JPH06502836A - Method and apparatus for forming double-layer glass panels - Google Patents
Method and apparatus for forming double-layer glass panelsInfo
- Publication number
- JPH06502836A JPH06502836A JP4502255A JP50225591A JPH06502836A JP H06502836 A JPH06502836 A JP H06502836A JP 4502255 A JP4502255 A JP 4502255A JP 50225591 A JP50225591 A JP 50225591A JP H06502836 A JPH06502836 A JP H06502836A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- glass
- film
- assembly
- polyvinyl butyral
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000011521 glass Substances 0.000 title claims description 78
- 238000000034 method Methods 0.000 title claims description 31
- 239000010410 layer Substances 0.000 claims description 154
- 239000004814 polyurethane Substances 0.000 claims description 54
- 229920002635 polyurethane Polymers 0.000 claims description 51
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims description 50
- 229920003023 plastic Polymers 0.000 claims description 31
- 239000004033 plastic Substances 0.000 claims description 31
- 239000002131 composite material Substances 0.000 claims description 22
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 21
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 21
- -1 polyethylene terephthalate Polymers 0.000 claims description 17
- 229920002799 BoPET Polymers 0.000 claims description 15
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- 238000010438 heat treatment Methods 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 238000003856 thermoforming Methods 0.000 claims description 9
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- 238000000465 moulding Methods 0.000 claims description 7
- 229920000728 polyester Polymers 0.000 claims description 7
- 238000007789 sealing Methods 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 238000004873 anchoring Methods 0.000 claims description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 3
- 230000000712 assembly Effects 0.000 claims description 3
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- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 125000003158 alcohol group Chemical group 0.000 claims description 2
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- 239000000806 elastomer Substances 0.000 claims description 2
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 239000004698 Polyethylene Substances 0.000 claims 3
- 229920000573 polyethylene Polymers 0.000 claims 3
- 238000003825 pressing Methods 0.000 claims 2
- CBECDWUDYQOTSW-UHFFFAOYSA-N 2-ethylbut-3-enal Chemical compound CCC(C=C)C=O CBECDWUDYQOTSW-UHFFFAOYSA-N 0.000 claims 1
- 238000005452 bending Methods 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000000835 fiber Substances 0.000 claims 1
- JTHNLKXLWOXOQK-UHFFFAOYSA-N n-propyl vinyl ketone Natural products CCCC(=O)C=C JTHNLKXLWOXOQK-UHFFFAOYSA-N 0.000 claims 1
- 239000002985 plastic film Substances 0.000 claims 1
- 229920006255 plastic film Polymers 0.000 claims 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 1
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical class CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
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- 125000006850 spacer group Chemical group 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
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- 230000008859 change Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- OJXOOFXUHZAXLO-UHFFFAOYSA-M magnesium;1-bromo-3-methanidylbenzene;bromide Chemical compound [Mg+2].[Br-].[CH2-]C1=CC=CC(Br)=C1 OJXOOFXUHZAXLO-UHFFFAOYSA-M 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 239000005336 safety glass Substances 0.000 description 2
- 229920002379 silicone rubber Polymers 0.000 description 2
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- 229920001169 thermoplastic Polymers 0.000 description 2
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- 238000013022 venting Methods 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- JVGPVVUTUMQJKL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl thiocyanate Chemical compound CCCCOCCOCCSC#N JVGPVVUTUMQJKL-UHFFFAOYSA-N 0.000 description 1
- BJUPZVQSAAGZJL-UHFFFAOYSA-N 2-methyloxirane;propane-1,2,3-triol Chemical compound CC1CO1.OCC(O)CO BJUPZVQSAAGZJL-UHFFFAOYSA-N 0.000 description 1
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 1
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000972773 Aulopiformes Species 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- 235000014653 Carica parviflora Nutrition 0.000 description 1
- 244000132059 Carica parviflora Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920013701 VORANOL™ Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000005328 architectural glass Substances 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
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- 238000005266 casting Methods 0.000 description 1
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- 239000003431 cross linking reagent Substances 0.000 description 1
- KQWGXHWJMSMDJJ-UHFFFAOYSA-N cyclohexyl isocyanate Chemical compound O=C=NC1CCCCC1 KQWGXHWJMSMDJJ-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000002355 dual-layer Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
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- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
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- CLXOLTFMHAXJST-UHFFFAOYSA-N esculentic acid Natural products C12CC=C3C4CC(C)(C(O)=O)CCC4(C(O)=O)CCC3(C)C1(C)CCC1C2(C)CCC(O)C1(CO)C CLXOLTFMHAXJST-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 201000003373 familial cold autoinflammatory syndrome 3 Diseases 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 239000005329 float glass Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
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- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
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- 229920000515 polycarbonate Polymers 0.000 description 1
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- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
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Classifications
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- B32—LAYERED PRODUCTS
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- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
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- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
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- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/10009—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets
- B32B17/10018—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets comprising only one glass sheet
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- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
- B32B17/10761—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing vinyl acetal
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
- B32B17/1077—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing polyurethane
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/10807—Making laminated safety glass or glazing; Apparatus therefor
- B32B17/10816—Making laminated safety glass or glazing; Apparatus therefor by pressing
- B32B17/10825—Isostatic pressing, i.e. using non rigid pressure-exerting members against rigid parts
- B32B17/10834—Isostatic pressing, i.e. using non rigid pressure-exerting members against rigid parts using a fluid
- B32B17/10844—Isostatic pressing, i.e. using non rigid pressure-exerting members against rigid parts using a fluid using a membrane between the layered product and the fluid
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B38/00—Ancillary operations in connection with laminating processes
- B32B2038/0052—Other operations not otherwise provided for
- B32B2038/0076—Curing, vulcanising, cross-linking
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2305/00—Condition, form or state of the layers or laminate
- B32B2305/72—Cured, e.g. vulcanised, cross-linked
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/40—Properties of the layers or laminate having particular optical properties
- B32B2307/412—Transparent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/514—Oriented
- B32B2307/518—Oriented bi-axially
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2367/00—Polyesters, e.g. PET, i.e. polyethylene terephthalate
Landscapes
- Joining Of Glass To Other Materials (AREA)
- Laminated Bodies (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるため要約のデータは記録されません。 (57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】 二層ガラスパネルを成5するためのア び装置見凱A1遣 本発明は二層ガラスパネル、特にこのようなパネルを成形するための方法及び装 置に関する。[Detailed description of the invention] Apparatus and equipment for forming double-layer glass panels A1 The present invention relates to double-layer glass panels, particularly methods and apparatus for forming such panels. Regarding the location.
車のフロントガラス、サイドウィンドウ、リアウィンドウ及びサンルーフ並びに 建物の建築用ガラス(例えば天窓、耐衝撃安全ガラス(1ntrusion 5 ecurity glass) 、サンルームのドア等)として使用される合わ せガラスパネルはよく知られている。これらのパネルはガラスの他に、ガラスパ ネルに物体を貫通させずに物体からの打撃を吸収して、周辺区域にいる人に安全 性を提供することのできるエネルギ吸収プラスチック層を含んでいる。Car windshields, side windows, rear windows, sunroofs, and Architectural glass for buildings (e.g. skylights, impact-resistant safety glass (1ntrusion 5) safety glass), sunroom doors, etc.) Glass panels are well known. These panels are made of glass as well as Absorbs blows from objects without penetrating the flannel, making it safe for people in the surrounding area Contains an energy-absorbing plastic layer that can provide
市販の合わせガラスパネルは通常、エネルギ吸収層の両側に夫々一枚のガラスを 有する。この三層構造に代わる構造は、通常二つ以上の層からなるプラスチック 内層に対して一枚のガラスを有する二層である。内側のガラス層がないために、 軽量化される他に、二層ガラスを壊すのに十分な衝撃が生じたときに、室内又は 車室内でガラスの破片から被る危険性が大幅に減少する。Commercially available laminated glass panels typically have one sheet of glass on each side of the energy absorbing layer. have An alternative to this three-layer structure is a plastic that typically consists of two or more layers. It is two layers with one piece of glass for the inner layer. Because there is no inner glass layer, In addition to being lighter, when an impact sufficient to break double-layered glass occurs, the interior or The risk of exposure to broken glass inside the vehicle is greatly reduced.
前述した三層構造のエネルギ吸収層としては、可塑化ポリビニルブチラールが最 もよく使用されている。このようなポリビニルブチラールは、ガラスと相互作用 して、ラミネートの強力な結合を生じるためにポリビニルアルコール(゛部分P VB”)として表されるヒドロキシルな約15〜30重1%含み、(更にはポリ 酢酸ビニルとして表される酢酸塩を0〜2.5重量%含み、残りはポリビニルブ チラールとして表されるブチラールである)。可塑化部分PVBシートは三層ガ ラスパネルで長い間商業的に使用されているので、合わせガラスの製造者はこの シートの取り扱い及び特性な十分熟知している。またこのシートは二層で使用す るように提案されている。米国特許第4.937,147号は二層での部分PV Bとポリウレタンとの結合に注目し、米国特許第4,952,457号は二層の 可塑化部分PVBシートの湿気許容度に注目している。これらの特許に開示され ているように、二層を含んでいる車室又は部屋の内部に面する耐損傷性内面とし て二層で架橋ポリウレタンを使用することも知られている。Plasticized polyvinyl butyral is the best choice for the energy absorption layer of the three-layer structure mentioned above. is also commonly used. Such polyvinyl butyral interacts with glass and polyvinyl alcohol (part P) to create a strong bond in the laminate. Contains about 15-30 1% by weight of hydroxyl expressed as VB" Contains 0 to 2.5% by weight of acetate expressed as vinyl acetate, with the remainder being polyvinyl vinyl. butyral, expressed as tyral). The plasticized part PVB sheet is made of three layers. Since it has been used commercially for a long time in laminated glass panels, manufacturers of laminated glass Must have sufficient knowledge of handling and properties of sheets. This sheet can also be used in two layers. It is proposed that U.S. Pat. No. 4,937,147 describes partial PV in two layers. Focusing on the bond between B and polyurethane, U.S. Patent No. 4,952,457 describes a two-layer We are looking at the moisture tolerance of plasticized PVB sheets. disclosed in these patents A damage-resistant inner surface facing the interior of the passenger compartment or room containing two layers, as shown in It is also known to use crosslinked polyurethane in two layers.
