The present disclosure relates generally to cold bent glass and, more specifically, to a curved structural glazing composite, a method of preparing the curved structural glazing composite, and a building including the curved structural glazing composite.
Modern construction has increasingly utilized free form (curved) glass façades in building architecture. Structural sealant glazing (SSG), for example, involves the use of large glass panels that are integral to the design of a building. The glass panels are bonded back to a support structure such as an aluminum frame using a silicone sealant. The glass panels are then bent into the desired curved shape. Cold bending and hot bending are two methods of forming the bent glass panels. Cold bending processes are more cost efficient than hot bending processes. In cold bending, a flat glass panel (either monolithic glass or laminated glass) is bonded to a metal frame by a silicone sealant, and then elastically deformed without the application of heat to follow the desired façade contours.
Unlike hot bending processes, cold bending imposes a permanent bending force onto the silicone sealant as the bent glass naturally attempts to return to its initial flat shape, stressing the sealant joint. Thus, two technical challenges in cold bent glass applications using silicone structural sealant are silicone sealant creep and silicone sealant tear failure. Silicone sealant creep is driven by the relaxation of silicone sealant under constant load, and it increases proportionally in relation to the initial strain applied onto the silicone sealant during the cold bending operation. Sealant creep can lead to deformation of the cold bent glass structure. Tear failure can occur in the silicone sealant after the cold bending operation. Sealant tear failure is caused by an excessive maximum principal strain inside the sealant layer, and is directed related to the durability (i.e. longevity) of the cold bent glass structure. Minimizing sealant creep and tear failure are therefore important to increasing the service life of cold bent glass structures.
The present disclosure provides a method of preparing a curved structural glazing composite. The method comprises providing an initial composite comprising a metal frame and a glass panel with a silicone sealant disposed therebetween. The method further comprises cold bending the initial composite to give the curved structural glazing composite. A ratio of a thickness of the metal frame to a thickness of the silicone sealant in the curved structural glazing composite is less than 10.
In specific embodiments, cold bending is carried out without the application of heat.
In particular embodiments, the metal frame defines an internal cavity, and the ratio of a thickness of the metal frame to a thickness of the silicone sealant is less than 7.
In particular embodiments, the ratio of a thickness of the metal frame to a thickness of the silicone sealant is less than 4.
In particular embodiments, the metal frame and the silicone sealant are continuous about a perimeter of the glass panel and define an internal gap adjacent the glass panel.
In particular embodiments, the silicone sealant is only disposed along a portion of the perimeter of the glass panel.
In particular embodiments, the method further includes preparing the initial composite by sandwiching a silicone sealant composition between the metal frame and the glass panel and curing the silicone sealant composition to give the silicone sealant and the initial composite.
In particular embodiments, the metal frame defines a plurality of substantially parallel grooves oriented in a direction transverse to the direction that the initial composite is bent, and the grooves are located on a side of the metal frame opposite of the silicone sealant.
In particular embodiments, the grooves are configured to reduce peak maximum principal strain in the silicone sealant by at least 8 percentage points.
In particular embodiments, the method further includes calculating a correlation between the peak maximum principal strain and the durability of the silicone sealant of the curved structural glazing composite.
In certain embodiments, the peak maximum principal strain is less than 35%.
A curved structural glazing composite formed in accordance with the method is also provided, along with a building comprising the curved structural glazing composite. The curved structural glazing composite includes a metal frame and a glass panel with a silicone sealant disposed therebetween. A ratio of a thickness of the metal frame to a thickness of the silicone sealant is less than 10.
Various advantages and aspects of this disclosure may be understood in view of the following detailed description when considered in connection with the accompanying drawings, wherein:
A method of preparing a curved structural glazing composite (the “curved composite”) and the curved composite formed thereby is provided herein. As will be understood from the description herein, the curved composite provides for improved durability of a silicone sealant bond between a glass panel and a metal frame of the curved composite. The curved composite reduces both sealant creep (deformation of the silicone sealant in the curved composite) as well as sealant tear failure in the curved composite. The curved composite may therefore have an increased longevity as compared to conventional curved structural glazing composites formed via a cold bending process.
