JPH03164452A - Production of safety sandwich glass plate - Google Patents
Production of safety sandwich glass plateInfo
- Publication number
- JPH03164452A JPH03164452A JP30120789A JP30120789A JPH03164452A JP H03164452 A JPH03164452 A JP H03164452A JP 30120789 A JP30120789 A JP 30120789A JP 30120789 A JP30120789 A JP 30120789A JP H03164452 A JPH03164452 A JP H03164452A
- Authority
- JP
- Japan
- Prior art keywords
- glass plate
- punching
- vinyl chloride
- metal
- punching metal
- 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 abstract description 27
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000002184 metal Substances 0.000 claims abstract description 42
- 229910052751 metal Inorganic materials 0.000 claims abstract description 42
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229920005989 resin Polymers 0.000 claims abstract description 22
- 239000011347 resin Substances 0.000 claims abstract description 22
- 229920001944 Plastisol Polymers 0.000 claims abstract description 19
- 239000004999 plastisol Substances 0.000 claims abstract description 19
- 125000003700 epoxy group Chemical group 0.000 claims description 19
- 239000005340 laminated glass Substances 0.000 claims description 18
- 238000004080 punching Methods 0.000 abstract description 24
- 238000010438 heat treatment Methods 0.000 abstract description 9
- 239000004593 Epoxy Substances 0.000 abstract description 4
- 238000009826 distribution Methods 0.000 abstract description 4
- 239000000853 adhesive Substances 0.000 abstract description 3
- 230000001070 adhesive effect Effects 0.000 abstract description 3
- 238000003475 lamination Methods 0.000 abstract description 2
- 230000007547 defect Effects 0.000 abstract 1
- 239000000178 monomer Substances 0.000 description 11
- 239000004014 plasticizer Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 7
- -1 glycidyl Glycidyl esters Chemical class 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000011229 interlayer Substances 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 2
- JQCXWCOOWVGKMT-UHFFFAOYSA-N diheptyl phthalate Chemical compound CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 description 2
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- BMASLOOHTMQIGP-ZOKJKDLISA-H (z)-but-2-enedioate;butyltin(3+) Chemical compound CCCC[Sn+3].CCCC[Sn+3].[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O BMASLOOHTMQIGP-ZOKJKDLISA-H 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- SFUDBXKBPOKIIW-ARJAWSKDSA-N 1-o-ethyl 4-o-(oxiran-2-ylmethyl) (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCC1CO1 SFUDBXKBPOKIIW-ARJAWSKDSA-N 0.000 description 1
- ARNSVGUHSKJJNE-UHFFFAOYSA-N 1-o-methyl 4-o-(oxiran-2-ylmethyl) 2-methylidenebutanedioate Chemical compound COC(=O)C(=C)CC(=O)OCC1CO1 ARNSVGUHSKJJNE-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- LQZDDWKUQKQXGC-UHFFFAOYSA-N 2-(2-methylprop-2-enoxymethyl)oxirane Chemical compound CC(=C)COCC1CO1 LQZDDWKUQKQXGC-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- QARRDVBZMBYNFA-UHFFFAOYSA-N 2-pent-3-enyloxirane Chemical compound CC=CCCC1CO1 QARRDVBZMBYNFA-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- ALKCLFLTXBBMMP-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl hexanoate Chemical compound CCCCCC(=O)OC(C)(C=C)CCC=C(C)C ALKCLFLTXBBMMP-UHFFFAOYSA-N 0.000 description 1
- FASUFOTUSHAIHG-UHFFFAOYSA-N 3-methoxyprop-1-ene Chemical compound COCC=C FASUFOTUSHAIHG-UHFFFAOYSA-N 0.000 description 1
