CN109355037A - A kind of ultraviolet light solidification packaging adhesive film and solar cell module - Google Patents
A kind of ultraviolet light solidification packaging adhesive film and solar cell module Download PDFInfo
- Publication number
- CN109355037A CN109355037A CN201811216248.6A CN201811216248A CN109355037A CN 109355037 A CN109355037 A CN 109355037A CN 201811216248 A CN201811216248 A CN 201811216248A CN 109355037 A CN109355037 A CN 109355037A
- Authority
- CN
- China
- Prior art keywords
- adhesive film
- packaging adhesive
- ultraviolet light
- bis
- mass parts
- 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
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- 238000004806 packaging method and process Methods 0.000 title claims abstract description 40
- 239000002313 adhesive film Substances 0.000 title claims abstract description 38
- 238000007711 solidification Methods 0.000 title claims abstract description 11
- 230000008023 solidification Effects 0.000 title claims abstract description 11
- 239000003292 glue Substances 0.000 claims abstract description 29
- 239000003999 initiator Substances 0.000 claims abstract description 15
- 150000003254 radicals Chemical class 0.000 claims abstract description 15
- 239000004611 light stabiliser Substances 0.000 claims abstract description 13
- 229940123973 Oxygen scavenger Drugs 0.000 claims abstract description 11
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 11
- 150000001768 cations Chemical class 0.000 claims abstract description 9
- 239000000463 material Substances 0.000 claims abstract description 5
- -1 Alkyl sulfur compounds Chemical class 0.000 claims description 44
- 238000002156 mixing Methods 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 12
- 238000001125 extrusion Methods 0.000 claims description 11
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 11
- 238000001816 cooling Methods 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 10
- 238000005453 pelletization Methods 0.000 claims description 10
- 238000005096 rolling process Methods 0.000 claims description 10
- 238000005266 casting Methods 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 8
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 150000002978 peroxides Chemical class 0.000 claims description 7
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- 239000012965 benzophenone Substances 0.000 claims description 6
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 5
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 claims description 4
- YKTNISGZEGZHIS-UHFFFAOYSA-N 2-$l^{1}-oxidanyloxy-2-methylpropane Chemical group CC(C)(C)O[O] YKTNISGZEGZHIS-UHFFFAOYSA-N 0.000 claims description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 4
- 229920000305 Nylon 6,10 Polymers 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 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 claims description 4
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 229920001684 low density polyethylene Polymers 0.000 claims description 4
- 239000004702 low-density polyethylene Substances 0.000 claims description 4
- 150000002903 organophosphorus compounds Chemical class 0.000 claims description 4
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 4
- ODKXGEBKLRHKGQ-UHFFFAOYSA-N C(C)(C)(C)OO.C(O)(O)=O Chemical compound C(C)(C)(C)OO.C(O)(O)=O ODKXGEBKLRHKGQ-UHFFFAOYSA-N 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 3
- 244000028419 Styrax benzoin Species 0.000 claims description 3
- 235000000126 Styrax benzoin Nutrition 0.000 claims description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 3
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 3
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 claims description 3
- PQMPFRMDGVOBGL-UHFFFAOYSA-N (1,2,2,6,6-pentamethylpiperidin-4-yl) dihydrogen phosphite Chemical class CN1C(CC(CC1(C)C)OP(O)O)(C)C PQMPFRMDGVOBGL-UHFFFAOYSA-N 0.000 claims description 2
- ZKSVYBRJSMBDMV-UHFFFAOYSA-N 1,3-diphenyl-2-benzofuran Chemical compound C1=CC=CC=C1C1=C2C=CC=CC2=C(C=2C=CC=CC=2)O1 ZKSVYBRJSMBDMV-UHFFFAOYSA-N 0.000 claims description 2
- VNQXSTWCDUXYEZ-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2(C)C(=O)C(=O)C1C2(C)C VNQXSTWCDUXYEZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 claims description 2
- OLPZCIDHOZATMA-UHFFFAOYSA-N 2,2-dioxooxathiiran-3-one Chemical compound O=C1OS1(=O)=O OLPZCIDHOZATMA-UHFFFAOYSA-N 0.000 claims description 2
- IIXGAMLWYYNCHK-UHFFFAOYSA-N 2-ethylhexyl 2-methylbutan-2-yl carbonate Chemical compound C(OC(C)(C)CC)(OCC(CCCC)CC)=O IIXGAMLWYYNCHK-UHFFFAOYSA-N 0.000 claims description 2
- BWMXRNGZUDOSJR-UHFFFAOYSA-N 3,3,5-trimethylhexanoic acid Chemical compound CC(C)CC(C)(C)CC(O)=O BWMXRNGZUDOSJR-UHFFFAOYSA-N 0.000 claims description 2
- ODJQKYXPKWQWNK-UHFFFAOYSA-L 3-(2-carboxylatoethylsulfanyl)propanoate Chemical compound [O-]C(=O)CCSCCC([O-])=O ODJQKYXPKWQWNK-UHFFFAOYSA-L 0.000 claims description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 claims description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 claims description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Substances CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 2
