to improve vehicle fuel efficiency, there is an increasing demand for multi-layer panels that are lighter in weight than conventional panels. Generally, the multilayer panels used in vehicles (which may include, for example, their windshields, side windows and other panels) constitute a significant portion of the total weight of the vehicle-sometimes up to 5%. Thus, a reduction in the overall weight of these panels typically results in a reduction in vehicle weight and a corresponding increase in fuel efficiency. The weight of these panels is largely not in the interlayer, but is attributed to the substrate, which typically comprises glass.

Thus, there is a need for polymer interlayers suitable for HUD applications that can also be used in lightweight multilayer panels. Such interlayers should exhibit desirable optical, acoustic, and visual properties while mitigating ghost image separation and allowing the use of thinner substrates.

SUMMARY

One embodiment of the present invention is directed to a tapered interlayer comprising at least one polymer layer comprising a poly (vinyl acetal) resin and at least one plasticizer. The polymer layer has a refractive index of at least about 1.480 and the interlayer comprises a tapered zone having an overall wedge angle of no greater than 0.85 mrad.

Another embodiment of the present invention is directed to a substrate comprising a pair of rigid substrates; and an interlayer disposed between the substrates. The interlayer comprises tapered zones having an overall wedge angle of less than 0.85 mrad and the multilayer sheet has an equivalent refractive index that is at least 0.010 higher than the refractive index of each rigid substrate.

Yet another embodiment of the present invention is directed to a multi-layer board comprising a pair of rigid substrates and a tapered interlayer disposed between the substrates. The tapered interlayer comprises at least one polymer resin. The refractive index of the interlayer is at least 5% higher than the refractive index of each rigid substrate.

Brief Description of Drawings

Various embodiments of the present invention are described in detail below with reference to the attached drawing figures, wherein:

FIG. 1 is a cross-sectional view of a tapered interlayer configured in accordance with one embodiment of the present invention, with various features of the tapered interlayer labeled for reference;

FIG. 2 is a cross-sectional view of a tapered interlayer having a tapered zone extending across the width of the interlayer, wherein the entire tapered zone has a constant wedge angle and a linear thickness profile;

FIG. 3 is a cross-sectional view of a tapered interlayer having a tapered zone extending across a portion of the width of the interlayer and a flat edge zone extending across a portion of the width of the interlayer, wherein the tapered zone comprises a constant angle zone and a variable angle zone;

FIG. 4 is a cross-sectional view of a tapered interlayer having a tapered zone extending across a portion of the width of the interlayer and two flat edge zones extending across a portion of the width of the interlayer, wherein the tapered zone comprises a constant angle zone and two variable angle zones;

FIG. 5 is a cross-sectional view of a tapered interlayer having a tapered zone extending across a portion of the width of the interlayer and two flat edge zones extending across a portion of the width of the interlayer, wherein the tapered zone is formed entirely by a tapered zone having a curved thickness profile;

FIG. 6 is a cross-sectional view of a tapered interlayer having a tapered zone extending the entire width of the interlayer, wherein the tapered zone comprises three constant angle zones separated from each other by two variable angle zones;

FIG. 7 is a cross-sectional view of a tapered interlayer having a tapered zone extending across a portion of the width of the interlayer and two flat edge zones extending across a portion of the width of the interlayer, wherein the tapered zone comprises three constant angle zones and four variable angle zones;

FIG. 8a is a plan view of a tapered interlayer configured for a vehicle windshield, wherein the interlayer has a thickness profile similar to that depicted in FIG. 2;

FIG. 8b is a cross-sectional view of the interlayer of FIG. 8a showing the thickness profile of the interlayer;

FIG. 9 is a schematic view of an apparatus for measuring ghost separation distances of a multilayer board;

fig. 10 is an example of a projected image formed when the ghost separation distance of the multilayer board is measured using the apparatus of fig. 9;

fig. 11 is an example of a graph (profile) formed by analyzing the projection image shown in fig. 10 by plotting the number of pixels as a function of intensity;

FIG. 12 is a graphical depiction of the results of the inter-ghost distance analysis performed on several comparative and public samples as described in example 11, particularly showing the inter-ghost distance of several samples with different wedge angles as a function of total thickness;

FIG. 13 is a graphical depiction of the results of the inter-ghost distance analysis performed on several comparative and public samples as described in example 11, particularly showing the inter-ghost distances of several samples with different glass configurations as a function of wedge angle; and

figure 14 is a graphical depiction of the results of the inter-ghost distance analysis performed in example 13, particularly showing the inter-ghost distance of several plates using plates with different glass thicknesses as a function of equivalent refractive index.

Detailed description of the invention

Resin compositions, layers and interlayers according to various embodiments of the present invention may comprise one or more thermoplastic polymers and a Refractive Index (RI) balancing agent. The term "refractive index balancer" or "RI balancer" as used herein refers to any component or additive included in the composition, layer or interlayer that is used to adjust the refractive index of at least one resin or layer. The RI balancing agent can increase or decrease the refractive index of at least one resin or layer within the interlayer, which can improve the optical properties of the interlayer, including mottle, haze, and/or clarity, as compared to the same interlayer formed without the RI balancing agent.

As used herein, the terms "polymeric resin composition" and "resin composition" refer to compositions comprising one or more polymeric resins. The polymer composition may optionally comprise other components, such as plasticizers and/or other additives. As used herein, the terms "polymer resin layer", "polymer layer" and "resin layer" refer to one or more polymer resins, optionally in combination with one or more plasticizers, that have been formed into a polymer sheet. The polymer layer may still contain additional additives, although these are not required. The term "interlayer" as used herein refers to a single or multi-layer polymeric sheet suitable for use with at least one rigid substrate to form a multi-layer sheet. The terms "monolithic" interlayer and "monolithic" interlayer refer to interlayers formed from a single resin sheet, while the term "multilayer" interlayer refers to interlayers having two or more resin sheets that are coextruded, laminated, or otherwise bonded to each other.

The resin compositions, layers, and interlayers described herein can comprise one or more thermoplastic polymers. Examples of suitable thermoplastic polymers may include, but are not limited to, poly (vinyl acetal) resins, Polyurethanes (PU), poly (ethylene-co-vinyl acetate) (EVA), polyvinyl chloride (PVC), poly (vinyl chloride-co-methacrylate), polyethylene, polyolefins, ethylene acrylate copolymers, poly (ethylene-co-butyl acrylate), silicone elastomers, epoxy resins, and acid copolymers, such as ethylene/carboxylic acid copolymers and ionomers thereof, derived from any of the above-listed polymers, and combinations thereof. In some embodiments, the thermoplastic polymer may be selected from poly (vinyl acetal) resins, polyvinyl chloride, and polyurethanes, or the resin may comprise one or more poly (vinyl acetal) resins. Although described herein with respect to poly (vinyl acetal) resins, it is to be understood that one or more of the above-described polymeric resins may be included with or in place of the poly (vinyl acetal) resins described below in accordance with various embodiments of the present invention.

When the resin compositions, layers, and interlayers described herein comprise a poly (vinyl acetal) resin, the poly (vinyl acetal) resin can be formed according to any suitable method. Poly (vinyl acetal) resins can be formed by acetalizing polyvinyl alcohol with one or more aldehydes in the presence of an acid catalyst. The resulting resin may then be cured according to known methods, for example, U.S. Pat. Nos. 2,282,057 and 2,282,026 andEncyclopedia of Polymer Science & Technologyisolation, stabilization and drying by the method described in "Vinyl acid Polymers" in 3 rd edition, volume 8, page 381-399, B.E. Wade (2003). Unless otherwise indicated, the resulting poly (vinyl acetal) resin can have a total acetalization percentage of at least about 50, at least about 60, at least about 70, at least about 75, at least about 80, at least about 85 weight percent, measured according to ASTM D1396. The total amount of aldehyde residues in the poly (vinyl acetal) resin, the balance of which are residual hydroxyl groups and residual acetate groups, may be collectively referred to as the acetal component, which will be discussed in more detail below.

According to some embodiments, the resin composition, layer or interlayer may comprise at least one poly (vinyl acetal) resin, which may be present in the composition, layer or interlayer in an amount of at least about 0.5, at least about 1, at least about 2, at least about 3, at least about 5, at least about 10, at least about 15, at least about 20, at least about 30, at least about 40, or at least about 45 weight percent based on the total weight of all resins in the composition, layer or interlayer. The at least one poly (vinyl acetal) resin, in total, may comprise at least about 10, at least about 20, at least about 30, at least about 40, at least about 50, at least about 60, at least about 70, or at least about 80 weight percent of the composition, layer, or interlayer, based on the total weight of all resins. In some embodiments, the amount of resin other than the at least one poly (vinyl acetal) resin may be no greater than about 20, no greater than about 15, no greater than about 10, no greater than about 5, no greater than about 2, or no greater than about 1 weight percent, based on the total weight of all resins.

In some embodiments, the resin composition, layer, or interlayer may comprise at least a first poly (vinyl acetal) resin and a second poly (vinyl acetal) resin, each of which may be present in the composition, layer, or interlayer in an amount of at least about 0.5, at least about 1, at least about 2, at least about 3, at least about 5, at least about 10, at least about 15, at least about 20, at least about 30, at least about 40, or at least about 45 weight percent based on the total weight of all resins in the composition, layer, or interlayer. The first and second poly (vinyl acetal) resins, in total, may comprise at least about 10, at least about 20, at least about 30, at least about 40, at least about 50, at least about 60, at least about 70, or at least about 80 weight percent of the composition, layer, or interlayer, based on the total weight of all resins. In some embodiments, the amount of resin other than the first and second poly (vinyl acetal) resins can be no greater than about 20, no greater than about 15, no greater than about 10, no greater than about 5, no greater than about 2, or no greater than about 1 weight percent, based on the total weight of all resins.

In some embodiments, one of the first and second poly (vinyl acetal) resins may be present in the composition, layer, or interlayer in an amount of less than 12 weight percent based on the total weight of the first and second poly (vinyl acetal) resins. For example, the first or second poly (vinyl acetal) resin can be present in the composition, layer, or interlayer in an amount of at least about 0.5, at least about 1, at least about 1.5, at least about 2, at least about 2.5, at least about 3, at least about 3.5, at least about 4, at least about 4.5, at least about 5, at least about 5.5, at least about 6, at least about 6.5, at least about 7 weight percent, and/or not greater than about 12, not greater than about 11.5, not greater than about 11, not greater than about 10.5, not greater than about 10, not greater than about 9.5, not greater than about 9, not greater than about 8.5, not greater than about 8, not greater than about 7.5 weight percent, based on the total weight of the first and second poly (vinyl acetal) resins. In some embodiments, one of the first and second poly (vinyl acetal) resins may be present in the composition, layer or interlayer in an amount of about 0.5 to about 12, about 1.5 to about 11.5, about 2 to about 11, about 2.5 to about 10 weight percent, based on the total weight of the first and second poly (vinyl acetal) resins.

The first and second poly (vinyl acetal) resins may comprise residues of any suitable aldehyde, and in some embodiments may comprise at least one C₁To C₁₀Aldehyde, or at least one C₄To C₈A residue of an aldehyde. Suitable C₄To C₈Examples of aldehydes may include, but are not limited to, n-butyraldehyde, isobutyraldehyde, 2-methylpentanal, n-hexanal, 2-ethylhexanal, n-octanal, and combinations thereof. At least one of the first and second poly (vinyl acetal) resins may comprise at least about 20, at least about 30, at least about 40, at least about 50, at least about 60, or at least about 70 weight percent of at least one C, based on the total weight of aldehyde residues of the resin₄To C₈A residue of an aldehyde, and/or may comprise no greater than about 90, no greater than about 85, no greater than about 80, no greater than about 75, no greater than about 70, or no greater than about 65 weight percent of at least one C₄To C₈An aldehyde or about 20 to about 90, about 30 to about 80, or about 40 to about 70 weight percent of at least one C₄To C₈An aldehyde. The C is₄To C₈The aldehyde may be selected from the above group, or it may be selected from n-butyraldehyde, isobutyraldehyde, 2-ethylhexanal, and combinations thereof.

In various embodiments, the first and/or second poly (vinyl acetal) resin can be a polyvinyl n-butyraldehyde (PVB) resin. In other embodiments, the first and/or secondThe second poly (vinyl acetal) resin can be a poly (vinyl butyral) resin that comprises predominantly residues of n-butyraldehyde and can, for example, comprise no more than about 50, no more than about 40, no more than about 30, no more than about 20, no more than about 10, no more than about 5, or no more than about 2 weight percent, based on the total weight of all aldehyde residues of the resin, of residues of aldehydes other than n-butyraldehyde. When the first and/or second poly (vinyl acetal) resin is a PVB resin, the molecular weight of the resin can be at least about 50,000, at least about 70,000, at least about 100,000 daltons, and/or not more than about 600,000, not more than about 550,000, not more than about 500,000, not more than about 450,000, or not more than 425,000 daltons, as measured by size exclusion chromatography (SEC/LALLS) using low angle laser light scattering by Cotts and Ouano. The term "molecular weight" as used herein refers to the weight average molecular weight (M)_w). The molecular weight of the first and/or second poly (vinyl acetal) resin can be from about 50,000 to about 600,000, from about 70,000 to about 450,000, or from about 100,000 to about 425,000 daltons.

Although generally described herein with respect to first and second poly (vinyl acetal) resins, it should be understood that in some embodiments, an equivalent single poly (vinyl acetal) resin comprising first and second acetal moieties may be substituted for the first and second poly (vinyl acetal) resins with similar results. The term "poly (vinyl acetal) resin component" as used herein may refer to the separate poly (vinyl acetal) resins present in the resin blend or to the acetal moieties present on a single poly (vinyl acetal) resin. In various embodiments, the weight ratio of the amount of the first poly (vinyl acetal) resin component to the second poly (vinyl acetal) resin component in a layer, interlayer, or blend may be about 0.5:99.5 to about 99.5:0.5, about 1:99 to 99:1, about 10:90 to about 90:10, about 25:75 to about 75:25, or about 40:60 to about 60: 40.

In some embodiments, at least one resin composition, layer, or interlayer may comprise at least a first poly (vinyl acetal) resin component and a second poly (vinyl acetal) resin component. In some embodiments, the first and second resin components may comprise first and second poly (vinyl acetal) resins, which may be physically mixed to form a resin blend, which may be combined with one or more plasticizers or other additives to provide a blended polymer layer or interlayer. In other embodiments, the first and second poly (vinyl acetal) resin components may be present as first and second acetal moieties, respectively, in a single poly (vinyl acetal) resin. With respect to resin blends, such a single "hybrid" poly (vinyl acetal) resin may optionally be blended with plasticizers and used in polymer layers and interlayers.

In some embodiments, when the resin component comprises a poly (vinyl acetal) resin, the first and second poly (vinyl acetal) resins can be blended to disperse one of the first and second resins within the other of the first and second resins, which can form domains (domains) of one of the first and second poly (vinyl acetal) resins within the other of the first and second poly (vinyl acetal) resins. Such a blended resin may be used as a single layer interlayer or it may be combined with one or more adjacent layers to form a multiple layer interlayer. In other embodiments, the first and second poly (vinyl acetal) resins may be present in adjacent layers of a multilayer interlayer such that one layer of the interlayer comprises the first poly (vinyl acetal) resin and another layer of the interlayer comprises the second poly (vinyl acetal) resin. Additional layers may also be present adjacent to at least one of these layers.

The resin compositions, layers and interlayers according to various embodiments of the present invention may further comprise at least one plasticizer. Depending on the specific composition of the resin or resins in the composition, layer or interlayer, the plasticizer may be present in an amount of at least about 5, at least about 10, at least about 15, at least about 20, at least about 25, at least about 30, at least about 35, at least about 40, at least about 45, at least about 50, at least about 55, at least about 60 parts per hundred resin (phr) and/or not more than about 120, not more than about 110, not more than about 105, not greater than about 100, not greater than about 95, not greater than about 90, not greater than about 85, not greater than about 75, not greater than about 70, not greater than about 65, not greater than about 60, not greater than about 55, not greater than about 50, not greater than about 45, or not greater than about 40 phr, or from about 5 to about 120, from about 10 to about 110, from about 20 to about 90, or from about 25 to about 75 phr. Specific embodiments are discussed in detail immediately.

As used herein, the term "parts per hundred resin" or "phr" refers to the amount of plasticizer present as compared to one hundred parts of resin on a weight basis. For example, if 30 grams of plasticizer is added to 100 grams of resin, the plasticizer is present in an amount of 30 phr. If the resin composition, layer or interlayer comprises two or more resins, the weight of plasticizer is compared to the total amount of all resins present to determine parts per hundred resin. Further, when the plasticizer content of a layer or interlayer is provided herein, it is provided with reference to the amount of plasticizer in the mixture or melt used to make the layer or interlayer.