As shown in
The metal frame 32 may be made primarily of aluminum, although the metal frame is not limited to aluminum and may include other metals or alloys or may be made primarily of another metal. The metal frame 32 also may have either a solid cross-section as shown in the initial composite 30′ of
The metal frame 32, 32′ and the silicone sealant 36 may be continuous along a perimeter of the glass panel 34 and may define an internal gap 40 adjacent the glass panel as shown in
The initial composite 30, 30′, 30″ may be obtained commercially or, in other embodiments, the method further comprises forming or preparing the initial composite. The initial composite is typically formed by sandwiching a silicone sealant composition between the metal frame and the glass panel and curing the silicone sealant composition to give the silicone sealant and the initial composite. By way of example, the silicone sealant composition is typically applied on the metal frame, and the glass panel is disposed on the silicone sealant composition to sandwich the silicone sealant composition between the metal frame and the glass panel. In other embodiments, however, the silicone sealant composition may be disposed on the glass panel, with the metal frame disposed on the silicone sealant composition to sandwich the silicone sealant composition between the metal frame and the glass panel. The order of addition with respect to preparing the initial composite is not limited.
In some embodiments, the silicone sealant composition is cured after being sandwiched between the metal frame and the glass panel, to form the initial composite prior to cold bending. However, the silicone sealant composition can be cured contemporaneously with cold bending the initial composite and/or after cold bending the initial composite. Further still, the silicone sealant composition may initiate cure prior to cold bending the initial composite, and continue to cure throughout any step of the method of preparing the curved composite.
In certain embodiments, the silicone sealant composition comprises a condensation-curable silicone composition.
The condensation-curable silicone composition typically comprises (A) an organopolysiloxane having an average of at least two silicon-bonded hydroxyl or hydrolysable groups per molecule; optionally (B) an organosilicon compound having an average of at least two silicon-bonded hydrogen atoms, hydroxyl groups, or hydrolysable groups per molecule; and (C) a condensation catalyst. Although any parameter or condition may be selectively controlled during the inventive method or any individual step thereof, relative humidity and/or moisture content of ambient conditions may be selectively controlled to further impact a cure rate of condensation-curable silicone compositions.
The organopolysiloxane (A) and the organosilicon compound (B) may independently be linear, branched, cyclic, or resinous. In particular, the organopolysiloxane (A) and the organosilicon compound (B) may comprise any combination of M, D, T, and Q units. The symbols M, D, T, and Q represent the functionality of structural units of organopolysiloxanes. M represents the monofunctional unit R03SiO1/2. D represents the difunctional unit R02SiO2/2. T represents the trifunctional unit R0SiO3/2. Q represents the tetrafunctional unit SiO4/2. Generic structural formulas of these units are shown below:
In these structures/formulae, each R0 may be any hydrocarbon, aromatic, aliphatic, alkyl, alkenyl, or alkynl group.
The particular organopolysiloxane (A) and organosilicon compound (B) may be selected based on desired properties of the silicone sealant.
For example, in certain embodiments, one of the organopolysiloxane (A) and the organosilicon compound (B) comprises a silicone resin, which typically comprises T and/or Q units in combination with M and/or D units. When the organopolysiloxane (A) and/or organosilicon compound (B) comprises a silicone resin, the silicone resin may be a DT resin, an MT resin, an MDT resin, a DTQ resin, an MTQ resin, an MDTQ resin, a DQ resin, an MQ resin, a DTQ resin, an MTQ resin, or an MDQ resin. Generally, when the condensation-curable silicone composition comprises a resin, the silicone sealant has increased rigidity.
Alternatively, in other embodiments, the organopolysiloxane (A) and/or the organosilicon compound (B) is an organopolysiloxane comprising repeating D units. Such organopolysiloxanes are substantially linear but may include some branching attributable to T and/or Q units. Alternatively, such organopolysiloxanes are linear. In these embodiments, the silicone sealant is elastomeric.
The silicon-bonded hydroxyl groups and silicon-bonded hydrogen atoms, hydroxyl groups, or hydrolysable groups of the organopolysiloxane (A) and the organosilicon compound (B), respectively, may independently be pendent, terminal, or in both positions.
As known in the art, silicon-bonded hydroxyl groups result from hydrolyzing silicon-bonded hydrolysable groups. These silicon-bonded hydroxyl groups may condense to form siloxane bonds with water as a byproduct.
Examples of hydrolysable groups include the following silicon-bonded groups: H, a halide group, an alkoxy group, an alkylamino group, a carboxy group, an alkyliminoxy group, an alkenyloxy group, or an N-alkylamido group. Alkylamino groups may be cyclic amino groups.