- 150000004056 anthraquinones Chemical class 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 claims description 2
- 229960002130 benzoin Drugs 0.000 claims description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 2
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 claims description 2
- 229930006711 bornane-2,3-dione Natural products 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 claims description 2
- 125000005520 diaryliodonium group Chemical group 0.000 claims description 2
- MZRQZJOUYWKDNH-UHFFFAOYSA-N diphenylphosphoryl-(2,3,4-trimethylphenyl)methanone Chemical compound CC1=C(C)C(C)=CC=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MZRQZJOUYWKDNH-UHFFFAOYSA-N 0.000 claims description 2
- 230000032050 esterification Effects 0.000 claims description 2
- 238000005886 esterification reaction Methods 0.000 claims description 2
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 claims description 2
- 239000008103 glucose Substances 0.000 claims description 2
- 235000019382 gum benzoic Nutrition 0.000 claims description 2
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 229920001083 polybutene Polymers 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- UIDUKLCLJMXFEO-UHFFFAOYSA-N propylsilane Chemical compound CCC[SiH3] UIDUKLCLJMXFEO-UHFFFAOYSA-N 0.000 claims description 2
- 229920002379 silicone rubber Polymers 0.000 claims description 2
- 239000001384 succinic acid Substances 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- 125000005409 triarylsulfonium group Chemical group 0.000 claims description 2
- 238000002211 ultraviolet spectrum Methods 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 238000001429 visible spectrum Methods 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims 2
- KCZIUKYAJJEIQG-UHFFFAOYSA-N 1,3,5-triazin-2-amine Chemical class NC1=NC=NC=N1 KCZIUKYAJJEIQG-UHFFFAOYSA-N 0.000 claims 1
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 claims 1
- DZRUNSUYJCQUIG-UHFFFAOYSA-N 2-methylbutan-2-yl hydrogen carbonate Chemical compound CCC(C)(C)OC(O)=O DZRUNSUYJCQUIG-UHFFFAOYSA-N 0.000 claims 1
- YEKZPZKFJZWQLH-UHFFFAOYSA-N C(CC)[Si](C)(C)C.[O] Chemical compound C(CC)[Si](C)(C)C.[O] YEKZPZKFJZWQLH-UHFFFAOYSA-N 0.000 claims 1
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- 239000002344 surface layer Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/10—Adhesives in the form of films or foils without carriers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/08—Copolymers of ethene
- C09J123/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C09J123/0815—Copolymers of ethene with aliphatic 1-olefins
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/08—Copolymers of ethene
- C09J123/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
- C09J123/0853—Vinylacetate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/08—Copolymers of ethene
- C09J123/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
- C09J123/0869—Acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J129/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Adhesives based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Adhesives based on derivatives of such polymers
- C09J129/14—Homopolymers or copolymers of acetals or ketals obtained by polymerisation of unsaturated acetals or ketals or by after-treatment of polymers of unsaturated alcohols
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- 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
- H01L31/0481—Encapsulation of modules characterised by the composition of the encapsulation material
-
- 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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
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- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
The invention discloses a kind of ultraviolet light solidification packaging adhesive film and solar cell module, which causes crosslinking agent, 0.01-1 mass parts light stabilizer, 0.01-1 mass parts tackifier by 100 mass parts packaging adhesive film basis materials, 0.1-5 mass parts free radical photo-initiation, 0.1-5 mass parts cation light initiator, 0.01-1 mass parts oxygen scavenger, 0.01-1 mass parts heat and forms.The present invention obtains good synergistic effect, and be equipped with oxygen scavenger, weakens molecular oxygen to the inhibitory effect of irradiation, improve ultra-violet curing efficiency by the way that free radical photo-initiation and cation light initiator is added.Meanwhile it adding a small amount of thermal initiator and can be further improved the gel content after solidifying.Compared with conventional package glue film, curing time greatly shortens glue film of the present invention, and crosslink density is high and uniformity is good.Component manufacturer packaging efficiency and yield are improved, production energy consumption is reduced, reduces production cost.
