POLYCARBONATE BASED RAPID DEPLOYMENT COVER SYSTEM
20170074034 ยท 2017-03-16
Assignee
Inventors
- James M. Lorenzo (Mars, PA, US)
- Robert A. Pyles (Bethel Park, PA)
- David Rocco (Bridgeville, PA, US)
- Jessica Boyer (Coraopolis, PA, US)
- Keith Whalen (Great Barrington, MA, US)
Cpc classification
E06B5/10
FIXED CONSTRUCTIONS
E06B9/02
FIXED CONSTRUCTIONS
E06B3/30
FIXED CONSTRUCTIONS
International classification
E06B9/02
FIXED CONSTRUCTIONS
E06B3/30
FIXED CONSTRUCTIONS
E04H9/14
FIXED CONSTRUCTIONS
Abstract
The present invention provides a rapid deployment cover system comprising a polycarbonate laminate or a glass-clad polycarbonate laminate in combination with a versatile and cushioned mounting system to yield a highly durable cover which provides protection from forced-entry, blast, ballistics and/or extreme storms in a wide range of climates.
Claims
1. A rapid deployment cover system for a wall having an opening, the system comprising: a mounting track attached to the wall; a polycarbonate laminate having a first side adjacent to the mounting track, a second side and a plurality of holes through the first and second sides; a pressure plate adjacent to the second side of the polycarbonate laminate; a first plurality of bolts, wherein each such bolt is fixedly attached to the pressure plate, and passes through a corresponding hole in the polycarbonate laminate; and a plurality of elastomeric sleeves, wherein each such sleeve is situated substantially around a bolt and within a hole of the polycarbonate laminate.
2. The rapid deployment cover system of claim 1, wherein the first plurality of bolts is fixedly attached to both the pressure plate and the mounting track, and the mounting track is attached to the wall by a second plurality of bolts.
3. The rapid deployment cover system of claim 2, wherein the mounting track is attached to the wall by 4 to 8 bolts of the second plurality of bolts.
4. The rapid deployment cover system of claim 1, wherein the first plurality of bolts is fixedly attached to the wall.
5. The rapid deployment cover system of claim 4, wherein the mounting track is attached to the wall by 4 to 8 bolts.
6. The rapid deployment cover system of claim 1, further comprising one or more shims disposed between the mounting plate and the wall.
7. The rapid deployment cover system of claim 6, wherein the shims are constructed of an elastomeric material.
8. The rapid deployment cover system of claim 6, wherein the shims create a space of at least 0.25 inches between the wall and the mounting plate.
9. The rapid deployment cover system of claim 1, wherein the first plurality of bolts are spaced at least 3 inches apart from each another.
10. The rapid deployment cover system of claim 9, wherein the first plurality of bolts are spaced at least 6 inches apart from each another.
11. The rapid deployment cover system of claim 1, wherein the plurality of holes in the polycarbonate laminate are about 2 inches in diameter.
12. The rapid deployment cover system of claim 1, wherein at least one of the plurality of holes in the polycarbonate laminate has a diameter of about 3.7 times the thickness of an elastomeric sleeve.
13. The rapid deployment cover system of claim 1, wherein at least one of the elastomeric sleeves has a thickness of about 0.535 inches.
14. The rapid deployment cover system of claim 1, wherein at least one of the elastomeric sleeves has a Shore A hardness of about 35 to about 45.
15. The rapid deployment cover system of claim 1, wherein at least one of the elastomeric sleeves has a tensile strength of about 1450 psi.
16. The rapid deployment cover system of claim 1, wherein at least one of the elastomeric sleeves is constructed of ethylene propylene diene monomer (EPDM).
17. The rapid deployment cover system of claim 1, further comprising at least one bushing disposed between a bolt and an elastomeric sleeve.
18. The rapid deployment cover system of claim 1, wherein the polycarbonate laminate comprises at least one edge, and the plurality of holes in the polycarbonate laminate are located at least 0.25 inches away from the at least one edge of the polycarbonate laminate.