In a specific embodiment, the organopolysiloxane (A) has the general formula:
(R1R32SiO1/2)w(R32SiO2/2)x(R3SiO3/2)y(SiO4/2)z (II)
wherein each R1 is defined above and each R3 is independently selected from R1 and a hydroxyl group, a hydrolysable group, or combinations thereof with the proviso that at least two of R3 are hydroxyl groups, hydrolysable groups, or combinations thereof, and w, x, y, and z are mole fractions such that w+x+y+z=1. As understood in the art, for linear organopolysiloxanes, subscripts y and z are generally 0, whereas for resins, subscripts y and/or z>0. Various alternative embodiments are described below with reference to w, x, y and z. In these embodiments, the subscript w may have a value of from 0 to 0.9999, alternatively from 0 to 0.999, alternatively from 0 to 0.99, alternatively from 0 to 0.9, alternatively from 0.9 to 0.999, alternatively from 0.9 to 0.999, alternatively from 0.8 to 0.99, alternatively from 0.6 to 0.99. The subscript x typically has a value of from 0 to 0.9, alternatively from 0 to 0.45, alternatively from 0 to 0.25. The subscript y typically has a value of from 0 to 0.99, alternatively from 0.25 to 0.8, alternatively from 0.5 to 0.8. The subscript z typically has a value of from 0 to 0.99, alternatively from 0 to 0.85, alternatively from 0.85 to 0.95, alternatively from 0.6 to 0.85, alternatively from 0.4 to 0.65, alternatively from 0.2 to 0.5, alternatively from 0.1 to 0.45, alternatively from 0 to 0.25, alternatively from 0 to 0.15.
As set forth above, the condensation-curable silicone composition further comprises the organosilicon compound (B). The organosilicon compound (B) may be linear, branched, cyclic, or resinous. In one embodiment, the organosilicon compound (B) has the formula R1qSix4-q, wherein R1 is defined above, X is a hydrolysable group, and q is 0 or 1.
Specific examples of organosilicon compounds (B) include alkoxy silanes such as MeSi(OCH3)3, CH3Si(OCH2CH3)3, CH3Si(OCH2CH2CH3)3, CH3Si[O(CH2)3CH3]3, CH3CH2Si(OCH2CH3)3, C6H5Si(OCH3)3, C6H5CH2Si(OCH3)3, C6H5Si(OCH2CH3)3, CH2═CHSi(OCH3)3, CH2═CHCH2Si(OCH3)3, CF3CH2CH2Si(OCH3)3, CH3Si(OCH2CH2OCH3)3, CF3CH2CH2Si(OCH2CH2OCH3)3, CH2═CHSi(OCH2CH2OCH3)3, CH2═CHCH2Si(OCH2CH2OCH3)3, C6H5Si(OCH2CH2OCH3)3, Si(OCH3)4, Si(OC2H5)4, and Si(OC3H7)4; organoacetoxysilanes such as CH3Si(OCOCH3)3, CH3CH2Si(OCOCH3)3, and CH2═CHSi(OCOCH3)3; organoiminooxysilanes such as CH3Si[O—N═C(CH3)CH2CH3]3, Si[O—N═C(CH3)CH2CH3]4, and CH2═CHSi[O—N=C(CH3)CH2CH3]3; organoacetamidosilanes such as CH3Si[NHC(═O)CH3]3 and C6H5Si[NHC(═O)CH3]3; amino silanes such as CH3Si[NH(C4H9)]3 and CH3Si(NHC6H11)3; and organoaminooxysilanes.
The organosilicon compound (B) can be a single organosilicon compound or a mixture of two or more different organosilicon compounds, each as described above. Also, methods of preparing organosilicon compounds are well known in the art; many organosilicon compounds are commercially available.
When present, the concentration of the organosilicon compound (B) in the condensation-curable silicone composition is sufficient to cure (cross-link) the organopolysiloxane (A). The particular amount of the organosilicon compound (B) utilized depends on the desired extent of cure, which generally increases as the ratio of the number of moles of silicon-bonded hydrolysable groups in the organosilicon compound (B) to the number of moles of silicon-bonded hydroxy groups in the organopolysiloxane (A) increases. The optimum amount of the organosilicon compound (B) can be readily determined by routine experimentation.