Description
Technical field
The invention belongs to photovoltaic encapsulation glue film field, it is related to a kind of ultraviolet light solidification packaging adhesive film and solar battery group
Part.
Background technique
The energy is valuable source for the survival of mankind, and the environmental problem increasingly shown then discloses conventional energy resource can not be again
Raw drawback and its subsidiary using environment as the sky high cost of cost.In order to realize the sustainable development of the energy and environment, various countries
It all promotes the use of clean energy in Devoting Major Efforts To Developing, photovoltaic power generation is also one of prior development direction.However, although photovoltaic power generation is in the energy
Middle accounting is significantly increased, but relies primarily on support on policy and subsidy of the government to new energy, and market development is still limited by solar energy
Battery component is at high cost.One of an important factor for influencing component cost is exactly production efficiency, this mainly depends on packaging adhesive film again
Curing time.General components curing time is up to 15-25 minutes at present, has seriously affected component package efficiency, in automation journey
It spends under environment higher and higher, packaging efficiency is particularly important.Packaging adhesive film curing time is shorter, and efficiency is higher, energy consumption is smaller, band
The benefit come is self-evident.
Current most widely used glue film curing method is that heat causes chemical method, this is a kind of traditional cross-linking method, main
Peroxide decomposition is set to generate free radicals and cause a series of free radical at high temperature by adding peroxide initiator
Reaction, makes polymeric matrix crosslink to form reticular structure.This method development is very mature, but time consumption and energy consumption, and not easily-controllable
Crosslinking degree processed.In order to improve curing efficiency, also usually uses raising laminating temperature and increases the means of peroxide additive amount,
But the problems such as both methods generates bubble when being easy to cause lamination, remains excessive peroxide damage component ageing-resistant performance.
In recent years solar double-glass assemblies with photovoltaic glass replace backboard, because its without frame, stronger anti-PID ability, reliability,
The advantages that weatherability, becomes photovoltaic industry development trend.But it is limited by process conditions, bubble, broken is easy to produce in production process
The bad phenomenons such as piece, displacement cause yield rate lower, and production cost increases.Solidify packaging adhesive film according to ultraviolet light, introduces purple
External irradiation technique can greatly shorten lamination times, component lamination temperature be reduced, to avoid bubble, excessive glue, displacement etc. bad
Phenomenon.
There are also patents to propose the preparation method of UV crosslinking glue film at present, and patent CN 102689386A is by adding
Enter photoinitiator and photosensitizer preparation UV crosslinking type EVA adhesive film, but it only passes through addition free radical photo-initiation and reaches purple
The effect of external crosslinking, cross-linking efficiency may be lower, and not can avoid the oxygen inhibition in ultraviolet irradiation.The ground state of general substance
It is singlet, O2Stable state be triplet state, there are two the identical unpaired electron of spin direction.Therefore, it can be with freedom
The polymerization reaction of base competes and consumes free radical.Oxygen inhibition can frequently result in that glue film surface layer is uncured and stickness or solidification path
The problems such as low is spent, to influence the long-term reliability of glue film.
Summary of the invention
The purpose of the present invention is being directed to existing ultra-violet curing technical deficiency, such as crosslinking is caused to be imitated using single initiator system
Rate is low, leads to surfaces of tacky or the low problem of curing degree because of oxygen inhibition, provide a kind of ultraviolet light solidification packaging adhesive film and
Solar cell module, the glue film curing degree is uniform, and cross-linking efficiency is high, and curing time is short, when can greatly shorten component package
Between, improve production efficiency.It is not necessarily to very high laminating temperature simultaneously, and is remained without excess peroxide.