なかなかの成功を収めたこれらの特許のシステムは、二層のプラスチック成分の 特性をうまく処理しているが、商業規模での二層の経済的な製造には向かない。These patented systems, which have been quite successful, consist of two layers of plastic components. Although the properties are well handled, they are not suitable for economical production of two layers on a commercial scale.
凡Jしυ1力 さて、商業的に魅力のある二層ガラスパネルの製造シスな。Ordinary J υ1 force Now, there is a commercially attractive manufacturing system for double-layer glass panels.
従って、本発明の主な目的は二層ガラスパネルを製造するための方法及び装置を 提供することである。Therefore, the main object of the present invention is to provide a method and apparatus for manufacturing double-layer glass panels. It is to provide.
他の目的は、このようなパネルを製造するための商業的に有意義で、手順取り扱 いの簡単な方法及び装置を提供することである。Other purposes include commercially meaningful and procedural handling for producing such panels. It is an object of the present invention to provide a simple method and apparatus for this purpose.
他の目的は、部分PVB及びポリウレタンを構造成分として使用している二層ガ ラスパネルに改良を加えることである。Another purpose is to create a double-layered structure using partial PVB and polyurethane as structural components. This is an improvement to the last panel.
以下の説明及び請求の範囲によって本発明の他の目的が一部分明白となろう。Other objects of the invention will become apparent in part from the following description and claims.
前記目的及び他の目的は、二層ガラスパネルを成形するための方法を提供するこ とによって達成される0本方法は、a)架橋セルフヒーリング(self−he aling)ポリウレタン層−で被覆した延伸ポリエステルフィルム、好ましく は二軸延伸ポリエチレンテL・フタレートフィルムの光学的に透明なプレラミネ ートを提供し、b)ポリウレタン層ではなく、ポリエステルフィルムの側面を部 分ポリビニルブチラール層の下方組織化(textured )面に対面接触さ せて、好ましくはガラスパネルで使用すべき区域の外側に脱気穴を有する可塑化 部分ポリビニルブチラール層とプレラミネートとを結合し、C)段階b)の結合 層を周囲固着装置内で締付け、d)引き続き、i)好ましくは脱気穴を通じて排 気することによってポリエステルフィルムと可塑化ポリビニルブチラールとの界 面から脱気し、ii)周囲固着装置内にある段階C)の層の局限区域をガラスシ ートに押圧し、次いで1ii)プラスチック層とガラスシートとを結合するため にプラスチック層は周囲固着装置内に締付けた状態にして、段Ill i i )のアセンブリを高温高圧下に置くという段階i)、ii) 、1ii) 、及 び場合によっては前記段階C)をエアオートクレーブ内で実施することからなる 。The above object and other objects are to provide a method for forming double-layer glass panels. The method achieved by a) cross-linking self-healing (self-healing) oriented polyester film coated with a polyurethane layer, preferably is an optically transparent prelaminated biaxially oriented polyethylenetetraphthalate film. b) the sides of the polyester film rather than the polyurethane layer; face-to-face contact with the textured surface of the polyvinyl butyral layer. plasticized with degassing holes on the outside of the area to be used, preferably in glass panels bonding the partial polyvinyl butyral layer and the prelaminate; C) bonding step b); tightening the layer in a peripheral fixing device; d) subsequently i) venting, preferably through a venting hole; The interface between polyester film and plasticized polyvinyl butyral by ii) glass shield the localized area of the layer of step C) in the surrounding fixation device; 1ii) to bond the plastic layer and the glass sheet; The plastic layer is then tightened into the surrounding fixing device and the stage Ill Steps i), ii), 1ii) of placing the assembly of ) under high temperature and pressure; and optionally carrying out step C) in an air autoclave. .
二層ガラスパネルを成形するための装置は、a)オートクレーブチャンバと、b )i)多層複合シート用周囲固着装置、ii)周囲固着装置の周辺内の支持台及 び1ii)熟成形アセンブリに負圧をかけるための支持台関連手段を含んでいる オートクレーブチャンバ内の熱成形アセンブリと、C)オートクレーブチャンバ 内に正圧を生じるための手段と、d)オートクレーブチャンバ内に負圧を生じる ための手段と、e)オートクレーブチャンバ内の空気含制御しながら加熱するた めの手段とを含んでいる。The apparatus for forming double-layer glass panels comprises: a) an autoclave chamber; b ) i) a peripheral fastening device for the multilayer composite sheet; ii) a support and a support within the periphery of the peripheral fastening device; and 1ii) support associated means for applying negative pressure to the ripener assembly. a thermoformed assembly within the autoclave chamber; and C) the autoclave chamber. d) means for creating a negative pressure in the autoclave chamber; e) means for controlled heating of the air content in the autoclave chamber; including means for
11立1皇11思 本発明全体を説明するに当たって、以下の添付図面を参照する。11 years 1 emperor 11 thoughts In describing the invention as a whole, reference is made to the following accompanying drawings.
図1は本発明の装置アセンブリの流れ図である。FIG. 1 is a flow diagram of the device assembly of the present invention.
図2は図1の装置の部品の平面図である。2 is a plan view of parts of the apparatus of FIG. 1; FIG.
図3は図2の3−3での断面図である。FIG. 3 is a sectional view taken along line 3-3 in FIG.
図4は図3の代替例の部分断面図である。FIG. 4 is a partial cross-sectional view of an alternative to FIG.
図5は本発明の成形段階中におけるプラスチック層の一部分を示す拡大詳細断面 図である。Figure 5 is an enlarged detailed cross-section showing a portion of the plastic layer during the molding step of the present invention. It is a diagram.
図6は本発明の二層ガラスパネルを示す図5と同様の図である。FIG. 6 is a view similar to FIG. 5 showing a double layer glass panel of the present invention.
11血1亙11j これから図面を参照する。二層ガラスパネル100(図5)を成形するための装 置10全体を図1に示す、装置10は、壁13によって仕切られ、後述する結合 プロセス中に発生するかなりの真空及び圧力に耐えるのに十分な強度を有するエ アオートクレーブチャンバ12を含んでいる。11 blood 1 11j Reference is now made to the drawings. Equipment for forming double-layer glass panel 100 (FIG. 5) The apparatus 10, shown in its entirety in FIG. An erected material that is strong enough to withstand the significant vacuum and pressure generated during the process. It includes an autoclave chamber 12.
少なくと乙一つの、好ましくは慢数の熱成形アセンブリ14a、14b、14c がチャンバ12内に収納される。at least one, preferably a plurality of thermoforming assemblies 14a, 14b, 14c; is housed in the chamber 12.
熟成形アセンブリ14を供給するために、チャンバ12人口の適切な開閉可能手 段(図示せず)、例えば密閉式のヒンジ付きアクセスドアが壁13に備わってい る。A suitable retractable hand of the chamber 12 serves to feed the ripening assembly 14. A step (not shown), for example a closed hinged access door, is provided in the wall 13. Ru.
各熟成形アセンブリ14(図2及び図3)は、更に詳しく説明すべき層状複合シ ート用周囲固着装置16と、周囲固着装置16の周辺内の支持台18と、熱成形 アセンブリ14上を真空にするための支持台18と関連する手段20(図1)と を含んでいる1手段20は、浅い円筒形ハウジング26く図2)を形成するため に底部28にしっかりと固定された直立側壁24に開口部22(図3)を含んで いる。各熟成形アセンブリ14のハウジング26の側壁24にある手段20の開 口部22は、管29a、29b。Each aged assembly 14 (FIGS. 2 and 3) is a layered composite assembly, which will be described in more detail. a perimeter anchoring device 16 for the seat, a support 18 within the periphery of the perimeter anchoring device 16, and a thermoforming a support 18 and associated means 20 (FIG. 1) for creating a vacuum on the assembly 14; 2) to form a shallow cylindrical housing 26 (Figure 2). including an opening 22 (FIG. 3) in an upright side wall 24 secured to a bottom 28. There is. An opening of the means 20 in the side wall 24 of the housing 26 of each ripening mold assembly 14 The mouth portion 22 includes tubes 29a and 29b.
29C(図1)を介して真空ポンプ30に連通している。It communicates with the vacuum pump 30 via 29C (FIG. 1).
複数の熱成形アセンブリ14を使用するときには、各開口部22はマニホールド 27を通じて管29に接続される。When multiple thermoforming assemblies 14 are used, each opening 22 is connected to a manifold. It is connected to tube 29 through 27.
手段34(図1)は手段2oとは異なり、オ・−トラレープチャンバ12内を真 空にするために備わり、且つ一方の端部38がチャンバ12内部に、他方の端部 が真空ポンプ30に連通している管36を大んている。The means 34 (FIG. 1) differs from the means 2o in that the means 34 (FIG. provided for emptying and having one end 38 inside the chamber 12 and the other end 38 inside the chamber 12; is extending through a tube 36 that communicates with the vacuum pump 30.
