JPH0969646A - Solar battery module - Google Patents
Solar battery moduleInfo
- Publication number
- JPH0969646A JPH0969646A JP8135995A JP13599596A JPH0969646A JP H0969646 A JPH0969646 A JP H0969646A JP 8135995 A JP8135995 A JP 8135995A JP 13599596 A JP13599596 A JP 13599596A JP H0969646 A JPH0969646 A JP H0969646A
- Authority
- JP
- Japan
- Prior art keywords
- solar cell
- resin
- adhesive resin
- cell module
- solar battery
- 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.)
- Granted
Links
- 239000004840 adhesive resin Substances 0.000 claims abstract description 17
- 229920006223 adhesive resin Polymers 0.000 claims abstract description 17
- 150000001451 organic peroxides Chemical class 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims abstract description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 38
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 38
- 239000004745 nonwoven fabric Substances 0.000 claims description 7
- 239000003365 glass fiber Substances 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 239000012784 inorganic fiber Substances 0.000 claims description 3
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical class C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims 3
- 239000002759 woven fabric Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 abstract description 48
- 239000011347 resin Substances 0.000 abstract description 48
- 239000003063 flame retardant Substances 0.000 abstract description 15
- 239000000463 material Substances 0.000 abstract description 7
- 238000003475 lamination Methods 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 238000005470 impregnation Methods 0.000 abstract description 2
- 239000003566 sealing material Substances 0.000 abstract description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 12
- -1 polyethylene Polymers 0.000 description 12
- 238000004132 cross linking Methods 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000006087 Silane Coupling Agent Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000008393 encapsulating agent Substances 0.000 description 3
- 238000005538 encapsulation Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000003504 photosensitizing agent Substances 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- 230000003712 anti-aging effect Effects 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- 239000012796 inorganic flame retardant Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 238000010248 power generation Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 2
- DJKGDNKYTKCJKD-BPOCMEKLSA-N (1s,4r,5s,6r)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene-5,6-dicarboxylic acid Chemical compound ClC1=C(Cl)[C@]2(Cl)[C@H](C(=O)O)[C@H](C(O)=O)[C@@]1(Cl)C2(Cl)Cl DJKGDNKYTKCJKD-BPOCMEKLSA-N 0.000 description 1
- QEQBMZQFDDDTPN-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy benzenecarboperoxoate Chemical compound CC(C)(C)OOOC(=O)C1=CC=CC=C1 QEQBMZQFDDDTPN-UHFFFAOYSA-N 0.000 description 1
- QXSZNDIIPUOQMB-UHFFFAOYSA-N 1,1,2,2-tetrabromoethane Chemical group BrC(Br)C(Br)Br QXSZNDIIPUOQMB-UHFFFAOYSA-N 0.000 description 1
- HSLFISVKRDQEBY-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)cyclohexane Chemical compound CC(C)(C)OOC1(OOC(C)(C)C)CCCCC1 HSLFISVKRDQEBY-UHFFFAOYSA-N 0.000 description 1
- ZNCDSAZBKYUMAB-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)octane Chemical compound CCCCCCCC(OOC(C)(C)C)OOC(C)(C)C ZNCDSAZBKYUMAB-UHFFFAOYSA-N 0.000 description 1
- DEIGXXQKDWULML-UHFFFAOYSA-N 1,2,5,6,9,10-hexabromocyclododecane Chemical group BrC1CCC(Br)C(Br)CCC(Br)C(Br)CCC1Br DEIGXXQKDWULML-UHFFFAOYSA-N 0.000 description 1
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- NZUPFZNVGSWLQC-UHFFFAOYSA-N 1,3,5-tris(2,3-dibromopropyl)-1,3,5-triazinane-2,4,6-trione Chemical compound BrCC(Br)CN1C(=O)N(CC(Br)CBr)C(=O)N(CC(Br)CBr)C1=O NZUPFZNVGSWLQC-UHFFFAOYSA-N 0.000 description 1
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
- XZNGUVQDFJHPLU-UHFFFAOYSA-N 1,3-dibromobutane Chemical group CC(Br)CCBr XZNGUVQDFJHPLU-UHFFFAOYSA-N 0.000 description 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N 1,4-Benzenediol Natural products OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
- ULTHEAFYOOPTTB-UHFFFAOYSA-N 1,4-dibromobutane Chemical group BrCCCCBr ULTHEAFYOOPTTB-UHFFFAOYSA-N 0.000 description 1
- IBODDUNKEPPBKW-UHFFFAOYSA-N 1,5-dibromopentane Chemical group BrCCCCCBr IBODDUNKEPPBKW-UHFFFAOYSA-N 0.000 description 1
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
- HQOVXPHOJANJBR-UHFFFAOYSA-N 2,2-bis(tert-butylperoxy)butane Chemical compound CC(C)(C)OOC(C)(CC)OOC(C)(C)C HQOVXPHOJANJBR-UHFFFAOYSA-N 0.000 description 1