- XAYDWGMOPRHLEP-UHFFFAOYSA-N 6-ethenyl-7-oxabicyclo[4.1.0]heptane Chemical compound C1CCCC2OC21C=C XAYDWGMOPRHLEP-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- PYGXAGIECVVIOZ-UHFFFAOYSA-N Dibutyl decanedioate Chemical compound CCCCOC(=O)CCCCCCCCC(=O)OCCCC PYGXAGIECVVIOZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 101001034845 Mus musculus Interferon-induced transmembrane protein 3 Proteins 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- FKXJWELJXMKBDI-UHFFFAOYSA-K [butyl-di(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(OC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC FKXJWELJXMKBDI-UHFFFAOYSA-K 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- OCWYEMOEOGEQAN-UHFFFAOYSA-N bumetrizole Chemical compound CC(C)(C)C1=CC(C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O OCWYEMOEOGEQAN-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- PUFGCEQWYLJYNJ-UHFFFAOYSA-N didodecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCC PUFGCEQWYLJYNJ-UHFFFAOYSA-N 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- XWVQUJDBOICHGH-UHFFFAOYSA-N dioctyl nonanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCC(=O)OCCCCCCCC XWVQUJDBOICHGH-UHFFFAOYSA-N 0.000 description 1
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- UCAOGXRUJFKQAP-UHFFFAOYSA-N n,n-dimethyl-5-nitropyridin-2-amine Chemical compound CN(C)C1=CC=C([N+]([O-])=O)C=N1 UCAOGXRUJFKQAP-UHFFFAOYSA-N 0.000 description 1
- ZMHZSHHZIKJFIR-UHFFFAOYSA-N octyltin Chemical compound CCCCCCCC[Sn] ZMHZSHHZIKJFIR-UHFFFAOYSA-N 0.000 description 1
- 150000004967 organic peroxy acids Chemical class 0.000 description 1
- YCNNCJXFNCVEOL-UHFFFAOYSA-N oxiran-2-ylmethyl ethenesulfonate Chemical compound C=CS(=O)(=O)OCC1CO1 YCNNCJXFNCVEOL-UHFFFAOYSA-N 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 239000005336 safety glass Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Joining Of Glass To Other Materials (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は安全合わせガラス板用プラスチゾルに関するも
のであり、施錠の安全、侵入防止などができる頑丈なパ
ンチングメタル内蔵の安全合わせガラス板の製造方法に
関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a plastisol for safety laminated glass plates, and a method for producing safety laminated glass plates with built-in sturdy punched metal that can be locked safely and prevented from entering. It is related to.
〔従来の技術]
従来、ガラス板とパンチングメタルの間に柔軟で強靭な
中間膜、例えばポリビニルブチラール膜やエチレンー酢
酸ビニル共重合体膜が使われているが、パンチングメタ
ルのパンチングの大きさやパンチングの分布に制限があ
り、上部だけパンチングしたものや、パンチングのサイ
ズの大きいものと小さいものが分布したものを用いると
、合わせガラス板の厚みが不均一になる欠点やガラス板
間に気泡が残る欠点がある。[Conventional technology] Conventionally, a flexible and strong interlayer film such as a polyvinyl butyral film or an ethylene-vinyl acetate copolymer film has been used between a glass plate and a punched metal, but the size of the punching in the punching metal and the strength of the punching There is a limit to the distribution, and if you use a type with punching only in the upper part or a type with large and small punches distributed, the thickness of the laminated glass plate will be uneven, or air bubbles will remain between the glass plates. There is.
本発明は、合わせガラス板の間にある金属網の網目の寸
法及びパンチングメタルのパンチングの形状、大きさ、
分布の影響を受けない均一な厚さヲ有し、パンチングメ
タルとガラス板が強固な接i度を有する安全合わせガラ
ス板の製造方法を提供することを目的とするものである
。The present invention relates to the dimensions of the metal mesh between the laminated glass plates, the shape and size of the punching of the punched metal,
The object of the present invention is to provide a method for manufacturing a safety laminated glass plate that has a uniform thickness that is not affected by distribution and has a strong bond between the punched metal and the glass plate.
[課題を解決するための手段]
本発明者らは、上記欠点を解決するために、流動性のよ
いプラスチゾルにエボキシ基含有の塩化ビニル樹脂を用
いれば、流動不良による気泡の混入や厚みの不均一さを
改善できることに着目して、本発明製造方法を完威した
。[Means for Solving the Problems] In order to solve the above-mentioned drawbacks, the present inventors have found that if an epoxy group-containing vinyl chloride resin is used in plastisol with good fluidity, air bubbles may be mixed in due to poor flow and the thickness may be insufficient. Focusing on the ability to improve uniformity, the manufacturing method of the present invention was successfully applied.