装置10は更に、オートクレーブチャンバ12内の空気を制御しながら加熱する ための手段40(図1)を備えており、この手段はチャンバ12内の導電性加熱 コイルアセンブリ42及び空気循環用ファン44として図示されている。コイル 42は通常、機能時には電源(図示せず)に電気接続されている。The apparatus 10 also provides controlled heating of the air within the autoclave chamber 12. means 40 (FIG. 1) for conductive heating in chamber 12; Illustrated as a coil assembly 42 and an air circulation fan 44. coil 42 is typically electrically connected to a power source (not shown) when functional.
支持台18(図3)の支持面46は、支持面に固定され、例えばシリコーンゴム のようなエラストマ材料からなり、且つガラス層102の表面形状に適合するよ うに図示するような外形を有する湾曲可能支持層(yieldable bea ringlayer) 48を有する。The support surface 46 of the support base 18 (FIG. 3) is fixed to the support surface and is made of, for example, silicone rubber. The glass layer 102 is made of an elastomer material such as A yieldable support layer having an outer shape as shown in FIG. ring layer) 48.
各周囲固着装置16(図3)は、密封リング49と、)Sウジフグ26の周辺に 均等に配置された複数のねじ切りノブ50a、50bとを含んでいる。これらの ノブは、ハウジング26の側壁24に固定されたブラケットの54にある回転付 属部品を介して矢印52の方向に旋回移動して、リング49との係合及び係合解 除の機能を果たす。Each peripheral fixing device 16 (FIG. 3) includes a sealing ring 49 and a and a plurality of evenly spaced threading knobs 50a, 50b. these The knob is a rotatable knob located at 54 on a bracket secured to the side wall 24 of the housing 26. Pivoting movement in the direction of arrow 52 through the attached parts to engage and disengage the ring 49 Performs the function of elimination.
ハウジング26内の支持台18の垂直軸上にある先細ボア56は、ボルト62に よって底部28に固定された部材60のねじ山58とtl、mLで係合する。ハ ウジング26内の支持台18の垂直方向位置は、台18を回転させて、ねじ山5 9t!0:ねじ山58に沿って協働的に上方又は下方に移動させることによって 設定される。周囲に間隔をあけて配置され且つ水平方向に調整可能な複数の位置 決めボルト64は、側壁24の内面との係合によって、支持台18を円筒形ハウ ジング26内の同心上に設置する。支持台、周囲のハウジング及び協働する周囲 固着装置の形状が円形でない(例えば長方形の)場合、支持台の垂直方向位置は 、代替手段(例えば台とハウジングの底部との間のジムストック)によって決定 される。A tapered bore 56 on the vertical axis of the support 18 within the housing 26 allows the bolt 62 to Therefore, it engages with the thread 58 of the member 60 fixed to the bottom part 28 at tl, mL. C The vertical position of the support base 18 within the housing 26 can be adjusted by rotating the base 18 to 9t! 0: by cooperatively moving upward or downward along the thread 58 Set. Multiple circumferentially spaced and horizontally adjustable positions The dowel bolt 64 moves the support base 18 into a cylindrical housing by engagement with the inner surface of the side wall 24. It is installed concentrically within the ring 26. Support platform, surrounding housing and cooperating surroundings If the shape of the anchoring device is not circular (e.g. rectangular), the vertical position of the support is , determined by alternative means (e.g. gym stock between the platform and the bottom of the housing) be done.
制御バルブ74を含んでいるライン72を通じて70でオートクレーブチャンバ 12に連通ずる空気圧縮器68を含んでいる手段66(図1)は、成形プロセス の適切な段階でチャンバ12内に正圧を発生させる。Autoclave chamber at 70 through line 72 containing control valve 74 Means 66 (FIG. 1) including an air compressor 68 communicating with A positive pressure is generated within the chamber 12 at an appropriate stage.
各熟成形アセンブリ14は適切な支持11!ff(図示せず)上に取出せるよう に配置されるか又はその代わりに、チャンバ12内に一つ以上が互いに積重ねら れる。Each ripening assembly 14 has a suitable support 11! so that it can be taken out on the ff (not shown) or alternatively, one or more may be stacked on top of each other within the chamber 12. It will be done.
図2及び図3と同一の部品を同じ番号で示している図4の実施例では、熱成形ア センブリ14は場合によって、真空開口部22と支持台18とを連通させるため に排気孔(weep hole) 77 ’i:有するスペーサ76を側壁24 と支持台18との間に含んでいる0層状複合材料32の区域7つを支持するスペ ーサ76の輪郭面78によって、成形中に支持されない広範な区域は回避される 。この区域が存在すると、複合材料を破壊し得る。例えば周辺二層形状が異なる ものを、従って輪郭の異なる支持台18を収納するために単一の共通ハウジング 26を使用するときには、形状及び周辺範囲が適切なスペーサ76を使用するこ とができる。従って、このような共通ハウジングで特殊な二層形状を成形すると きには、スペーサ76を使用して、前述したように実質的に支持されない区域を 回避することができるが、図3に示すように周辺がより大きい形状では、不要物 として除去することができる。In the embodiment of FIG. 4, in which parts identical to those of FIGS. 2 and 3 are designated with the same numbers, the thermoforming Assembly 14 optionally provides communication between vacuum opening 22 and support platform 18. A spacer 76 having a weep hole 77'i on the side wall 24 and the support platform 18 for supporting seven areas of the layered composite material 32. The contoured surface 78 of the supporter 76 avoids extensive unsupported areas during molding. . The presence of this zone can destroy the composite material. For example, the shape of the peripheral two layers is different. A single common housing for accommodating supports 18 of different shapes and therefore different contours. 26, use a spacer 76 with an appropriate shape and peripheral range. I can do it. Therefore, when molding a special two-layer shape with such a common housing, In some cases, spacers 76 may be used to provide substantially unsupported areas as described above. However, in a shape with a larger periphery as shown in Figure 3, unnecessary objects can be avoided. It can be removed as
これから、ガラスとプラスチックとの二層ガラスパネル100(区5)を装置t loを使用して成形するための方法を説明する。From now on, a double-layer glass panel 100 (section 5) of glass and plastic will be manufactured using the equipment t. A method for molding using lo will be explained.
ガラスと合わせて二層ガラスパネルを製造するために装置110に供給される光 学的に透明なプレラミネートは、架橋セルフヒーリングポリウレタン(PU)で 被覆され、場合によっては持に可塑化部分P ”v’ Bへの付着と促進するた めに反対側が処理又は被覆された延伸ポリエステル(例えばポリエチレンテレフ タレー) (PET))のフィルムを含んでいる。プレラミネートの成形につい ては後で説明する。Light supplied to apparatus 110 for manufacturing double-layer glass panels with glass The chemically transparent pre-laminate is made of cross-linked self-healing polyurethane (PU). coated and, in some cases, to promote adhesion to the plasticized portion P”v’B. Oriented polyester (e.g. polyethylene terephthalate) that has been treated or coated on the opposite side to (PET)) film. About pre-laminate molding will be explained later.
PUてはなく、PETの側面を可塑化部分PVB層の下方面に対面させて、プレ ラミネートを可塑化部分PVB[と結合する。このアセンブリ全体を1状複合材 料32として図3に概略的に示し、詳しくは図5に示す。図5の80は可塑化部 分PVB層であり、82はPET層であり、84はPU層である。PET層82 の面86は90層84に当接し、層82の面88は、好ましくは可塑化部分PV B層80の組織化した下方側面90と対面接触する。Instead of PU, the PET side faces the lower side of the plasticized PVB layer. The laminate is bonded with the plasticized part PVB. This entire assembly is made of single composite material. It is shown schematically in FIG. 3 as material 32 and in detail in FIG. 80 in Fig. 5 is a plasticizing part 82 is a PET layer, and 84 is a PU layer. PET layer 82 The surface 86 of 90 abuts the layer 84, and the surface 88 of the layer 82 preferably faces the plasticized portion PV. Face-to-face contact is made with the textured lower side surface 90 of the B layer 80.
間隔をあけて配置された複数の脱気穴92(図5)が、二層ガラスパネルで使用 すべき層80の区域の外側(図2)に、可塑化PVB層80の厚さ全体を貫通し て伸びている。Multiple spaced vent holes 92 (Figure 5) are used in double-layer glass panels. Outside the area of the layer 80 to be treated (FIG. 2), it penetrates the entire thickness of the plasticized PVB layer 80. It's growing.
穴92の開口寸法は重要ではなく、単なる実験によって決定することができる。The aperture size of hole 92 is not critical and can be determined by mere experimentation.
約3〜10mmの開口部の使用に成功したが、開口部は手で軟質PVB材料内に 形成してもよいし、例えば先鋭突起部分を備えた動力シリンダ上に層80を通過 させてシートに穿孔するか又は同等の代替手段を用いて成形してもよい。We have successfully used openings of approximately 3-10mm, but the openings were manually inserted into the soft PVB material. For example, layer 80 may be formed on a power cylinder with a sharp protrusion. The sheet may be perforated or formed using equivalent alternatives.
脱気穴92は層80と層82との界面に連通している。Degassing holes 92 communicate with the interface between layers 80 and 82.
このような穴の代わりに、この界面から脱気するために、装置に結合された代替 手段、例えば別個の(5eparete )脱気リングく図示せず)を、このよ うな界面上を真空にすることのできるボートを有する側面24の上部と締付はリ ング49との間の界面の向かい側に備えることができる。Instead of such a hole, an alternative coupled to the device to degas from this interface A means, e.g. a separate degassing ring (not shown), is provided in this manner. The upper part of the side surface 24 with a boat that can create a vacuum on the interface and the tightening are removed. It can be provided on the opposite side of the interface with the ring 49.