19. The rapid deployment cover system of claim 18, wherein the plurality of holes in the polycarbonate laminate are located at least 3 inches away from the at least one edge of the polycarbonate laminate.
20. The rapid deployment cover system of claim 1, further comprising a pressure plate cover.
21. A method for installing a cover to a wall having an opening, the method comprising: A) drilling and installing 4 to 8 anchor holes in the wall around the opening; B) fixing a mounting track to the 4 to 8 anchor holes in the wall; and C) hanging a polycarbonate laminate having a first side adjacent to the mounting track, a second side and a plurality of holes through the first and second sides, (i) through the use of a pressure plate adjacent to the second side of the polycarbonate laminate, and (ii) also through the use of a first plurality of bolts, wherein each such bolt is fixedly attached to the pressure plate at one end, and passes through an elastomeric sleeve and a hole of the polycarbonate laminate.
22. The method of claim 21, wherein the first plurality of bolts is fixedly attached to both the pressure plate and the mounting track, and the mounting track is attached to the wall by a second plurality of bolts.
23. The method of claim 19, wherein the first plurality of bolts is fixedly attached to the wall.
24. The method of claim 19, further comprising: D) installing one or more shims between the mounting plate and the wall.
25. The method of claim 24, wherein the shims create a space of at least 0.25 inches between the wall and the mounting plate.
26. The method of claim 21, wherein the first plurality of bolts are spaced at least 3 inches apart from each another.
27. The method of claim 26, wherein the first plurality of bolts are spaced at least 6 inches apart from each another.
28. The method of claim 21, wherein the plurality of holes in the polycarbonate laminate are about 2 inches in diameter.
29. The method of claim 21, wherein at least one of the plurality of holes in the polycarbonate laminate has a diameter of about 3.7 times the thickness of an elastomeric sleeve.
30. The method of claim 21, wherein each of the first plurality of bolts passes through a bushing.
31. The method of claim 21, wherein the polycarbonate laminate comprises at least one edge, and the plurality of holes in the polycarbonate laminate are located at least 0.25 inches away from the at least one edge of the polycarbonate laminate.
32. The method of claim 31, wherein the plurality of holes in the polycarbonate laminate are located at least 3 inches away from the at least one edge of the polycarbonate laminate.
33. The method of claim 21, further comprising: E) installing a pressure plate cover.
Description
BRIEF DESCRIPTION OF THE FIGURES
[0046] The present invention will now be described for purposes of illustration and not limitation in conjunction with the figures, wherein:
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DETAILED DESCRIPTION OF THE INVENTION
[0127] The present invention will now be described for purposes of illustration and not limitation. Except in the operating examples, or where otherwise indicated, all numbers expressing quantities, percentages, and so forth in the specification are to be understood as being modified in all instances by the term about.
[0128] The present invention provides a rapid deployment cover system comprising a polycarbonate laminate or a glass-clad polycarbonate laminate in combination with a versatile and cushioned mounting system to provide a highly durable cover over building openings (e.g., architectural openings such as windows and doors, and non-architectural openings such as those openings created by bullets, shells and explosives) which provides protection from forced-entry, ballistics and/or extreme storms in a wide range of climates. The polycarbonate laminate or glass-clad polycarbonate laminate may be opaque, translucent or transparent.
[0129] Such laminates may be designed to be held in place by a framing system attached to the building, and surrounding the individual building openings. The framing system must compensate for the following: the coefficient of thermal expansion of polymeric materials, and associated expansion and contraction; the weight of the covers, some in excess of 750 lbs. (340 kg); different building architectures and materials of construction; chemical compatibility of all components; and potential for fastener misalignments and lack of building wall flatness and squareness. Moreover, the installed panels and framing must be forced entry and ballistics certified. The present invention also provides an adjustable framing system and a cushioned mounting system that meets all the above criteria.
[0130] The polycarbonate panels useful in the inventive laminate are preferably transparent, but there are situations where the panels may be translucent, or even opaque.