すなわち、本発明は、ガラス板とガラス板の間にパンチ
ングメタル又は金属網を挟み込んだ合わせガラス板にお
いて、ガラス板とパンチングメタルの間にエポキシ基含
有塩化ビニル樹脂を必須戊分とする戊膜性プラスチゾル
を介在させて積層し、加熱圧着することを特徴とする安
全合わせガラス板の製造方法を提供するものである。That is, the present invention provides a laminated glass plate in which a punched metal or a metal mesh is sandwiched between the glass plates, and a film-forming plastisol that essentially contains an epoxy group-containing vinyl chloride resin between the glass plate and the punched metal. The present invention provides a method for manufacturing a safety laminated glass sheet, which is characterized by laminating the sheets with the glass sheets interposed therebetween and bonding them under heat and pressure.
本発明において用いられるエポキシ基含有塩化ビニル系
樹脂とは、1)塩化ビニルと、エボキシ基を有する単量
体と、任意成分であるこれらと共重合可能な単量体との
共重合体、2)塩化ビニル単量体を主成分とする塩化ビ
ニル系共重合体にエポキシ基を付加せしめたもの、3)
塩化ビニル系共重合体に、これと相溶するエポキシ基含
有樹脂を分散させた組成物を使用することができる。The epoxy group-containing vinyl chloride resin used in the present invention is: 1) a copolymer of vinyl chloride, a monomer having an epoxy group, and an optional monomer copolymerizable with these; ) A vinyl chloride copolymer containing vinyl chloride monomer as the main component with an epoxy group added, 3)
A composition in which a vinyl chloride copolymer is dispersed with an epoxy group-containing resin that is compatible with the vinyl chloride copolymer can be used.
いずれのエボキシ基含有塩化ビニル系樹脂においても、
エポキシ基含有量は、0.05〜5重量%のものを使用
することができる。In any epoxy group-containing vinyl chloride resin,
An epoxy group content of 0.05 to 5% by weight can be used.
エボキシ基含有量が少ないと、ガラスへの接着力が劣り
、多すぎると、接着力が強すぎ耐貫通性が劣る。If the epoxy group content is too low, the adhesive strength to glass will be poor, and if it is too high, the adhesive strength will be too strong and the penetration resistance will be poor.
1)の型のエポキシ含有塩化ビニル系樹脂において用い
るエポキシ基を有する単量体の例としては、アリルグリ
シジルエーテル、メタリルグリシジルエーテルなどの不
飽和アルコールのグリシジルエーテル類、グリシジルメ
タクリレート、グリシジルアクリレート、グリシジルー
p−ビニルベンゾエート、メチルグリシジルイタコネー
ト、グリシジルエチルマレート、グリシジルビニルスル
ホネート、グリシジル(メタ)アリルスルホネートなど
の不飽和酸のグリシジルエステル類、ブタジエンモノオ
キサイド、ビニルシクロヘキセンモノオキサイド、2−
メチル−5.6−エポキシヘキセンなどのエポキシドオ
レフィン類などが挙げられる。Examples of monomers having epoxy groups used in the epoxy-containing vinyl chloride resin of type 1) include glycidyl ethers of unsaturated alcohols such as allyl glycidyl ether and methallyl glycidyl ether, glycidyl methacrylate, glycidyl acrylate, and glycidyl Glycidyl esters of unsaturated acids such as p-vinyl benzoate, methyl glycidyl itaconate, glycidyl ethyl maleate, glycidyl vinyl sulfonate, glycidyl (meth)allylsulfonate, butadiene monoxide, vinylcyclohexene monooxide, 2-
Examples include epoxide olefins such as methyl-5,6-epoxyhexene.
まt;、本発明において、エポキシ基を有する単量体及
び塩化ビニルと必要に応じて共重合させる単量体として
は、酢酸ビニル、ブロピオン酸ビニルなどの脂肪酸ビニ
ル類、エチレン、プロピレンなどのオレフィン類、塩化
ビニリデン、フッ化ビニリデンなどのハロゲン化ビニリ
デン類、インプチルビニルエーテル、メチルビニルエー
テル、エチルビニルエーテルなどのビニルエーテル類、
塩化アリル、メチルアリルエーテルなどのアリル化合物
類などが挙げられる。In the present invention, monomers having an epoxy group and monomers to be copolymerized as necessary with vinyl chloride include fatty acid vinyls such as vinyl acetate and vinyl propionate, and olefins such as ethylene and propylene. vinylidene halides such as vinylidene chloride and vinylidene fluoride; vinyl ethers such as imptyl vinyl ether, methyl vinyl ether, and ethyl vinyl ether;
Examples include allyl compounds such as allyl chloride and methyl allyl ether.