- QWQNFXDYOCUEER-UHFFFAOYSA-N 2,3-ditert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1C(C)(C)C QWQNFXDYOCUEER-UHFFFAOYSA-N 0.000 description 1
- IAHOUQOWMXVMEH-UHFFFAOYSA-N 2,4,6-trinitroaniline Chemical compound NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O IAHOUQOWMXVMEH-UHFFFAOYSA-N 0.000 description 1
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 1
- JGBAASVQPMTVHO-UHFFFAOYSA-N 2,5-dihydroperoxy-2,5-dimethylhexane Chemical compound OOC(C)(C)CCC(C)(C)OO JGBAASVQPMTVHO-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- OXYZDRAJMHGSMW-UHFFFAOYSA-N 3-chloropropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCl OXYZDRAJMHGSMW-UHFFFAOYSA-N 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical group C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- LHMRXAIRPKSGDE-UHFFFAOYSA-N benzo[a]anthracene-7,12-dione Chemical compound C1=CC2=CC=CC=C2C2=C1C(=O)C1=CC=CC=C1C2=O LHMRXAIRPKSGDE-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- WOXXJEVNDJOOLV-UHFFFAOYSA-N ethenyl-tris(2-methoxyethoxy)silane Chemical compound COCCO[Si](OCCOC)(OCCOC)C=C WOXXJEVNDJOOLV-UHFFFAOYSA-N 0.000 description 1
- XIMFCGSNSKXPBO-UHFFFAOYSA-N ethyl 2-bromobutanoate Chemical group CCOC(=O)C(Br)CC XIMFCGSNSKXPBO-UHFFFAOYSA-N 0.000 description 1
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- VUNCWTMEJYMOOR-UHFFFAOYSA-N hexachlorocyclopentadiene Chemical compound ClC1=C(Cl)C(Cl)(Cl)C(Cl)=C1Cl VUNCWTMEJYMOOR-UHFFFAOYSA-N 0.000 description 1
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 229910001853 inorganic hydroxide Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- GVYLCNUFSHDAAW-UHFFFAOYSA-N mirex Chemical compound ClC12C(Cl)(Cl)C3(Cl)C4(Cl)C1(Cl)C1(Cl)C2(Cl)C3(Cl)C4(Cl)C1(Cl)Cl GVYLCNUFSHDAAW-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910001392 phosphorus oxide Inorganic materials 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical class [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 description 1
- AUHHYELHRWCWEZ-UHFFFAOYSA-N tetrachlorophthalic anhydride Chemical compound ClC1=C(Cl)C(Cl)=C2C(=O)OC(=O)C2=C1Cl AUHHYELHRWCWEZ-UHFFFAOYSA-N 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
Classifications
-
- 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
- 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
- B32B17/10788—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 ethylene vinylacetate
-
- 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
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/02—Layered products essentially comprising sheet glass, or glass, slag, or like fibres in the form of fibres or filaments
- B32B17/04—Layered products essentially comprising sheet glass, or glass, slag, or like fibres in the form of fibres or filaments bonded with or embedded in a plastic substance
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/048—Encapsulation of modules
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02B—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
- Y02B10/00—Integration of renewable energy sources in buildings
- Y02B10/10—Photovoltaic [PV]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、太陽電池モジュー
ルに関し、特に太陽電池モジュールの難燃・不燃化技術
に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a solar cell module, and more particularly to a flame retardant / non-combustible technology for a solar cell module.
【0002】[0002]
【従来の技術及び発明が解決しようとする課題】近年、
クリーンなエネルギーとして太陽光発電システムに対す
る期待は非常に高く、各方面からその普及が強く望まれ
ている。特に住宅の屋根に太陽電池モジュールを設置す
ることにより、電力のピークカット対策として期待が大
きい。しかし、現状ではそのコストが高く、普及の阻害
要因となっている。このため、この対策として太陽電池
モジュールを屋根材替わりに使用することが提案されて
いる。2. Description of the Related Art In recent years,
There are very high expectations for solar power generation systems as clean energy, and their widespread use is strongly desired. Especially, by installing a solar cell module on the roof of a house, there are great expectations as a measure to reduce the peak of electric power. However, at present, the cost is high, which is an obstacle to the spread. Therefore, as a countermeasure against this, it has been proposed to use a solar cell module instead of a roof material.
【0003】しかしながら、従来の太陽電池モジュール
は、図4に示すように、太陽電池用セル1と白板ガラス
板2及び耐候性バックカバー3との間にこれらを接着、
封止させるためにEVA樹脂(エチレン−酢酸ビニル共
重合体)封止材膜4をそれぞれ介装することが行われて
いたが、この太陽電池モジュール内でセルとガラスの接
着材等に使用されているEVA樹脂封止材膜が可燃であ
り、太陽電池モジュール燃焼試験時にEVA樹脂が加熱
されて滴下し、このEVA樹脂が燃焼するため、直接屋
根材として使用できないのが現状であった。However, in the conventional solar cell module, as shown in FIG. 4, the solar cell 1 and the white glass plate 2 and the weather resistant back cover 3 are adhered to each other.