[0131] All panels, whether transparent, translucent or opaque, may be also fabricated to include decorative elements such as artwork, graphics and natural grasses. Further, the transparent panels may be fabricated to include mirrored surfaces or graphics which permit one-way viewing from inside a darkened building to the brighter exterior.
[0132] Suitable polycarbonate resins for preparing the panels useful in the laminates of the present invention are homopolycarbonates and copolycarbonates, both linear or branched resins and mixtures thereof. Such polycarbonates have a weight average molecular weight (as determined by gel permeation chromatography, or size-exclusion chromatography) of preferably 10,000 to 200,000, more preferably 20,000 to 80,000 and a melt flow rate, per ASTM D-1238 at 300 C., of preferably 1 to 65 g/10 min., more preferably 2 to 35 g/10 min. The polycarbonates may be prepared, for example, by the known diphasic interface process from a carbonic acid derivative such as phosgene and dihydroxy compounds by polycondensation (See, German Offenlegungsschriften 2,063,050; 2,063,052; 1,570,703; 2,211,956; 2,211,957 and 2,248,817; French Patent 1,561,518; and the monograph by H. Schnell, Chemistry and Physics of Polycarbonates, Interscience Publishers, New York, N.Y., 1964).
[0133] In the present context, dihydroxy compounds suitable for the preparation of the polycarbonates of the invention conform to the structural formulae (1) or (2) below.
##STR00001##
[0134] Wherein A denotes an alkylene group with 1 to 8 carbon atoms, an alkylidene group with 2 to 8 carbon atoms, a cycloalkylene group with 5 to 15 carbon atoms, a cycloalkylidene group with 5 to 15 carbon atoms, a carbonyl group, an oxygen atom, a sulfur atom, SO or SO.sub.2 or a radical conforming to (3)
##STR00002##
[0135] e and g both denote the number 0 to 1;
[0136] Z denotes F, Cl, Br or C.sub.1-C.sub.4-alkyl and if several Z radicals are substituents in one aryl radical, they may be identical or different from one another;
[0137] d denotes an integer of from 0 to 4; and
[0138] f denotes an integer of from 0 to 3.
[0139] Among the dihydroxy compounds useful in the practice of the invention are hydroquinone, resorcinol, bis-(hydroxyphenyl)-alkanes, bis-(hydroxyl-phenyl)-ethers, bis-(hydroxyphenyl)-ketones, bis-(hydroxyl-phenyl)-sulfoxides, bis-(hydroxyphenyl)-sulfides, bis-(hydroxyphenyl)-sulfones, and ,-bis-(hydroxyphenyl)-diisopropylbenzenes, as well as their nuclear-alkylated compounds. These and further suitable aromatic dihydroxy compounds are described, for example, in U.S. Pat. Nos. 5,401,826, 5,105,004; 5,126,428; 5,109,076; 5,104,723; 5,086,157; 3,028,356; 2,999,835; 3,148,172; 2,991,273; 3,271,367; and 2,999,846, the contents of which are incorporated herein by reference.
[0140] Further examples of suitable bisphenols are 2,2-bis-(4-hydroxyphenyl)-propane (bisphenol A), 2,4-bis-(4-hydroxyphenyl)-2-methyl-butane, 1,1-bis-(4-hydroxyphenyl)-cyclohexane, ,-bis-(4-hydroxy-phenyl)-p-diisopropylbenzene, 2,2-bis-(3-methyl-4-hydroxyphenyl)-propane, 2,2-bis-(3-chloro-4-hydroxyphenyl)-propane, 4,4-dihydroxy-diphenyl, bis-(3,5-dimethyl-4-hydroxyphenyl)-methane, 2,2-bis-(3,5-dimethyl-4-hydroxyphenyl)-propane, bis-(3,5-dimethyl-4-hydroxyphenyl)-sulfide, bis-(3,5-dimethyl-4-hydroxy-phenyl)-sulfoxide, bis-(3,5-dimethyl-4-hydroxyphenyl)-sulfone, dihydroxy-benzophenone, 2,4-bis-(3,5-dimethyl-4-hydroxyphenyl)-cyclohexane, ,-bis-(3,5-dimethyl-4-hydroxyphenyl)-p-diisopropyl-benzene and 4,4-sulfonyl diphenol.