これらの単量体を用いて、本発明に用いる塩化ビニル系
共重合体は、懸濁重合、乳化重合など塩化ビニルの重合
法としてよく知られている方法゜が採用可能である。例
えば、プラスチゾルとして使用する場合は、プラスチゾ
ルの流動性を適当に保つ目的から、ペースト加工用塩化
ビニル樹脂の製法として常用の乳化重合あるいはミクロ
懸濁重合で製造することができる。Using these monomers, well-known vinyl chloride polymerization methods such as suspension polymerization and emulsion polymerization can be used to produce the vinyl chloride copolymer used in the present invention. For example, when used as a plastisol, it can be produced by emulsion polymerization or microsuspension polymerization, which is a commonly used method for producing vinyl chloride resin for paste processing, in order to maintain appropriate fluidity of the plastisol.
2)の型のエポキシ基含有塩化ビニル系樹脂において、
エポキシ基の付加方法としては、塩化ビニル系樹脂を熱
処理やアルカリ化合物との接触により脱塩化水素した後
、これを有機過酸などによりエポキシ化する方法などが
挙げられる。In the epoxy group-containing vinyl chloride resin of type 2),
Examples of the method for adding an epoxy group include a method in which a vinyl chloride resin is dehydrochlorinated by heat treatment or contact with an alkali compound, and then epoxidized with an organic peracid or the like.
ここに用いる塩化ビニル系樹脂は、塩化ビニル単量体単
位を主体とし、1)において所望により用いる単量体成
分単位を構成単位とする共重合体体を使用することがで
きる。The vinyl chloride resin used here may be a copolymer mainly composed of vinyl chloride monomer units and having as a constituent unit the monomer component units optionally used in 1).
3)の型のエポキシ基含有樹脂とは、例えば、エポキシ
基を有する単量体と共重合可能な単量体との共重合体で
あって、2)で用いた塩化ビニル系樹脂と相溶性のある
ものを該塩化ビニル系樹脂に混合したm戊物などを使用
することができる。The epoxy group-containing resin of the type 3) is, for example, a copolymer of a monomer having an epoxy group and a copolymerizable monomer, and is compatible with the vinyl chloride resin used in 2). It is possible to use a mixture of the vinyl chloride resin and the like.
本発明に使用されるエポキシ基含有塩化ビニル系樹脂に
は、可塑剤以外に目的に応じて、安定剤、紫外線吸収剤
、酸化防止剤、滑剤、充填剤、着色剤などを混合するこ
とができる。In addition to plasticizers, stabilizers, ultraviolet absorbers, antioxidants, lubricants, fillers, colorants, etc. can be mixed with the epoxy group-containing vinyl chloride resin used in the present invention, depending on the purpose. .
さらに、別の塩化ビニル系樹脂、アクリル樹脂、エポキ
シ樹脂などの塩化ビニルと相溶し得る樹脂などの混用も
可能である。Furthermore, it is also possible to use a resin compatible with vinyl chloride, such as another vinyl chloride resin, acrylic resin, or epoxy resin.