The condensation catalyst (C) can be any condensation catalyst typically used to promote condensation of silicon-bonded hydroxy (silanol) groups to form Si—O—Si linkages. Examples of condensation catalysts include, but are not limited to, amines; and complexes of lead, tin, zinc, and iron with carboxylic acids. In particular, the condensation catalyst (C1) can be selected from tin (II) and tin (IV) compounds such as tin dilaurate, tin dioctoate, and tetrabutyl tin; and titanium compounds such as titanium tetrabutoxide.
When present, the concentration of the condensation catalyst (C) is typically from 0.1 to 10% (w/w), alternatively from 0.5 to 5% (w/w), alternatively from 1 to 3% (w/w), based on the total weight of the organopolysiloxane (A) in the condensation-curable silicone composition.
When the condensation-curable silicone composition includes the condensation catalyst (C), the condensation-curable silicone composition is typically a two-part composition where the organopolysiloxane (A) and condensation catalyst (C) are in separate parts. In this embodiment, the organosilicon compound (B) is typically present along with the condensation catalyst (C). Alternatively still, the condensation-curable silicone composition may be a three-part composition, where the organopolysiloxane (A), the organosilicon compound (B) and condensation catalyst (C) are in separate parts.
Solidification conditions for such condensation-curable silicone compositions may vary. For example, condensation-curable silicone composition may be solidified or cured upon exposure to ambient conditions and/or heat, although heat is commonly utilized to accelerate solidification and curing.
In specific embodiments, the silicone sealant composition comprises a room temperature vulcanizable (RTV) silicone compositions (hereinafter referred to as “RTV compositions”). Generally, such RTV compositions are condensation-curable and comprise an —OH end-blocked diorganopolysiloxane polymer or an alkoxy end-blocked polydiorganosiloxane which may have an alkylene link between the end silicon atoms and one or more suitable cross-linking agents designed to react with the —OH and/or alkoxy groups and thereby cross-link the composition to form an elastomeric sealant product. One or more additional ingredients such as catalysts, reinforcing fillers, non-reinforcing fillers, diluents (e.g. plasticisers and/or extenders), chain extenders, flame retardants, solvent resistant additives, biocides and the like are often also incorporated into these compositions as and when required. They may be one-part compositions or multiple-part compositions. One-part compositions are generally stored in a substantially anhydrous form to prevent premature cure. In certain embodiments, the primary, if not sole, source of moisture in these compositions are the inorganic fillers, e.g. silica when present. Such fillers may be rendered anhydrous before inter-mixing with other ingredients or water/moisture may be extracted from the mixture during the mixing process to ensure that the resulting silicone sealant composition is substantially anhydrous. RTV silicone compositions are advantageous for the silicone sealant composition given that no discrete or external curing condition, e.g. heat, is necessary to cure. As such, when the silicone sealant composition comprises the RTV composition, no curing condition need be applied to form the silicone sealant from the silicone sealant composition.
The method comprises cold bending the initial composite. In certain embodiments, cold bending is carried out in the absence of any application of heat, e.g. from an external heat source. In particular, the method involves a cold bending process as distinguished from a hot bending process, as known in the art. Cold bending is typically carried out at natural room or ambient temperature (i.e. without the application of heat energy from any external source) to impart a curve in the entire unit as shown by example in
Methods of cold bending are generally known in the art. For example, in one embodiment, cold bending is carried out via a cantilevered beam assembly in which one edge of the initial composite is fixed and an opposite edge is subjected to a bending force. The force utilized to bend the initial composite can be, for example, pneumatically applied, hydraulically applied, or applied via other suitable techniques. Typically, the bending force is applied to one end of the initial composite, and may be repeated at each end of the initial composite, depending on the desired shape and configuration of the curved composite. Alternatively, the bending force may be applied to only one corner of the initial composite while holding the other corners of the composite fixed in a plane (corner clamping). In yet other alternatives, two edges of the initial composite may be fixed, and the free corner may be bent.