プラスチック層のアセンブリ32を側聞固着装置16内において図3に示す実質 的に水平な状慧に締付ける。各ノブ50を図3の位Wに旋回させ、次にノブを下 方に回転させて、図示するワッシャを図示するような密封リング面と圧縮係合さ せることによって密封リング49と側壁24の上面との締付けを行う。The assembly 32 of plastic layers is placed within the lateral anchorage device 16 as shown in FIG. Tighten it in a horizontal position. Turn each knob 50 to the position W shown in Figure 3, then lower the knob. until the washer shown is in compression engagement with the sealing ring surface as shown. This tightens the sealing ring 49 and the upper surface of the side wall 24.
オートクレーブチャンバ12を密閉した後に、引き続き以下の段階を好ましくは 自動化方式で実施する。手段20(図1)の真空ポンプ30と開口部38との間 のバルブを開放し、ポンプ30に給電して、オートクレーブチャンバ12内を真 空にする。熱成形アセンブリ14上を真空にするための手段のバルブ31を開放 して、固着装置16内に締付けられた層状複き材r132の下側も開口部223 通じて選択的にほぼ同様に真空にする。延伸を容易にするために場合によって複 合材料32を加熱してもよいが、プロセスのこの段階で加熱しないことが好まし い。アセンブリ16内で密封された複合材料32の下側が真空になると、最も下 側の可塑化PVB層8層内0内92を通じて排気され、それによってPET層8 層上2塑化PVB層80との界面から脱気されるが、複合材料32の上方はボー ト38を通じて同様に真空にされるので、複合材料32は図3に示すように殆ど 水平のままである0次に真空ポンプ30への給電が解除されると、接続された圧 縮器68が(制御バルブ74を介して)脱気したプラスチック層アセンブリに徐 々に差圧を発生させて、周囲固着装置の周辺内部の局限区域(I2!3の94) 及びPVBV6O13気穴92の内部を、湾曲可能層48の耐破損性面上に予め 配置された下方の透明なフロートガラスシート102の面に押圧する3区域94 がガラス層102と係合した後の層状複合材料32の延伸値1はほぼ、図3の点 線96内に示す通りである。After sealing the autoclave chamber 12, the following steps are preferably carried out: Implemented in an automated manner. Between the vacuum pump 30 and the opening 38 of the means 20 (FIG. 1) open the valve, supply power to the pump 30, and make the inside of the autoclave chamber 12 vacuum. empty. Opening the valve 31 of the means for creating a vacuum over the thermoforming assembly 14 Then, the lower side of the layered composite material r132 tightened in the fixing device 16 also has an opening 223. Through the vacuum selectively in much the same way. In some cases, multiple The composite material 32 may be heated, but is preferably not heated at this stage of the process. stomach. When a vacuum is applied to the underside of the sealed composite material 32 within the assembly 16, the lowest The plasticized PVB layer 8 on the side is evacuated through the 0 inside 92, thereby the PET layer 8 The air is degassed from the interface with the upper layer 2 plasticized PVB layer 80, but the upper part of the composite material 32 is Similarly, a vacuum is applied through port 38 so that composite material 32 is almost completely evacuated as shown in FIG. When the power supply to the vacuum pump 30 is removed, the connected pressure A condenser 68 (via control valve 74) applies a gradual pressure to the degassed plastic layer assembly. A localized area (94 in I2!3) inside the periphery of the surrounding fixing device and the inside of the PVBV6O13 pores 92 on the breakage-resistant surface of the bendable layer 48 in advance. Three areas 94 press against the surface of the lower transparent float glass sheet 102 disposed The elongation value 1 of the layered composite material 32 after the is engaged with the glass layer 102 is approximately equal to the point in FIG. As shown within line 96.
プラスチック層が殆ど点線位置96にあって、周囲固着装置16内で絶えず締付 けられた状態にある一方で、チャンバ12内の温度及び圧力を、部分PVB層の ポリビニルアルコール基との相互作用を通じて可塑化部分PVB層80をガラス 層102に強く結合し且つポリエチレンテレフタレート層82を部分PVB層8 0に溶融結合するのに適した時間維持されるレベルまで上昇させる。コイル42 (図1)に給電して高温空気を提供し、ファン44を介してチャンバ12内に循 環させる。圧縮器68及び制御バルブ74を使用して、チャンバ12内の圧力を 制御しながら徐々に所望のレベルまで上昇させる。このような圧力が上昇すると 、差圧制御バルブ98は、ポート22を通じてアセンブリ14にかけられる延伸 複合材料96の下側への圧力を、延伸複合材料の上側で発生される上昇するオー トクレーブ圧力よりも大幅に低く維持するように機能する。この処理は、バルブ 37を開放した状態で、制御バルブ98を制御しながら開放して、ライン29( 図1)を通じて熱成形アセンブリ14内の圧力を徐々に上昇させることによって 行われる。この特徴は、締付けられた延伸複合材料が支持層48から密封リング 49の内側に突出している区域で破断するか又はガラスが破損する傾向を回避す るのに役立つ。The plastic layer is mostly at the dotted line position 96 and is constantly tightened within the peripheral fastening device 16. While the temperature and pressure within the chamber 12 are kept Glass plasticized portion PVB layer 80 through interaction with polyvinyl alcohol groups The polyethylene terephthalate layer 82 is strongly bonded to the layer 102 and the polyethylene terephthalate layer 82 is bonded to the partial PVB layer 8. 0 to a level maintained for a suitable time to melt bond. coil 42 (FIG. 1) to provide hot air and circulate it into the chamber 12 via the fan 44. make a circle Compressor 68 and control valve 74 are used to reduce the pressure within chamber 12. Gradually increase to desired level in a controlled manner. When such pressure increases , differential pressure control valve 98 is connected to the extension applied to assembly 14 through port 22. Pressure on the underside of the composite material 96 is applied to the rising orifice generated on the upper side of the stretched composite material. functions to maintain the pressure significantly lower than the toclave pressure. This process 37 is open, control valve 98 is opened under control to open line 29 ( By gradually increasing the pressure within the thermoforming assembly 14 through FIG. It will be done. This feature allows the tightened expanded composite material to be removed from the support layer 48 by the sealing ring. 49 to avoid the tendency to break or break the glass in areas that protrude inwardly. It will help you.
部分PVBとガラス層との望ましい結合を生じるためのオートりし−ブの条件は 、約1・10°C11135kraて約30分とする。The auto-recess conditions for producing the desired bond between the partial PVB and the glass layer are: , about 30 minutes at about 1.10°C and 11135 kra.
ナヤンバ12内の条件を大気楽件まで下げ、アセンブリ14からラミネー1−を 取出し、ガラス層102の周囲の外側の不要のプラスチック部分をトリミングし た後のプロセスの生成物は、ガラスシート102と、ガラス層102に強く結合 した可塑化部分PVBの成形層104と、透明ポリエステルフィルム106と、 架橋セルフヒーリングポリウレタン層108とを続けて含んでいるしわのない二 層ガラスパネル100(図6)である0図3に示すように、ガラスシート102 <従って二層ガラスパネル100)は好ましくは複心曲率(compound curvature )を有する。このことは、このような熱可塑性層を複心 曲率面と表面接触させるのに複合材料32の平坦な熱可塑性層をある程度延伸さ せる必要があることを意味する。これに代えて、平坦なガラスシートを使用して 、実質的に平坦な二層ガラスパネルを製造してもよい、これは例えば自動車のサ イドウィンドウとして非常に適し得る。The conditions inside Nayamba 12 are lowered to atmospheric conditions, and the laminate 1- is removed from assembly 14. Take it out and trim the unnecessary plastic part on the outside around the glass layer 102. The products of the subsequent process are strongly bonded to the glass sheet 102 and the glass layer 102. a molded layer 104 of the plasticized portion PVB, a transparent polyester film 106, A wrinkle-free double layer successively comprising a cross-linked self-healing polyurethane layer 108. As shown in FIG. 3, a layered glass panel 100 (FIG. 6) is a glass sheet 102. <Therefore, the double-layer glass panel 100) preferably has a compound curvature. curvature). This means that such a thermoplastic layer can be The flat thermoplastic layer of composite material 32 is stretched to some extent to bring it into surface contact with the curved surface. This means that it is necessary to Alternatively, use a flat glass sheet , substantially flat double-layer glass panels may be manufactured, which may be used, for example, in automotive panels. It can be very suitable as an id window.