[0141] Examples of particularly preferred aromatic bisphenols are 2,2-bis-(4-hydroxyphenyl)-propane, 2,2-bis-(3,5-dimethyl-4-hydroxyphenyl)-propane, 1,1-bis-(4-hydroxyphenyl)-cyclohexane and 1,1-bis-(4-hydroxy-phenyl)-3,3,5-trimethylcyclohexane. The most preferred bisphenol is 2,2-bis-(4-hydroxyphenyl)-propane (bisphenol A).
[0142] The polycarbonates useful in producing the laminates of the invention may entail in their structure units derived from one or more of the suitable bisphenols.
[0143] Among the resins suitable in the practice of the invention are phenolphthalein-based polycarbonate, copolycarbonates and terpolycarbonates such as are described in U.S. Pat. Nos. 3,036,036 and 4,210,741, both of which are incorporated by reference herein.
[0144] The polycarbonates useful in preparing the laminates of the invention may also be branched by condensing therein small quantities, e.g., 0.05 to 2.0 mol % (relative to the bisphenols) of polyhydroxyl compounds. Polycarbonates of this type have been described, for example, in German Offenlegungsschriften 1,570,533; 2,116,974 and 2,113,374; British Patents 885,442 and 1,079,821 and U.S. Pat. No. 3,544,514, which is incorporated herein by reference. The following are some examples of polyhydroxyl compounds which may be used for this purpose: phloroglucinol; 4,6-dimethyl-2,4,6-tri-(4-hydroxy-phenyl)-heptane; 1,3,5-tri-(4-hydroxyphenyl)-benzene; 1,1,1-tri-(4-hydroxyphenyl)-ethane; tri-(4-hydroxyphenyl)-phenyl-methane; 2,2-bis-[4,4-(4,4-dihydroxydiphenyl)]-cyclohexyl-propane; 2,4-bis-(4-hydroxy-1-isopropylidine)-phenol; 2,6-bis-(2-dihydroxy-5-methylbenzyl)-4-methyl-phenol; 2,4-dihydroxybenzoic acid; 2-(4-hydroxy-phenyl)-2-(2,4-dihydroxy-phenyl)-propane and 1,4-bis-(4,4-dihydroxytri-phenylmethyl)-benzene. Some of the other polyfunctional compounds are 2,4-dihydroxy-benzoic acid, trimesic acid, cyanuric chloride and 3,3-bis-(4-hydroxyphenyl)-2-oxo-2,3-dihydroindole.
[0145] In addition to the polycondensation process mentioned above, other processes for the preparation of the polycarbonates of the invention are polycondensation in a homogeneous phase and transesterification. Suitable processes are disclosed in U.S. Pat. Nos. 3,028,365; 2,999,846; 3,153,008; and 2,991,273 which are incorporated herein by reference.
[0146] The preferred process for the preparation of polycarbonates is the interfacial polycondensation process. Other methods of synthesis in forming the polycarbonates useful in the invention, such as disclosed in U.S. Pat. No. 3,912,688, incorporated herein by reference, may be used. Suitable polycarbonate resins are available in commerce, for instance, from Bayer MaterialScience under the MAKROLON trademark. The polycarbonate is preferably used in the form of panels, (sheets) or films in the laminates. Suitable polycarbonate laminates are available from Bayer MaterialScience under the HYGARD trademark.
[0147] Aliphatic thermoplastic polyurethanes are preferred in the laminate useful in the present invention such as those prepared according to U.S. Pat. No. 6,518,389, the entire contents of which are incorporated herein by reference. Particularly preferred are thermoplastic polyurethane based on aliphatic chemistries to resist color changes from ultraviolet radiation exposure, especially ultraviolet radiation such as found in natural sunlight.