本発明のエポキシ基含有塩化ビニル系樹脂に配合される
可塑剤は一般にポリ塩化ビニル用可塑剤と称されている
ものが広く使用できる。例えば、脂肪族系可塑剤として
はジオクチルアジペート、プチルジグリコールアジペー
ト、ジオクチルアゼレート、ジブチルセバケート、アジ
ピン酸ジイソデシルなどが挙げられ、フタル酸系可塑剤
としてはジオクチルフタレート、ジブチル7タレート、
ジイソプチルフタレート、プチルベンジルフタレート、
ジラウリルフタレート、ジヘプチルフタレートなどが挙
げられ、り冫酸系可塑剤としてはトリキシレニルホス7
エート、トリクレジルホスフェート、タレジルジフエニ
ルホス7エート、トリスクロロエチルホスフエート、ト
リスクロロエチルホスファイト、トリブチルホス7エー
トなどが挙げられる。エポキシ誘導体としてはエポキシ
化大豆油、エボキシ脂肪酸モノエステルなどがある。ポ
リエステル系可塑剤も場合によっては使用可能である。As the plasticizer to be added to the epoxy group-containing vinyl chloride resin of the present invention, those generally referred to as plasticizers for polyvinyl chloride can be widely used. For example, aliphatic plasticizers include dioctyl adipate, butyl diglycol adipate, dioctyl azelate, dibutyl sebacate, diisodecyl adipate, etc., and phthalate plasticizers include dioctyl phthalate, dibutyl heptalate,
diisobutyl phthalate, butyl benzyl phthalate,
Examples of dilauryl phthalate and diheptyl phthalate include trixylenyl phos 7 as a phosphoric acid plasticizer.
ate, tricresyl phosphate, talesyl diphenyl phos7ate, trischloroethyl phosphate, trischloroethyl phosphite, tributyl phos7ate, and the like. Examples of epoxy derivatives include epoxidized soybean oil and epoxy fatty acid monoester. Polyester plasticizers can also be used in some cases.
可塑剤の配合量は塩化ビニル系樹脂100重量部に対し
、20〜120重量部が適当である。可塑剤が多すぎる
と膜強度が低下し、少なすぎるとグラスチゾルの粘度が
高くなり、塗布の作業性が悪くなる。The appropriate amount of the plasticizer to be blended is 20 to 120 parts by weight per 100 parts by weight of the vinyl chloride resin. If there is too much plasticizer, the film strength will decrease, and if it is too little, the viscosity of Glastisol will increase and the workability of coating will deteriorate.
所望によりプラスチゾルに添加する熱安定剤としてはブ
チル錫ラウレート、ブチル錫マレート、オクチル錫マレ
ートなどの脂肪酸のアルキル化錫化合物や、ジノルマル
オクチル錫のビス(インオクチルチオグリコール酸エス
テル)塩などのアルキル錫含有硫黄化合物が好適に用い
られる。これらと共に金属石けん系の安定剤を併用する
ことも可能である。Heat stabilizers that may be added to plastisol if desired include alkylated tin compounds of fatty acids such as butyltin laurate, butyltin maleate, and octyltin maleate, and alkyl compounds such as di-normal octyltin bis(in-octylthioglycolic acid ester) salt. Tin-containing sulfur compounds are preferably used. It is also possible to use a metal soap type stabilizer together with these.
本発明グラスチゾルに添加する紫外線吸収剤としてはペ
ンゾトリアゾール系が優れており、例えば2(2’−ヒ
ドロキシ−5′−メチルフエニル)ペンゾトリアゾール
、2 (2’−ヒドロキシ−3′ターシャリーブチル−
5゛−メチルフエニル)−5−クロロベンゾトリアゾー
ル、2(2’−ヒドロキシ−3′,5″一ターシャリー
プチルフエニル)−5−クロローベンゾトリアゾール、
2(2゜−ヒドロキシ−4″−オクトキシ7エニル)ペ
ンゾトリアゾールなどを好適に使用することができる。Penzotriazole-based UV absorbers are excellent as UV absorbers to be added to Glastisol of the present invention, such as 2(2'-hydroxy-5'-methylphenyl)penzotriazole, 2(2'-hydroxy-3'tert-butyl-
5′-methylphenyl)-5-chlorobenzotriazole, 2(2′-hydroxy-3′,5″-tertiarybutylphenyl)-5-chlorobenzotriazole,
2(2°-hydroxy-4″-octoxy7enyl)penzotriazole and the like can be preferably used.
また、本発明プラスチゾルに用いる酸化防止剤としては
7エノール系酸化防止剤が優れており、例えば2,6−
ジターシャリーブチルーp−クレゾール.2,2゜−メ
チレンビス(4−メチル−6−ターシャリープチル7エ
ノール)、4.4″プチリデンビス(3−メチル−6−
ターシャリープチル7エノール),4.4’−チオビス
(3−メチル−6−ターシャリープチル7エノール)な
どが挙げられる。In addition, 7-enol antioxidants are excellent as antioxidants used in the plastisol of the present invention, such as 2,6-
Ditertiary butyl p-cresol. 2,2°-methylenebis(4-methyl-6-tert-butyl-7enol), 4.4″butylidenebis(3-methyl-6-
tert-butyl 7-enol), 4,4'-thiobis(3-methyl-6-tert-butyl 7-enol), and the like.