これから、装置10で処理する光学的に透明なポリエステルとポリウレタンとの プレラミネートの製造について説明する。ポリエステルは、付着を促進するため に、特に可塑化部分PVBへの付着を促進するために、場合によって片側又は両 側が例えば感圧接着材で被覆されているか又は例えばプラズマ放電、フレーム( Name)放電、コロナ放電、グロー放電等で処理されている約0.0125〜 0.175mm厚さの延伸フィルム、好ましくは光学的に透明な二軸延伸ポリエ チレンテレフタレートフィルムである。このようなポリエチレンテレフタレート は、反復するエチレンテレフタレート単位を含み、また約10モル%までのエス テル化グリコール単位がジエチレングリコール;プロパン−1,3ジオール;ブ タン−1,4ジオール;ポリテトラメチレングリコール;ポリエチレングリコー ル等から得られ、約10モル%までの酸性成分が酸く例えばイソフタル酸、二安 息香酸、ナフタレン1.4=又は2,6−ジカルボン酸、アジピン酸、セバシン 酸等)から得られるエチレンテレフタレートのコポリマーを含んでいる。From now on, the optically transparent polyester and polyurethane to be processed in the device 10 will be combined. The production of prelaminate will be explained. Polyester to promote adhesion optionally on one or both sides, in particular to promote adhesion to the plasticized part PVB. The sides are coated with e.g. a pressure-sensitive adhesive or e.g. with a plasma discharge, flame ( Name) Approximately 0.0125 ~ processed by discharge, corona discharge, glow discharge, etc. 0.175 mm thick stretched film, preferably optically clear biaxially oriented polyester It is a tylene terephthalate film. Such polyethylene terephthalate contains repeating ethylene terephthalate units and also contains up to about 10 mole percent ester The tellurized glycol unit is diethylene glycol; propane-1,3 diol; Tan-1,4 diol; polytetramethylene glycol; polyethylene glycol up to about 10 mol% of acidic components, such as isophthalic acid, dianic acid, etc. Zozoic acid, naphthalene 1.4= or 2,6-dicarboxylic acid, adipic acid, sebacin It contains copolymers of ethylene terephthalate obtained from
ポリエステルフィルムを、必ずしもそうではないが、通常゛単層である透明な架 橋性ポリウレタンで被覆する。耐損傷非黄変性の架橋セルフヒーリング面が二層 ガラスパネルの内側に露出した面、即ち窓のような二層パネルを含んでいる車又 は部屋の中にいる人に面している面として硬(ヒj麦に得られるならば、ポリウ レタンの化学的構造は大幅に変動し得る。ポリエステル支持体と一緒に使用する のに必要であり得るとして後で説明するように製造される好ましいポリウレタン 組成物及び性能強化剤は、米国特許第4.937,147号の第・1項45行か ら第7項20行、米lII特許第4,923,757号の第3項45行から第5 項37行、並びに米国特許第4,925,734号の第4項31行及び第5項3 0行に開示されている。これらは参照によって本明細書の一部をなすものとする 。Polyester film is usually, but not always, a transparent film that is a single layer. Cover with cross-linking polyurethane. Dual layers of damage-resistant, non-yellowing, cross-linked self-healing surface The inside exposed surface of a glass panel, i.e. a car or vehicle containing a double layer panel such as a window. The surface facing the people in the room should be hard (or polyurethane, if available in oats). The chemical structure of lethane can vary widely. Use with polyester support A preferred polyurethane manufactured as described below as may be necessary for The compositions and performance enhancers are described in U.S. Pat. No. 4,937,147, paragraph 1, line 45. Paragraph 7, line 20 of US Patent No. 4,923,757, Paragraph 3, lines 45 to 5 Section 37, and Section 4, Line 31 and Section 5, Section 3 of U.S. Pat. No. 4,925,734. It is disclosed on line 0. They are incorporated herein by reference. .
厚さが約0.25〜1.5mm、好ましくは約0.35〜0.75mmの可塑化 部分PVBシートがMon5ant。Plasticized with a thickness of about 0.25-1.5 mm, preferably about 0.35-0.75 mm Partial PVB sheet is Mon5ant.
Co+apany製5aflex (登録商標)シート及びE、1.duPon t deNemours & Company製Butacite (登録商標 )ポリビニルブチラール樹脂シートとして市販されている。市販されているこの ようなシートは可塑剤を含み、各主要側面上の組織が細かく又は粗くなっている 0部分ポリビニルブチラール用可塑剤はよく知られており、米国特許第4,90 2,464号の第5項11〜21行に開示されている。同特許は参照によって本 明細書の一部となすものとする。可塑化部分PVBシ・−1の表面を組織化する ための技術も知られており、米国特許第2,904,844号、本田特許第2, 909,810号、米国特許第3.994,654号、米国特許第4,575, 540号、ヨーロッパ特許第0185.863号に開示されている。これらは9 照によって本明細書の一部をなすものとする。Co+apany 5aflex (registered trademark) sheet and E, 1. duPon Butacite (registered trademark) manufactured by deNemours & Company ) It is commercially available as a polyvinyl butyral resin sheet. This commercially available Such sheets contain plasticizers and have a fine or coarse texture on each major side. Plasticizers for 0-part polyvinyl butyral are well known and are described in U.S. Pat. No. 2,464, paragraph 5, lines 11-21. The patent is incorporated herein by reference. It shall be made a part of the specification. Texturing the surface of plasticized part PVB-1 Techniques for this are also known, such as U.S. Pat. No. 909,810, U.S. Patent No. 3,994,654, U.S. Patent No. 4,575, No. 540, European Patent No. 0185.863. These are 9 is incorporated herein by reference.
ローリング、噴霧、流延、スピニング、押出し、ロッド又はプレードコーチング 、スライド又はカスケードコーチング等によってPU組成物をポリエステルフィ ルムに付着させる。大規模の付着を簡単にするには、フローコーチングが好まし い。Rolling, spraying, casting, spinning, extrusion, rod or plaid coating , slide or cascade coating etc. Attach it to the lum. Flow coating is preferred to facilitate large-scale deposition. stomach.
市販の自蔵式フローコーチングシステムが使用可能である。通常のシステムでは 、成分は撹拌容器内で混合されて、被覆される支持体を支持する供給及び引取り コンベヤの前進方向に垂直に伸びている受容トラフの上方に配置されたコーチン グヘッドにフィルタを通じて注入される。トラフはコーチングヘッドから重力に よって供給を受け、PU配合物の液体カーテンがトラフ底部の調節可能な間隙開 口部を通じて流出する。支持体は支持体面上に均一厚さの層を付着させるために トラフの底部を通じて運搬される。配合物の粘度及び厚さ並びに支持体の物理的 性質によって、支持体上ての平滑4“被膜の付着を促進するように支持体フィル ム登!&!遣するのにある程度の措1が必要となり得る。Commercially available self-contained flow coaching systems are available. In a normal system , the components are mixed in a stirred vessel and the feed and take-off supports the substrate to be coated. Cochin located above the receiving trough running perpendicular to the direction of conveyor advance is injected through a filter into the processing head. Trough from coaching head to gravity Thus, the liquid curtain of PU formulation is fed through an adjustable gap opening at the bottom of the trough. It flows out through the mouth. The support is used to deposit a layer of uniform thickness on the support surface. Conveyed through the bottom of the trough. The viscosity and thickness of the formulation and the physical properties of the support. Depending on the nature of the support film, it is possible to Mu climb! &! Some measures may be required to provide assistance.
PU配合物の付着後に、被覆したボリエステルフイ/Lムを配合物中で架橋剤を 活性化させて、被膜を硬化、架橋させるのに十分な時間だけ高温、電子ビーム若 しく番よ紫タト線(UV)に暴露するか又はこれらの要素を組み合わせて処理す る。連続硬化を容易にするために、熱硬化炉及び/又は一つ以上の紫外線バンク を、フローコータの弓i取りコンベヤの下流に、またコンベヤと一列になるよう に機能的Gこ配置してもよい。After application of the PU formulation, the coated polyester film/L film is treated with a crosslinker in the formulation. High temperature, electron beam, and Exposure to UV radiation or a combination of these factors should be avoided. Ru. A thermosetting oven and/or one or more UV banks to facilitate continuous curing. downstream of the flow coater's bow conveyor and in line with the conveyor. A functional G may be placed in the
単に例示的であって、本発明を限定しなし)以下の実施例によって本発明を更に 詳しく説明する。測定した分子量を測定した1分子当たりの官能基の数で割るこ とGこよって量(当量として示す)が得られる。The invention is further illustrated by the following examples (which are illustrative only and do not limit the invention). explain in detail. Divide the measured molecular weight by the measured number of functional groups per molecule. and G gives the amount (expressed as equivalent weight).
以下の試験を使用して、実施例に示す結果を得た。The following tests were used to obtain the results shown in the Examples.
暴露安定性−Xeronウエザロメータに特定時間暴露した二層ラミネートの黄 色度指数(YI)として特徴付(すられる黄色度と曇り度(以下参照)とを検査 した。tlunter 025分光計を用いてYIを測定した。16未満のYI を許容できるとみなす。Exposure stability - yellow of two-layer laminate exposed to Xeron Weatherometer for a specified time Characterized as chromaticity index (YI) (examines yellowness and cloudiness (see below)) did. YI was measured using a tlunter 025 spectrometer. YI less than 16 is considered acceptable.
曇り度O6−^STM D1003−61 (1977年再認可)−手順A−曇 り度肝 Hunter 八5sociaLes Inc、、 Re5ton、 V^製Huntcrlab Model 0251使用する。4%未満の曇り度 は光学的に透明であるとして許容できるとみなす。Cloudiness O6-^STM D1003-61 (Reauthorized in 1977) - Procedure A - Cloudy Re5ton Hunter 85socialLes Inc, Re5ton Huntcrlab Model 0251 manufactured by V^ is used. Haze level less than 4% is considered acceptable as being optically transparent.
100回の牽耗サイクル後の曇り度%の変化として測定する耐摩耗性:4 in x 4 in(10cm x 10cm)のガラス/可塑化PVB/PET/ PU二層ラミネートの試料を製造し、Te1edyne Taber Abra der 5130、研削砥石No、C5−10Fを500gの荷重下で使用して PU層を研磨した。ラミネートを45度の角度で甫に向けてフロリダ暴露した。Abrasion resistance measured as change in % haze after 100 drag cycles: 4 in. x 4 in (10cm x 10cm) glass/plasticized PVB/PET/ A sample of PU double layer laminate was manufactured and Te1edyne Taber Abra Using der 5130, grinding wheel No. C5-10F under a load of 500g. The PU layer was polished. The laminate was exposed to water at a 45 degree angle.