Examples of suitable plasticizers may include, but are not limited to, triethylene glycol di- (2-ethylhexanoate) ("3 GEH"), triethylene glycol di- (2-ethylbutyrate), triethylene glycol diheptanoate, tetraethylene glycol di- (2-ethylhexanoate) ("4 GEH"), dihexyl adipate, dioctyl adipate, hexylcyclohexyl adipate, diisononyl adipate, heptylnonyl adipate, di (butoxyethyl) adipate, and bis (2- (2-butoxyethoxy) ethyl) adipate, dibutyl sebacate, dioctyl sebacate, and mixtures thereof. The plasticizer may be selected from triethylene glycol di- (2-ethylhexanoate) and tetraethylene glycol di- (2-ethylhexanoate), or the plasticizer may comprise triethylene glycol di- (2-ethylhexanoate).

According to some embodiments, the first and second poly (vinyl acetal) resins in the compositions, layers, and interlayers described herein may have different compositions. For example, in some embodiments, the first poly (vinyl acetal) resin may have a residual hydroxyl content and/or a residual acetate group content that is at least about 2, at least about 3, at least about 4, at least about 5, at least about 6, or at least about 8 weight percent higher or lower than the residual hydroxyl content and/or the residual acetate group content of the second poly (vinyl acetal) resin. The terms "residual hydroxyl content" and "residual acetate group content" as used herein refer to the amount of hydroxyl and acetate groups, respectively, that are left on the resin after processing is complete. For example, polyvinyl n-butyraldehyde can be produced by hydrolyzing polyvinyl acetate to polyvinyl alcohol, and then acetalizing the polyvinyl alcohol with n-butyraldehyde to form polyvinyl n-butyraldehyde. During hydrolysis of polyvinyl acetate, not all acetate groups are converted to hydroxyl groups and residual acetate groups remain on the resin. Similarly, not all hydroxyl groups are converted to acetal groups during acetalization of polyvinyl alcohol, which also leaves residual hydroxyl groups on the resin. Thus, most poly (vinyl acetal) resins contain residual hydroxyl groups (as vinyl hydroxyl groups) and residual acetate groups (as vinyl acetate groups) as part of the polymer chain. Unless otherwise indicated, residual hydroxyl content and residual acetate group content are expressed in weight percent based on the weight of the polymer resin and measured according to ASTM D1396.

The difference between the residual hydroxyl content of the first and second poly (vinyl acetal) resins can also be at least about 2, at least about 5, at least about 10, at least about 12, at least about 15, at least about 20, or at least about 30 weight percent. The term "different in weight percent" or "at least … weight percent difference" as used herein refers to the difference between two given weight percent calculated by subtracting one value from the other. For example, a poly (vinyl acetal) resin having a residual hydroxyl content of 12 wt.% has a residual hydroxyl content that is 2 wt.% lower than a poly (vinyl acetal) resin having a residual hydroxyl content of 14 wt.% (14 wt.% to 12 wt.% = 2 wt.%). The term "different" as used herein may refer to a numerical value that is higher or lower than another numerical value.

At least one of the first and second poly (vinyl acetal) resins can have a residual hydroxyl content of at least about 14, at least about 14.5, at least about 15, at least about 15.5, at least about 16, at least about 16.5, at least about 17, at least about 17.5, at least about 18, at least about 18.5, at least about 19, at least about 19.5, and/or not more than about 45, not more than about 40, not more than about 35, not more than about 33, not more than about 30, not more than about 27, not more than about 25, not more than about 22, not more than about 21.5, not more than about 21, not more than about 20.5, or not more than about 20 wt.%, or in the range of about 14 to about 45, about 16 to about 30, about 18 to about 25, about 18.5 to about 24, or about 19.5 to about 21 wt.%.

The further poly (vinyl acetal) resin may have a residual hydroxyl content of at least about 8, at least about 9, at least about 10, at least about 11 weight percent, and/or not more than about 16, not more than about 15, not more than about 14.5, not more than about 13, not more than about 11.5, not more than about 11, not more than about 10.5, not more than about 10, not more than about 9.5, or not more than about 9 weight percent or in the range of about 8 to about 16, about 9 to about 15, or about 9.5 to about 14.5 weight percent and may be selected such that the difference between the residual hydroxyl content of the first and second poly (vinyl acetal) resins is at least about 2 weight percent as noted above. One or more other poly (vinyl acetal) resins may also be present in the resin composition, layer or interlayer and may have residual hydroxyl groups within the ranges provided above. Additionally, the residual hydroxyl content of the one or more other poly (vinyl acetal) resins may be the same as or different from the residual hydroxyl content of the first and/or second poly (vinyl acetal) resins.

In some embodiments, at least one of the first and second poly (vinyl acetal) resins may have a residual acetate group content that is different from the other. For example, in some embodiments, the difference between the residual acetate group content of the first and second poly (vinyl acetal) resins can be at least about 2, at least about 3, at least about 4, at least about 5, at least about 8, at least about 10 weight percent. One of the poly (vinyl acetal) resins can have a residual acetate group content of no greater than about 4, no greater than about 3, no greater than about 2, or no greater than about 1 weight percent, measured as described above. In some embodiments, at least one of the first and second poly (vinyl acetal) resins can have a residual acetate group content of at least about 5, at least about 8, at least about 10, at least about 12, at least about 14, at least about 16, at least about 18, at least about 20, or at least about 30 weight percent. The difference in residual acetate group content between the first and second poly (vinyl acetal) resins can be within the ranges provided above, or the difference can be less than about 3, not greater than about 2, not greater than about 1, or not greater than about 0.5 weight percent. The additional poly (vinyl acetal) resin present in the resin composition or interlayer may have a residual acetate group content that is the same as or different from the residual acetate group content of the first and/or second poly (vinyl acetal) resin.

In some embodiments, the difference between the residual hydroxyl content of the first and second poly (vinyl acetal) resins may be less than about 2, not greater than about 1, not greater than about 0.5 weight percent, and the difference in residual acetate group content between the first and second poly (vinyl acetal) resins may be at least about 3, at least about 5, at least about 8, at least about 15, at least about 20, or at least about 30 weight percent. In other embodiments, the difference in residual acetate group content of the first and second poly (vinyl acetal) resins may be less than about 3, not greater than about 2, not greater than about 1, or not greater than about 0.5 weight percent and the difference in residual hydroxyl group content of the first and second poly (vinyl acetal) resins may be at least about 2, at least about 5, at least about 10, at least about 12, at least about 15, at least about 20, or at least about 30 weight percent.

In various embodiments, the difference in residual hydroxyl and/or residual acetate content of the first and second poly (vinyl acetal) resins may be selected to control or provide certain performance properties to the final composition, layer, or interlayer, such as strength, impact resistance, penetration resistance, processability, or acoustical properties. For example, a poly (vinyl acetal) resin having a relatively high residual hydroxyl content, typically greater than about 16 wt%, may promote high impact resistance, penetration resistance, and strength of the resin composition or layer, while a lower hydroxyl content resin, typically having a residual hydroxyl content of less than 16 wt%, may improve the acoustic properties of the interlayer or blend.

Poly (vinyl acetal) resins having higher or lower residual hydroxyl content and/or residual acetate group content may also ultimately contain different amounts of plasticizer when combined with at least one plasticizer. Thus, layers or domains formed from first and second poly (vinyl acetal) resins having different compositions may also have different properties within a single polymer layer or interlayer. While not wishing to be bound by theory, it is speculated that the compatibility of a given plasticizer with a poly (vinyl acetal) resin may depend at least in part on the composition of the polymer, particularly its residual hydroxyl content. In general, poly (vinyl acetal) resins with higher residual hydroxyl content tend to exhibit lower compatibility (or capacity) for a given plasticizer than similar resins with lower residual hydroxyl content. Thus, poly (vinyl acetal) resins with higher residual hydroxyl content tend to plasticize to a lower degree and exhibit higher stiffness than similar resins with lower residual hydroxyl content. In contrast, poly (vinyl acetal) resins with lower residual hydroxyl content may tend to incorporate higher amounts of plasticizer when plasticized with a given plasticizer, which may result in softer polymer layers exhibiting lower glass transition temperatures than polymer layers comprising similar resins with higher residual hydroxyl content. These trends can be reversed depending on the particular resin and plasticizer.

When two poly (vinyl acetal) resins having different levels of residual hydroxyl content are blended with a plasticizer, the plasticizer can be partitioned between the polymer layers or domains such that more plasticizer can be present in the layer or domain having the lower residual hydroxyl content and less plasticizer can be present in the layer or domain having the higher residual hydroxyl content. Eventually an equilibrium state is achieved between the two resins. The correlation between the residual hydroxyl content of the poly (vinyl acetal) resin and the plasticizer compatibility/capacity can facilitate the addition of an appropriate amount of plasticizer to the polymer resin. Such correlation also helps to stably maintain the plasticizer content difference between two or more resins as the plasticizer would otherwise migrate between the resins.

In some embodiments, the polymer layer or interlayer can include at least a first polymer layer comprising a first poly (vinyl acetal) resin and a first plasticizer and a second polymer layer adjacent to the first polymer layer comprising a second poly (vinyl acetal) resin and a second plasticizer. The first and second plasticizers may be the same type of plasticizer, or the first and second plasticizers may be different. In some embodiments, at least one of the first and second plasticizers may also be a blend of two or more plasticizers, which may be the same or different from one or more other plasticizers. When one of the first and second poly (vinyl acetal) resins has a residual hydroxyl content that is at least 2 wt% higher or lower than the residual hydroxyl content of the other resin, the difference in plasticizer content between the polymer layers may be at least about 2, at least about 5, at least about 8, at least about 10, at least about 12, or at least about 15 phr. In most embodiments, a polymer layer comprising a resin having a lower hydroxyl content can have a higher plasticizer content. To control or maintain other properties of the polymer layer or interlayer, the difference in plasticizer content between the first and second polymer layers may be no greater than about 40, no greater than about 30, no greater than about 25, no greater than about 20, or no greater than about 17 phr. In other embodiments, the difference in plasticizer content between the first and second polymeric layers may be at least about 40, at least about 50, at least about 60, or at least about 70 phr.

Thus, in some embodiments where the first and second poly (vinyl acetal) resins are present in adjacent layers of a multilayer interlayer, the first and second polymer layers may exhibit different glass transition temperatures. Similarly, when first and second poly (vinyl acetal) resins are present in the blend, the domains of one of the first and second poly (vinyl acetal) resins may exhibit a different glass transition temperature than the other of the first and second poly (vinyl acetal) resins. Glass transition temperature or T_gIs the temperature that marks the transition from the glassy state to the rubbery state of the polymer. The glass transition temperatures of the resins and layers described herein were determined by Dynamic Mechanical Thermal Analysis (DMTA). DMTA measures the storage (elastic) modulus (G') in pascals, the loss (viscous) modulus (G ") in pascals, and the likeThe temperature-dependent sample tan δ (G "/G') at a constant oscillation frequency and temperature sweep rate. The glass transition temperature was then determined by the position of the tan delta peak on the temperature scale. The glass transition temperatures provided herein are determined in shear mode at an oscillation frequency of 1 Hz and a temperature sweep rate of 3 deg.C/min.

The difference in glass transition temperatures between the first polymer layer and the second polymer layer, or various regions of the blended resin or polymer layer, can be at least about 3, at least about 5, at least about 8, at least about 10, at least about 12, at least about 15, at least about 18, at least about 20, at least about 22, or at least about 25 ℃. One of the first and second polymer layers can have a glass transition temperature of at least about 26, at least about 28, at least about 30, at least about 33, at least about 35 ℃, and/or not more than about 70, not more than about 65, not more than about 60, not more than about 55, not more than about 50 ℃, or in the range of about 26 to about 70, about 30 to about 60, about 35 to about 50 ℃. The other of the first and second poly (vinyl acetal) resins can have a glass transition temperature of no greater than 25, no greater than about 20, no greater than about 15, no greater than about 10, no greater than about 5, no greater than about 0, no greater than about-5, or no greater than about-10 ℃.

When the first and second poly (vinyl acetal) resins are blended with each other such that the domains of one resin are dispersed within the other, such differences in plasticizer content and/or glass transition temperature may also exist between the domains of the first and second resins. For example, in some embodiments, the polymer layer or interlayer can include various domains with higher or lower plasticizer content and/or domains with higher or lower glass transition temperatures, as described above. In some embodiments, at least a portion of the polymeric layer or interlayer can have a glass transition temperature of at least about 26, at least about 28, at least about 30, at least about 33, at least about 35 ℃, and/or not more than about 70, not more than about 65, not more than about 60, not more than about 55, not more than about 50 ℃, or in the range of about 26 to about 70, about 28 to about 60, about 35 to about 50 ℃, and/or at least a portion of the polymeric layer or interlayer can have a glass transition temperature of not more than 25, not more than about 20, not more than about 15, not more than about 10, not more than about 5, not more than about 0 ℃, not more than about-5 ℃, or not more than about-10 ℃.

One or more of the resin blends, layers, and interlayers described herein can include various other additives to impart specific properties or characteristics to the interlayer. Such additives may include, but are not limited to, dyes, pigments, stabilizers such as ultraviolet stabilizers, antioxidants, antiblocking agents, flame retardants, IR absorbers or blockers such as indium tin oxide, antimony tin oxide, lanthanum hexaboride (LaB)₆) And cesium tungsten oxide, processing aids, flow enhancement additives, lubricants, impact modifiers, nucleating agents, heat stabilizers, UV absorbers, dispersants, surfactants, chelating agents, coupling agents, adhesives, primers, enhancement additives, and fillers.

In addition, various adhesion control agents ("ACA") may be used in the interlayers of the present disclosure to control the adhesion of the sheet to the glass. In various embodiments, the ACA may be present in the resin composition, layer or interlayer in an amount of at least about 0.003, at least about 0.01, at least about 0.025, and/or not greater than about 0.15, not greater than about 0.10, or not greater than about 0.04 phr, or in a range of about 0.003 to about 0.15, about 0.01 to about 0.10, or about 0.025 to about 0.04 phr. Suitable ACAs may include, but are not limited to, sodium acetate, potassium acetate, magnesium bis (2-ethylbutyrate), magnesium bis (2-ethylhexanoate), and combinations thereof, as well as the ACAs disclosed in U.S. patent No. 5,728,472.

Resins having different compositions and plasticized polymer layers having different properties also tend to exhibit different refractive indices, which can reduce the optical quality of the resulting layer or blend. While not wishing to be bound by theory, it is believed that this difference in refractive index may cause light transmitted through different polymer layers or domains to be refracted in different directions, which may cause haze in the final product. Sometimes, the absolute value of the difference between the refractive index of the first poly (vinyl acetal) resin or layer and the refractive index of the second poly (vinyl acetal) resin or layer, as measured at a wavelength of 589 nanometers and 25 ℃, according to ASTM D542, may exceed 0.010. Thus, these compositions, layers or interlayers can have a haze value of greater than 5% and/or a mottle value of greater than 3.

However, in various embodiments of the present invention, compositions, layers and interlayers comprising poly (vinyl acetal) resins can further comprise at least one Refractive Index (RI) balancing agent for adjusting the refractive index of the composition, layer or interlayer. In some embodiments, the composition, layer, or interlayer can comprise at least a first poly (vinyl acetal) resin and a second poly (vinyl acetal) resin and at least one RI balancing agent. In other embodiments, the composition, layer, or interlayer may comprise a single poly (vinyl acetal) resin and at least one RI balancing agent. As discussed above, the RI balancing agent can be any suitable agent present in a resin or resin blend, layer or interlayer, or portion thereof, that increases or decreases the refractive index of at least one resin or layer, which can improve the optical properties of the interlayer as compared to the same interlayer formed without the RI balancing agent. In some embodiments, the resin blend, layer, or interlayer may have a haze value of at least 5% when formed in the absence of a RI balancing agent.

The RI balancer can be in any suitable form and can be physically blended with one or more resins or it can be chemically bonded or reacted with at least one resin to incorporate the RI balancer into a polymer chain. Examples of RI balancing agents can include, but are not limited to, liquid RI additives, solid RI additives, and residues of at least one aldehyde present in one or more poly (vinyl acetal) resins. Various embodiments of RI balancing agents are discussed in detail below, as well as resin compositions, layers, and interlayers comprising the same.