The structural durability of the silicone sealant 36 of the curved composite 38 is related to the relative thicknesses of the metal frame 32 and the silicone sealant 36 as measured in a direction from the metal frame through the silicone sealant 36 and glass panel 34 that is perpendicular to the face of the glass panel, as shown in
For example, a 914.4 mm×1524 mm×12 mm glass panel bonded on a 75 mm×20 mm aluminum frame with a 6 mm×20 mm layer of silicone sealant was modeled as shown in
It is believed that the thickness ratio of the metal frame to the silicone sealant is significant to the strain distribution and durability of the curved composite due to its effect on the location of the neutral plane in the curved composite. The neutral plane is a conceptual, imaginary plane within a structure that is stress-free under loading. The neutral plane thereby separates compression and tension regions. When the thickness ratio of the metal frame to the silicone sealant is high (e.g. above 10), the neutral plane is located within the metal frame as shown in
Thus, the peak maximum principal strain in the silicone sealant of the curved composite increases with thickness of the metal frame and decreases with thickness of the silicone sealant, for a given amount of cold bend deflection imparted upon the curved composite. The peak strain is also dependent upon the dimensions of the glass panel, and the type of metal frame (i.e., whether the metal frame is solid or hollow). The definition of maximum principal strain in a simple plane strain state is shown in
where ε1 is the maximum principal strain, εx is the strain in the x-axis, εy is the strain in the y-axis, and γxy is the shear strain. The peak maximum principal strain is the highest value (of maximum principal strain) in the whole structure.
An optimized design formula was established by conducting a simulation-based DOE study. The parameters used in this study are summarized in Table 2 below. It was surprisingly found that in addition to the level of cold bend glass deflection, thicknesses of both the metal frame and the silicone sealant had the most significant effect on the peak strain in the sealant in the cold bent glass operation. The peak maximum principal strain increased with thickness of the metal frame (i.e., peak maximum principal strain was directly proportional to the thickness of the metal frame) and decreased with thickness of the silicone sealant (i.e., peak maximum principal strain was inversely proportional to the thickness of the silicone sealant), as shown in the main effect plot of
The peak strain in the silicone sealant for a curved composite with a solid metal frame subjected to cold bending may thus be calculated according to the following Equation (2):
Based on Equation 2 above, the durability of the silicone sealant in the curved composite can be calculated through a strain-durability relationship established for the silicone sealant, as shown in Tables 3-5 below as well as
An optimized design formula for a curved composite where the metal frame was hollow was also established by conducting a simulation-based DOE study, as shown in the main effect plot in
Based on Equation 3 above, the durability of the silicone sealant joint can be calculated through a strain-durability relationship established for the silicone sealant, as shown in Tables 6 and 7 below as well as
A case study was further performed to test the efficacy of the obtained design equations. Specifically, a cold bent glass design was evaluated using Equation (3) and compared with the durability/sealant failure for this design observed in the field. The effective thickness of the metal frame was 130 mm, the metal frame was hollow, the thickness ratio was 16.25, the glass panel had dimensions of 1535 mm×1632 mm, and the curved composite was subjected to a deflection of 23.9 mm. The peak strain was calculated by Equation (3) to be 52.37%. The corresponding durability of the silicone sealant was estimated to be 1.4 years. This durability estimate was close to the actual service life of this design reported from the field, which was approximately 1 year. These results are summarized in Table 8 below.
In certain embodiments, the peak strain may also be reduced by providing a plurality of substantially parallel grooves 52 in the metal frame 32″, the grooves being oriented in a direction transverse to the direction of cold bending of the curved composite. The grooves 52 may be located on a side of the metal frame 32″ opposite the silicone sealant 36 as shown in
The groove depth is a distance from a groove opening in the surface of the frame to the bottom of the groove opposite the groove opening, and the groove spacing is a distance between two adjacent grooves.
The grooves may have one of a variety of configurations that affects the level of peak strain, such as but not limited to a round groove chamfer 52 shown in
The curved composites of this disclosure can be utilized in myriad end use applications, including residential and commercial buildings, passenger and commercial vehicles, public transportation, and any other end use applications requiring bent glass.
The invention has been described in an illustrative manner, and it is to be understood that the terminology which has been used is intended to be in the nature of words of description rather than of limitation. Obviously, many modifications and variations of the present invention are possible in light of the above teachings. The invention may be practiced otherwise than as specifically described.
This application claims the benefit of U.S. Provisional Application No. 63/295,549, filed Dec. 31, 2021, the disclosure of which is incorporated by reference in its entirety.
Filing Document | Filing Date | Country | Kind |
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PCT/US2022/054169 | 12/28/2022 | WO |
Number | Date | Country | |
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63295549 | Dec 2021 | US |