曇り度%の4%未満の変化を許容できるとみなす。A change in % haze of less than 4% is considered acceptable.
変形回復−ガラス/可塑化PVB/PET/PUの二層ラミネート試料のPU面 を、20ミル(0,51mm)厚さの刃を用いて室温で5分間500gの負荷を かけて変形させる。変形を回復するのに必要な時間を測定する。24時間以内の 回復時間を許容できるとみなす。Deformation recovery - PU side of glass/plasticized PVB/PET/PU bilayer laminate sample was applied with a 500 g load for 5 minutes at room temperature using a 20 mil (0.51 mm) thick blade. Transform it by applying it. Measure the time required to recover the deformation. within 24 hours Consider recovery time acceptable.
−耐溶剤性一種々の溶剤(例えばメタノール、メチレンクロライド、クロロホル ム、トルエン等)の液滴を続けてPU画面上5秒間保持して、拭き取る6表面へ の作用及び膨潤からの回復時間を記録する。12時間以内の回復を許容できると みなす。-Solvent resistance to various solvents (e.g. methanol, methylene chloride, chloroform) 6. Hold a droplet of water (toluene, etc.) on the PU screen for 5 seconds and wipe it onto the 6 surface. The action and recovery time from swelling are recorded. Recovery within 12 hours is allowed. I reckon.
蝕旦ニュ この対照例は、米国特許第4,937,147号の可塑化PVB支持体上のPU 被被膜iAI露面の老化後の品質を示している。Eclipse This control example is based on the PU on plasticized PVB support of U.S. Pat. No. 4,937,147. It shows the quality of the exposed surface of the coating iAI after aging.
支持体は、厚さが0.75mm、ヒドロキシル含量が18.2%で、100部の 樹脂当たり35部のアジピン酸ジヘキシルで可塑化したMon5anto Co mpany製部分PVB樹脂シート: 5aflex (登録商標)TGレシー トあった。使用したPUは米[El特許第4,937,147号の実施例6に開 示されている。PUレシート実施例6に開示されているように製造し、可塑化P VBシート上に付着させて、50℃で熱硬化させた。このPVB/PU構造を含 むガラスとの二層ラミネート3製造し、長時間50℃に暴露して、PU被被膜の PVB可塑剤の作用を評価した。約30日後に、暴露したPU面の手触りはすべ すべしているように惑じられた。The support had a thickness of 0.75 mm, a hydroxyl content of 18.2%, and 100 parts of Mon5anto Co plasticized with 35 parts dihexyl adipate per resin Partial PVB resin sheet made by mpany: 5aflex (registered trademark) TG receipt There was. The PU used was disclosed in Example 6 of the US patent No. 4,937,147. It is shown. PU receipt produced as disclosed in Example 6 and plasticized P It was deposited on a VB sheet and heat cured at 50°C. Including this PVB/PU structure. A two-layer laminate with PU glass3 was prepared and exposed to 50°C for a long time, resulting in the formation of a PU coating. The effect of PVB plasticizer was evaluated. After about 30 days, the exposed PU surface will be smooth to the touch. I was fooled into thinking it was smooth.
これはアジピン酸ジヘキシルがポリウレタンによって吸収され、次いで暴露面に 移動したために摩擦係数が下がったことを意味している。This is because the dihexyl adipate is absorbed by the polyurethane and then onto the exposed surface. This means that the coefficient of friction has decreased due to movement.
え族勇ユ これは本発明に基づく。Ezoku Yuyu This is based on the invention.
光学的等級(Optical grade)が透明で0.1mm厚の二軸延伸ポ リエチレンテレフタレート(PET)フィルムを市販のHoechst Ce1 anese製Ho5taphan 4400として入手した。表面には手を加え ず、前述したようなフローコータを使用して、このPETフィルムをPUで被覆 した。被覆中のPETフィルムの支持体を以下のように製造した。約45cm幅 の板上のガラス層に平滑面を提供し、ガラス上に多孔質クロスを延伸させて、板 に固定させた1次いで、クロス上に置かれたPETフィルムの部分を板に固定し た。Biaxially stretched polyester with transparent optical grade and 0.1mm thickness. Hoechst Ce1 commercially available polyethylene terephthalate (PET) film It was obtained as Ho5taphan 4400 manufactured by Anese. touch the surface First, coat this PET film with PU using a flow coater as described above. did. The PET film support during coating was prepared as follows. Approximately 45cm wide The glass layer on the plate is provided with a smooth surface, and the porous cloth is stretched over the glass to form the plate. 1 Next, the part of the PET film placed on the cloth was fixed to the board. Ta.
このアセンブリを熱風炉内に置き、加熱手段が即座に遮断される150℃まで温 度を上昇させた。この事前の熱処理でPETの応力が除去されて、フィルムは軽 い張力下でぴんと張って、支持体上で平坦になった。下層の多孔質クロスによっ て、熱処理中におけるPETフィルムの下方からの排気が簡単になった。これら の製造方法は、可動真空プレート又はテンタフレームのような適切な手段によっ て水平位置にぴんと張られるフィルムの連続ウェブを使用する連続する全規模プ ロセスでは不要となり得る0次に、約0.25〜0.5mm厚さの被膜を形成す るのに適し且つ以下のPtJ配合物が流出する間隙放出用開口部含有するフロー コータの槽の下方において約19mm、7分で移動する45cm1gのコンベヤ 上に前述したような支持されたPETフィルムを置いた。Place this assembly in a hot air oven and heat it to 150°C, where the heating means are immediately shut off. increased the level. This pre-heat treatment removes stress from the PET, making the film lighter. taut under high tension and flattened on the support. The lower layer of porous cloth This makes it easier to exhaust air from below the PET film during heat treatment. these The method of manufacturing the Continuous full-scale printing using a continuous web of film stretched taut in a horizontal position. A coating with a thickness of approximately 0.25 to 0.5 mm is formed on the 0th order, which may be unnecessary in the process. Flow containing interstitial discharge openings suitable for discharging and through which the PtJ formulation flows. A 45cm 1g conveyor that moves approximately 19mm in 7 minutes below the coater tank. On top was placed a supported PET film as described above.
成分 含有量 化、l Gms。Ingredient content ization, l Gms.
メチレンビス(4−0,13 シクロヘキシルイソシアネート) (Desmodur H) 1ポリエーテルトリオール 0.04252ポリエーテルをキャッピングした トリオール 0.0075 1エトキシル化トリメチロール プロパン(架橋剤) (ETMP) 0.07ジブチルスズジアセテート 20 0ppm(触媒) 鑑尿上二 ’Tinuvin 765 (0,25重量%)0.5’Tinuvin 32 8 (0,25重量%)0.5@IrHanox 245 (0,25重量%) o、5Dos Corning 57 300ppm(均展剤) ’N1ax LG−168、分子量= 1000、Union Carbide Corp、。Methylenebis(4-0,13 cyclohexyl isocyanate) (Desmodur H) 1 polyether triol capped with 0.04252 polyether Triol 0.0075 1-ethoxylated trimethylol Propane (crosslinking agent) (ETMP) 0.07 dibutyltin diacetate 20 0ppm (catalyst) Urinary examination 2 'Tinuvin 765 (0.25% by weight) 0.5'Tinuvin 32 8 (0.25% by weight) 0.5 @ IrHanox 245 (0.25% by weight) o, 5Dos Corning 57 300ppm (leveling agent) 'N1ax LG-168, molecular weight = 1000, Union Carbide Corp.
(Dabury、 CT)製、グリセリンと酸化プロピレンとを縮きさせて合成 する。(Dabury, CT), synthesized by condensing glycerin and propylene oxide do.
2Niax 11−27、分子31 = 6200、Union Carbid e Corp、製、グリセリン−酸化プロピレン付加物を酸化エチレンてキャン ピングして合成する。2Niax 11-27, Molecule 31 = 6200, Union Carbid e Corp., glycerin-propylene oxide adduct can be used with ethylene oxide. Ping and synthesize.
’Voranol 234−630.Dow Che+5ical Co。'Voranol 234-630. Dow Che+5ical Co.
”Tinuvin 765:C1ba Geigy Corp製ビス(1,2, 2,6゜6−ベンタメチルー4−ピペリジビニル)セバケート。“Tinuvin 765: C1ba Geigy Corp screws (1, 2, 2,6°6-bentamethyl-4-piperidivinyl) sebacate.
’Tinuvin 328:C1ba Ge’+gy Corp、製2− (2 ’ヒドロキシ−3’ 、5’−ジ−t−アミルフェニル)ベンゾトリアゾルビス (3−(3°−t−ブチル−4′ヒドロキシ−5゜メチルフェニル〕10ビオネ ート。'Tinuvin 328: C1ba Ge'+gy Corp, 2-(2 'Hydroxy-3',5'-di-t-amylphenyl)benzotriazorbis (3-(3°-t-butyl-4′hydroxy-5°methylphenyl)10 Bione To.
フローコーチングしたPETフィルムを70℃で1時間硬化させた。この温度は 、PETフィルムの応力が実質的に除去されて、PUが架橋して、不活着PU面 が得られる温度範囲よりも低い、支持体から取出した後の被覆フィルムは、前述 した装置を使用して形成される二層ガラスで使用すべきプレラミネートを構成し ていた。これから再度図面を参照して特に装置について説明する。The flow coated PET film was cured at 70° C. for 1 hour. This temperature is , the stress in the PET film is substantially removed and the PU crosslinks to form a non-active PU surface. The coated film after removal from the support is lower than the temperature range in which Pre-laminates should be used with double glazing that is formed using equipment that was. The apparatus will now be specifically described with reference to the drawings again.