The purpose of the present invention is what is be achieved through the following technical solutions: a kind of ultraviolet light solidifies packaging adhesive film, mainly by with
The raw material of lower quality proportioning is prepared:
Further, the oxygen scavenger is by ethers acrylate, organic phosphorus compound, organic phosphorus compound, phosphorous
Hydrochlorate, thiodipropionate, thiophosphoric acid and its derivative, alkyl sulfur compounds, aromatic yl sulfide, tertiary amine, mercaptan, 1,3- hexichol
Base isobenzofuran, 1,2- diphenylisobenzofuran, 2,3- diphenylisobenzofuran, cyclic annular vinyl compound, acetal ring class
It closes the one or more of object, polynary straight chain alcohols, polyether compound, glucose and its oxidizing ferment and presses any proportion mixing group
At.
Further, the free radical photo-initiation is by benzoin and its derivative, benzil ketals derivative, α, α-two
Acetophenone, 2- dimethyl-alpha-hydroxyacetophenone, 1- hydroxy cyclohexyl phenylketone, 1- are to methyl mercapto phenyl -2- methyl -
2- morpholinyl -1- acetone, 2- benzyl -2-N, N- dimethylamino -1- (4- morpholinyl phenyl) butanone, alpha-hydroxyalkyl benzophenone, α-amine alkane
Base benzophenone, trimethylbenzoyl diphenyl phosphine oxide, bis(benzoylphenyl) phosphine oxide, Sulfo-benzophenone class compound, ester
Change oximinoketone compound, aryl peroxide ester compounds, halogenated methyl arone, benzoyl formiate, benzophenone and its derivative, sulphur
Miscellaneous anthrone and its derivative, anthraquinone and its derivative, benzofuran, the one or more of camphorquinone press any proportion mixing group
At.
Further, the cation light initiator is by aromatic diazo salt, diaryl iodonium salt, triaryl sulfonium salts, alkane
Base sulfosalt, iron arene salt, sulfonyloxy ketone and the one or more of triaryl silicon oxygen ether are formed by the mixing of any proportion.
Further, the packaging adhesive film basis material is by ethylene-vinyl acetate copolymer, low density polyethylene (LDPE), poly-
Propylene, polybutene, polyvinyl butyral, polyurethane elastomer, organic silicon rubber, metallocene catalysed polyethylene, ethylene octene
Copolymer, the one or more of ethylene pentene copolymer are formed by the mixing of any proportion.
Further, it is bis- by tert-butyl hydroperoxide propylene carbonate, 2,5- dimethyl -2,5- to cause crosslinking agent for the heat
(tert-butyl peroxy base) hexane, bis- (tert-butyl peroxide) -3 1-, 3,5- trimethyl-cyclohexanes, tert-butyl hydroperoxide carbonic acid -2- second
Bis- (t-butyl peroxy) -3 the own ester of base, 1,1-, bis- (t-amyl peroxy) -3 3,5- trimethyl-cyclohexanes, 1,1-, 3,5- trimethyls
Bis- (t-amyl peroxy) hexamethylenes of hexamethylene, 1,1-, bis- (t-butyl peroxy) hexamethylenes of 1,1-, bis- (t-butyl peroxy) fourths of 2,2-
Alkane, peroxidating 2- ethylhexyl carbonate tert-pentyl ester, 2,5- dimethyl 2, bis- (benzoyl the peroxide)-hexanes of 5-, peroxidating carbonic acid uncle
Pentyl ester, the one or more of 3,3,5 trimethylhexanoate of peroxidating are formed by the mixing of any proportion;The light stabilizer is
Hindered amine light stabilizer, by 3,5- di-t-butyl -4- hydroxy-benzoic acid cetyl ester, three (1,2,2,6,6- pentamethyls -
4- piperidyl) phosphite ester, decanedioic acid double -2,2,6,6- tetramethyl piperidine alcohol esters, double -1- decane oxygroups -2,2,6,6- tetramethyls
Phenylpiperidines -4- alcohol sebacate, succinic acid and 4- hydroxyl -2,2, polymer, the N of 6,6- tetramethyl -1- piperidine alcohols, N '-it is bis- (2,
2,6,6- tetramethyl -4- piperidyls) -1,6- hexamethylene diamine and 2,4- bis- chloro- 6- (1,1,3,3- tetramethyl butyl) amino -1,3,5-
Bis- (2,2,6,6- tetramethyl -4- piperidyl) -1, the 6- hexamethylene diamines of polymer, the N of triazine, N '-and morpholine -2,4,6- tri- chloro- 1,
The one or more of the polymer of 3,5- triazines are formed by the mixing of any proportion;The tackifier are by gamma-aminopropyl-triethoxy
Silane, γ-methacryloxypropyl trimethoxy silane, γ-(the third oxygen of 2,3- epoxy) propyl trimethoxy silicane, ethylene
Base trimethoxy silane, N- (β-aminoethyl)-γ-aminopropyltrimethoxysilane, γ-glycidyl ether oxygen propyl trimethyl silicane
Alkane, the one or more of 3- propyl silane are formed by the mixing of any proportion.