The EVA resin (ethylene-vinyl acetate copolymer) encapsulant film 4 has been interposed for encapsulation, but it is used as an adhesive between cells and glass in this solar cell module. The existing EVA resin encapsulant film is inflammable, and the EVA resin is heated and dropped during the solar cell module combustion test, and this EVA resin burns, so that it cannot be directly used as a roofing material.
【0004】本発明は上記事情に鑑みなされたもので、
難燃・不燃化され、直接屋根材等として使用することが
可能な太陽電池モジュールを提供することを目的とす
る。The present invention has been made in view of the above circumstances.
It is an object of the present invention to provide a solar cell module which is flame-retardant / non-combustible and can be directly used as a roof material or the like.
【0005】[0005]
【課題を解決するための手段及び発明の実施の形態】本
発明は、上記目的を達成するため、太陽電池用セルとこ
れを被覆する透明板及びバックカバーとの間のいずれか
一方又は双方に接着性樹脂を含浸させた網状体を介装し
てなることを特徴とする太陽電池モジュールを提供す
る。Means for Solving the Problems and Embodiments of the Invention In order to achieve the above object, the present invention provides a solar cell and a transparent plate and a back cover which cover the solar cell, or both. Provided is a solar cell module including a mesh body impregnated with an adhesive resin.
【0006】本発明によれば、このようにエチレン−酢
酸ビニル共重合体(EVA樹脂)等の接着性樹脂をガラ
ス繊維不織布等の網状体に含浸させて用いるので、燃焼
試験時に樹脂の滴下が防止され、その燃焼が防止され
て、太陽電池モジュールが難燃乃至は不燃化されるもの
で、これにより太陽電池モジュールを屋根材として使用
することを可能にしたものである。According to the present invention, since an adhesive resin such as an ethylene-vinyl acetate copolymer (EVA resin) is impregnated into a reticulated body such as a glass fiber non-woven fabric as described above, the resin is not dropped during the combustion test. The solar cell module is prevented from burning, and the solar cell module is made flame-retardant or non-combustible, which makes it possible to use the solar cell module as a roofing material.
【0007】以下、本発明につき更に詳しく説明する
と、本発明の太陽電池モジュールは、図1にその一例を
示したように、太陽電池用セル11と透明板12との間
及び該セル11とバックカバー13との間に接着性樹脂
を含浸させた網状体14をそれぞれ介装したものであ
る。The present invention will be described in more detail below. As shown in FIG. 1, the solar cell module of the present invention has a space between the solar cell 11 and the transparent plate 12 and between the cell 11 and the back plate. A mesh body 14 impregnated with an adhesive resin is interposed between the cover 13 and the cover 13.
【0008】ここで、上記セル11、透明板12、バッ
クカバー13としては公知のものを使用できる。この場
合、バックカバーとしては、一フッ化ポリエチレン、二
フッ化ポリエチレン、三フッ化ポリエチレンなどのフッ
素系ポリエチレンフィルム、ポリエステルフィルムや、
アルミ箔の両面又は片面に一フッ化ポリエチレン等の上
記した耐候性に富むフィルムを貼り合せたものを使用す
ることができる。Here, as the cell 11, the transparent plate 12, and the back cover 13, known ones can be used. In this case, as the back cover, a fluorinated polyethylene film such as monofluorinated polyethylene, difluorinated polyethylene, or trifluorinated polyethylene, a polyester film,
It is possible to use a laminate of the above-mentioned film having high weather resistance such as polyethylene monofluoride on both sides or one side of an aluminum foil.
【0009】また、上記網状体14としては、織布、不
織布、フォーム体等、樹脂を含浸し得るものであればい
ずれのものでもよいが、織布、不織布が好適であり、特
に光線透過性が優れる点から不織布が好ましく使用され
る。この網状体14の材料としては、不燃性のものであ
ることが推奨され、無機繊維を用いたものが好適に使用
されるが、光線透過を阻害しないガラス繊維を材料とし
たもの、とりわけガラス繊維不織布がより好ましく用い
られる。The mesh 14 may be woven cloth, non-woven cloth, foam or the like as long as it can be impregnated with a resin, but woven cloth and non-woven cloth are preferable, and particularly light-transmissive. Nonwoven fabrics are preferably used because of their excellent properties. It is recommended that the material of the reticulate body 14 is nonflammable, and those using inorganic fibers are preferably used, but those using glass fibers that do not inhibit light transmission, especially glass fibers. Nonwoven fabric is more preferably used.
【0010】この場合、不織布は、10〜1000g/
m2、特に10〜100g/m2の密度範囲であるものが
特に好ましい。10g/m2未満であると燃焼時の樹脂
の保持能力が低下し、燃焼試験時に樹脂の滴下が生じる
場合がある。また、1000g/m2を越えると光線透
過率が著しく低下してしまい、太陽電池の発電効率が低
下する場合がある。In this case, the non-woven fabric is 10 to 1000 g /
Those having a density range of m 2 , particularly 10 to 100 g / m 2 , are particularly preferred. If it is less than 10 g / m 2 , the resin holding capacity during combustion may be lowered, and the resin may drop during the combustion test. On the other hand, if it exceeds 1000 g / m 2 , the light transmittance may remarkably decrease, and the power generation efficiency of the solar cell may decrease.