[0148] Thermoplastic polyurethane elastomers are well known to those skilled in the art. They are of commercial importance due to their combination of high-grade mechanical properties with the known advantages of cost-effective thermoplastic processability. A wide range of variation in their mechanical properties can be achieved by the use of different chemical synthesis components. A review of thermoplastic polyurethanes, their properties and applications is given in Kunststoffe [Plastics] 68 (1978), pages 819 to 825, and in Kautschuk, Gummi, Kunststoffe [Natural and Vulcanized Rubber and Plastics] 35 (1982), pages 568 to 584.
[0149] Thermoplastic polyurethanes are synthesized from linear polyols, mainly polyester diols or polyether diols, organic diisocyanates and short chain diols (chain extenders). Catalysts may be added to the reaction to speed up the reaction of the components.
[0150] The relative amounts of the components may be varied over a wide range of molar ratios in order to adjust the properties. Molar ratios of polyols to chain extenders from 1:1 to 1:12 have been reported. These result in products with hardness values ranging from 80 Shore A to 75 Shore D.
[0151] Thermoplastic polyurethanes can be produced either in stages (prepolymer method) or by the simultaneous reaction of all the components in one step (one shot). In the former, a prepolymer formed from the polyol and diisocyanate is first formed and then reacted with the chain extender. Thermoplastic polyurethanes may be produced continuously or batch-wise. The best-known industrial production processes are the so-called belt process and the extruder process.
[0152] Examples of the suitable polyols include difunctional polyether polyols, polyester polyols, and polycarbonate polyols. Small amounts of trifunctional polyols may be used, yet care must be taken to make certain that the thermoplasticity of the thermoplastic polyurethane remains substantially un-effected.
[0153] Suitable polyester polyols include those which are prepared by polymerizing -caprolactone using an initiator such as ethylene glycol, ethanolamine and the like. Further suitable examples are those prepared by esterification of polycarboxylic acids. The polycarboxylic acids may be aliphatic, cycloaliphatic, aromatic and/or heterocyclic and they may be substituted, e.g., by halogen atoms, and/or unsaturated. The following are mentioned as examples: succinic acid; adipic acid; suberic acid; azelaic acid; sebacic acid; phthalic acid; isophthalic acid; trimellitic acid; phthalic acid anhydride; tetrahydrophthalic acid anhydride; hexahydrophthalic acid anhydride; tetrachlorophthalic acid anhydride, endomethylene tetrahydrophthalic acid anhydride; glutaric acid anhydride; maleic acid; maleic acid anhydride; fumaric acid; dimeric and trimeric fatty acids such as oleic acid, which may be mixed with monomeric fatty acids; dimethyl terephthalates and bis-glycol terephthalate. Suitable polyhydric alcohols include, e.g., ethylene glycol; propylene glycol-(1,2) and -(1,3); butylene glycol-(1,4) and -(1,3); hexanediol-(1,6); octanediol-(1,8); neopentyl glycol; (1,4-bis-hydroxy-methylcyclohexane); 2-methyl-1,3-propanediol; 2,2,4-tri-methyl-1,3-pentanediol; triethylene glycol; tetraethylene glycol; polyethylene glycol; dipropylene glycol; polypropylene glycol; dibutylene glycol and polybutylene glycol, glycerine and trimethlyolpropane.