Further, the preparation process specifically: raw material is used to double screw extruder extruding pelletization after mixing.It will
The particle made is squeezed out with single screw extrusion machine, and for extrudate through casting film-forming, rolling after cooling obtains the glue with a thickness of 0.5mm
Film.
The present invention also provides a kind of solar cell modules for solidifying packaging adhesive film with above-mentioned ultraviolet light, by following
Method is prepared: solidifying packaging adhesive film according to lower cover plate, the first ultraviolet light solidification packaging adhesive film, cell piece, the second ultraviolet light
Sequence successively organize arrangement, be put into ultraviolet irradiation room, irradiated 1 minute under 100 DEG C of -100wUVA ultraviolet lamp tubes.Later
Covers upper cover plate on two ultraviolet lights solidification packaging adhesive film, is sent into vacuum laminator, 130-150 DEG C laminated 3-5 minutes.
The present invention also provides a kind of solar cell modules for solidifying packaging adhesive film with above-mentioned ultraviolet light, by following
Method is prepared: according to lower cover plate, the first ultraviolet light solidification packaging adhesive film, cell piece, the second ultraviolet light solidification packaging adhesive film,
The sequence of upper cover plate successively organizes arrangement, is sent into vacuum laminator, 130-150 DEG C laminated 3-5 minutes, using ultraviolet spoke
According to device, irradiated 1 minute under 100 DEG C of -100wUVA ultraviolet lamp tubes.
Further, transmitance >=85% of the visible spectrum wave band of the upper cover plate, the transmitance of ultraviolet spectra wave band
>=60%.
The beneficial effects of the present invention are: the present invention is obtained by the way that free radical photo-initiation and cation light initiator is added
Good synergistic effect, and it is equipped with oxygen scavenger, weaken molecular oxygen to the inhibitory effect of irradiation, improves ultra-violet curing efficiency.Together
When, adding a small amount of thermal initiator can be further improved the gel content after solidifying.By the addition of other auxiliary agents, guarantee ultraviolet
Insulating properties, weatherability of photocuring packaging adhesive film etc. meet the requirement in photovoltaic encapsulation field.Glue film of the present invention and tradition are sealed
Dress glue film is compared, and curing time greatly shortens, and crosslink density is high and uniformity is good.Component manufacturer packaging efficiency and yield are improved,
Production energy consumption is reduced, production cost is reduced.
Specific embodiment
The present invention will be further described below with reference to examples, but protection scope of the present invention is not only limited to implement
Example:
Embodiment 1:
In terms of mass fraction, to 100 parts of ethylene-vinyl acetate copolymers (mass content of vinyl acetate VA is 33%)
In, it is added 5 parts of free radical photo-initiation benzophenone, 0.1 part of cationic initiator diphenyl iodine hexafluorophosphate, 0.5 part
Oxygen scavenger n,N-Dimethylaniline, 0.1 part of thermal cross-linking agent 2, bis- (tert-butyl peroxy base) hexanes of 5- dimethyl -2,5-, 0.1 part
Double -2,2,6, the 6- tetramethyl piperidine alcohol esters of light stabilizer decanedioic acid, 0.1 part of tackifier gamma-aminopropyl-triethoxy-silane, mixing
Double screw extruder extruding pelletization is used after uniformly.The particle made is squeezed out with single screw extrusion machine, extrudate through casting film-forming,
Rolling after cooling obtains the glue film with a thickness of 0.5mm, is denoted as S1.