【0011】上記網状体に含浸される接着性樹脂として
は、ポリビニルブチラール樹脂、塩化ビニル樹脂、EV
A樹脂、変性EVA樹脂等、光線透過率がよく、かつ布
に含浸できるものであればいかなる樹脂であっても構わ
ないが、特にEVA樹脂が好ましい。ここで、本発明に
用いられるEVA樹脂は、酢酸ビニル含有率が10〜5
0重量%であることが好ましく、より好ましくは15〜
40重量%である。また、本発明で用いられるEVA樹
脂は、メルトフローレートが0.7〜20であることが
好ましく、より好ましくは1.5〜10である。As the adhesive resin impregnated in the reticulated body, polyvinyl butyral resin, vinyl chloride resin, EV
Any resin can be used as long as it has good light transmittance and can impregnate a cloth, such as A resin and modified EVA resin, but EVA resin is particularly preferable. The EVA resin used in the present invention has a vinyl acetate content of 10-5.
0% by weight, more preferably 15 to
40% by weight. Further, the EVA resin used in the present invention preferably has a melt flow rate of 0.7 to 20, and more preferably 1.5 to 10.
【0012】このEVA樹脂には、架橋構造を持たせる
ことが、耐候性の点から好ましい。架橋構造を持たせる
方法としては、予めEVA樹脂に有機過酸化物を添加
し、その後100〜200℃程度に加熱して架橋する方
法が好ましい。EVA樹脂に添加する有機過酸化物とし
ては、100℃以上でラジカルを発生するものであれば
いずれでも使用可能であるが、配合時の安定性を考慮に
いれれば、半減期10時間の分解温度が70℃以上であ
ることが好ましく、例えば2,5−ジメチルへキサン−
2,5−ジハイドロパーオキサイド;2,5−ジメチル
−2,5−ジ(t−ブチルパーオキシ)ヘキサン−3、
ジ−t−ブチルパーオキサイド;t−ジクミルパーオキ
サイド;2,5ジメチル−2,5−ジ(t−ブチルパー
オキシ)ヘキサン;ジクミルパーオキサイド;α,α’
−ビス(t−ブチルパーオキシイソプロピル)ベンゼ
ン;n−ブチル−4,4−ビス(t−ブチルパーオキ
シ)ブタン;2,2−ビス(t−ブチルパーオキシ)ブ
タン;1,1−ビス(t−ブチルパーオキシ)シクロヘ
キサン;1,1−ビス(t−ブチルパーオキシ)3,
3,5−トリメチルシクロヘキサン;t−ブチルパーオ
キシベンゾエート;ベンゾイルパーオキサイド等を用い
ることができる。これらの有機過酸化物の配合量はEV
A樹脂対比(100重量部当り、以下同様)5重量部以
下、好ましくは1〜3重量部で十分である。From the viewpoint of weather resistance, it is preferable that the EVA resin has a crosslinked structure. As a method for providing a crosslinked structure, it is preferable to add an organic peroxide to EVA resin in advance and then heat it to about 100 to 200 ° C. to crosslink it. As the organic peroxide to be added to the EVA resin, any one can be used as long as it generates a radical at 100 ° C. or higher, but if the stability at the time of compounding is taken into consideration, the decomposition temperature with a half-life of 10 hours is used. Is preferably 70 ° C. or higher, for example, 2,5-dimethylhexane-
2,5-dihydroperoxide; 2,5-dimethyl-2,5-di (t-butylperoxy) hexane-3,
Di-t-butyl peroxide; t-dicumyl peroxide; 2,5 dimethyl-2,5-di (t-butylperoxy) hexane; dicumyl peroxide; α, α ′
-Bis (t-butylperoxyisopropyl) benzene; n-butyl-4,4-bis (t-butylperoxy) butane; 2,2-bis (t-butylperoxy) butane; 1,1-bis ( t-butylperoxy) cyclohexane; 1,1-bis (t-butylperoxy) 3,3
3,5-Trimethylcyclohexane; t-butyl peroxybenzoate; benzoyl peroxide and the like can be used. The blending amount of these organic peroxides is EV
5 parts by weight or less, preferably 1 to 3 parts by weight (100 parts by weight, the same applies hereinafter) to resin A is sufficient.