The RI balancing agent may be present in the poly (vinyl acetal) resin, polymer layer, or interlayer in an amount sufficient to alter the refractive index of the resin, polymer layer, or interlayer. The RI balancing agent may also be present in the composition, layer or interlayer in an amount sufficient to modify the refractive index of at least one of the two poly (vinyl acetal) resins, thereby minimizing the difference between the refractive indices of two poly (vinyl acetal) polymer layers having different refractive indices. The RI balancing agent may also minimize the difference between the refractive indices of the one or more poly (vinyl acetal) resins and the one or more plasticizers within the resin composition, layer or interlayer. In some embodiments, the RI balancing agent can be present in an amount sufficient to reduce the absolute value of the difference between the refractive index of the first poly (vinyl acetal) polymer layer and the refractive index of the second poly (vinyl acetal) polymer layer to no greater than 0.010, no greater than about 0.009, no greater than about 0.008, no greater than about 0.007, no greater than about 0.006, no greater than about 0.005, no greater than about 0.004, or no greater than about 0.003. When the multilayer interlayer comprises two or more polymer layers, the RI balancing agent may be present in one or both layers, and in some embodiments may be present in one layer in a higher amount than in one or more other layers.

In some embodiments, the RI balancing agent can comprise one or more residues of an aldehyde having a refractive index of at least 1.421 as measured by ASTM D542 at a wavelength of 589 nanometers and a temperature of 25 ℃. The RI-balancing aldehydes, which may also be referred to herein as "high refractive index aldehydes" or "high RI aldehydes," may have a refractive index of at least about 1.425, at least about 1.450, at least about 1.475, at least about 1.500, at least about 1.510, or at least about 1.515 and/or not greater than about 1.675, not greater than about 1.650, or not greater than about 1.625, or in the range of about 1.425 to about 1.675, about 1.475 to about 1.650, or about 1.515 to about 1.625. The high RI aldehyde may be an aromatic aldehyde comprising at least one aromatic ring or aromatic group. Examples of aromatic aldehydes may include, but are not limited to, C₇To C₃₀Aromatic aldehyde, C₈To C₂₅Aromatic aldehydes or C₉To C₂₀An aromatic aldehyde. Specific examples of high RI aldehydes that may be used as RI balancing agents in various embodiments of the present invention are listed in table 1 below.

TABLE 1 exemplary high RI aldehydes

When the RI balancing agent comprises residues of at least one high RI aldehyde, at least one of the first and second poly (vinyl acetal) resins can comprise at least about 0.5, at least about 1, at least about 5, at least about 10, at least about 15, at least about 20, at least about 25, at least about 30, at least about 35, at least about 40, at least about 45, at least about 50, at least about 55, at least about 60, at least about 65, at least about 70, at least about 75, at least about 80, at least about 85, at least about 90, at least about 95%, and/or not more than about 99.5, not more than about 99, not more than about 97, not more than about 95, not more than about 90, not more than about 85, not more than about 80, not more than about 75, not more than about 70, at least about 90, and/or not more than about 99.5, not more than about 99, not more than about 97, not, Residues of at least one high RI aldehyde in an amount of no greater than about 65 or no greater than about 60 wt.%. At least one of the first and second poly (vinyl acetal) resins may comprise residues of at least one high RI aldehyde in an amount of about 0.5 to about 99.5, about 10 to about 90, about 25 to about 75, or about 40 to about 60 weight percent, based on the total weight of aldehyde residues of the first or second poly (vinyl acetal) resin.

The amount of high RI aldehyde residues can be determined using a combination of fourier transform infrared spectroscopy (FT-IR) and size exclusion chromatography with UV detection (SEC). In particular, the residual hydroxyl content of the resin was measured using FT-IR and the amount of high RI aldehyde residues was determined using SEC, the amount of any other aldehyde residues being determined by difference. FT-IR analysis was performed using a Perkin Elmer Spectrum 100 FT-IR Spectrometer (available from Perkin Elmer, Waltham, Massachusetts) with ATR sampling accessory. Analysis was performed using 8 scans at 4 cm-1 resolution. Before testing, calibrations were generated from several samples of poly (vinyl n-butyraldehyde) with different residual hydroxyl group contents that had been dried overnight with silica at room temperature in a desiccator to remove excess moisture. The peak maximum wavenumber of the hydroxyl stretching vibration band was correlated with the molar vinyl alcohol content of each sample previously determined by ASTM D1396, and the molar residual hydroxyl content of the analyzed sample was predicted using the resulting linear curve fit. These values can be converted to weight percent by calculation after the composition of the poly (vinyl acetal) resin is determined using SEC analysis as described below.

SEC analysis was performed using a Waters 2695 Alliance pump and autosampler with a Waters 410 online differential refractive index detector and a Waters 2998 PDA online UV detector (available from Waters Corporation, Milford, Mass.) and Dionex Chromeleon v.6.8 data acquisition software with extender kit (available from Thermo Fischer Scientific, Sunnyvale, Calif.). Analysis was performed with a PL Gel Mixed C (5 micron) column and a Mixed E (3 micron) column at a flow rate of 1.0 mL/min in a 50 microliter sample volume. Samples were prepared by dissolving 0.03 to 0.09 grams of the resin in 10-15 milliliters of stabilized tetrahydrofuran, then filtering each through a 0.22 micron PTFE filter. Initial calibration of the chromatograph was performed using narrow molecular weight polystyrene standards and poly (vinyl acetal) resin containing only the residues of the high RI aldehyde, and subsequent samples were calibrated with broad molecular weight polystyrene (available as PSBR250K from American Polymer Standard Corporation, Mentor, Ohio).

In some embodiments, only one of the first and second poly (vinyl acetal) resins comprises residues of a high RI aldehyde, while in other embodiments both resins may comprise such residues. The refractive index of the resin comprising residues of the high RI aldehyde may be at least about 1.492, at least about 1.495, at least about 1.500, at least about 1.505, at least about 1.510, or at least about 1.515.

In various embodiments, at least one of the first and second poly (vinyl acetal) resins can further comprise residues of at least one aldehyde having a refractive index of less than 1.421. Examples of such aldehydes may include, for example, aliphatic aldehydes, such as C discussed above₄To C₈An aldehyde. The aldehydes having a refractive index of less than 1.421 may be selected from the group consisting of n-butyraldehyde, isobutyraldehyde, and 2-ethylhexanal.

When present, the first and/or second poly (vinyl acetal) resin can comprise at least about 10, at least about 15, at least about 20, at least about 25, at least about 30, at least about 35, at least about 40, at least about 45, at least about 50, at least about 55, at least about 60, at least about 65, at least about 70, at least about 75, at least about 80, at least about 85, at least about 90, at least about 95%, and/or not more than about 99, not more than about 97, not more than about 95, not more than about 90, not more than about 85, not more than about 80, not more than about 75, not more than about 70, not more than about 65, or not more than about 60 weight percent of the aldehydes, based on the total weight of the aldehyde residues of the first or second poly (vinyl acetal) resin.

The amount of residues of aldehydes having a refractive index of less than 1.421 is then determined by calculation according to the following formula using the FT-IR/SEC method described above: 100 wt% -wt% residual hydroxyl groups (from FT-IR) -wt% high RI aldehyde residues (from SEC) -wt% residual acetate groups (from FT-IR) = wt% of residues of aldehydes having a refractive index of less than 1.421. The first and/or second poly (vinyl acetal) resin can comprise residues of an aldehyde having a refractive index of less than 1.421 in an amount of from about 10 to about 99, from about 25 to about 75, or from about 40 to about 60 weight percent, based on the total weight of aldehyde residues of the first or second poly (vinyl acetal) resin. The refractive index of one of these resins, measured as described above, may be less than about 1.492, less than about 1.491, or less than about 1.490.

According to some embodiments, one of the first and second poly (vinyl acetal) resins comprises predominantly residues of a high RI aldehyde, while the other of the first and second poly (vinyl acetal) resins comprises predominantly residues of at least one aldehyde having a refractive index of less than 1.421. The term "predominantly" as used herein means at least 75 percent by weight, such that a poly (vinyl acetal) resin comprising predominantly residues of the specified aldehyde comprises at least 75 percent by weight residues of the specified aldehyde, based on the total weight of aldehyde residues in the resin. The poly (vinyl acetal) resin comprising predominantly residues of high RI aldehydes may comprise no greater than about 25, no greater than about 20, no greater than about 15, no greater than about 10, no greater than about 5, no greater than about 2, or no greater than about 1 weight percent, based on the total weight of aldehyde residues of the resin, of residues of other aldehydes having a refractive index of less than 1.421.

Similarly, another poly (vinyl acetal) resin that can predominantly comprise residues of aldehydes having a refractive index of less than 1.421 can comprise no greater than about 25, no greater than about 20, no greater than about 15, no greater than about 10, no greater than about 5, no greater than about 2, or no greater than about 1 weight percent of residues of high RI aldehydes, based on the total weight of aldehyde residues of the resin, and can comprise at least about 75, at least about 80, at least about 85, at least about 90, at least about 95, at least about 97, or at least about 99% of residues of one or more aldehydes having a refractive index of less than 1.421. In some embodiments, the ratio of resin comprising primarily residues of high RI aldehydes to another resin or other resins in the composition can be at least about 1:99, at least about 5:95, at least about 10:90, at least about 20:80, at least about 25:75, at least about 30:70, at least about 40:60, and/or not greater than about 99:1, not greater than about 95:5, not greater than about 90:10, not greater than about 85:15, not greater than about 75:25, not greater than about 70:30, or not greater than about 60:40, or in the range of about 1:99 to 99:1, about 10:90 to about 90:10, about 25:75 to 75:25, or about 40:60 to 60: 40.

In other embodiments, at least one of the first and second poly (vinyl acetal) resins comprises residues of a high RI aldehyde and at least one aldehyde having a refractive index of less than 1.421, thereby forming a "hybrid" resin comprising residues of high and low RI aldehydes. According to these embodiments, the amount of high RI aldehyde residues and residues of aldehydes having a refractive index of less than 1.421 in the hybrid resin and the weight ratio of one to the other may be within the same ranges provided above for the resin blend. When the first or second poly (vinyl acetal) resin comprises residues of both high RI and lower RI aldehydes, the other of the two poly (vinyl acetal) resins may also comprise residues of at least one high RI aldehyde. Alternatively, the other of the two resins may contain little or no high RI aldehyde residues such that it contains less than about 10, less than about 5, less than about 2, or less than about 1 weight percent of residues of high RI aldehydes, the balance being aldehydes having a refractive index of less than 1.421, including for example residues of aldehydes selected from the group consisting of n-butyraldehyde, isobutyraldehyde, 2-ethylhexanal, and combinations thereof.

When the interlayer is a multilayer interlayer, it may comprise at least one polymer layer having at least a first poly (vinyl acetal) resin and another polymer layer comprising at least a second poly (vinyl acetal) resin, wherein the difference between the residual hydroxyl content of the first poly (vinyl acetal) resin and the second poly (vinyl acetal) resin is at least 2 weight percent. One or both of these poly (vinyl acetal) resins can comprise residues of high RI aldehydes, and one of the polymer layers can have a refractive index that is higher or lower than the other by an amount that is at least about 0.002, at least about 0.003, at least about 0.004, and/or not more than about 0.010, not more than about 0.009, not more than about 0.008 or not more than about 0.007, or in the range of about 0.002 to about 0.010, about 0.003 to about 0.009, or about 0.004 to about 0.007. In some embodiments, when the interlayer comprises at least three polymer layers, the innermost polymer layer may have a higher refractive index, while in other embodiments, the refractive index of one or both of the outer polymer layers may be higher. In some embodiments, only one of the first and second poly (vinyl acetal) resins may comprise residues of a high RI aldehyde. In other embodiments, both poly (vinyl acetal) resins may comprise the residue of at least one high RI aldehyde, but these resins may still exhibit refractive index differences within the ranges provided above.

One or both of the poly (vinyl acetal) resins may comprise residues of at least one high RI aldehyde. In some embodiments, when a poly (vinyl acetal) resin comprising such residues has a residual hydroxyl content of no greater than, for example, 15 wt.%, a polymer layer comprising such resin can have a glass transition temperature of less than 20, no greater than about 15, no greater than about 10, no greater than about 5, no greater than about 0, no greater than about-5, or no greater than about-10 ℃, and a refractive index of at least about 1.465, at least about 1.470, at least about 1.475, at least about 1.480, at least about 1.485, at least about 1.490, at least about 1.495, at least about 1.500, at least about 1.510, at least about 1.520, at least about 1.525, at least about 1.540, at least about 1.550, at least about 1.575, at least about 1.590, at least about 1.600, at least about 1.615, at least about 1.625, or at least about 1.650, each measured as described above. According to various embodiments, the plasticizer content of the layer may be at least about 50, at least about 55, at least about 60, at least about 65 phr and/or not more than about 120, not more than about 110, not more than about 90, not more than about 85, not more than about 80, or not more than about 75 phr, or in the range of about 50 to about 120, about 55 to about 110, about 60 to about 90, or about 65 to about 75 phr.

When the resin having residues of high RI aldehydes in the multi-layer interlayers discussed above has a residual hydroxyl content of greater than, for example, 16 wt%, the polymer layer comprising the resin may have a glass transition temperature of at least about 26, at least about 30, at least about 33, or at least about 35 ℃, and a refractive index of at least about 1.470, at least about 1.475, at least about 1.480, at least about 1.485, at least about 1.490, at least about 1.495, at least about 1.500, at least about 1.510, at least about 1.520, at least about 1.525, at least about 1.540, at least about 1.550, at least about 1.575, at least about 1.590, at least about 1.600, at least about 1.615, at least about 1.625, or at least about 1.650, each measured as described above. According to some embodiments, the plasticizer content of the layer may be less than 50 phr, not greater than about 45 phr, not greater than about 40 phr, not greater than about 30, not greater than about 20 phr.

The refractive index of the overall interlayer measured as described above can be at least about 1.477, at least about 1.478, at least about 1.480, at least about 1.485, at least about 1.490, at least about 1.495, at least about 1.500, at least about 1.505, at least about 1.510, at least about 1.515, at least about 1.520, at least about 1.540, at least about 1.550, at least about 1.575, at least about 1.580, at least about 1.590, at least about 1.600, at least about 1.610, at least about 1.620, at least about 1.630, at least about 1.640, or at least about 1.650.

According to various embodiments of the present invention, the RI balancing agent may comprise a liquid RI balancing agent. The term "liquid RI balance" as used herein refers to a RI balance that is liquid at standard conditions of 25 ℃ and 1 atm. In some embodiments, the liquid RI balancing agent can be, for example, a high RI plasticizer. The term "high RI plasticizer" as used herein refers to a plasticizer having a refractive index of at least 1.460, measured as described above. High RI plasticizers suitable for use as RI balancing agents may have a refractive index measured as described above of at least about 1.470, at least about 1.480, at least about 1.490, at least about 1.500, at least about 1.510, at least about 1.520, and/or not greater than about 1.600, not greater than about 1.575, or not greater than about 1.550. The refractive index of the high RI plasticizer may be in the range of about 1.460 to about 1.600, about 1.470 to about 1.575, about 1.480 to about 1.550, about 1.490 to about 1.525.

Examples of types or classes of high RI plasticizers may include, but are not limited to, polyadipates (RI of about 1.460 to about 1.485); epoxides, such as epoxidized soybean oil (RI of about 1.460 to about 1.480); phthalates and terephthalates (RI of about 1.480 to about 1.540); benzoate and toluate esters (RI of about 1.480 to about 1.550); and other specialty plasticizers (RI of about 1.490 to about 1.520). Specific examples of suitable RI plasticizers may include, but are not limited to, dipropylene glycol dibenzoate, tripropylene glycol dibenzoate, polypropylene glycol dibenzoate, isodecyl benzoate, 2-ethylhexyl benzoate, diethylene glycol benzoate, butoxyethyl benzoate, butoxyethoxyethyl benzoate, butoxyethoxyethoxyethyl benzoate, propylene glycol dibenzoate, 2, 4-trimethyl-1, 3-pentanediol benzoate isobutyrate, 1, 3-butanediol dibenzoate, diethylene glycol di-o-toluate, triethylene glycol di-o-toluate, dipropylene glycol di-o-toluate, 1, 2-octyl dibenzoate, tri-2-ethylhexyl trimellitate, and mixtures thereof, Di-2-ethylhexyl terephthalate, bisphenol A bis (2-ethylhexanoate), bis- (butoxyethyl) terephthalate, bis- (butoxyethoxyethyl) terephthalate, and mixtures thereof. The high RI plasticizer may be selected from dipropylene glycol dibenzoate and tripropylene glycol dibenzoate and/or 2,2, 4-trimethyl-1, 3-pentanediol dibenzoate.