さらに必要に応じ、架橋剤、増粘剤、希釈剤、シラン系
やチタ不−ト系のカップリング剤などが配合される。Further, if necessary, a crosslinking agent, a thickener, a diluent, a silane type or a titanoate type coupling agent, etc. are blended.
プラスチゾルの調製は、常法に従い、樹脂、可塑剤、諸
配合材料などを混合、脱泡して行われる。Plastisol is prepared by mixing a resin, a plasticizer, various compounded materials, etc. and defoaming according to a conventional method.
プラスチゾルは液状であるため、ゴミ、異物の除去はフ
ィルターなどで行い得るし、保管輸送もタンク、パイプ
ラインといった閉鎖系での取り扱いとなるため、品質管
理が容易であるうえ、自動化にも適している。Since plastisol is in liquid form, dust and foreign matter can be removed using filters, etc., and storage and transportation are handled in closed systems such as tanks and pipelines, making quality control easy and suitable for automation. There is.
また、本発明で使用されるパンチングメタルとは、金属
板をパンチングにより穴をあけたものであり、パンチン
グメタル、パンチング板と呼ばれているものであり、本
発明に使用される金属網は、金属線を網目状にしたもの
である。金属の種類に特に制限なく使用することができ
る。Furthermore, the punching metal used in the present invention is a metal plate with holes made by punching, and is called a punching metal or a punching plate, and the metal mesh used in the present invention is It is a mesh of metal wires. The type of metal can be used without any particular restrictions.
本発明において、グラスチゾルをパンチングメタル等と
ガラス板間に介在させて積層する方法としては、ガラス
板にブレードコーター、ロールコ−’l−、7.’)+
J−ンコーター、ブローコータースプレーコーターなど
の塗工機によりプラスチゾルを塗布し、その上にパンチ
ングメタル又は金属網を気泡が入らないように貼り合わ
せ、さらにその上に上記塗工機によりプラスチゾルを塗
布し、ガラス板を気泡が入らないように貼り合わせ、積
層体としたり、ガラス板に上記塗工機によりプラスチゾ
ルを塗布、加熱ゲル化させたのち、パンチングメタル等
をのせ再度プラスチゾルを塗布し、ガラス板を気泡が入
らないように貼り合わせ、積層体としたりする方法など
、従来から公知の積層方法が挙げられる。In the present invention, the method of laminating Glastisol with punching metal or the like interposed between the glass plates is as follows: coat the glass plate with a blade coater, roll coater, 7. ')+
Plastisol is applied using a coating machine such as a J-n coater or a blow coater spray coater, and then a punched metal or metal mesh is pasted on top of it to avoid air bubbles, and then plastisol is applied on top of that using the above coating machine. , Glass plates are bonded together to prevent air bubbles from forming into a laminate, or plastisol is applied to the glass plate using the above coating machine, heated to gel, and then a punching metal etc. is placed on it and plastisol is applied again to form a glass plate. Conventionally known lamination methods, such as a method of laminating the materials without air bubbles to form a laminate, can be used.
こうして積層した安全ガラス板は次に加熱されて、プラ
スチゾル層をゲル化し、強固な弾性膜とされる。ここで
加熱する方法としては、熱風循環加熱、(遠)赤外線加
熱、誘電加熱、誘導加熱など、通常のペースト加工に用
いられる加熱装置を使用できる。The laminated safety glass sheets are then heated to gel the plastisol layer and form a strong, elastic membrane. As a heating method here, heating devices used in normal paste processing, such as hot air circulation heating, (far) infrared heating, dielectric heating, and induction heating, can be used.
以下に実施例を挙げて本発明をさらに具体的に説明する
。The present invention will be explained in more detail with reference to Examples below.