【0013】また、本発明ではEVA樹脂に光増感材を
予め加え、これに光照射することで分解し、EVA樹脂
に架橋構造を持たせることもできる。本発明で用いられ
る光増感材としては光照射でラジカルを生じるものであ
ればいかなるものでもよく、例えばベンゾイン、ベンゾ
インメチルエーテル、ベンゾインイソエチルエーテル、
ベンゾインイソプロピルエーテル、ベンゾインイソブチ
ルエーテル、ジベンゾイル、5−ニトリアセナフテン、
ヘキサクロロシクロペンタジエン、パラニトロジフェニ
ル、パラニトロアニリン、2,4,6トリニトロアニリ
ン、1,2−ベンズアントラキノン等がある。これらの
光増感材はEVA対比10重量部以下、好ましくは1〜
3重量部で十分である。In the present invention, it is also possible to add a photosensitizer to the EVA resin in advance and decompose it by irradiating it with light to give the EVA resin a crosslinked structure. The photosensitizer used in the present invention may be any as long as it produces a radical upon irradiation with light, for example, benzoin, benzoin methyl ether, benzoin isoethyl ether,
Benzoin isopropyl ether, benzoin isobutyl ether, dibenzoyl, 5-nitriacenaphthene,
Examples include hexachlorocyclopentadiene, paranitrodiphenyl, paranitroaniline, 2,4,6 trinitroaniline, and 1,2-benzanthraquinone. These photosensitizers are 10 parts by weight or less with respect to EVA, preferably 1 to
3 parts by weight is sufficient.
【0014】また、EVA樹脂とバックカバー及び発電
素子との接着力を更に向上せしめる目的でEVA樹脂に
シランカップリング剤を添加することができる。この目
的に供されるシランカップリング剤としては公知のも
の、例えばγ−クロロプロピルトリメトキシシラン;ビ
ニルトリクロロシラン;ビニルトリエトキシシラン;ビ
ニル−トリス(β−メトキシエトキシ)シラン;γ−メ
タクリロキシプロピルトリメトキシシラン;β−(3,
4−エトキシシクロヘキシル)エチルトリメトキシシラ
ン;γ−グリシドキシプロピルトリメトキシシラン;ビ
ニルトリアセトキシシラン;γ−メルカプトプロピルト
リメトキシシラン;γ−アミノプロピルトリメトキシシ
ラン;N−β−(アミノエチル)−γ−アミノプロピル
トリメトキシシラン等を挙げることができる。これらの
シランカップリング剤の配合量はEVA樹脂対比5重量
部以下、好ましくは0.1〜2重量部で十分である。Further, a silane coupling agent may be added to the EVA resin for the purpose of further improving the adhesion between the EVA resin and the back cover and the power generating element. Known silane coupling agents used for this purpose, for example, γ-chloropropyltrimethoxysilane; vinyltrichlorosilane; vinyltriethoxysilane; vinyl-tris (β-methoxyethoxy) silane; γ-methacryloxypropyl. Trimethoxysilane; β- (3,
4-ethoxycyclohexyl) ethyltrimethoxysilane; γ-glycidoxypropyltrimethoxysilane; vinyltriacetoxysilane; γ-mercaptopropyltrimethoxysilane; γ-aminopropyltrimethoxysilane; N-β- (aminoethyl)- γ-aminopropyltrimethoxysilane and the like can be mentioned. The amount of these silane coupling agents to be compounded is 5 parts by weight or less, preferably 0.1 to 2 parts by weight relative to the EVA resin.
【0015】更に、EVA樹脂のゲル分率を向上させ、
耐久性を向上するためにEVA樹脂に架橋助剤を添加で
きる。この目的に供せられる架橋助剤としては、公知の
ものとしてトリアリルイソシアヌレート;トリアリルイ
ソシアネート等の3官能の架橋助剤のほかNKエステル
等の単官能の架橋助剤等も挙げることができる。これら
の架橋助剤は配合量としてはEVA樹脂対比10重量部
以下で十分であり、好ましくは1〜5重量部である。Further, by improving the gel fraction of EVA resin,
A crosslinking aid can be added to the EVA resin to improve durability. As the cross-linking aid used for this purpose, known ones include triallyl isocyanurate; trifunctional cross-linking aids such as triallyl isocyanate, and monofunctional cross-linking aids such as NK ester. . The amount of these cross-linking aids is 10 parts by weight or less, preferably 1 to 5 parts by weight, relative to the EVA resin.
【0016】なおまた、本発明では安定性を向上する目
的でハイドロキノン、ハイドロキノンモノメチルエーテ
ル、p−ベンゾキノン、メチルハイドロキノン等をEV
A樹脂対比5重量部以下で加えることができる。Furthermore, in the present invention, EV is selected from hydroquinone, hydroquinone monomethyl ether, p-benzoquinone, methylhydroquinone and the like for the purpose of improving stability.
It can be added in an amount of 5 parts by weight or less relative to the A resin.