Embodiment 2:
In terms of mass fraction, into 100 parts of ethylene octene copolymer, the double first of 2 parts of free radical photo-initiation styraxes are added
Ether, 0.5 part of cation light initiator isopropylbenzene cyclopentadienyl iron hexafluorophosphate, 0.5 part of oxygen scavenger 4- dimethyl ethyl aminobenzoate,
0.1 part of thermal cross-linking agent tert-butyl hydroperoxide propylene carbonate, 0.1 part of light stabilizer 3,5- di-t-butyl -4- hydroxy-benzoic acid ten
Six Arrcostabs, 0.1 part of tackifier γ-methacryloxypropyl trimethoxy silane, use twin-screw extrusion after mixing
Machine extruding pelletization.The particle made is squeezed out with single screw extrusion machine, extrudate obtains thickness through casting film-forming, rolling after cooling
For the glue film of 0.5mm, it is denoted as S2.
Embodiment 3:
In terms of mass fraction, into 100 parts of ethylene methyl methacrylate copolymers, it is light-initiated that 0.1 part of free radical is added
Agent 2- benzyl -2-N, N- dimethylamino -1- (4- morpholinyl phenyl) butanone, is added 5 parts of cationic initiator triphenyl sulfosalts, adds
Enter 1 part of oxygen scavenger triphenyl phosphorus, 0.1 part of thermal cross-linking agent 1, bis- (t-butyl peroxy) -3 1-, 3,5- trimethyl-cyclohexanes, 0.1
Part light stabilizer three (1,2,2,6,6- pentamethyl -4- piperidyl) phosphite ester, 0.1 part of tackifier γ-(2,3- the third oxygen of epoxy)
Propyl trimethoxy silicane uses double screw extruder extruding pelletization after mixing.The particle single screw extrusion machine that will have been made
It squeezes out, for extrudate through casting film-forming, rolling after cooling obtains the glue film with a thickness of 0.5mm, is denoted as S3.
Embodiment 4:
In terms of mass fraction, into 100 parts of polyvinyl butyrals, 0.5 part of free radical photo-initiation isopropyl sulphur is added
0.01 part of oxygen scavenger triethanolamine, 0.1 part of thermal cross-linking agent is added in miscellaneous anthrone, 0.5 part of cation light initiator sulfonyloxy ketone
Tert-butyl hydroperoxide carbonic acid -2- ethylhexyl, the double -1- decane oxygroups -2,2 of 0.1 part of light stabilizer, 6,6- tetramethyl piperidine -4-
Alcohol sebacate, 0.1 part of tackifier vinyltrimethoxysilane use double screw extruder extruding pelletization after mixing.It will
The particle made is squeezed out with single screw extrusion machine, and for extrudate through casting film-forming, rolling after cooling obtains the glue with a thickness of 0.5mm
Film is denoted as S4.
Embodiment 5:
In terms of mass fraction, into 100 parts of metallocene catalysed polyethylenes, the double benzoyls of 1 part of free radical photo-initiation are added
Base phenyl phosphine oxide, 1.5 parts of cation light initiator tetrafluoro boric acid diphenyl iodniums, 0.5 part of oxygen scavenger 1,3- diphenyl
Isobenzofuran, 0.1 part of thermal cross-linking agent 1, bis- (t-amyl peroxy) -3 1-, 3,5- trimethyl-cyclohexanes, 0.1 part of light stabilizer last of the ten Heavenly stems
Double -2,2,6, the 6- tetramethyl piperidine alcohol esters of diacid, 0.1 part of tackifier N- (β-aminoethyl)-γ-aminopropyltrimethoxysilane,
Double screw extruder extruding pelletization is used after mixing.The particle made is squeezed out with single screw extrusion machine, extrudate is through being cast
Film forming, rolling after cooling obtain the glue film with a thickness of 0.5mm, are denoted as S5.