熱成形アセンブリの外周形状は円形であり、ハウジング26の内径は36.8c mであった。支持台18の直径は35.6cmであり、湾曲可能面48は、成形 され、室温加硫したショアーA押込硬度が約65のシリコーンエラストマであっ た0面48のくぼんだ上面は球状であり、曲率半径は48.3cmであった。ハ ウジング26内での台18の垂直位置は、面48の上方リムがハウジング26の 側壁24の上部から約0.32cmはど下になるように調整した。ハウジング2 6の側壁24の内面に対して位置決めねじ64を締め付けて、支持台18をハウ ジング26内の同心上に固定した。The outer circumferential shape of the thermoformed assembly is circular, and the inner diameter of the housing 26 is 36.8 cm. It was m. The diameter of the support base 18 is 35.6 cm, and the bendable surface 48 is molded. The silicone elastomer has a Shore A indentation hardness of about 65 and is cured at room temperature. The concave upper surface of the surface 48 was spherical and had a radius of curvature of 48.3 cm. C The vertical position of platform 18 within housing 26 is such that the upper rim of surface 48 is It was adjusted to be approximately 0.32 cm below the top of the side wall 24. housing 2 Tighten the positioning screw 64 against the inner surface of the side wall 24 of It was fixed concentrically within the ring 26.
支持体102は、透明なフローガラスからなり、角に丸みのある0、23cm厚 さの長方形プレート(約22.2am x 27.9cm)であった、このプレ ートを、支持部材48の曲率半径とほぼ一致するように炉内で約48.3cmの 曲率半径になるまで曲げた。くぼんだ側を上にして、プレート102を部材48 上の中央に置いた。The support 102 is made of transparent flow glass and has a thickness of 0.23 cm with rounded corners. This plate was a large rectangular plate (approximately 22.2am x 27.9cm). 48.3 cm in the furnace to approximately match the radius of curvature of the support member 48. Bend it until it reaches the radius of curvature. Place plate 102 on member 48 with the recessed side up. I placed it in the top center.
層状複合材料32は、組織化された両面を有し且つ前述した特定プレラミネート 、即ちその上側が約0125mm厚さの架橋PU層でVc覆された0、05mm 厚さのPETフィルムに対面接触する実施例C−1で使用した型及び厚さの可塑 化部分PVB下層を含んでいた。可塑化部分PVB層は、直径34cmの円上に 均等に間隔をあけて配置された直径6mmのスルーホールを八つ有していた0層 状複合材料は締付はリング49と側壁24の上面との間に締付けられて、締付け られた周囲の周りに気密シールを形成した。The layered composite material 32 has both textured surfaces and the specific prelaminate described above. , i.e. 0.05 mm whose upper side is covered with a cross-linked PU layer approximately 0.0125 mm thick. The mold and thickness used in Example C-1 for face-to-face contact with the thick PET film contained a PVB underlayer. The plasticized part PVB layer is placed on a circle with a diameter of 34 cm. Layer 0 had eight evenly spaced 6mm diameter through holes. The shaped composite material is tightened between the ring 49 and the top surface of the side wall 24. formed an airtight seal around the exposed perimeter.
次に、締付けられた熱成形アセンブリをオートクレーブチャンバ12内に置き、 マニホールド27に真空接続したく図1)、オートクレーブを密封し、室温で又 は室温付近で真空ポンプ30を介して1.33kPa未満の圧力で、熱成形アセ ンブリ及びオートクレーブチャンバから同時に排気した。排気が完了すると、オ ートクレーブチャンバへの真空接続を閉鎖しく図1のバルブ37)、チャンバ1 2内の圧力が約97kPaに達するまでチャンバ12にゆっくりと空気を導入し た。複合シート32上で発生した差圧によって、シートは強く延伸されて、ガラ ス102の湾曲面と整合接触した。締付けられた複合材料32とガラス支持体と の間の空間及びシート80とフィルム82との界面から排気されたので、この成 形段術中のエアトラップは取るに足らないものであった。次に、オートクレーブ の圧力を約10分以上1136kPaに上げ、ガラス層102の破損又は層10 2の縁部と締付はリングとの間の区域での複合シートの破断を防止するために、 熱成形アセンブリ内の圧力をオートクレーブの圧力よりも35〜135kPaは ど低く維持するように差圧コントローラ98をセットした。オートクレーブの圧 力が1136kPaに達すると、圧力差はゼロに下がった。The tightened thermoformed assembly is then placed in the autoclave chamber 12; To make a vacuum connection to the manifold 27 (Fig. 1), seal the autoclave and store it again at room temperature. The thermoforming assembly is heated at a pressure of less than 1.33 kPa via the vacuum pump 30 at around room temperature. The assembly and autoclave chamber were evacuated simultaneously. When exhausting is complete, turn on the Close the vacuum connection to the autoclave chamber (valve 37 in Figure 1), chamber 1. Air is slowly introduced into chamber 12 until the pressure inside chamber 2 reaches approximately 97 kPa. Ta. Due to the differential pressure generated on the composite sheet 32, the sheet is strongly stretched and becomes glassy. It made alignment contact with the curved surface of the base 102. The clamped composite material 32 and the glass support This formation Air traps during Gedanjutsu were insignificant. Then autoclave The pressure of 2 edges and tightening to prevent breakage of the composite sheet in the area between the ring and The pressure within the thermoforming assembly should be 35 to 135 kPa below the autoclave pressure. The differential pressure controller 98 was set to keep the pressure as low as possible. autoclave pressure When the force reached 1136 kPa, the pressure difference dropped to zero.
オートクレーブの圧力が上昇し始めると同時に、オートクレーブ内の温度は5℃ /分の速度で上昇し、145℃で横ばい状態になり、そこで30分間保持した0 次いで、オートクレーブを5〜b なるまで約5分間排気し、開放した。熱成形アセンブリを取出し、クランプをゆ るめ、ガラス/複合材料シートを取出した。過剰プラスチックをトリミングして 、二層ガラスパネルを残した。このガラスパネルはガラス層に完全に適合するプ ラスチック層を含み、パネルの一方の側には反対側から見たときに目に見えるし わも物体の光学的歪みもなかった。At the same time as the pressure in the autoclave begins to rise, the temperature inside the autoclave reaches 5℃. /min, plateaued at 145°C and held there for 30 min. Then autoclave for 5~b It was evacuated for about 5 minutes until it became saturated and then opened. Remove the thermoform assembly and loosen the clamp. Then, the glass/composite material sheet was taken out. Trim excess plastic , leaving a double-layer glass panel. This glass panel is made of plastic that perfectly fits the glass layer. Contains a plastic layer on one side of the panel that is visible when viewed from the opposite side. There was also no optical distortion of the object.
実施例C−1で使用した同じ50°Cという高温にJ%露した前記二層パネルの 切片は、約30日後に完全に屹燥したポリウレタン暴露面を有していた。このこ とは、部分PVB層の可塑剤の移動が生じなかったことを示している。The two-layer panel exposed to J% of the same high temperature of 50°C used in Example C-1 The sections had completely dried polyurethane exposed surfaces after about 30 days. this child indicates that no migration of the plasticizer in the partial PVB layer occurred.
本実施例のしわのない二層ガラスパネルでの特性試験の結果は以下の通りであっ た。The results of the characteristic test on the wrinkle-free double-layer glass panel of this example are as follows. Ta.
特性 結果 暴露安定性 時間 黄色度 0.8 −1.52 −1.95曇り度% 0.88 1.2 0.9 9耐摩耗性 1.07 @ 0時間;6力月のフロラダ暴露後は1.67 変形回復 15分 耐溶剤性 最初の膨潤後に表面は溶剤が蒸発すると正常に戻った 前記結果は、本発明の二層ガラスパネルの優れた機械性能を示している。 Xe nonウェザロメータに5000時間暴露した後のYrの増加は5%未満であっ た。Characteristics Results Exposure stability time Yellowness 0.8 -1.52 -1.95 Haze% 0.88 1.2 0.9 9 Abrasion resistance 1.07 @ 0 hours; 1.67 after 6 days of Florada exposure Deformation recovery 15 minutes Solvent resistance After initial swelling, the surface returned to normal when the solvent evaporated. The above results demonstrate the excellent mechanical performance of the double layer glass panel of the present invention. Xe The increase in Yr after 5000 hours of exposure to a non-weatherometer was less than 5%. Ta.
この対照例は、ポリエステルフィルムを含まない二層の製造に対する作用を示し ている。This control example shows the effect on the production of a bilayer without polyester film. ing.
実施例1の装置及び方法を用いて、実施例C−1の部分PVB−PUプラスチッ クラミネート含ガラスと貼り合わせて二層にした。ポリエステルフィルムは使用 しなかった。Using the apparatus and method of Example 1, the partial PVB-PU plastic of Example C-1 was prepared. It was laminated with glass-containing laminate to form two layers. Polyester film is used I didn't.