【0017】また、必要に応じ、上記以外に着色剤、紫
外線吸収剤、老化防止剤、変色防止剤等を添加すること
ができる。着色剤の例としては、金属酸化物、金属粉等
の無機顔料、アゾ系、フタロシアニン系、アチ系、酸
性、または塩基染料系レーキ等の有機顔料がある。紫外
線吸収剤には、2−ヒドロキシ−4−オクトキシベンゾ
フェノン、2−ヒドロキシ−4−メトキシ−5−スルフ
ォベンゾフェノン等のベンゾフェノン系、2−(2’−
ヒドロキシ−5−メチルフェニル)ベンゾトリアゾール
等のベンゾトリアゾール系、フェニルサルシレート、p
−t−ブチルフェニルサリシレート等のヒンダードアミ
ン系がある。老化防止剤としては、アミン系、フェノー
ル系、ビスフェニル系、ヒンダードアミン系があり、例
えばジ−t−ブチル−p−クレゾール、ビス(2,2,
6,6−テトラメチル−4−ピペラジル)セバケート等
がある。In addition to the above, a colorant, an ultraviolet absorber, an antiaging agent, a discoloration preventing agent, etc. may be added, if necessary. Examples of colorants include inorganic pigments such as metal oxides and metal powders, and organic pigments such as azo-based, phthalocyanine-based, achi-based, acidic or basic dye-based lakes. Examples of the ultraviolet absorber include benzophenone-based compounds such as 2-hydroxy-4-octoxybenzophenone and 2-hydroxy-4-methoxy-5-sulfobenzophenone, 2- (2′-).
Benzotriazoles such as hydroxy-5-methylphenyl) benzotriazole, phenyl salsylates, p
There are hindered amines such as -t-butylphenyl salicylate. As the antiaging agent, there are amine type, phenol type, bisphenyl type, hindered amine type, for example, di-t-butyl-p-cresol, bis (2,2,2,2
6,6-tetramethyl-4-piperazyl) sebacate and the like.
【0018】本発明において、含浸する樹脂にはハロゲ
ン原子を含む難燃剤を添加することができ、これによ
り、太陽電池モジュールの難燃・不燃性を更に向上でき
る。本発明で用いられる有機難燃剤の例としては、塩素
原子や臭素原子を分子中に1個以上含むもの、例えば塩
素化パラフィン、塩素化ポリエチレン、ヘキサクロロエ
ンドメチレンテトラヒドロフタル酸、パークロロペンタ
シクロデカン、四塩化無水フタール酸などや、トリス
(2,3−ジブロモプロピル)イソシアヌレート等の芳
香環を有しかつ該芳香環に直接ハロゲン原子が結合して
いないモノマーやポリマー、1,1,2,2−テトラブ
ロモエタン、1,4−ジブロモブタン、1,3−ジブロ
モブタン、1,5−ジブロモペンタン、α−ブロモ酪酸
エチル、1,2,5,6,9,10−ヘキサブロモシク
ロデカン等の芳香環を持たないものが挙げられる。これ
らの難燃剤の配合量は、EVA樹脂100重量部に対し
て20重量部以下、好ましくは1〜20重量部で十分で
ある。In the present invention, a flame retardant containing a halogen atom can be added to the resin to be impregnated, whereby the flame retardancy / nonflammability of the solar cell module can be further improved. Examples of the organic flame retardant used in the present invention include those containing at least one chlorine atom or bromine atom in the molecule, for example, chlorinated paraffin, chlorinated polyethylene, hexachloroendomethylenetetrahydrophthalic acid, perchloropentacyclodecane, Monomers or polymers having an aromatic ring such as tetrachlorophthalic anhydride or tris (2,3-dibromopropyl) isocyanurate and having no halogen atom directly bonded to the aromatic ring, 1,1,2,2 -Tetrabromoethane, 1,4-dibromobutane, 1,3-dibromobutane, 1,5-dibromopentane, ethyl α-bromobutyrate, 1,2,5,6,9,10-hexabromocyclodecane, etc. The thing which does not have an aromatic ring is mentioned. The amount of these flame retardants to be blended is 20 parts by weight or less, preferably 1 to 20 parts by weight, based on 100 parts by weight of the EVA resin.
【0019】この場合、本発明において含浸する樹脂に
おいて、非受光面側に積層される樹脂には難燃化助剤と
して三酸化アンチモンや膨張黒鉛を添加することができ
る。その添加量は10重量%以下で十分である。また、
本発明において含浸する樹脂において、非受光面側に積
層される樹脂には難燃剤として無機系の難燃剤が添加で
きる。無機難燃剤の例としては、水酸化アルミニウム、
水酸化マグネシウムなどの水酸化無機塩、リン酸アンモ
ニウム、リン酸亜鉛などのリン酸化物、赤リンなどが挙
げられる。In this case, in the resin to be impregnated in the present invention, antimony trioxide or expanded graphite can be added as a flame retardant aid to the resin laminated on the non-light-receiving surface side. The addition amount of 10% by weight or less is sufficient. Also,
In the resin to be impregnated in the present invention, an inorganic flame retardant can be added as a flame retardant to the resin laminated on the non-light-receiving surface side. Examples of inorganic flame retardants include aluminum hydroxide,
Examples thereof include inorganic hydroxide salts such as magnesium hydroxide, ammonium phosphate, phosphorus oxides such as zinc phosphate, and red phosphorus.