Embodiment 6:
In terms of mass fraction, into 100 parts of polyurethane elastomers, 0.2 part of free radical photo-initiation esterification oximinoketone is added
Object is closed, 0.8 part of cation light initiator 3- nitrobenzophenone diphenyl sulphur hexafluorophosphate is added, 0.05 part of oxygen scavenger four is added
(3- mercaptopropionic acid) pentaerythritol ester, 0.1 part of thermal cross-linking agent 1, bis- (t-amyl peroxy) hexamethylenes of 1-, 0.1 part of light stabilizer fourth
Diacid and 4- hydroxyl -2,2, the polymer of 6,6- tetramethyl -1- piperidine alcohols, 0.1 part of tackifier N- (β-aminoethyl)-γ-ammonia third
Base trimethoxy silane uses double screw extruder extruding pelletization after mixing.The particle made is squeezed with single screw extrusion machine
Out, for extrudate through casting film-forming, rolling after cooling obtains the glue film with a thickness of 0.5mm, is denoted as S6.
Comparative example 1:
In terms of mass fraction, to 100 parts of ethylene-vinyl acetate copolymers (mass content of vinyl acetate VA is 18%)
In, it is added 5 parts of thermal cross-linking agents 2, bis- (tert-butyl peroxy base) hexanes of 5- dimethyl -2,5-, 0.1 part of light stabilizer decanedioic acid double -2,
2,6,6- tetramethyl piperidine alcohol esters, 0.1 part of tackifier gamma-aminopropyl-triethoxy-silane, use twin-screw extrusion after mixing
Machine extruding pelletization.The particle made is squeezed out with single screw extrusion machine, extrudate obtains thickness through casting film-forming, rolling after cooling
For the glue film of 0.5mm, it is denoted as C1.
Comparative example 2:
In terms of mass fraction, into 100 parts of polyvinyl butyrals, 5 parts of thermal cross-linking agent tert-butyl hydroperoxide carbonic acid are added
Isopropyl ester, 0.1 part of light stabilizer 3,5- di-t-butyl -4- hydroxy-benzoic acid cetyl ester, 0.1 part of tackifier γ-methyl-prop
Alkene acryloxypropylethoxysilane trimethoxy silane uses double screw extruder extruding pelletization after mixing.By the single spiral shell of the particle made
Bar extruder squeezes out, and for extrudate through casting film-forming, rolling after cooling obtains the glue film with a thickness of 0.5mm, is denoted as C2.
The packaging adhesive film obtained through the foregoing embodiment with comparative example is assessed, assessment result through following test methods
It is listed in table 1:
1, the degree of cross linking
Sample making: taking 3mm heavy sheet glass, packaging adhesive film, TPT backboard, according to lower glass-release film-glue film-release film
Sequence place, be put into ultraviolet irradiation room, irradiated 1 minute under 100 DEG C of -100wUVA ultraviolet lamp tubes.Backboard is covered later, is sent
Enter vacuum laminator, 150 DEG C laminated 5 minutes.Glue film after lamination is taken out to test from release film.Comparative example 1 and 2 is pressed
Be put into vacuum laminator according to glass-release film-glue film-release film-backboard sequence, 150 DEG C laminated 6 minutes.
Test method refers to national standard GB/T 29848-2013 " photovoltaic module ethylene-vinyl acetate copolymer
(EVA) glue film " in degree of cross linking part.
2, light transmittance
Sample making: the same degree of cross linking of method.
Test method is with reference to light transmittance in national standard GB/T 2410-2008 " measurement of transparent plastic light transmittance and mist degree "
Part.
3, glass/packaging adhesive film adhesion strength
" 180 ° of peeling strength test method flexible materials of adhesive are to rigidity with reference to standard GB/T/T2790 for test method
Material ".
Sample making: taking 3mm heavy sheet glass, packaging adhesive film, TPT backboard, places, is put into ultraviolet by glass-glue film order
Radiation chamber irradiates 1 minute under 100 DEG C of -100wUVA ultraviolet lamp tubes.Backboard is covered later, vacuum laminator is sent into, at 150 DEG C
Laminated 5 minutes.Comparative example 1 and 2 is put into vacuum laminator according to glass-glue film-backboard sequence, divides in 150 DEG C of laminateds 6
Clock.
It is tested on puller system, peeling rate 100mm/min, records tensile strength numerical value.