実施例\l
塩化ビニル90重量%、グリシジルメタクリレート10
重量%よりなる平均粒径1μm1平均重合度800のエ
ポキシ基含有塩化ビニル樹脂100重量部に、ジオクチ
ルアジペート45重量部、ジオクチル7タレート15重
量部、ジブチル錫ポリメルカプタイド4重量部、2,2
′−メチレンビス−4−メチル−6−ターシャリーブチ
ルフェノール0.3重量部などを真空式高速脱泡混合機
に入れ、混合、脱泡する。Example\l Vinyl chloride 90% by weight, glycidyl methacrylate 10
To 100 parts by weight of an epoxy group-containing vinyl chloride resin with an average particle diameter of 1 μm and an average degree of polymerization of 800, 45 parts by weight of dioctyl adipate, 15 parts by weight of dioctyl 7-talate, 4 parts by weight of dibutyltin polymercaptide, 2,2
0.3 parts by weight of '-methylenebis-4-methyl-6-tert-butylphenol and the like are placed in a vacuum high-speed defoaming mixer, mixed, and defoamed.
次に、3 0 0+*mX 3 0 0ars,厚み3
1RrRのガラス板に上記プラスチゾルをブレードコー
ターで0.4+u+の厚みになるように塗布し、第1図
のパターンのパンチングメタル(2 9 5miX 2
9 5m屑、厚さ0 . 3 term、孔径3旧、
孔間距離5■)をのせ、次いで、そのパンチングメタル
の上にプラスチゾルをナイ7コーターで0.4mmの厚
さになるように塗布し、最後に、その上に、ガラス板を
気泡が入らないように積層して貼り合わせた。この積層
体を180℃で30分間加熱し、安全合わせガラス板を
得t;。Next, 300+*mX300ars, thickness 3
The above plastisol was applied to a 1RrR glass plate using a blade coater to a thickness of 0.4+u+, and punched metal (2 9 5mi x 2
9 5m scrap, thickness 0. 3 terms, hole diameter 3 old,
Then, apply plastisol on the punched metal to a thickness of 0.4 mm using a Ny7 coater, and finally, place a glass plate on top of it to prevent air bubbles. Laminated and pasted together like this. This laminate was heated at 180°C for 30 minutes to obtain a safety laminated glass plate.
実施例2
実施例lのパンチングメタルの代わりに第2図のパター
ンのパンチングメタノレ(295mmX295ms,厚
さ0 . 3 rtrtas孔径6 111%孔間距離
8■)を用いた以外は実施例1と同様に操作し、安全合
わせガラス板を得た。Example 2 The same as Example 1 except that punched methanol (295 mm x 295 ms, thickness 0.3 rtrtas hole diameter 6, 111% hole distance 8 cm) having the pattern shown in Fig. 2 was used instead of the punched metal of Example 1. A safety laminated glass plate was obtained.
実施例3
実施例1のパンチングメタルの代わりに第3図に示すよ
うに、右側にか第1図のパンチング形状があり、左側に
第2図のパンチング形状があるパターンのパンチングメ
タル(2 9 5m+*x 2 9 5ms+、厚さ0
.3++v+、左半分6amd、右半分3mmu)を用
いた以外は実施例lと同様に操作し、安全合わせガラス
板を得た。Example 3 Instead of the punched metal of Example 1, as shown in Figure 3, a punched metal (295m + *x 2 9 5ms+, thickness 0
.. A safety laminated glass plate was obtained in the same manner as in Example 1, except that 3++v+, 6 amd for the left half, and 3 mmu for the right half) were used.
実施例4
実施例lのパンチングメタルの代わりに第4図に示すよ
うに、半面だけ第1図パンチン゜グ形状のあるパターン
のパンチングメタル(295**x2 9 5 +u+
,厚さ0 . 3 yarns上半分3I+llII1
下半分パンチングなし)を用いた以外は実施例1と同様
に操作し、安全合わせガラス板を得た。Example 4 Instead of the punching metal of Example 1, as shown in FIG. 4, a punching metal (295**x2 9 5 +u+
, thickness 0. 3 yarns upper half 3I+llII1
A safety laminated glass plate was obtained in the same manner as in Example 1 except that the lower half (without punching) was used.
実施例5
実施例lのパンチングメタルの代わりに碁盤の目状の網
目間隔20mm,線の径0.5開のステンレス製金属網
を用いt;以外は実施例1と同様に操作し、安全合わせ
ガラス板を得た。Example 5 Instead of the punched metal of Example 1, a stainless steel metal mesh with a grid pattern of 20 mm in pitch and a wire diameter of 0.5 was used. I got a glass plate.