【0020】本発明の太陽電池モジュールの製造方法は
特に制限されず、予め接着性樹脂を含浸した網状体をセ
ル透明板、バックカバーと積層するようにしてもよい
が、太陽電池モジュールは、通常その生産時に真空ラミ
ネート処理を施すのが通常であるから、部材積層時に、
図2、3に示すように、セル11と透明板12との間及
びセル11とバックカバー13との間にそれぞれ網状体
14aと接着性樹脂膜14bとを介装し(なお、網状体
14aと樹脂膜14bとはどちらがセル11側に配置さ
れていてもよい)、次いで真空ラミネートを行い、加熱
して上記接着性樹脂膜14bを溶融すれば、接着性樹脂
が網状体14a中に含浸され、容易に難燃・不燃化され
た太陽電池モジュールが得られる。この場合、上記樹脂
膜14bとして有機過酸化物が添加されたEVA封止材
膜を用いれば、含浸加熱時にEVAが同時に架橋され
る。The method for manufacturing the solar cell module of the present invention is not particularly limited, and the mesh body previously impregnated with the adhesive resin may be laminated with the cell transparent plate and the back cover. Since vacuum laminating is usually applied at the time of production,
As shown in FIGS. 2 and 3, a mesh body 14a and an adhesive resin film 14b are interposed between the cell 11 and the transparent plate 12 and between the cell 11 and the back cover 13, respectively (note that the mesh body 14a Whichever of the resin film 14b and the resin film 14b may be disposed on the cell 11 side) is then vacuum laminated and heated to melt the adhesive resin film 14b, the adhesive resin is impregnated into the mesh body 14a. Thus, a flame-retardant / non-combustible solar cell module can be easily obtained. In this case, if an EVA sealing material film to which an organic peroxide is added is used as the resin film 14b, EVA is simultaneously cross-linked during impregnation heating.
【0021】なお、上記例では、セルと透明板及びセル
とバックカバーとの間にいずれも樹脂含浸網状体を介装
したが、場合によっては、いずれか一方を樹脂含浸網状
体に代えて難燃化処理した接着性樹脂封止膜を配設する
ことができる(この場合の難燃化処理した樹脂封止膜と
しては、例えばEVA封止材膜に上記したような難燃剤
を添加したものを挙げることができる)が、少なくとも
受光面側(透明板側)は上記樹脂含浸網状体を配設する
ことが好適である。この場合、受光面側の樹脂含浸網状
体は光透過性が必要であるが、バックカバー側の樹脂含
浸網状体は必ずしも光透過性は必要ない。In the above example, the resin-impregnated mesh is interposed between the cell and the transparent plate and between the cell and the back cover, but it is difficult to replace one of them with the resin-impregnated mesh. A flame-retardant adhesive resin encapsulation film can be provided (as the flame-retardant resin encapsulation film in this case, for example, an EVA encapsulant film to which the above-mentioned flame retardant is added. However, it is preferable to dispose the resin-impregnated mesh body on at least the light-receiving surface side (transparent plate side). In this case, the resin-impregnated network on the light-receiving surface side needs to be light transmissive, but the resin-impregnated network on the back cover side is not necessarily required to be light transmissive.
【0022】[0022]
【実施例】以下、実施例及び比較例を示し、本発明を具
体的に説明するが、本発明は下記の実施例に制限される
ものではない。EXAMPLES The present invention will be specifically described below by showing Examples and Comparative Examples, but the present invention is not limited to the following Examples.
【0023】〔実施例、比較例〕表1に示す通り、EV
A樹脂を主成分とし、各成分を80℃に加熱したロール
ミルにて混合して、EVA樹脂組成物を調製した。これ
らの組成物を90℃に設定したプレスで0.5mm厚
(150mm角)のシートとした。[Examples, Comparative Examples] As shown in Table 1, EV
An EVA resin composition was prepared by mixing A resin as a main component and each component with a roll mill heated to 80 ° C. A sheet having a thickness of 0.5 mm (150 mm square) was formed from these compositions by a press set at 90 ° C.
【0024】[0024]
【表1】 [Table 1]
【0025】次に、実施例1、2のシートを図3に示す
ように積層した。即ち、図3において、11は太陽電池
用セル、12は白板ガラス板、13は耐候性バックカバ
ー、14aはガラス繊維不織布(密度75g/m2)、
14bは上記シートである。この積層体を真空ラミネー
ターで予備圧着(温度150℃、脱気3分、プレス3
分)し、その後30分、150℃に加熱して評価サンプ
ルを作成した。比較のため、ガラス繊維不織布14bを
積層しない以外は上記と同様にして評価サンプルを作成
した。Next, the sheets of Examples 1 and 2 were laminated as shown in FIG. That is, in FIG. 3, 11 is a solar cell, 12 is a white glass plate, 13 is a weather resistant back cover, 14a is a glass fiber non-woven fabric (density 75 g / m 2 ),
14b is the sheet. This laminated body is pre-compressed with a vacuum laminator (temperature 150 ° C., deaeration 3 minutes, press 3
Minutes) and then heated to 150 ° C. for 30 minutes to prepare an evaluation sample. For comparison, an evaluation sample was prepared in the same manner as above except that the glass fiber nonwoven fabric 14b was not laminated.