When the polymer layer or interlayer comprises a high RI plasticizer, the plasticizer may be present in the layer alone or it may be blended with one or more additional plasticizers. The one or more other plasticizers may also comprise a high RI plasticizer, or the one or more may be a lower RI plasticizer having a refractive index of less than 1.460. In some embodiments, the lower RI plasticizer may have a refractive index of less than about 1.450, less than about 1.445, or less than about 1.442 and may be selected from the above groups. When a mixture of two or more plasticizers is used as the RI balancing agent, the mixture can have a refractive index within one or more of the above ranges.

When used as an RI balancer in a multilayer interlayer, the high RI plasticizer may be present in two or more polymer layers in varying amounts. Similarly, when used as an RI balancer in a resin composition or blended polymer layer, the high RI plasticizer may be partitioned as described above so that a polymer layer or domain with a lower residual hydroxyl content may have a higher amount of high RI plasticizer. In some embodiments, at least one layer or a portion of a polymer layer or interlayer can comprise a high RI plasticizer as a RI balancer in an amount of at least about 5, at least about 10, at least about 15, at least about 20, at least about 25, at least about 30, at least about 35, and/or not greater than about 50, not greater than about 45, or not greater than about 40 phr. The high RI plasticizer may be present in the polymer layer or interlayer in an amount of about 5 to about 50, about 10 to about 45, about 20 to about 40 phr. In some embodiments, one or more other layers or portions may comprise a high RI plasticizer in an amount of at least about 50, at least about 55, at least about 60, at least about 65, at least about 70, and/or not more than about 120, not more than about 110, not more than about 100, not more than about 90, or not more than about 75 phr, or in a range of about 50 to about 120, about 55 to about 110, about 60 to about 90, about 65 to about 75 phr. These amounts may include any other plasticizers present in the composition, including those having a refractive index of less than 1.460, or may include only high RI plasticizers.

When a high RI plasticizer is used as the RI balancer in a multilayer interlayer, the interlayer can include at least one polymer layer having a first poly (vinyl acetal) resin and another polymer layer comprising a second poly (vinyl acetal) resin, wherein the difference between the residual hydroxyl content of the first poly (vinyl acetal) resin and the second poly (vinyl acetal) resin is at least 2 weight percent. At least one of the polymer layers may contain a high RI plasticizer in an amount sufficient to provide an absolute value of the difference between the refractive index of the polymer layer and the refractive index of the other polymer layer of no greater than 0.010. In some embodiments, when the interlayer comprises at least three polymer layers, the innermost polymer layer may have a higher refractive index, while in other embodiments, the refractive index of one or both of the outer polymer layers may be higher.

When a high RI plasticizer is included in a polymer layer comprising at least one poly (vinyl acetal) resin having a relatively low residual hydroxyl content, at least a portion of the polymer layer can have a glass transition temperature of no greater than 25, no greater than about 20, no greater than about 15, no greater than about 10, no greater than about 5, no greater than about 0, no greater than about-5, or no greater than about-10 ℃, and the layer may have a refractive index measured as described above of at least about 1.465, at least about 1.470, at least about 1.475, at least about 1.480, at least about 1.485, at least about 1.490, at least about 1.495, at least about 1.500, at least about 1.510, at least about 1.520, at least about 1.525, at least about 1.540, at least about 1.550, at least about 1.575, at least about 1.590, at least about 1.600, at least about 1.615, at least about 1.625, or at least about 1.650. In some embodiments, the plasticizer content of the layer may be at least about 50, at least about 55, at least about 60 phr and/or not more than about 120, not more than about 110, not more than about 90, not more than about 85, not more than about 80, or not more than about 75 phr, or in the range of about 50 to about 120, about 55 to about 110, about 60 to about 90, or about 60 to about 75 phr.

When a high RI plasticizer is present in a polymer layer comprising a poly (vinyl acetal) resin having a relatively high residual hydroxyl content, at least a portion of the layer can have a glass transition temperature of at least about 26, at least about 30, at least about 33, or at least about 35 ℃, and the layer can have a refractive index measured as described above of at least about 1.470, at least about 1.475, at least about 1.480, at least about 1.485, at least about 1.490, at least about 1.495, at least about 1.500, at least about 1.510, at least about 1.520, at least about 1.525, at least about 1.540, at least about 1.550, at least about 1.575, at least about 1.590, at least about 1.600, at least about 1.615, at least about 1.625, or at least about 1.650. According to some embodiments, the plasticizer content of the layer may be less than 50 phr, not greater than about 45 phr, not greater than about 40 phr, not greater than about 30, or not greater than about 20 phr.

According to various embodiments of the present invention, the RI balancing agent may be a solid RI additive present in one or more layers or in one or more portions of a layer or interlayer. The term "solid RI additive" as used herein refers to an additive used to adjust the refractive index of a poly (vinyl acetal) resin, polymer layer or interlayer and is solid at ambient conditions of 25 ℃ and 1 atm. In various embodiments, the solid RI additive may have a melting point of at least about 27, at least about 30, at least about 35, at least about 40, at least about 45, at least about 50, at least about 55, at least about 60, at least about 75, at least about 80, at least about 85, at least about 90, at least about 95, or at least about 100 ℃. When used in a resin blend, layer or interlayer, the solid RI additive may be present in an amount sufficient to provide an absolute value of the difference in refractive indices of the first and second polymer layers of no greater than about 0.010. When formulated into the same polymer layer in the absence of the solid RI additive, the difference between the refractive indices of the first and second polymer layers may be greater than 0.010.

In some embodiments, the solid RI additive may be a high RI solid additive for increasing the refractive index of at least one polymer layer or interlayer. The refractive index of the high RI solid additive, measured as described above, may be at least about 1.460, at least about 1.465, at least about 1.470, at least about 1.475, at least about 1.480, at least about 1.485, at least about 1.490, at least about 1.495, at least about 1.500, at least about 1.505, at least about 1.510, at least about 1.525, at least about 1.550, at least about 1.575, or at least about 1.600. In other embodiments, the solid RI additive may be an RI-reducing solid additive for reducing the refractive index of at least one resin or polymer layer. The solid RI-reducing additive can have a refractive index, measured as described above, of less than 1.460, no greater than about 1.455, no greater than about 1.450, no greater than about 1.445, or no greater than about 1.440. Whether higher or lower, the solid RI additive can have a refractive index that differs from the refractive index of the poly (vinyl acetal) resin by at least about 0.005, at least about 0.010, at least about 0.050, at least about 0.10, and/or not greater than about 0.50, not greater than about 0.35, or not greater than about 0.20. The refractive index difference between the solid RI additive and the poly (vinyl acetal) resin can be in the range of about 0.005 to about 0.50, about 0.010 to about 0.35, or about 0.050 to about 0.35.

In various embodiments, the solid RI additive may be present in the resin composition or interlayer in an amount of at least about 0.5, at least about 1, at least about 1.5, at least about 2, or at least about 5 phr, depending on the particular type of additive and layer or interlayer. The solid RI additive, whether a high RI additive or an RI-reducing additive, may comprise a physical solid RI additive that is capable of being physically mixed or blended with at least one poly (vinyl acetal) resin in a resin composition or layer, or it may be a reactive solid RI additive that is reactive with one or more poly (vinyl acetal) resins and incorporated into the backbone of the one or more poly (vinyl acetal) resins.

The solid RI additive may be used in combination with one or more low RI plasticizers. Examples of low RI plasticizers may include, but are not limited to, triethylene glycol di- (2-ethylhexanoate) ("3 GEH"), triethylene glycol di- (2-ethylbutyrate), triethylene glycol diheptanoate, tetraethylene glycol di- (2-ethylhexanoate) ("4 GEH"), dihexyl adipate, dioctyl adipate, hexylcyclohexyl adipate, diisononyl adipate, heptylnonyl adipate, di (butoxyethyl) adipate, and bis (2- (2-butoxyethoxy) ethyl) adipate, dibutyl sebacate, dioctyl sebacate, and mixtures thereof. The plasticizer may be selected from triethylene glycol di- (2-ethylhexanoate) and tetraethylene glycol di- (2-ethylhexanoate), or the plasticizer may comprise triethylene glycol di- (2-ethylhexanoate). The solid RI additive may also be used in combination with one or more of the high RI plasticizers mentioned above.

When the solid RI additive is a physical solid RI additive, it may be combined with one or more poly (vinyl acetal) resins or layers in the interlayer. In some embodiments, the physical solid RI additive may be present in at least one layer or interlayer in an amount of at least about 1, at least about 2, at least about 3, at least about 5, at least about 8, at least about 10, at least about 12, at least about 15, at least about 20, and/or not more than about 60, not more than about 55, not more than about 50, not more than about 45, not more than about 40, not more than about 35, not more than about 30, not more than about 25, not more than about 20, or not more than about 15 phr, or in an amount within a range of about 1 to about 60, about 5 to about 50, or about 10 to about 45 phr. Examples of suitable physical solid high RI additives may include, but are not limited to, polyadipates, polystyrenes having a molecular weight of less than 2500, epoxides, phthalates, benzoates, inorganic oxides such as zirconia, and combinations thereof. The physical solid RI-reducing additive may be selected from halogenated additives and silicon-containing additives.

When used in a multilayer interlayer, the physical solid RI additive may be present in one of the polymer layers in a higher amount than in one or more of the other layers. The difference between the amount of physical solid RI additive present in one of the polymer layers and the amount of physical solid RI additive present in another layer (including, for example, an adjacent layer) can be at least about 2, at least about 5, at least about 8, at least about 10 phr, and/or not greater than about 30, not greater than about 25, or not greater than about 20 phr, or it can be in the range of about 2 to about 30, about 5 to about 25, or about 10 to about 20 phr. According to some embodiments, at least one layer may comprise at least about 1, at least about 5, at least about 10, at least about 15 phr and/or not greater than about 60, not greater than about 55, not greater than about 50, not greater than about 45 phr of the physical solid RI additive, or the physical solid RI additive may be present in an amount of about 1 to about 60, about 10 to about 50, or about 15 to about 45 phr. In some embodiments, the physical solid RI additive may be present in one or more layers in an amount of at least about 5, at least about 10, at least about 15, at least about 20 phr and/or not more than about 60, not more than about 55, not more than about 50 phr or in an amount within the range of about 5 to about 60, about 15 to about 55, or about 20 to about 50 phr.

When the multilayer interlayer comprises three or more polymer layers and the solid RI additive is a solid high RI additive, one or more of the inner or core layers may comprise a higher amount of the physical solid RI additive than the outer or skin layers. However, if the solid RI additive is a RI-reducing solid additive, the outer skin layer can comprise a higher amount of the solid RI additive than the inner core layer. The core layer may comprise at least about 30, at least about 40, at least about 50, at least about 60, at least about 70, or at least about 80% of the total amount of the physical solid RI additive present in the interlayer.

When the solid RI additive is a reactive solid RI additive, it may be reacted with at least one poly (vinyl acetal) resin to incorporate at least a portion of the additive into the polymer chain. The reactive RI additive may be an aromatic additive and may in some embodiments comprise phthalic anhydride and a phenylalkoxysilane, including, for example, diphenyldimethoxysilane.

In some embodiments, the reactive RI additive may be present in one layer of a multilayer interlayer in an amount that is higher than the amount present in one or more other layers of the interlayer. In some embodiments, it may be absent or substantially absent from one or more of the polymer layers. For example, when the interlayer is a multilayer interlayer comprising at least three polymeric layers, the inner core layer may comprise at least about 0.5, at least about 1, at least about 1.5, at least about 2, at least about 2.5, at least about 3, and/or not more than about 50, not more than about 30, not more than about 20, not more than about 15, not more than about 12, not more than about 10, or not more than about 8 phr of one or more reactive solid RI additives, or in an amount of about 0.5 to about 20, about 1 to about 12, or about 2 to about 8 phr. The one or more outer skin layers can comprise not greater than about 10, not greater than about 5, not greater than about 2, not greater than about 1, or not greater than about 0.5 phr of the reactive solid RI additive. The core layer may comprise at least about 65, at least about 75, at least about 85, at least about 95, or at least about 99% of the total amount of reactive RI additive present in the interlayer.

When a solid RI additive is used as an RI balancer in a multilayer interlayer, the interlayer can include at least one polymer layer having a first poly (vinyl acetal) resin and another polymer layer comprising a second poly (vinyl acetal) resin, wherein the difference between the residual hydroxyl content of the first poly (vinyl acetal) resin and the second poly (vinyl acetal) resin is at least 2 weight percent. At least one of the polymer layers may include a high RI additive in an amount sufficient to provide an absolute value of the difference between the refractive index of the first polymer layer and the refractive index of the second polymer layer of no greater than 0.010. In some embodiments, when the interlayer comprises at least three polymer layers, the innermost polymer layer may have a higher refractive index, while in other embodiments, the refractive index of one or both of the outer polymer layers may be higher.

When the solid RI additive is included in a polymer layer comprising a poly (vinyl acetal) resin having a relatively low residual hydroxyl content, the polymer layer can have a glass transition temperature of no greater than 25, no greater than about 20, no greater than about 15, no greater than about 10, no greater than about 5, no greater than about 0, no greater than about-5, or no greater than about-10 ℃, and a refractive index of at least about 1.465, at least about 1.470, at least about 1.475, at least about 1.480, at least about 1.485, at least about 1.495, at least about 1.500, at least about 1.510, at least about 1.520, at least about 1.525, at least about 1.540, at least about 1.550, at least about 1.575, at least about 1.590, at least about 1.600, at least about 1.615, at least about 1.625, or at least about 1.650, each measured as described above. In some embodiments, the plasticizer content of the layer may be at least about 50, at least about 55, at least about 60, at least about 65 phr and/or not more than about 120, not more than about 110, not more than about 90, not more than about 85, not more than about 80, or not more than about 75 phr, or in the range of about 50 to about 120, about 55 to about 110, about 60 to about 90, about 65 to about 75 phr.

When the solid RI additive is present in a polymer layer comprising a poly (vinyl acetal) resin having a relatively high residual hydroxyl content, the layer can have a glass transition temperature of at least about 26, at least about 30, at least about 33, or at least about 35 ℃. In some embodiments, the layer can have a refractive index of at least about 1.470, at least about 1.475, at least about 1.480, at least about 1.485, at least about 1.490, at least about 1.500, at least about 1.510, at least about 1.520, at least about 1.525, at least about 1.540, at least about 1.550, at least about 1.575, at least about 1.590, at least about 1.600, at least about 1.615, at least about 1.625, or at least about 1.650. According to some embodiments, the plasticizer content of the layer may be less than 50 phr, not greater than about 45 phr, not greater than about 40 phr, not greater than about 30, or not greater than about 20 phr.

According to some embodiments, the interlayer can have a refractive index greater than 1.475, at least about 1.480, at least about 1.490, at least about 1.500, at least about 1.510, at least about 1.520, at least about 1.530, at least about 1.540, at least about 1.550, at least about 1.560, at least about 1.570, at least about 1.580, at least about 1.590, at least about 1.600, at least about 1.610, at least about 1.620, at least about 1.630, at least about 1.640, at least about 1.650, at least about 1.660, or at least about 1.670, measured as described above. The interlayer may comprise one or more RI balancing agents as described herein or one or more other RI balancing agents not specifically mentioned. As discussed herein, the interlayer may be a single layer (or a monolithic interlayer) or it may comprise two or more layers adjacent to each other.

Resin compositions, layers, and interlayers formulated according to various embodiments of the present invention to comprise at least two poly (vinyl acetal) resins and an RI balancing agent can exhibit enhanced optical properties without sacrificing other properties, such as impact resistance and acoustic performance. As discussed above, due to differences in the properties or composition of the resins, such as residual hydroxyl content, residual acetate content, or aldehyde residues, the same blend of the same resins formulated without RI balancing agents can provide compositions, layers, and interlayers with reduced optical performance.

Clarity is a parameter used to describe the optical properties of the compositions, layers and interlayers described herein and can be determined by measuring haze values or percentages. The haze value represents a quantification of the light scattered by the sample compared to the incident light. In some embodiments, the resin blends, layers, and interlayers described herein can have a haze value of less than 5%, less than about 4%, less than about 3%, less than about 2%, less than about 1%, or less than about 0.5% as measured according to ASTM D1003-13-Procedure B using Illuminant C at a 2 ° observation angle. The test is performed on a polymer sample having a thickness of 0.76 mm that has been laminated between two sheets of clear Glass each having a thickness of 2.3 mm (available from Pittsburgh Glass Works of Pennsylvania) using a spectrophotometer, such as a Hunterlab UltraScan XE instrument (available from Hunter Associates, Reston, VA).