比較例1
3 0 0mmX 3 0 0ars1厚さ:3+mの
ガラス板の上に、市販の合わせガラス板用中間膜1 5
mil1(ポリビニルブチラール製)を0.5wt%の
水分に調湿したものをのせ、次にその上に第1図のパタ
ーンのパンチングメタル(295+uix295mm、
厚さ0 . 3 am)をのせ、さらに上記中間膜と同
様に調整した膜、ガラス板をのせて、70〜75℃のゴ
ムローラー間を通し、予備圧着を行った。その後、13
0°0,13〜1 4 kg/ cra”の空気圧式オ
ートクレープで30分間加熱圧着し、安全合わせガラス
板を得た。Comparative Example 1 A commercially available interlayer film for laminated glass plate 15 was placed on a glass plate of 300mm x 300ars1 thickness: 3+m
Place mil1 (made of polyvinyl butyral) with a moisture content of 0.5 wt%, and then punch metal with the pattern shown in Figure 1 (295 + uix 295 mm,
Thickness 0. 3 am) was placed thereon, and a film prepared in the same manner as the above-mentioned interlayer film and a glass plate were placed thereon, and the mixture was passed between rubber rollers at 70 to 75°C for preliminary pressure bonding. After that, 13
A safety laminated glass plate was obtained by heating and pressing in a pneumatic autoclave at 0°0.13 to 14 kg/cra for 30 minutes.
比較例2
比較例1のパンチングメタルの代わりに第4図のパター
ンのパンチングメタル(295m+*x295開、厚さ
0.3m屠、上半分3ravgl、下半分パンチングな
し)を用いた他は比較例lと同様に操作して、安全合わ
せガラス板を得た。ところが、この合わせガラス板の下
部は上部よりも厚くなり、気泡も残ってしまった。Comparative Example 2 Comparative Example 1 except that a punching metal with the pattern shown in Figure 4 (295m + * 295 open, 0.3m thick, upper half 3 ravgl, lower half without punching) was used instead of the punched metal of Comparative Example 1. A safety laminated glass plate was obtained in the same manner as above. However, the bottom of this laminated glass plate was thicker than the top, and air bubbles remained.
本発明製造方法によれば、気泡がなく、パンチングメタ
ルのパンチングの形状、大きさ、分布の変化に影響され
ないで常に正確な均一の厚さの安全合わせガラス板を得
ることができる。According to the manufacturing method of the present invention, it is possible to obtain a safety laminated glass plate without bubbles and always having an accurate uniform thickness without being affected by changes in the shape, size, and distribution of punches in the punched metal.
第1図、第2図、第3図及び第4図は本発明に用いる実
施例のパンチングメタルの平面図である。
第
l
図
第
3
図
第
2
図
弔
4
図FIG. 1, FIG. 2, FIG. 3, and FIG. 4 are plan views of punched metals according to embodiments of the present invention. Figure l Figure 3 Figure 2 Figure 4
Claims (1)
属網を挟み込んだ合わせガラス板において、ガラス板と
パンチングメタルの間にエポキシ基含有塩化ビニル樹脂
を必須成分とする成膜性プラスチゾルを介在させて積層
し、加熱圧着することを特徴とする安全合わせガラス板
の製造方法。1. In a laminated glass plate in which a punched metal or metal mesh is sandwiched between glass plates, a film-forming plastisol containing an epoxy group-containing vinyl chloride resin as an essential component is interposed between the glass plate and the punched metal, and laminated, A method for producing a safety laminated glass plate, which is characterized by heat-press bonding.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30120789A JPH03164452A (en) | 1989-11-20 | 1989-11-20 | Production of safety sandwich glass plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30120789A JPH03164452A (en) | 1989-11-20 | 1989-11-20 | Production of safety sandwich glass plate |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03164452A true JPH03164452A (en) | 1991-07-16 |
Family
ID=17894072
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30120789A Pending JPH03164452A (en) | 1989-11-20 | 1989-11-20 | Production of safety sandwich glass plate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03164452A (en) |
-
1989
- 1989-11-20 JP JP30120789A patent/JPH03164452A/en active Pending
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