[0154] Suitable polyisocyanates for producing the thermoplastic polyurethanes useful in the laminates may be, for example, organic aliphatic diisocyanates including, for example, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 2,2,4-trimethyl-1,6-hexamethylene diisocyanate, 1,12-dodecamethylene diisocyanate, cyclohexane-1,3- and -1,4-diisocyanate, 1-isocyanato-2-isocyanatomethylcyclopentane, 1-isocyanato-3-isocyanatomethyl-3,5,5-trimethyl-cyclohexane (isophorone diisocyanate or IPDI), bis-(4-isocyanatocyclohexyl)-methane, 2,4-dicyclohexylmethane diisocyanate, 1,3- and 1,4-bis-(isocyanatomethyl)-cyclohexane, bis-(4-isocyanato-3-methylcyclohexyl)-methane, ,,,-tetramethyl-1,3- and/or -1,4-xylylene diisocyanate, 1-isocyanato-1-methyl-4(3)-isocyanatomethyl cyclohexane, 2,4- and/or 2,6-hexahydrotoluylene diisocyanate, and mixtures thereof.
[0155] Preferred chain extenders with molecular weights of 62 to 500 include aliphatic diols containing 2 to 14 carbon atoms, such as ethanediol, 1,6-hexanediol, diethylene glycol, dipropylene glycol, and 1,4-butanediol in particular, for example. However, diesters of terephthalic acid with glycols containing 2 to 4 carbon atoms are also suitable, such as terephthalic acid-bis-ethylene glycol or -1,4-butanediol for example, or hydroxyalkyl ethers of hydroquinone, such as 1,4-di-(-hydroxyethyl)-hydroquinone for example, or (cyclo)aliphatic diamines, such as isophorone diamine, 1,2- and 1,3-propylenediamine, N-methyl-propylenediamine-1,3 or N,N-dimethyl-ethylenediamine, for example, and aromatic diamines, such as toluene 2,4- and 2,6-diamines, 3,5-diethyltoluene 2,4- and/or 2,6-diamine, and primary ortho-, di-, tri- and/or tetraalkyl-substituted 4,4-diaminodiphenylmethanes, for example. Mixtures of the aforementioned chain extenders may also be used. Optionally, triol chain extenders having a molecular weight of 62 to 500 may also be used. Moreover, customary monofunctional compounds may also be used in small amounts, e.g., as chain terminators or demolding agents. Alcohols such as octanol and stearyl alcohol or amines such as butylamine and stearylamine may be cited as examples.
[0156] To prepare the thermoplastic polyurethanes, the synthesis components may be reacted, optionally in the presence of catalysts, auxiliary agents and/or additives, in amounts such that the equivalent ratio of NCO groups to the sum of the groups which react with NCO, particularly the OH groups of the low molecular weight diols/triols and polyols, is 0.9:1.0 to 1.2:1.0, preferably 0.95:1.0 to 1.10:1.0.
[0157] Suitable catalysts include tertiary amines which are known in the art, such as triethylamine, dimethyl-cyclohexylamine, N-methylmorpholine, N,N-dimethyl-piperazine, 2-(dimethyl-aminoethoxy)-ethanol, diazabicyclo-(2,2,2)-octane and the like, for example, as well as organic metal compounds in particular, such as titanic acid esters, iron compounds, tin compounds, e.g., tin diacetate, tin dioctoate, tin dilaurate or the dialkyltin salts of aliphatic carboxylic acids such as dibutyltin diacetate, dibutyltin dilaurate or the like. The preferred catalysts are organic metal compounds, particularly titanic acid esters and iron and/or tin compounds.
[0158] In addition to difunctional chain extenders, small quantities of up to about 5 mol. %, based on moles of the bifunctional chain extender used, of trifunctional or more than trifunctional chain extenders may also be used.
[0159] Trifunctional or more than trifunctional chain extenders of the type in question are, for example, glycerol, trimethylolpropane, hexanetriol, pentaerythritol and triethanolamine.
[0160] Suitable thermoplastic polyurethanes are available in commerce, for example, from Bayer MaterialScience under the TEXIN and DUREFLEX trademarks. The thermoplastic polyurethanes are preferably used in the present invention in the form of films or sheets.