Additionally, the polymeric layers and interlayers described herein can have a mottle value of no greater than 3, no greater than 2, or no greater than 1. Mottle is another measure of optical quality, which is measured as texture or granularity. If the level is too high or too severe, mottle is a visual defect, thereby causing an unpleasant visual appearance. Mottle is assessed and classified by side-by-side qualitative comparison of the image projection of the tested laminate with a set of standard laminate images representing a range or scale of mottle values from 1 to 4, where 1 represents a low mottle criterion (i.e., low interference count) and 4 represents a high mottle criterion (i.e., high interference count). High mottle is generally considered undesirable, particularly in automotive and architectural applications. Optionally, a model laminate with a single ply interlayer mottled 0 (no mottled) is used to facilitate evaluation of test laminates with a mottled rating lower than the standard set scale, such as lower than rating 1. The laminates tested, which exhibited image projections similar to 0 mottled laminates, were evaluated as having mottled or the likeStage 0. The laminates tested were prepared from two sheets of clear Glass (commercially available from Pittsburgh Glass Works of Pennsylvania) each having a thickness of 2.3 millimeters and an interlayer. The interlayer typically has a random rough surface R of about 35 to 40 microns_zAnd a thickness of 0.76 to 0.86 millimeters.

The Mottle values provided herein were determined using a Clear Mottle Analyzer (CMA) including a xenon arc lamp, sample holder, projection screen, and digital camera. An image of the laminated sample was projected onto a screen using a xenon arc lamp and a camera was configured to capture an image of the resulting image. The image is then digitally analyzed using computer imaging software and compared to previously captured images of standard samples to determine the mottle of the sample. The method of measuring mottle using CMA is described in detail in U.S. patent application publication US 2012-0133764.

Another parameter used to determine optical performance is the transparency or percent visible light transmission (% T)_vis) It is measured using a spectrophotometer such as HunterLab UltraScan EX according to ASTM D1003, Procedure B using Illuminant C at a 2 ° viewing angle. The values provided herein were obtained by analyzing Glass laminate samples having an interlayer thickness of about 0.76 mm and a clear Glass thickness of 2.3 mm (available from Pittsburgh Glass Works of Pennsylvania). In some embodiments, the polymeric layers and interlayers of the present invention can have a percent transmission of visible light of at least about 70, at least about 75, at least about 80, at least about 81, at least about 82, at least about 83, at least about 84, at least about 85, at least about 85.5, at least about 86, at least about 86.5, at least about 87, at least about 87.5, at least about 88, or at least about 88.5%. More specifically, the polymer layers and interlayers of the present invention have a% T of greater than 85% for interlayers containing only ACA, UV stabilizer and antioxidant additives or greater than 80% for interlayers containing additional additives such as the pigments, IR absorbers or blockers mentioned above_vis. Polymer interlayers containing high amounts of pigments and/or dyes can optionally have a lower% T_visValues, such as in a mass pigmented or colored polymer interlayer.

In addition to exhibiting one or more optical properties within the above ranges, the polymeric layers and interlayers described herein can also exhibit acoustic properties within a desired range. In some embodiments, as discussed above, at least a portion of the polymeric layer or interlayer can have a glass transition temperature of no greater than 25, no greater than about 20, no greater than about 15, no greater than about 10, no greater than about 5, no greater than about 0, no greater than about-5, or no greater than about-10 ℃, which can facilitate the acoustic performance of the layer or interlayer. Also, at least a portion of the layer or interlayer can have a glass transition temperature of at least about 26, at least about 30, at least about 35 ℃, which can contribute to impact resistance and strength.

In some embodiments, a polymer layer or interlayer according to the present invention can have a tan delta value of at least about 0.70. tan δ is the ratio of the loss modulus in pascals (G ") of the sample to the storage modulus in pascals (G') of the sample as measured by Dynamic Mechanical Thermal Analysis (DMTA). DMTA was performed in shear mode at an oscillation frequency of 1 Hz and a temperature sweep rate of 3 deg.C/min. The G '/G' curve has a peak at the glass transition temperature of tan delta. A polymeric layer or interlayer as described according to various embodiments herein can have a tan δ of at least about 1.0, at least about 1.05, at least about 1.10, at least about 1.25, at least about 1.50, at least about 1.75, at least about 2.0, or at least about 2.25.

Additionally, the polymer layers and interlayers can have a damping or loss factor of at least about 0.10, at least about 0.15, at least about 0.17, at least about 0.20, at least about 0.25, at least about 0.27, at least about 0.30, at least about 0.33, or at least about 0.35. The loss factor is measured by mechanical impedance measurements as described in ISO standard 16940. The polymer sample was laminated between two pieces of transparent glass each having a thickness of 2.3 mm, and prepared to have a width of 25 mm and a length of 300 mm. The laminated samples were then excited at the center point using a vibrator available from Bruel and Kj æ r (N æ rum, Netherlands) and the force and vibration speed required to excite the bar to vibrate was measured using an impedance head (Bruel and Kj æ r). The resulting transfer function was recorded on a National Instrument data acquisition and analysis system and the loss factor in the first vibration mode was calculated using a half power method. In some embodiments, when the RI balancer is a high RI plasticizer, the layer or interlayer can have a dissipation factor at 20 ℃ of greater than 0.25, greater than 0.27, greater than 0.30, or greater than 0.35, while in other embodiments, when the RI balancer is a residue of a solid RI additive or at least one high RI aldehyde, the layer or interlayer can have a dissipation factor at 20 ℃ of at least about 0.10, at least about 0.15, at least about 0.20, at least about 0.25, or at least about 0.30.

Similar to two different resins: blending two or more different polymer layers or interlayers with a resin blend of a first poly (vinyl acetal) resin and a second poly (vinyl acetal) resin can generally produce one or more new polymer layers or interlayers having unexpected properties and performance attributes. For example, a polymer layer or interlayer having a lower residual hydroxyl content and a lower glass transition temperature can be blended with another polymer layer or interlayer having a higher residual hydroxyl content and a higher glass transition temperature to produce a new polymer layer or interlayer having soft domains with a lower glass transition temperature that enhance its acoustic properties and hard domains with a higher glass transition temperature that impart enhanced processability, strength and impact resistance to the polymer layer or interlayer. Other examples include blending a monolithic interlayer with a multiple layer interlayer, blending two multiple layer interlayers, or blending one multiple layer interlayer into a polymer layer of another multiple layer interlayer. Basically, the effect resulting from blending two materials can also be achieved by blending two or more resins, plasticizers, and other additives according to the material content. As used herein, "blended resin material" or "blended material" refers to a resin composition, polymer layer, or interlayer that is to be blended into another resin composition, polymer layer, or interlayer. When blending two polymer layers or two interlayers, at least one of the two materials to be blended may comprise a polymer layer or interlayer of the present invention. In other embodiments, both materials may comprise a polymer layer or interlayer of the present invention.

According to some embodiments, at least a portion of the resin composition, layer or interlayer described herein may comprise a further resin, layer or interlayer. In some embodiments, at least about 0.5, at least about 1, at least about 5, at least about 10, at least about 15, at least about 20, at least about 25, at least about 30, or at least about 50% of the total amount of resin in the composition, layer, or interlayer can be derived from the blended resin material.

In general, when the type and/or amount of resin and plasticizer in the blended resin material is significantly different from the type and/or amount of resin or plasticizer in manufacture to which the blended resin material is added, the optical properties, as measured by clarity or haze, of the resulting resin composition, layer or interlayer comprising the blended resin material may be adversely affected. In accordance with embodiments of the present invention, polymer layers and interlayers comprising higher levels of blended resin material can be produced using one or more of the RI balancing agents discussed above.

When the RI balancing agent comprises a high RI plasticizer, higher amounts of blended resin materials can be added to the process of making the resin compositions, layers, or interlayers described herein without reducing the clarity or increasing the haze of the final composition, layer, or interlayer. In some embodiments, a composition comprising the blended material may comprise a first poly (vinyl acetal) resin and a second poly (vinyl acetal) resin, wherein one of the resins may have a residual hydroxyl content that is at least 2 weight percent lower than the residual hydroxyl content of the other resin. Such compositions may further comprise at least one high RI plasticizer having a refractive index of 1.460, and in some embodiments, more than 3% of the total amount of the first and second poly (vinyl acetal) resins present in the composition, layer or interlayer may be derived from the blend composition, layer or interlayer. Despite the difference in residual hydroxyl content of the first and second poly (vinyl acetal) resins, compositions comprising more than 0.5 wt.% of the blended resin material can have a haze value of no greater than about 5, no greater than about 4, no greater than about 3, no greater than about 2, or no greater than about 1, or no greater than about 0.5.

The high RI plasticizer used in the blend resin composition as the RI balancer may have a refractive index within one or more of the above ranges. The high RI plasticizer may be added with the blending material during the manufacture of the composition, layer or interlayer and/or at least a portion of the high RI plasticizer may be present in the blended resin material added to the process. Additionally, one or more other plasticizers may also be present in the blended resin material and/or in the resin composition, layer or interlayer in manufacture, including, for example, those having a refractive index measured as described above of less than about 1.450, less than about 1.445, or less than about 1.442. In some embodiments, one or more additional high RI plasticizers may also be present in the blended material and/or the resin composition, layer or interlayer into which the material is blended.

Resin compositions comprising the blended resin materials as described above may be used to form layers and interlayers according to various embodiments of the present invention. For example, a resin composition comprising a blended resin material may be used to form a single monolithic interlayer, or it may be used to form one or more layers of a multi-layer interlayer. When used in various layers and interlayers, additional plasticizers may be added such that the total amount of plasticizer present in the polymer layer or interlayer may be within the ranges described above. Similarly, the glass transition temperature and refractive index of the polymer layers and interlayers formed from the composition comprising the blended resin material may also be within the ranges provided above. In addition, the polymeric layers and interlayers formed from the compositions comprising the blended materials may also exhibit acoustic properties as described above and may be included in any of the applications described below.

According to some embodiments, at least a portion of the resin compositions, layers, or interlayers described herein can comprise one or more recycled resin materials, including, for example, recycled layers or interlayers. The term "recycle" as used herein refers to removal from the process line and subsequent return to the process line. In general, the use of recycled materials can adversely affect the optical properties of the final composition, layer or interlayer as measured by clarity or haze, due to the different compositions and properties of the blended or combined materials. However, in some embodiments, a layer or interlayer as described herein may comprise at least one recycled resin material while still exhibiting the same optical and/or acoustic properties as described herein. The type and/or amount of recycled resin material may fall within one or more of the above ranges and the layer or interlayer may further comprise at least one RI balancing agent. In addition, the polymer layers and interlayers comprising recycled resin material may also have optical and/or acoustical properties in one or more of the ranges described below.

The above-described resin compositions, layers and interlayers may be made according to any suitable method. In various embodiments, methods of making these compositions, layers, and interlayers can comprise providing two or more poly (vinyl acetal) resins, blending at least one resin with an RI balancer and optionally, at least one plasticizer or other additive to form a blended composition, and forming a layer from the blended composition.

In some embodiments, the resin provided in the initial step of the process may be in the form of one or more poly (vinyl acetal) resins, while in other embodiments, one or more resin precursors may also be provided. In some embodiments, when physically blending two or more poly (vinyl acetal) resins, the blending of the two resins may comprise melt blending and may be performed at a temperature of at least about 140, at least about 150, at least about 180, at least about 200, at least about 250 ℃. In other embodiments, when the provided poly (vinyl acetal) resin component comprises a resin precursor, the blending step can comprise reacting two or more aldehydes with polyvinyl alcohol to provide a single poly (vinyl acetal) resin having two or more aldehyde moieties. Additionally, a portion of the blending step may include blending one or more resins with at least one plasticizer and/or with one or more of the foregoing RI balancing agents.

The resulting blended resin may then be formed into one or more polymer layers according to any suitable method. Exemplary methods of forming the polymeric layers and interlayers can include, but are not limited to, solution casting, compression molding, injection molding, melt extrusion, melt blowing, and combinations thereof. The multilayer interlayer comprising two or more polymer layers may also be made according to any suitable method, such as coextrusion, blown film, melt blowing, dip coating, solution coating, doctor blade, air knife, printing, powder coating, spray coating, and combinations thereof. In various embodiments of the invention, the layer or interlayer may be formed by extrusion or coextrusion. In an extrusion process, one or more thermoplastic polymers, plasticizers, and optionally, at least one additive, including one or more RI balancing agents as described above, may be pre-mixed and fed to an extrusion device. Other additives, which may be in the form of liquid, powder or pellets, such as ACA, colorants and UV inhibitors, may also be used and may be mixed into the thermoplastic polymer or plasticizer prior to entering the extrusion device. These additives can be incorporated into the polymer resin and, by extension, the resulting polymer sheet, thereby enhancing certain properties of the polymer layer or interlayer and its performance in the final multiple layer glass panel or other final product.

In various embodiments, the thickness of the layer or interlayer can be at least about 10, at least about 15, at least about 20 mils and/or not greater than about 100, not greater than about 90, not greater than about 60, not greater than about 50, or not greater than about 35 mils, or it can be in the range of about 10 to about 100, about 15 to about 60, or about 20 to about 35 mils. The thickness of the polymer layer or interlayer, in millimeters, can be at least about 0.25, at least about 0.38, at least about 0.51 millimeters, and/or not more than about 2.54, not more than about 2.29, not more than about 1.52, or not more than about 0.89 millimeters, or in the range of about 0.25 to about 2.54 millimeters, about 0.38 to about 1.52 millimeters, or about 0.51 to about 0.89 millimeters. In some embodiments, the polymer layer or interlayer may comprise a flat polymer layer having substantially the same thickness along the length or longest dimension and/or width or next longest dimension of the sheet, while in other embodiments, one or more layers of a multi-layer interlayer may be tapered or may have a tapered profile, for example, such that the thickness of the interlayer varies along the length and/or width of the sheet, such that one side of the layer or interlayer is thicker than the other. When the interlayer is a multilayer interlayer, at least one, at least two, or at least three layers of the interlayer can comprise at least one tapered zone. When the interlayer is a monolithic interlayer, the polymer sheet may be flat or may comprise at least one tapered zone. The tapered interlayer can be used, for example, in head-up display (HUD) panels in automotive and aircraft applications.

Turning now to fig. 1 to 8, several embodiments of tapered interlayers according to the present invention are provided. FIG. 1 is a cross-sectional view of an exemplary tapered interlayer comprising tapered regions of different thicknesses. As shown in FIG. 1, the tapered zone has a minimum thickness T measured at a first boundary of the tapered zone_minAnd a maximum thickness T measured at a second boundary of the tapered region_max. In certain embodiments, T_minCan be at least about 0.25, at least about 0.40, or at least about 0.60 millimeters (mm) and/or not greater than 1.2, not greater than about 1.1, or not greater than about 1.0 mm. Furthermore, T_minMay be in the range of 0.25 to 1.2 mm, 0.4 to 1.1 mm, or 0.60 to 1.0 mm. In certain embodiments, T_maxMay be at least about 0.38, at least about 0.53, or at least about 0.76 mm and/or not greater than 2.2, not greater than about 2.1, or not greater than about 2.0 mm. Furthermore, T_maxMay be in the range of 0.38 to 2.2 mm, 0.53 to 2.1 mm, or 0.76 to 2.0 mm. In certain embodiments, T_maxAnd T_minThe difference may be at least about 0.13, at least about 0.15, at least about 0.2, at least about 0.25, at least about 0.3, at least about 0.35, at least about 0.4 mm and/or not more than 1.2, not more than about 0.9, not more than about 0.85, not more than about 0.8, not more than about 0.75, not more than about 0.7, not more than about 0.65, or not more than about 0.6 mm. Furthermore, T_maxAnd T_minThe difference may be in the range of 0.13 to 1.2 mm, 0.25 to 0.75 mm, or 0.4 to 0.6 mm. In certain embodiments, the distance between the first and second boundaries of the tapered zone (i.e., the "tapered zone width") can be at least about 5, at least about 10, at least about 15, at least about 20, or at least about 30 centimeters (cm) and/or not greater than about 200, not greater than about 150, not greater than about 125, not greater than about 100, or not greater than about 75 cm. Further, the tapered zone width can be in the range of 5 to 200 cm, 15 to 125 cm, or 30 to 75 cm.