形成された二層を外観検査したところ、PU層の周囲周りの縁部(図3の99) にかなりの波しわがあることが判明した。軟質PVBは下層の硬質ガラス層の縁 部上で延伸されると、ガラス層の厚みのある面97にぴったり一致した0部分P VBが局部的に過剰に伸張されると、部分PVBに直接強く結合され、従って部 分PVBの延伸運動を正確にフォローするPU層が好ましくないほど破断された 。実施例1ではPU層のこのような縁部の破断は認められなかった。実施例1の 場合、部分PVB層とPU層との間のPETフィルムが安定化の作用をして、局 部的な過剰延伸及びそれに関連するPU層縁縁部波しわが避けられた。When the formed two layers were visually inspected, the edges around the PU layer (99 in Figure 3) It was found that there were considerable waves and wrinkles. Soft PVB is the edge of the underlying hard glass layer When stretched over the part, the 0 part P closely corresponds to the thick surface 97 of the glass layer. When the VB is locally overstretched, it is strongly coupled directly to the partial PVB and thus the partial The PU layer, which accurately follows the stretching movement of the PVB, was unfavorably ruptured in minutes. . In Example 1, such edge breakage of the PU layer was not observed. Example 1 In this case, the PET film between the partial PVB layer and the PU layer has a stabilizing effect and the local Local overstretching and associated PU layer edge ripples were avoided.
更には、この実施例C−2では、PU被被膜化学的に結合されている悪態性部分 PVB下層の収縮運動によるPU面のしわ及び歪みを避けるために、PU被被膜 硬化温度を約50℃に制限せねばならなかった。これは、PETフィルム3含ん でいる実施例1の場合の70℃とは対照的である。硬1ヒは時間一温度に依存す るので、時間は使用する特定触媒及び濃度によって約110℃で約3分と短くな り得る。このように温度が高くなると、商業的に望ましい硬化サイクルの短縮が 簡単になり、しかもしわのない二層製品が得られる。Furthermore, in this Example C-2, the PU coating chemically bonded the swearing portion. To avoid wrinkles and distortion of the PU surface due to shrinkage movement of the PVB underlying layer, the PU coating is The curing temperature had to be limited to about 50°C. This includes PET film 3 This is in contrast to the temperature of 70° C. in Example 1. Hardness depends on time and temperature. Therefore, the time can be as short as about 3 minutes at about 110°C depending on the specific catalyst and concentration used. can be obtained. These higher temperatures reduce the commercially desirable curing cycle. This makes it easy and results in a crease-free two-layer product.
鮭qニュ ここでは、本発明の二層ガラスパネルで米国特許第4.937,147号に記載 の従来技術に基づ<PUU合物を使用したときのPU層の曇り度への影響を説明 する。salmon qyu Here, the present invention is described in U.S. Pat. No. 4,937,147 with a double layer glass panel. Based on the conventional technology of do.
実施例1のプレラミネート成形方法に基づいてPET−PUサラミートを製造し た。但し、トリメチロールプロパン架橋剤を含んでいる米国特許第4,937, 147号の実施例6に記載の従来技術の配合物を使用した。硬化後にPU被被膜 外観は肉眼で見ると非常に乳濁状なので、曇り度は4%よりも許容できないほど 大きいと推定された。対照的に、PETフィルム上のPU被被膜架橋剤が実施例 1と同様にエトキシル化トリメチロールプロパンのときには、プレラミネートの 曇り度及び二層ガラスの耐摩耗性は十分に許容できる品質の範囲内にあった。硬 化のために紫外線に暴露して製造した配合物中でエトキシル化トリメチロールプ ロパントリアクリし−1〜を使用した場き、同様の結果が子、忠される。PET-PU salamito was manufactured based on the pre-laminate molding method of Example 1. Ta. However, U.S. Pat. No. 4,937, which contains a trimethylolpropane crosslinker, The prior art formulation described in Example 6 of No. 147 was used. PU coating after curing Appearance is very opalescent to the naked eye, with haze levels unacceptable below 4%. estimated to be large. In contrast, the PU coated crosslinker on PET film Similarly to 1, when using ethoxylated trimethylolpropane, pre-laminate The haze and abrasion resistance of the double glazing were well within acceptable quality. hard Ethoxylated trimethylol in formulations prepared by exposure to UV light for oxidation. Similar results were obtained when using Ropantriacrylic-1.
本明細書ではガラスと特定の数及び型のプラスチック層とのために使用する本発 明の装置を開示したが、所望とあれば、形成される二層構造て場合によってプラ スチック層の数を増減させるか又はプラスチック若しくは他の材料からなる代替 機能層及び/若しくは被膜を使用してもよい。The invention herein uses glass and a specific number and type of plastic layers. However, if desired, the two-layer structure formed may be Alternatives that increase or decrease the number of stick layers or consist of plastic or other materials Functional layers and/or coatings may also be used.
同様にガラスの代わりに、代替硬質部材(例えばポリカーボネート又はポリメチ ルメタクリレート)の使用が可能であり得る。Similarly, instead of glass, alternative rigid materials (e.g. polycarbonate or polymethane) can be used. methacrylate) may be possible.
本明細書で説明した型の市販サイズの装置を使用すると、プレラミネートをロー ル形状に製造して、便宜的には場合によって二層ガラスパネルの局部製造のため に他の場所に運搬することができる。Using commercially sized equipment of the type described herein, prelaminates can be rolled for local manufacturing of double-layer glass panels for convenience and in some cases. can be transported to other locations.
前述した説明は例示的であって、非制限的である。当業者には種々の変形及び変 更が容易に提示されるであろう。The foregoing description is illustrative and non-limiting. Various modifications and variations will occur to those skilled in the art. Changes will be readily presented.
従って、前述した説明は単なる例とみなし、本発明の範囲は以下の請求の範囲で 明白となろう。Accordingly, the foregoing description should be considered as illustrative only and the scope of the invention is defined by the following claims. Let it be clear.
珊 N 国際調査報告 PCTAIS 91108262フロ〕lトページの続き (81)指定国 EP(AT、BE、CH,DE。coral N International search report PCTAIS 91108262 floor Continued from the first page (81) Designated countries EP (AT, BE, CH, DE.
DK、 ES、FR,GB、 GR,IT、 LU、 NL、SE)、AU、B R,C3,JP、KR (72)発明者 サイモン、ロバート・バーバート・メルビン アメリカ合衆国、マサチューセッツ・ 01106、ロングメドウ、キャラベル・ドライブ・23DK, ES, FR, GB, GR, IT, LU, NL, SE), AU, B R, C3, JP, KR (72) Inventor: Simon, Robert Barbert Melvin United States, Massachusetts 23 Caravel Drive, Longmeadow, 01106
Claims (19)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61773590A | 1990-11-26 | 1990-11-26 | |
| US617,735 | 1990-11-26 | ||
| US617,734 | 1990-11-26 | ||
| US07/617,734 US5082515A (en) | 1990-11-26 | 1990-11-26 | Method of forming a bilayer glazing panel |
| PCT/US1991/008262 WO1992009427A1 (en) | 1990-11-26 | 1991-11-06 | Method and apparatus for forming a bilayer glazing panel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH06502836A true JPH06502836A (en) | 1994-03-31 |
Family
ID=27088085
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4502255A Pending JPH06502836A (en) | 1990-11-26 | 1991-11-06 | Method and apparatus for forming double-layer glass panels |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0559759A1 (en) |
| JP (1) | JPH06502836A (en) |
| KR (1) | KR960004760B1 (en) |
| AU (1) | AU9049291A (en) |
| BR (1) | BR9107123A (en) |
| MX (1) | MX9102211A (en) |
| WO (1) | WO1992009427A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010533085A (en) * | 2007-07-09 | 2010-10-21 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Decorative polyvinyl butyral solar control laminate |
| JP2020160255A (en) * | 2019-03-26 | 2020-10-01 | 新光エンジニアリング株式会社 | Workpiece laminating device and work stage |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR9307804A (en) * | 1992-12-30 | 1995-11-14 | Jose R Mannheim | Curved unbreakable glass laminate and process to form the laminate |
| KR101795341B1 (en) | 2017-06-08 | 2017-11-07 | 김재욱 | Multistage degassing device available autoclave |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR192924A1 (en) * | 1971-04-20 | 1973-03-21 | Saint Gobain | LAMINATED SAFETY GLASS |
| GB2119704B (en) * | 1982-04-30 | 1985-09-11 | Glaverbel | Process of forming multi-ply laminates |
| EP0304898B1 (en) * | 1987-08-25 | 1994-11-02 | Asahi Glass Company Ltd. | Method for press-bonding laminated assembly |
-
1991
- 1991-11-06 AU AU90492/91A patent/AU9049291A/en not_active Abandoned
- 1991-11-06 KR KR1019930701550A patent/KR960004760B1/en not_active Expired - Fee Related
- 1991-11-06 WO PCT/US1991/008262 patent/WO1992009427A1/en not_active Ceased
- 1991-11-06 EP EP92900885A patent/EP0559759A1/en not_active Withdrawn
- 1991-11-06 BR BR919107123A patent/BR9107123A/en unknown
- 1991-11-06 JP JP4502255A patent/JPH06502836A/en active Pending
- 1991-11-25 MX MX9102211A patent/MX9102211A/en unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010533085A (en) * | 2007-07-09 | 2010-10-21 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Decorative polyvinyl butyral solar control laminate |
| JP2020160255A (en) * | 2019-03-26 | 2020-10-01 | 新光エンジニアリング株式会社 | Workpiece laminating device and work stage |
Also Published As
| Publication number | Publication date |
|---|---|
| WO1992009427A1 (en) | 1992-06-11 |
| KR960004760B1 (en) | 1996-04-13 |
| AU9049291A (en) | 1992-06-25 |
| BR9107123A (en) | 1993-11-03 |
| EP0559759A1 (en) | 1993-09-15 |
| KR930702153A (en) | 1993-09-08 |
| MX9102211A (en) | 1992-06-01 |
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