【0026】その結果、本実施例ではサンプルのエッジ
をガスバーナーで加熱した場合、EVA樹脂の融け出し
はなかった。これに対し、比較例で同様の実験を行った
場合、EVA樹脂は融け出し燃焼した。As a result, in this example, when the edge of the sample was heated by the gas burner, the EVA resin did not melt. On the other hand, when the same experiment was performed in the comparative example, the EVA resin melted and burned.
【0027】また、実施例3、4のシートを用い、上記
と同様の積層を行い、真空ラミネーターで圧着した。圧
着条件は設定温度150℃、脱気時間3分、プレス時間
15分であり、この段階で十分なEVA樹脂の架橋がな
された。上記実施例1と同じ試験をした結果、一部EV
A樹脂の滴下が見られたが、滴下したEVA樹脂が燃焼
することはなかった。なお、TAIC−6Bの代りに塩
素化パラフィン(塩素化率70%)を用いたものも同様
の結果を得た。Further, using the sheets of Examples 3 and 4, the same lamination as above was carried out, and the sheets were pressure-bonded with a vacuum laminator. The pressure bonding conditions were a set temperature of 150 ° C., a deaeration time of 3 minutes, and a pressing time of 15 minutes. At this stage, the EVA resin was sufficiently crosslinked. As a result of the same test as in Example 1, a partial EV
Although the A resin was found to be dropped, the dropped EVA resin was not burned. Similar results were obtained when chlorinated paraffin (chlorination rate 70%) was used instead of TAIC-6B.
【0028】[0028]
【発明の効果】本発明によれば、太陽電池モジュールが
確実に難燃乃至は不燃化され、このためこのモジュール
を屋根材として使用することが可能である。According to the present invention, the solar cell module is surely rendered flame-retardant or non-combustible, so that this module can be used as a roofing material.
【図1】本発明の一実施例を示す断面図である。FIG. 1 is a sectional view showing an embodiment of the present invention.
【図2】太陽電池モジュールの作成に用いる積層体の一
例を示す断面図である。FIG. 2 is a cross-sectional view showing an example of a laminated body used for producing a solar cell module.
【図3】同積層体の他の例を示す断面図である。FIG. 3 is a cross-sectional view showing another example of the same laminate.
【図4】従来の太陽電池モジュールの断面図である。FIG. 4 is a cross-sectional view of a conventional solar cell module.
11 太陽電池用セル 12 透明板 13 バックカバー 14 樹脂含浸網状体 11 Solar Cell 12 Transparent Plate 13 Back Cover 14 Resin Impregnated Mesh
Claims (7)
及びバックカバーとの間のいずれか一方又は双方に接着
性樹脂を含浸させた網状体を介装してなることを特徴と
する太陽電池モジュール。1. A solar cell comprising a solar cell, a transparent plate and a back cover which cover the solar cell, and one or both of which is provided with a mesh body impregnated with an adhesive resin. Battery module.
である請求項1記載の太陽電池モジュール。2. The solar cell module according to claim 1, wherein the mesh body is a woven or non-woven fabric of inorganic fibers.
1又は2記載の太陽電池モジュール。3. The solar cell module according to claim 1, wherein the inorganic fiber is glass fiber.
共重合体又は変性エチレン−酢酸ビニル共重合体である
請求項1、2又は3記載の太陽電池モジュール。4. The solar cell module according to claim 1, 2 or 3, wherein the adhesive resin is an ethylene-vinyl acetate copolymer or a modified ethylene-vinyl acetate copolymer.
エチレン−酢酸ビニル共重合体が架橋構造を有するもの
である請求項4記載の太陽電池モジュール。5. The solar cell module according to claim 4, wherein the ethylene-vinyl acetate copolymer or the modified ethylene-vinyl acetate copolymer has a crosslinked structure.
エチレン−酢酸ビニル共重合体を有機過酸化物の存在下
に加熱することにより架橋させた架橋構造を有する請求
項5記載の太陽電池モジュール。6. The solar cell module according to claim 5, which has a crosslinked structure in which an ethylene-vinyl acetate copolymer or a modified ethylene-vinyl acetate copolymer is crosslinked by heating in the presence of an organic peroxide.
のである請求項1乃至6のいずれか1項記載の太陽電池
モジュール。7. The solar cell module according to claim 1, wherein the adhesive resin contains a halogen atom.
Priority Applications (1)
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JP13599596A JP3687701B2 (en) | 1995-05-08 | 1996-05-02 | Solar cell module |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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JP13481295 | 1995-05-08 | ||
JP17813295 | 1995-06-21 | ||
JP7-178132 | 1995-06-21 | ||
JP7-134812 | 1995-06-21 | ||
JP13599596A JP3687701B2 (en) | 1995-05-08 | 1996-05-02 | Solar cell module |
Publications (2)
Publication Number | Publication Date |
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JPH0969646A true JPH0969646A (en) | 1997-03-11 |
JP3687701B2 JP3687701B2 (en) | 2005-08-24 |
Family
ID=27316959
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