As shown in fig. 1, the tapered interlayer includes opposing first and second outer end edges. In certain embodiments, the distance between the first and second outer edges (i.e., "the interlayer width") can be at least about 20, at least about 40, or at least about 60 cm and/or no greater than about 400, no greater than about 200, or no greater than about 100 cm. Further, the interlayer width may be in the range of 20 to 400 cm, 40 to 200 cm, or 60 to 100 cm. In the embodiment depicted in fig. 1, the first and second boundaries of the tapered zone are spaced inwardly from the first and second outer end edges of the interlayer. In such embodiments, only a portion of the interlayer is tapered. When the tapered zone constitutes only a portion of the interlayer, the ratio of the interlayer width to the tapered zone width can be at least about 0.05:1, at least about 0.1:1, at least about 0.2:1, at least about 0.3:1, at least about 0.4:1, at least about 0.5:1, at least about 0.6:1, or at least about 0.7:1 and/or not more than about 1:1, not more than about 0.95:1, not more than about 0.9:1, not more than about 0.8:1, or not more than about 0.7: 1. Further, the ratio of the interlayer width to the taper region width may be in the range of 0.05:1 to 1:1 or 0.3:1 to 0.9: 1. In another embodiment, discussed below, the entire sandwich is tapered. When the entire interlayer is tapered, the tapered zone width is equal to the interlayer width and the first and second boundaries of the tapered zone are located at the first and second terminal edges, respectively.

As illustrated in fig. 1, the tapered zone of the interlayer has a wedge angle defined as the angle formed between a first reference line passing through two points of the interlayer where the first and second tapered zone boundaries intersect the first (upper) surface of the interlayer and a second reference line passing through two points where the first and second tapered zone boundaries intersect the second (lower) surface of the interlayer. In certain embodiments, the wedge angle of the tapered zone can be at least about 0.13, at least about 0.15, at least about 0.2, at least about 0.25, at least about 0.3, at least about 0.35, at least about 0.4 milliradians (mrad), and/or not greater than about 1.2, not greater than about 1.0, not greater than about 0.9, not greater than about 0.85, not greater than about 0.8, not greater than about 0.75, not greater than about 0.7, not greater than about 0.65, not greater than about 0.6, not greater than about 0.55, not greater than about 0.5, or not greater than about 0.45 mrad. Further, the wedge angle of the tapered zone may be in the range of 0.13 to 1.2 mrad, 0.2 to 0.8 mrad, 0.25 to 0.75 mrad, 0.3 to 0.6, or 0.4 to 0.55 mrad.

When the first and second surfaces of the tapered zone are each planar, the wedge angle of the tapered zone is simply the angle between the first (upper) surface and the second (lower) surface. However, as discussed in more detail below, in certain embodiments, the tapered zone may include at least one variable angle zone having a curved thickness profile and a continuously varying wedge angle. Further, in certain embodiments, the tapered zone may include two or more fixed angle zones, wherein the fixed angle zones each have a linear thickness profile, but at least two fixed angle zones have different wedge angles.

Fig. 2-7 illustrate various tapered interlayers configured in accordance with embodiments of the present invention. Fig. 2 depicts an interlayer 20 that includes a tapered region 22 that extends completely from a first terminal edge 24a of interlayer 20 to a second terminal edge 24b of interlayer 20. In this configuration, the first and second boundaries of the tapered zone are located at the first and second end edges 24a, b of the interlayer. The entire tapered zone 22 of the sandwich interlayer 20 depicted in fig. 2 has a constant wedge angle Ѳ, which is simply the angle formed between the first (upper) plane and the second (lower) plane of the sandwich interlayer 20.

Fig. 3 illustrates a sandwich 30 including a tapered region 32 and a flat edge region 33. A first boundary 35a of tapered region 32 is located at a first end edge 34a of interlayer 30 and a second boundary 35b of tapered region 32 is located at the intersection of tapered region 32 and planar edge region 33. The tapered section 32 includes a constant angle section 36 and a variable angle section 37. The constant angle region 36 has a linear thickness profile and a constant wedge angle Ѳ_cWhile the varied angle region 37 has a curved thickness profile and a continuously varying wedge angle. The initial wedge angle of the variable angle section 37 is equal to the constant wedge angle Ѳ_cAnd the end wedge angle of the variable angle section 37 is 0. The interlayer 30 depicted in FIG. 3 has a constant wedge angle Ѳ that is greater than the overall wedge angle of the entire tapered zone 32_c。

Fig. 4 illustrates an interlayer 40 that includes a tapered region 42 located between first and second planar edge regions 43a, b. First boundary 45a of tapered region 42 is located where tapered region 42 meets first planar edge region 43a, and second boundary 45b of tapered region 42 is located where tapered region 42 meets second planar edge region 43bTo (3). The tapered section 42 includes a constant angle section 46 located between first and second variable angle sections 47a, b. The first variable angle region 47a forms a transition region between the first flat edge region 43a and the constant angle region 46. The second variable angle region 47b forms a transition region between the second flat edge region 43b and the constant angle region 46. The constant angle region 46 has a linear thickness profile and a constant wedge angle Ѳ_cWhile the first and second variable angle regions 47a, b have a curved thickness profile and a continuously varying wedge angle. The initial wedge angle of the first variable angle section 47a is equal to 0 and the final wedge angle of the first variable angle section 47b is equal to the constant wedge angle Ѳ_c. The initial wedge angle of the second variable angle section 47b is equal to the constant wedge angle Ѳ_cAnd the final wedge angle of the second variable angle section 47b is 0. The sandwich interlayer 40 depicted in FIG. 4 has a constant wedge angle Ѳ that is greater than the overall wedge angle of the entire tapered zone 42_c。

Fig. 5 illustrates a sandwich 50 including a tapered region 52 located between first and second planar edge regions 53a, b. The tapered region 52 of the interlayer 50 does not include a constant angle region. Instead, the entire tapered zone 52 of the interlayer 50 is a varied angle zone with a curved thickness profile and a continuously varying wedge angle. As described above, the overall wedge angle Ѳ of the tapered region 52 is measured as the angle between a first reference line "a" that runs through the two points where the first and second boundaries 55a, B of the tapered region 52 meet the first (upper) surface of the interlayer 50 and a second reference line "B" that runs through the two points where the first and second boundaries 55a, B of the tapered region 52 meet the second (lower) surface of the interlayer 50. However, within the tapered zone 52, the curved thickness profile provides an infinite number of wedge angles, which may be greater than, less than, or equal to the total wedge angle Ѳ of the entire tapered zone 52.

Fig. 6 illustrates an interlayer 60 that does not include any flat end portions. Instead, tapered region 62 of interlayer 60 forms the entire interlayer 60. Thus, the first and second boundaries 65a, b of the tapered region 60 are located at the first and second terminal edges 64a, b of the interlayer 60. The tapered section 62 of the interlayer 60 includes first, second and third constant angle sections 46a, b, c separated by first and second variable angle sections 47a, b. The first, second and third constant angle regions 46a, b, c each have a linear thickness profile and each have a unique first, second and third constant wedge angle Ѳ, respectively_c1、Ѳ_c2、Ѳ_c3. The first variable angle region 47a serves as first and secondThe transition between the fixed angle regions 46a, b. The second variable angle region 47b serves as a transition region between the second and third fixed angle regions 46b, c. As discussed above, the overall wedge angle Ѳ of the tapered zone 62 is measured as the angle between the first reference line "A" and the second reference line "B". First constant wedge angle Ѳ_c1Less than the overall wedge angle Ѳ of the tapered region 62. Second constant wedge angle Ѳ_c2Greater than the overall wedge angle Ѳ of the tapered region 62. Third constant wedge angle Ѳ_c3Less than the overall wedge angle Ѳ of the tapered region 62. The wedge angle of the first variable angle section 47a is changed from the first constant wedge angle Ѳ_c1Continuously increases to a second constant wedge angle Ѳ_c2. The wedge angle of the second variable angle section 47b is from the second constant wedge angle Ѳ_c2Continuously decreases to a third wedge angle Ѳ_c3。

Fig. 7 illustrates a sandwich interlayer 70 that includes a tapered region 72 located between first and second planar edge regions 73a, b. The first and second boundaries 75a, b of the tapered region 72 are spaced inwardly from the first and second outer edges 74a, b of the interlayer 70. The tapered zone 72 of the interlayer 70 includes first, second, third and fourth angled zones 77a, b, c, d and first, second and third angled zones 76a, b, c. The first angled region 77a serves as a transition region between the first flat edge region 73a and the first angled region 76 a. The second variable angle region 77b serves as a transition region between the first fixed angle region 76a and the second fixed angle region 76 b. The third variable angle region 77c serves as a transition region between the second constant angle region 76b and the third constant angle region 76 c. The fourth variable angle region 77d serves as a transition region between the third constant angle region 76c and the second flat edge region 73 b. The first, second and third constant angle regions 76a, b, c each have a linear thickness profile and each have a unique first, second and third constant wedge angle Ѳ, respectively_c1、Ѳ_c2、Ѳ_c3. As discussed above, the first, second, third and fourth variable angle regions 77a, b, c, d have wedge angles that continuously transition from the wedge angle of the constant angle region on one side of the variable angle region 77 to the wedge angle of the constant angle region on the other side of the variable angle region 77.

As discussed above, the tapered interlayer may include one or more constant angle tapered zones, each having a width less than the overall width of the entire tapered zone and each having a wedge angle that is the same or different than the overall wedge angle of the entire tapered zone. For example, the tapered zone may include one, two, three, four, five, or more fixed angle tapered zones. When multiple fixed angle tapered zones are used, the fixed angle tapered zones may be spaced apart from each other by variable angle tapered zones for transitioning between adjacent fixed angle tapered zones.

In certain embodiments, the width of each angled cone region may be at least about 2, at least about 5, at least about 10, at least about 15, or at least about 20 cm and/or not greater than about 150, not greater than about 100, or not greater than about 50 cm. In certain embodiments, the ratio of the width of each angled taper region to the total width of the entire taper region may be at least about 0.1:1, at least about 0.2:1, at least about 0.3:1, or at least about 0.4:1 and/or not greater than about 0.9:1, not greater than about 0.8:1, not greater than about 0.7:1, not greater than about 0.6:1, or not greater than about 0.5: 1.

In certain embodiments, the wedge angle of each constant angle tapered zone may be at least about 0.13, at least about 0.15, at least about 0.2, at least about 0.25, at least about 0.3, at least about 0.35, at least about 0.4 mrad, and/or not greater than about 1.2, not greater than about 1.0, not greater than about 0.9, not greater than about 0.85, not greater than about 0.8, not greater than about 0.75, not greater than about 0.7, not greater than about 0.65, or not greater than about 0.6 mrad. Further, the wedge angle of each constant angle tapered zone may be in the range of 0.13 to 1.2 mrad, 0.25 to 0.75 mrad, or 0.4 to 0.6 mrad. In certain embodiments, the wedge angle of at least one constant angle conical zone is at least about 0.01, at least about 0.05, at least about 0.1, at least about 0.2, at least about 0.3, or at least about 0.4 mrad greater than the total wedge angle of the entire conical zone. In certain embodiments, the wedge angle of at least one constant angle conical zone is at least about 0.01, at least about 0.05, at least about 0.1, at least about 0.2, at least about 0.3, or at least about 0.4 mrad less than the total wedge angle of the entire conical zone. In certain embodiments, the wedge angle of at least one constant angle conical zone is no greater than about 0.4, no greater than about 0.3, no greater than about 0.2, no greater than about 0.1, no greater than about 0.05, or no greater than about 0.01 mrad greater than the total wedge angle of the entire conical zone. In certain embodiments, the wedge angle of at least one constant angle conical zone is no greater than about 0.4, no greater than about 0.3, no greater than about 0.2, no greater than about 0.1, no greater than about 0.05, or no greater than about 0.01 mrad less than the total wedge angle of the entire conical zone.

Fig. 8a and 8b illustrate an interlayer 80 having a thickness profile similar to interlayer 30 of fig. 3. The interlayer 80 of fig. 8a and 8b is configured for use in a vehicle windshield by securing the interlayer between two sheets of glass. As depicted in fig. 8a, the first terminal edge 84a of the interlayer 80 may be located at the bottom of the windshield, while the second terminal edge 84b of the interlayer 80 may be located at the top of the windshield. The cone region 82 of the interlayer 80 is located in the region of the windshield where the head-up display is located. The tapered region 82 of the interlayer 80 includes a constant angle region 86 and a variable angle region 87. As depicted in fig. 8a, in certain embodiments, the tapered region 82 extends completely across the interlayer 80 between the first side edge 88a and the second side edge 88b of the interlayer 80. Fig. 8b, similar to fig. 3, shows the thickness distribution of the interlayer 80 between the bottom of the windshield and the top of the windshield.

Although not illustrated in the figures, it should be understood that in certain embodiments, the tapered interlayer may be a multi-layer interlayer. When the tapered interlayer comprises a plurality of individual layers, all of the individual layers may be tapered, some of the individual layers may be tapered or only one of the individual layers may be tapered. Further, in certain embodiments, the glass transition temperatures of the individual layers may be different from one another. For example, in one embodiment, the interlayer comprises a tapered interlayer having a lower glass transition temperature than the two tapered outer layers of the interlayer, wherein the glass transition temperature of one or both outer layers exceeds the glass transition temperature of the interlayer by at least about 10, at least about 20, at least about 30, at least about 40, or at least about 50 ℃.

In some embodiments, the polymer layer or interlayer may comprise a flat polymer layer having substantially the same thickness along the length or longest dimension and/or width or next longest dimension of the sheet, while in other embodiments, one or more layers of a multi-layer interlayer may be wedge-shaped or may have a wedge-shaped profile, for example, such that the thickness of the interlayer varies along the length and/or width of the sheet, such that one side of the layer or interlayer is thicker than the other. When the interlayer is a multilayer interlayer, at least one, at least two, or at least three layers of the interlayer may be wedge-shaped. When the interlayer is a monolithic interlayer, the polymer sheet may be flat or wedge-shaped. The wedge interlayer can be used, for example, in head-up display (HUD) panels in automotive and aircraft applications.

The resin compositions, layers and interlayers according to embodiments of the present invention can be used in multilayer boards comprising a polymer layer or interlayer and at least one rigid substrate. In some embodiments, the multilayer sheet includes a pair of rigid substrates and a resin interlayer disposed therebetween. The total thickness of the plate, measured as the total thickness of the substrate and interlayer, may be at least about 2, at least about 3, at least about 3.5, at least about 4, at least about 4.5, at least about 4.65, at least about 4.75, or at least about 5 mm and/or not more than about 6.5, not more than about 6.25, not more than about 6.0, not more than about 5.75, not more than about 5.5, or not more than about 5 mm. The thickness of one or both substrates can be significantly less than the expected thickness of a conventional multilayer board. For example, in some embodiments, the total thickness of each rigid substrate can be no greater than about 4.0, no greater than about 3.9, no greater than about 3.8, no greater than about 3.7, no greater than about 3.6, no greater than about 3.5, no greater than about 3.4 mm.

Any suitable rigid substrate may be used to form the multilayer sheet, and in some embodiments the substrate may comprise a material selected from the group consisting of glass, polycarbonate, biaxially oriented PET, copolyester, acrylic, and combinations thereof. When the rigid substrate comprises a polymeric material, the polymeric material may or may not include a hard-coated surface layer. In certain embodiments, the rigid substrate can have a refractive index that is less than the refractive index of the interlayer used to form the multilayer sheet. For example, the refractive index of the at least one rigid substrate measured as described above may be no greater than about 1.550, no greater than about 1.545, no greater than about 1.540, no greater than about 1.535, no greater than about 1.530, or no greater than about 1.525. In some embodiments, the refractive index of at least one rigid substrate may be at least about 5, at least about 10, at least about 15, at least about 20% lower than the refractive index of the interlayer used to form the multilayer sheet. In certain embodiments, the refractive index of one or both substrates may be at least about 0.25 units, at least about 0.50 units, at least about 0.75 units, at least about 1.0 unit, at least about 1.1 units, or at least about 1.5 units lower than the refractive index of the interlayer. Alternatively, it can be said that the interlayer has a refractive index that is higher than the refractive index of the at least one substrate by an amount or percentage described herein.

Multilayer boards configured in accordance with certain embodiments of the present invention can have an equivalent refractive index that is higher than the refractive index of one or more rigid substrates. The term "equivalent refractive index" as used herein refers to the overall refractive index of a composite material, such as a multilayer sheet. Specific equivalent refractive index of multilayer sheet: (n _eq) Calculated according to the following equations (1) and (2):

　　　　　　　　　　(1)

　　　　　　　　　　(2)

whereinx _TAndt _Tas defined below:

　　　　　　　　　　(3)

　　　　　　　　　　(4)。

in the above equation, θ_eqIs the equivalent angle of incidence of the composite material,x _Tis the distance the light travels through the entire composite,t _Tis provided withmThe total thickness of the composite material of the individual layers,n _Ais the refractive index of air, θ₁Is the angle of incidence of the light passing through the air-layer 1 interface,n _eqis the composition ofThe equivalent refractive index of the material is,t _iis a layeriAnd θ is_iIs through the layeriThe angle of incidence of the light. The equivalent refractive index of a multiwall sheet as described herein can be at least about 1.490, at least about 1.495, at least about 1.500, at least about 1.505, at least about 1.510, at least about 1.515, at least about 1.520, at least about 1.525, at least about 1.530, at least about 1.535, at least about 1.540, or at least about 1.545.