[0161] The polycarbonate laminate of the present invention may also include one or more additives that may inhibit harmful effects of sunlight or other radiation, such as UV or IR-blocking additives. In addition, the polycarbonate laminate may further comprise additives, or be composed of materials, which may inhibit the transmission of various radio frequencies, signals or RF-waves. Such compositions or additives may be incorporated into the polycarbonate laminate, or may be in an additional layer that is applied to the surface of the polycarbonate laminate.
[0162] As used herein, the term glass includes not only window glass, plate glass, silicate glass, aluminosilicate glasses, sheet glass, tempered glass, chemically treated glass and float glass, but also colored glass, specialty glass which includes ingredients to control, for example, solar heating, coated glass with, for example, sputtered metals, such as silver or indium tin oxide, for solar control purposes and other specialty glasses. The type and thickness of the glass selected for a particular laminate depends on the intended use.
Example
[0163] The present invention is further illustrated, but is not to be limited, by the following description. The thicknesses and other dimensions provided in describing the various aspects of the invention shown in the Figures are for descriptive purposes and those skilled in the art will recognize the invention is not limited to only those dimensions. The inventive rapid deployment cover system and its elements may be of those dimensions necessary to fulfill the intended purpose.
[0164] In the following descriptions and Figures, the reference numbers are used to refer to the following: 1wall; 21200 mm1200 mm Level 8 forced entry/blast resistant (FEBR) glass-clad polycarbonate laminate; 21200 mm1200 mm Level 3 forced entry/blast resistant (FEBR) polycarbonate laminate; 3track back plate; 4track bars; 5track front plate; 63.5 inch hex bolt; 74 inch hex bolt; 81.75 inch hex bolt; 9glazing tape; 10glazing tape; 11ethylene propylene diene monomer (EPDM) sleeve; 12bushing; 13pressure plate; 14glazing tape; 15glazing tape; 16air baffle; 17setting block; 18pressure plate cover; 19ethylene propylene diene monomer (EPDM) washer; 20lockout, nylon insert; 21steel washer; 22steel washer; 230.5 inch steel split lock washer; 24threaded sleeve element (HILTI HIS-RN); 25injectable mortar (HILTI HIT-HY 150 MAX); 26backer rod; 27perimeter silicone sealant (DOW 995); 28shims; 30tamper-proof nut and matching key (McGard); and 31mounting track.
[0165] In one embodiment of the present invention, as shown in
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[0186] The rapid deployment cover system of the present invention were tested for forced-entry, ballistics and blast resistance with the following results:
TABLE-US-00001 Severe Storm DoE Standard Forced-Entry Blast 1020* (*wind US Dept Ballistics UL (*laminant and tornado Cover Type of State Standard 752 only) hazard only) glass-clad 15R-minute UL 8 *>41 psi compliant polycarbonate simulated assault polycarbonate 15N-minute UL 3 *>41 psi compliant simulated assault
[0187] Also, it is contemplated that any optional feature of the inventive variations described may be set forth and claimed independently, or in combination with any one or more of the features described herein. Reference to a singular item, includes the possibility that there are plural of the same items present. More specifically, as used herein and in the appended claims, the singular forms a, an, said, and the include plural referents unless the specifically stated otherwise. In other words, use of the articles allow for at least one of the subject item in the description above as well as the claims below. It is further noted that the claims may be drafted to exclude any optional element. As such, this statement is intended to serve as antecedent basis for use of such exclusive terminology as solely, only and the like in connection with the recitation of claim elements, or use of a negative limitation. Without the use of such exclusive terminology, the term comprising in the claims shall allow for the inclusion of any additional elementirrespective of whether a given number of elements are enumerated in the claim, or the addition of a feature could be regarded as transforming the nature of an element set forth in the claims. Stated otherwise, unless specifically defined herein, all technical and scientific terms used herein are to be given as broad a commonly understood meaning as possible while maintaining claim validity.
[0188] The foregoing examples of the present invention are offered for the purpose of illustration and not limitation. It will be apparent to those skilled in the art that the embodiments described herein may be modified or revised in various ways without departing from the spirit and scope of the invention. The scope of the invention is to be measured by the appended claims.