In some embodiments, the multilayer sheet can have an equivalent refractive index that is at least about 0.25, at least about 0.5, at least about 0.75, at least about 1, or at least about 1.5% higher than the refractive index of at least one substrate used to form the multilayer interlayer. For example, the plate can have an equivalent index of refraction that is at least 0.010, at least about 0.015, at least about 0.020, or at least about 0.025 higher than the index of refraction of the rigid substrate or substrates used to form the plate. In certain embodiments, the multilayer sheet may have an equivalent refractive index that is less than the refractive index of the interlayer used to form the sheet and may, for example, be at least about 0.5, at least about 1, at least about 1.5, at least about 2, at least about 2.5, at least about 3, at least about 5, or at least about 7% lower than the refractive index of the interlayer used to form the multilayer sheet. The difference between the index of refraction of the interlayer and the equivalent index of refraction of the plate can be at least about 0.010, at least about 0.025, at least about 0.050, at least about 0.10, at least about 0.125, at least about 0.50, or at least about 0.75.

The multiwall sheets as described herein can be used in a variety of end applications, including, for example, in automotive windshields and windows, aircraft windshields and windows, sheets for various transportation applications such as marine applications, rail applications, and the like, structural building sheets such as windows, doors, stairs, walkways, railings, decorative building sheets, weather resistant sheets such as hurricane or tornado glasses, ballistic resistant sheets, and other similar applications.

In certain embodiments, a multiwall sheet as described herein can exhibit reduction of interfering ghosting or reflective "ghosting" when used, for example, to project a head-up display (HUD) image onto a windshield of an automobile or aircraft. In general, when the windshield has a substantially uniform thickness distribution, ghosting is most problematic due to differences in the position of the projected image when reflected from the inner and outer surfaces of the glass. However, in some embodiments, a multiwall sheet as described herein can minimize the projection of ghosting such that, for example, the distance between ghost images of the sheet is significantly less than that exhibited by conventional sheets.

A method of determining ghost pitch includes providing a multiwall sheet comprising at least a pair of rigid substrates and an interlayer disposed therebetween. The interlayer can comprise any property of or can be any interlayer described herein. In some embodiments, the interlayer can be a tapered interlayer comprising, for example, at least one tapered zone having a wedge angle of at least 0.05 mrad. The substrate may also include one or more properties of the substrates described herein and may include glass in certain embodiments.

To measure the ghost image pitch for a given panel, a projection image may be generated by passing light through at least a portion of the panel. In some embodiments, the light passing through the plate comprises an image, such as a grid, a line, a shape, or a graphic. In some embodiments, the image may be generated by reflecting the thin film transistor display from a substantially flat mirror, although other suitable methods of generating the image may be used. If a tapered interlayer is used to form a multilayer sheet, at least a portion of the light passing through the sheet may pass through at least a portion of the tapered region. Alternatively or additionally, light may be passed along the plate through one or more other relevant regions to determine the ghost pitch formed when the light is projected through these regions.

Once the light has passed through and reflected from the surface of the plate, the projected image may be projected onto the surface and then captured to form a captured image. In some embodiments, the projected image displayed on the surface may include a primary image as shown in fig. 10 and a secondary "ghost" image that is offset and slightly overlapping with the primary image. The projected image may be captured using a digital camera or other suitable device, and the capturing may include digitizing the projected image to form a digital projected image comprising a plurality of pixels.

Once digitized, the captured image may be quantitatively analyzed to form a graph including at least one primary image index and at least one secondary image index. The analysis may be performed by converting at least a portion of the digital projection image into a vertical image matrix comprising values representing intensities of pixels in the image portion. The columns of the matrix may then be extracted and plotted against the number of pixels as shown in fig. 11 to provide a graph. The primary image index of the graph is then compared to the secondary image index of the graph to determine a difference. In some embodiments, the primary image indicator may include a higher intensity peak of the curve, and the secondary image indicator may be a lower intensity peak. Any suitable difference between the two indices may be determined and in some embodiments may be the difference in position between the two indices in the graph. Based on the difference, a ghost image separation distance of the portion of the subject panel can be calculated. One specific application of the above method for determining ghost separation distance is described in example 11.

Multilayer boards configured in accordance with embodiments of the present invention can have ghost image separation distances that are significantly lower than conventionally formed boards. For example, in some embodiments, the ghost image separation distance of a plate as described herein can be at least about 10, at least about 20, at least about 30, at least about 40% less than the ghost image separation distance of a plate formed from a conventional interlayer, such as those having a refractive index of less than 1.480 (all other things being equal). The ghost image separation distance for a given plate can depend in part on its particular configuration, including the type and size of its interlayer and substrate. Several specific examples of ghost image separation distances for the inventive and comparative panels are provided in the examples.

When laminating the polymer layer or interlayer between two rigid substrates, such as glass, the method may comprise at least the following steps: (1) assembling the two substrates and the interlayer; (2) heating the assembly by infrared radiation or convection means for a first short time; (3) feeding the assembly to a pressure nip roll for a first degassing; (4) heating the assembly to about 60 ℃ to about 120 ℃ for a short period of time to impart sufficient temporary adhesion to the assembly to seal the interlayer edges; (5) feeding the assembly to a second pressure nip roller to further seal the interlayer edges and allow further processing; and (6) heat treating the assembly under pressure at a temperature of 135 ℃ to 150 ℃ and a pressure of 150 psig to 200 psig for about 30 to 90 minutes. Other methods of degassing the interlayer-glass interface, as described in accordance with some embodiments of steps (2) through (5) above, include vacuum bag and vacuum ring methods, both of which may also be used to form the interlayers of the present invention as described herein.

In some embodiments, the multilayer sheet can include at least one polymer film disposed on the layer or interlayer to form a multilayer sheet known as a "bilayer". In some embodiments, the interlayer used in the bilayer may comprise a multi-layer interlayer, while in other embodiments, a monolithic interlayer may be used. The use of polymer films in multilayer sheets as described herein can enhance the optical characteristics of the final sheet while also providing other performance improvements, such as infrared absorption. Polymer films are distinguished from polymer layers or interlayers in that the film alone does not provide the necessary penetration resistance and glass retention. The polymer film may also be thinner than the sheet material and may have a thickness of 0.001 to 0.25 millimeters. Poly (ethylene terephthalate) ("PET") is one example of a material used to form polymer films.

The following examples are intended to illustrate the present invention to teach one of ordinary skill in the art to make and use the invention and are not intended to limit the scope of the invention in any way.

Examples

The following examples describe the preparation of several resin compositions, layers and interlayers comprising various poly (vinyl acetal) resins. Several comparative materials and the materials of the present invention were evaluated for acoustic and optical properties using several tests performed on a number of compositions, layers and interlayers, as described below.

EXAMPLE 1 preparation of high refractive index Poly (vinyl Acetal) resin

Several comparative poly (vinyl acetal) resins, referred to in table 2 below as comparative resins CR-1 to CR-12, were prepared by acetalizing polyvinyl alcohol with one or more aldehydes, including n-butyraldehyde (nBuCHO; RI = 1.377), isobutyraldehyde (iBuCHO; RI = 1.374), and 2-ethylhexanal (2 EHCHO; RI = 1.414). Using the above detailsThe composition of the resulting resin was measured by the finely described ASTM D1396 or FT-IR/SEC method. The refractive index and glass transition temperature (T) of several resins were also measured according to the above method_g) The results are provided in table 2 below.

TABLE 2 Properties of several comparative poly (vinyl acetal) resins

nd = not determined.

In addition, several poly (vinyl acetal) resins according to embodiments of the invention were also prepared in a similar manner. These inventive resins, referred to in Table 3 as public resins DR-1 to DR-21, were formed by acetalizing polyvinyl alcohol with a mixture of n-butyraldehyde and various high refractive index aldehydes, including benzaldehyde (BzCHO RI = 1.545), cinnamaldehyde (CCHO; RI = 1.620), 4-chlorobenzaldehyde (4-ClBzCHO; RI = 1.5850), 2-phenylpropionaldehyde (2 PHPrCHO; RI = 1.517), and hydrocinnamaldehyde (HCCHO; RI = 1.523). The refractive indices of several of the disclosed resins were also determined and the results are summarized in table 3 below.

As shown in the above tables 2 and 3, the polyvinyl acetal resin containing residues of at least one high-refractive-index aldehyde (including those listed above) tends to exhibit a higher refractive index than those containing residues of aldehydes such as n-butyraldehyde, isobutyraldehyde, and 2-ethylhexanal.

Example 2 preparation of high refractive index resin interlayer

Several comparative and disclosed interlayers were formed by mixing and melt blending several comparative resins listed in table 2 and several disclosed resins listed in table 3 above with varying amounts of the plasticizer triethylene glycol bis (2-ethylhexanoate) (3 GEH). The composition, refractive index, and glass transition temperature of each of the resulting interlayers, referred to as comparative interlayers CL-1 through CL-14 and disclosed interlayers DL-1 through DL-26, were measured as described above and the results are summarized in tables 4 and 5, respectively, below.

TABLE 4 Properties of several comparative interlayers

nd = not determined.

TABLE 5 Properties of several disclosed interlayers

nd = not determined.

As shown in tables 4 and 5 above, the disclosed interlayers using the higher refractive index disclosed resins from table 3 exhibit higher refractive indices than the comparative interlayers formulated with the lower refractive index resins, such as the comparative resins listed in table 2. In addition, as shown by a comparison disclosing interlayers DL-1 and DL-2 and DL-6 and DL-23 to DL-25, the amount of plasticizer used to form the interlayers affects the glass transition temperature and refractive index of the layer, although not necessarily to the same extent for all resins. For example, as shown by a comparison of DL-1 (75 phr 3 GEH; DR-1) and DL-2 (50 phr 3 GEH; DR-1), reducing the amount of plasticizer by about 33% increases the glass transition temperature of the interlayer by 11 ℃ (from 1 ℃ to 12 ℃), but only by 0.006 (from 1.473 to 1.479) in refractive index. However, as shown by a comparison of DL-25 (60 phr 3 GEH; DR-5) and DL-6 (75 phr 3 GEH; DR-5), reducing the plasticizer content in the layer formed from this resin resulted in an increase in the glass transition temperature of only 1 deg.C (from 1 deg.C to 2 deg.C) while increasing the refractive index by 0.004 (from 1.484 to 1.488).

Example 3 preparation of interlayers using high refractive index resins

Several comparative and disclosed multi-layer interlayers were made using several comparative interlayers and disclosed interlayers formed in example 2 and summarized in tables 4 and 5, respectively, above. Each multi-layer interlayer comprises a pair of outer "skin" layers having a total thickness of 28 mils sandwiching an inner "core" layer having a thickness of 5 mils, typically formed of a resin having a relatively low residual hydroxyl content. The composition of the interlayers and several properties, including refractive index, glass transition temperature, mottle, and loss factor, were measured as described above, and the results for the comparative multiple layer interlayers (CI-1 through CI-16) and the disclosed multiple layer interlayers (DI-1 through DI-29) are summarized in tables 6 and 7 below.

As shown in table 6 above, the interlayer formed of the skin layer and the core layer having a refractive index difference of 0.010 or more exhibits optical defects as indicated by a mottle value of more than 5. However, as shown in table 7, the interlayer formed of the skin layer and the core layer having a refractive index difference of less than 0.010 exhibits a low mottle value of 1 or less. In addition, as shown in table 7, such low mottle values can be achieved by interlayers having a core layer with a refractive index higher or lower than the skin layer, as long as the absolute value of the difference between the refractive indices of adjacent layers is less than 0.010. As also shown in table 7, interlayers formed from a skin layer and a core layer both having a high RI aldehyde residue and having a refractive index difference greater than 0.010 exhibit high mottle values of 5 or greater.

EXAMPLE 4 stability of Multi-layer interlayers

Two comparative multiple interlayers, CI-2 and CI-7, and two disclosed multiple interlayers, DI-4 and DI-5, prepared as described in examples 1-3 above, were tested to determine the relative stability of the interlayers over time. Net plasticizer migration was measured by comparing the glass transition temperature of each layer at the initial time (t = 0) and after the layers reached equilibrium. The results are summarized in table 8 below.

TABLE 8 Net plasticizer migration and Properties of exemplary comparative and disclosed interlayers

It is disclosed that interlayer DI-4 (as well as comparative interlayers CI-2 and CI-7) exhibits minimal change in the glass transition temperatures of the skin and core layers of the interlayer at equilibrium. This indicates that traces of plasticizer migrate between the skin and core layers of each of the interlayers CI-2, CI-7, and DI-4. While the comparative interlayers CI-2 and CI-7 may be relatively stable, both exhibit a mottle value of greater than 5, which is unacceptable for most optical applications. In contrast, interlayer DI-4 was disclosed to exhibit a mottle value of less than 1.

It is disclosed that interlayer DI-5 exhibited a slight decrease in glass transition temperature at equilibrium indicating a small amount of plasticizer migration from the skin layer into the core layer. Such migration can be mitigated by using a smaller amount of plasticizer in the skin layer or a larger amount in the core layer. Nevertheless, the refractive indices of the core and skin layers of the disclosed interlayer DI-5 differ by only 0.004, and thus the interlayer also exhibits a mottle value of less than 1.

Example 5 blended Poly (vinyl Acetal) resins

Several comparative and published resins prepared as described above in example 1 were mixed and melt blended together with 38 phr of 3GEH plasticizer to form comparative blend layers CBL-16 and CBL-17 and published blend layers DBL-27 and DBL-28. Comparative polymer layer CL-2 is listed in table 4. Comparative polymer layer CL-15 was formulated with comparative resin CR-10 and 38 phr of 3GEH, while public polymer layers DL-27 and DL-28 were formulated with public resins DR-3 and DR-5 and 38 phr of 3GEH, respectively. Haze and percent visible light transmission (T) were measured for each of the blended resin interlayers_vis). The results are provided in table 9 below.

TABLE 9 haze and percent visible light transmittance of several Polymer layers

As shown in Table 9 above, the comparative blended interlayers CBL-16 and CBL-17 formed from a blend of comparative resins CR-2 and CR-10 exhibit high haze values and lower percentages of visible light transmission than the single polymer layer of comparative resin CR-2 (comparative layer CL-2) or the single polymer layer of CR-10 (comparative interlayer CL-15). In contrast, the disclosed blended interlayers DBL-27 and DBL-28 formed from a blend of the comparative resin CR-2 and a high refractive index disclosed resin (resin DR-3 in layer DBL-27 or resin DR-5 in layer DBL-28) exhibit substantially the same haze and percent visible light transmission as the comparative interlayer CL-2 formulated with comparative resin CR-2 alone. Thus, the addition of the high refractive index resin of the present invention to the comparative interlayer does not degrade the optical quality of the resulting interlayer.

Example 6 preparation of interlayers with high refractive index additives

Several poly (vinyl acetal) resins were prepared by acetalizing polyvinyl alcohol with n-butyraldehyde. Resins with different residual hydroxyl contents were melt blended with various amounts of 3GEH plasticizer and used to form the various layers of the multilayer interlayer. Each interlayer had an inner "core" layer of 5 mils thickness sandwiched between two outer "skin" layers each of 14 mils thickness. The poly (vinyl butyral) resin used to form the core layer had a hydroxyl content of 11 wt% and the resin used for the skin layer had a hydroxyl content of 19 wt%. Both resins had a residual acetate group content of about 2 wt.%.

Comparative interlayers CI-17 through CI-19 were formed from polymer layers plasticized with 3GEH present in various amounts in the core and skin layers. In addition to 3GEH, disclosed interlayers DI-30 through DI-38 also comprise various amounts of two different high refractive index additives, Benzoflex 2-45 (diethylene glycol dibenzoate; available from Eastman Chemical Company, Kingsport, Tennessee) (additive A-1), having a melting point of 28 ℃ and a refractive index of 1.542; and Benzoflex 352 (1, 4-cyclohexanedimethanol dibenzoate; commercially available from Eastman Chemical Company) (additive A-2) having a melting point of 118 ℃ and a refractive index of 1.554. The refractive indices and glass transition temperatures of the layers of the comparative interlayers CI-17 through CI-19 and the disclosed interlayers DI-30 through DI-38 were measured and the results are summarized in table 10 below.

As shown in table 10 above, increasing the plasticizer content of the core layer of the interlayer containing only 3GEH plasticizer reduces the glass transition temperature of the layer, which ultimately improves its acoustic properties. However, such an increase also broadens the difference in refractive index between the skin and core layers, thereby degrading the optical quality of the interlayer. As shown in table 10 by comparison with the disclosed interlayers DI-30 to DI-38, the refractive index of the core layer formulated with the additional high refractive index additive remains fairly constant with increasing plasticizer loading while still exhibiting a similar decrease in glass transition temperature. As a result, an interlayer having a core layer and a skin layer with almost the same refractive index is obtained, which greatly reduces optical defects such as mottle. At the same time, the core layer also exhibits a sufficiently low glass transition temperature, indicating that the resin also has acoustic properties.

Example 7 preparation of core layer with reactive high refractive index additive

Several polymer layers simulating the inner core layer of a multilayer interlayer were formed by melt blending a polyvinyl n-butyraldehyde resin having a residual hydroxyl content of 11 wt% and a residual acetate group content of about 2 wt% with various amounts of 3GEH plasticizer. The comparative layer CL-16 contained 75 phr of 3GEH, while the disclosed layers DL-29 to DL-31 were formulated with various mixtures of 3GEH and reactive high refractive index additives (reactive high RI additives). The reactive high RI additive (additive A) used in the disclosed layers DL-29 and DL-30 was diphenyldimethoxysilane (commercially available as SID4535.0 from Gelest, Inc., Morrisville, Pennsylvania) and the reactive high RI additive (additive B) used in the disclosed layer DL-31 was phthalic anhydride (commercially available from Sigma Aldrich Co., St. Louis, Missouri). The refractive indices of the comparative layer CL-16 and each of the disclosed layers DL-29 to DL-31 were measured and the results are provided in Table 11 below.

TABLE 11 refractive indices of the Polymer core layers are compared and disclosed

As shown in table 11, the polymer layers formed using 3GEH and one or more reactive high refractive index additives have a higher refractive index than the polymer layers formulated with 3GEH alone. Thus, when used as the inner core layer in a multilayer interlayer, the disclosed layers DL-29 to DL-31 have refractive indices that more closely match the refractive index of the skin layer formed of polyvinyl n-butyraldehyde (RI = 1.477). Thus, the multiple interlayers formed using the disclosed layers DL-29 through DL-31 as core layers exhibit fewer optical defects than the multiple interlayers formed using the comparative layer CL-16 as the core layer.

Example 8 various interlayers Using resin blends with high refractive index plasticizers

Two kinds of polyvinyl n-butyraldehyde resins R-1 and R-2 were prepared according to the procedure described above in example 1. Resin R-1 had a residual hydroxyl content of 19 wt.%, while resin R-2 had a residual hydroxyl content of 11 wt.%. Both resins had a residual acetate group content of 2 wt.%. Several resin blends were prepared containing various amounts of resins R-1 and R-2 to simulate various blending ratios. This blend was combined with 38 phr of a plasticizer selected from 3GEH (plasticizer P-1; RI = 1.442), dioctyl phthalate (plasticizer P-2; RI = 1.485), a blend of 30 weight percent 3GEH and 70 weight percent Benzoflex 2088 (available from Eastman Chemical Company, Kingsport, Tennessee) (plasticizer P-3; RI = 1.506) and nonylphenyl tetraethylene glycol (plasticizer P-4; RI = 1.500). The resulting plasticized resin is then formed into a single sheet comprising the resin and plasticizer. The refractive index, haze and percent visible light transmission of each sheet were determined and the results are provided in table 12 below.

As shown in Table 12 above, while the blended polymer layer formulated with plasticizer P-1 maintains a substantially constant refractive index as the amount of lower hydroxyl content resin R-2 increases, the optical properties of these resin blends with high R-2 content deteriorate as the amount of R-2 increases. For example, as shown in table 12, the haze of blends containing more than 1.1% resin R-2 increased, while the percent visible light transmission of these blends decreased from 88.5% to 81.7%.

In contrast, resin blends containing more than 2.2% of resin R-2 plasticized with higher refractive index plasticizers P-2 through P-4 each exhibited substantially the same haze values and percent visible light transmission as blends with lower amounts of resin R-2. Thus, it can be concluded that the use of higher refractive index plasticizers, such as resin blends of plasticizers P-2 to P-4, can allow the use of higher amounts of lower hydroxyl content resins without adversely affecting the optical properties of the final blend.

Example 9 Poly (vinyl butyral) layer comprising high refractive index plasticizer

Several poly (vinyl n-butyraldehyde) layers were formed by combining and melt blending three different poly (vinyl n-butyraldehyde) resins (PVB-1 to PVB-3) with different types and amounts of plasticizers. Each resin PVB-1 to PBV-3 had a different residual hydroxyl content of 11 to 20.4 wt% and all three resins had a residual vinyl acetate content of 1 wt%. Comparative layers CL-17 to CL-19 were formulated with various amounts of triethylene glycol di- (2-ethylhexanoate) ("3 GEH"; RI = 1.442), while public layers DL-32 to DL-37 comprised a mixture of 3GEH and Benzoflex 354 (available from Eastman Chemical Company, Kingsport, Tennessee) (RI = 1.53). The refractive index of each layer was measured and the results are summarized in table 13 below.

TABLE 13 layers of several poly (vinyl alcohol) butyrals with various plasticizers

As shown in table 13 above, the polymer layer containing the high refractive index plasticizer exhibited a higher refractive index than those containing only the low refractive index plasticizer.

Example 10 preparation of interlayers with high refractive index additives

Several comparative and disclosed multi-layer interlayers were made using the several comparative and disclosed interlayers formed in example 9 and summarized in table 13 above. Each multi-layer interlayer comprises a pair of outer "skin" layers, each having a thickness of 14 mils, sandwiching an inner "core" layer formed of a resin having a lower residual hydroxyl content, having a thickness of 5 mils. The composition and several properties of the multiple interlayers were measured as described above, including total plasticizer content, refractive index, glass transition temperature, mottle and loss factor, and the results for comparing the multiple interlayers CI-20 and CI-21 and disclosing the multiple interlayers DI-39 to DI-41 are summarized in table 14 below.

TABLE 14 several comparative and published interlayer Properties

As shown in table 14 above, interlayers formed from a skin layer and a core layer having a refractive index difference greater than 0.010 exhibit more optical defects as indicated by a mottle value of 5. In addition, the disclosed interlayers DI-39 through DI-41 using high refractive index plasticizers exhibit higher overall refractive indices than comparative interlayers CI-20 and CI-21 using only plasticizers having refractive indices less than 1.460.

Example 11 comparison of different thicknesses and wedge angles and measurement of ghost image separation distance of the disclosed multiwall sheet

Several interlayers were formed by combining a poly (vinyl butyral) resin having a residual hydroxyl content of 18.7 wt% with 38 phr of the plasticizer triethylene glycol bis (2-ethylhexanoate) (3 GEH) and extruding the resulting mixture to form a single layer sheet. A flat interlayer sheet, i.e. without a tapered zone, having a uniform thickness of about 30 mils (about 0.76 mm) was formed and cut to form several comparative interlayers having a wedge angle of 0 °.

Forming several sheets having tapered zones each having a different constant wedge angle, and cutting each sheet to form several tapered integral interlayers. The tapered interlayers each have a wedge angle of 0.30 to 0.73 mrad. Each interlayer sample was then laminated between a pair of 6 inch x 12 inch glass sheets, each glass/interlayer/glass multiwall sheet having a thickness of 3.0 mm, 4.32 mm, or 5.0 mm. The specific configuration of each of the comparative multiwall sheets (CP-1 to CP-3) and the disclosed multiwall sheets (DP-1 to DP-15) is shown in Table 15 below.

TABLE 15 ghost image spacing for several comparative and disclosed laminates

The laminates listed in table 15 were subjected to a ghost pitch test using apparatus 100 shown in fig. 9. As shown in FIG. 9, the assay device 100 includes a projector 130, an adjustable mirror 140, and a detector 120. The distance between the projector 130 and the adjustable mirror 140, shown as line segment a in fig. 9, is 43.8 cm, the distance between the adjustable mirror 140 and the plate 110, shown as line segment B in fig. 9, is 31.7 cm, and the distance between the plate 110 and the detector 120, shown as line segment C in fig. 9, is 47 cm. In addition, shown as θ in fig. 9₁Is directed at an angle of incidence of 30.11 deg. to the adjustable mirror 140, and the plate 110 is arranged so as to be shown as theta in figure 9₂The sum of the incident angles of the image from the mirror 140 on the plate 110 is shown as θ₂The incident angles of the light reflected from the plate 110 to the detector 120 of' are each approximately the same and equal to 24.8 °. Finally, as in FIG. 9 by θ₃The plate 110 is shown to be offset from vertical by an angle of 30.5 deg..

To measure the ghost image separation distance of the plate 110 using the apparatus 100 shown in fig. 9, an image is generated using a standard thin film transistor display and reflected onto the plate 110 through the plane of the mirror 140. The image is reflected by one or more surfaces of the plate 110 and projected onto the detector 120. The image is then recorded using a digital camera to form a captured image as shown in fig. 10, which is then analyzed to form a graph by converting the digital image into a matrix having elements representing the intensity (gray scale) of each pixel of the digital image. The matrix is then plotted column by column as a function of the number of pixels as shown in fig. 11. The higher intensity peaks shown in fig. 11 represent the primary image reflected from the plate, while the shorter, weaker peaks correspond to secondary or "heavy" images. The separation distance in pixels between the primary and secondary peaks was then determined to calculate the ghost separation distance (D) for each plate in minutes (arc min) according to the following equation:

。

using the above procedure, the ghost image separation distances of each of the comparative plates (CP-1 to CP-3) and each of the public plates (DP-1 to DP-15) were measured, and the results are provided in Table 15 above. The results are also summarized in figure 12 in the form of a graph.

In addition, several additional comparative multiwall sheets (CP-4 through CP-8) and the disclosed multiwall sheet (DP-16 through DP-29) were constructed in a similar manner as described above, but with different thicknesses at several different wedge angles. The ghost pitch test described above was then performed on each of the control panels CP-4 through CP-8 and the public panels DP-16 through DP-29, and the results are provided in Table 16 below. FIG. 13 shows ghost image separation distances as a function of wedge angle for the comparative plates CP-4 through CP-8 and the public plates DP-16 through DP-29 under different glass configurations.

TABLE 16 ghost image spacing for several comparative and disclosed laminates

Example 12 several comparisons and disclosures of the equivalent refractive index (n) of multilayer sheets_eq) Measurement of (2)

The equivalent refractive indices n of the comparative and disclosed multilayer sheets were determined in the following examples_eq. ｃA comparative panel (CP- ｃA) was formed by laminating PVB interlayers having ｃA uniform thickness of 0.76 mm and ｃA refractive index of 1.475 between glass plates, one having ｃA thickness of 1.6 mm and the other having ｃA thickness of 2.3 mm. The glass plates each have a refractive index of 1.52 measured at a wavelength of 589 nanometers and at 25 ℃ according to ASTM D542. Incident angle (theta) at 60 DEG₂) Next, the equivalent refractive index of the comparative plate was determined to be 1.512 according to the above equations (1) to (4).

Similarly, a disclosed multiwall sheet (DP-B) was formed by laminating another PVB interlayer having a uniform thickness of 0.76 mm between two glass sheets, each sheet having the same thickness as the sheet used to form the comparative multiwall sheet. However, the PVB interlayer used to form the disclosed multilayer sheet (DP-B) has a refractive index of 1.65. Using the above formula, the equivalent refractive index of the disclosed multilayer board was calculated to be 1.540. This disclosed multilayer sheet DP-B may represent the actual maximum (or practical limit) of equivalent refractive index that may be achieved in some cases. The results are summarized in table 17 below.

TABLE 17 refractive index Properties of interlayers (at an angle of incidence of 60 deg.)

Example 13 Effect of refractive index on ghost image spacing of various laminates

Several glass/air/glass laminates were formed to simulate multilayer sheets with different equivalent refractive indices. Each laminate was constructed by spacing several glass sheets of different thicknesses from one another using appropriately sized metal shims to establish and maintain an air gap between the glass sheets. The total thickness of the resulting glass/air/glass laminate was maintained between 4 and 5 mm and the respective equivalent refractive indices were calculated according to the above equations (1) to (4). The specific configurations of two exemplary panels AGL-1 and AGL-2 and the parameter values of the above equations (1) to (4) are summarized in the following tables 18 and 19, respectively.

TABLE 18 AGL-1 configuration and equivalent refractive index parameters

TABLE 19 AGL-2 configuration and equivalent refractive index parameters

Each glass/air/glass plate formed as described above was then subjected to a ghost image spacing test similar to that described in example 11 above using the apparatus shown in figure 9, except that the captured image formed when the plates were analysed comprised three ghost images instead of one, due to the large difference between the refractive indices of glass and air. For this analysis, the separation between the primary image and the last ghost image is analyzed in determining the ghost image separation distance for each plate. The results of these analyses are summarized in graph form in fig. 14.

While the present invention has been disclosed in connection with the description of certain embodiments, including those presently believed to be the preferred embodiments, the detailed description is intended to be illustrative and should not be taken to limit the scope of the disclosure. As will be appreciated by one of ordinary skill in the art, the present invention includes embodiments other than those described in detail herein. Modifications and variations of the described embodiments may be made without departing from the spirit and scope of the invention.

It is further understood that any range, value, or characteristic given for any single component of the present disclosure can be used interchangeably with any range, value, or characteristic given for any other component of the present disclosure, if compatible, to form embodiments having defined values for each component, as given throughout this document. For example, interlayers comprising poly (vinyl butyral) having a residual hydroxyl content within any of the ranges given, in addition to plasticizer within any of the ranges given, can be formed to form many permutations that are within the scope of the present disclosure but that are too cumbersome to list. Furthermore, unless otherwise indicated, the ranges provided for a genus or class, such as phthalates or benzoates, may also be used for materials within that genus or class members, such as dioctyl terephthalate.

Claims

1. A tapered interlayer comprising at least one polymer layer comprising a poly (vinyl acetal) resin and at least one plasticizer, wherein the polymer layer has a refractive index of at least 1.480, and wherein the interlayer comprises a tapered zone having an overall wedge angle of no greater than 0.85 mrad.

2. The interlayer of claim 1, wherein said tapered zone has an overall wedge angle of less than 0.55 mrad and wherein said polymer layer has a refractive index of at least 1.500.

3. The interlayer of claim 1 or 2, wherein said interlayer is a monolithic interlayer.

4. The interlayer of claim 1 or 2, wherein said interlayer is a multilayer interlayer comprising said polymer layer and another polymer layer adjacent to said polymer layer, wherein the difference between the glass transition temperature of said polymer layer and the glass transition temperature of said another polymer layer is at least 3 ℃.

5. The interlayer of claim 4, wherein said another polymer layer comprises a second poly (vinyl acetal) resin and at least one plasticizer, wherein the difference between the residual hydroxyl content of said poly (vinyl acetal) resin in said polymer layer and the residual hydroxyl content of said second poly (vinyl acetal) resin in said another polymer layer is at least 2 weight percent.

6. The interlayer of any of claims 1-5, wherein said tapered zone comprises at least one variable angle zone having a curved thickness profile and a continuously varying wedge angle.

7. The interlayer of any of claims 1-6, wherein said tapered zone comprises at least one constant angle zone having a linear thickness profile and a constant wedge angle.

8. A multiwall sheet comprising a pair of rigid substrates and the interlayer of any of claims 1-7, wherein the interlayer is disposed between the pair of rigid substrates and wherein the rigid substrates have a total thickness of less than 4.0 mm.

9. A multiwall sheet, comprising:

a pair of rigid substrates; and

the interlayer of any of claims 1-7 disposed between said substrates,

wherein the multilayer sheet has an equivalent refractive index that is at least 0.010 higher than the refractive index of each of the rigid substrates.

10. The sheet of claim 9 wherein the refractive index of each of said substrates is at least 20% lower than the refractive index of said interlayer.

11. The sheet of claim 9 wherein said interlayer has a refractive index of at least 1.600.

12. A multilayer sheet comprising

A pair of rigid substrates; and

the tapered interlayer of any of claims 1-7 disposed between said substrates,

wherein the refractive index of the interlayer is at least 5% higher than the refractive index of each of the rigid substrates.

13. The panel of claim 12, wherein said panel has an equivalent refractive index higher than said refractive index of each of said rigid substrates.

14. The panel of claim 12 wherein said interlayer has a minimum thickness of 0.25 to 1.2 mm and a maximum thickness of 0.38 to 2.2 mm, wherein the difference between the minimum thickness of said interlayer and the maximum thickness of said interlayer is at least 0.13 mm, and wherein the total thickness of each of said rigid substrates is less than 4.0 mm.