Table 1: embodiment and the resulting packaging adhesive film performance comparison of comparative example
Film sample | The degree of cross linking (%) | Light transmittance (%) | With glassy bond intensity (N/cm) |
S1 | 91.5 | 91.3 | 180 |
S2 | 85.7 | 90.5 | 157 |
S3 | 88.9 | 89.6 | 185 |
S4 | 83.3 | 89.1 | 132 |
S5 | 87.1 | 90.8 | 172 |
S6 | 84.9 | 88.9 | 135 |
C1 | 56.7 | 89.5 | 69 |
C2 | 53.5 | 90.1 | 60 |
By upper table 1 it is found that the present invention program can obtain the higher degree of cross linking within short curing time, shorten component package
Time greatly improves production efficiency.
Finally it should be noted that: above embodiments are only to illustrate the present invention and are not intended to limit the present invention described technology
Scheme;Therefore, although this specification is referring to above-mentioned each embodiment, the present invention has been described in detail, this
Field it is to be appreciated by one skilled in the art that still can modify to the present invention or equivalent replacement;And all do not depart from this
The technical solution and its improvement of spirit and range, should all cover within the scope of the claims of the present invention.
Claims (10)
1. a kind of ultraviolet light solidifies packaging adhesive film, which is characterized in that be mainly prepared by the raw material of following quality proportioning:
2. ultraviolet light according to claim 1 solidifies packaging adhesive film, which is characterized in that the oxygen scavenger can be by ethers third
Olefin(e) acid ester, organic phosphorus compound, organic phosphorus compound, phosphite, thiodipropionate, thiophosphoric acid and its derivative,
Alkyl sulfur compounds, aromatic yl sulfide, tertiary amine, mercaptan, 1,3- diphenyl isobenzofuran, 1,2- diphenylisobenzofuran, 2,3-
Diphenylisobenzofuran, cyclic annular vinyl compound, acetal cyclics, polynary straight chain alcohols, polyether compound, glucose
And its oxidizing ferment is one or more by any proportion mixing composition.
3. ultraviolet light according to claim 1 solidifies packaging adhesive film, which is characterized in that the free radical photo-initiation can be by
Benzoin and its derivative, benzil ketals derivative, α, α-diethoxy acetophenone, 2- dimethyl-alpha-hydroxyacetophenone, 1-
Hydroxy cyclohexyl phenylketone, 1- are to methyl mercapto phenyl -2- methyl -2- morpholinyl -1- acetone, 2- benzyl -2-N, N- dimethylamino -
1- (4- morpholinyl phenyl) butanone, alpha-hydroxyalkyl benzophenone, α-amine alkyl phenones, trimethylbenzoyl diphenyl phosphine oxide, double benzene first
Aminosulfonylphenyl phosphine oxide, Sulfo-benzophenone class compound, esterification oximinoketone compound, aryl peroxide ester compounds, halogenated methyl
Arone, benzoyl formiate, benzophenone and its derivative, thioxanthone and its derivative, anthraquinone and its derivative, benzo furan
It mutters, the one or more of camphorquinone are formed by any proportion mixing.
4. ultraviolet light according to claim 1 solidifies packaging adhesive film, which is characterized in that the cation light initiator can be by
Aromatic diazo salt, diaryl iodonium salt, triaryl sulfonium salts, alkyl sulfosalt, iron arene salt, sulfonyloxy ketone and triaryl silicon
The one or more of oxygen ether are formed by the mixing of any proportion.
5. ultraviolet light according to claim 1 solidifies packaging adhesive film, it is characterised in that: the packaging adhesive film basis material can
By ethylene-vinyl acetate copolymer, low density polyethylene (LDPE), polypropylene, polybutene, polyvinyl butyral, elastic polyurethane
Body, organic silicon rubber, metallocene catalysed polyethylene, ethylene octene copolymer, ethylene pentene copolymer it is one or more by appoint
Meaning proportion mixing composition.
6. ultraviolet light according to claim 1 solidifies packaging adhesive film, which is characterized in that the heat causes crosslinking agent can be by uncle
Bis- (tert-butyl peroxy base) hexanes of butyl peroxy propylene carbonate, 2,5- dimethyl -2,5-, bis- (tert-butyl peroxide) -3 1-,
3,5- trimethyl-cyclohexanes, tert-butyl hydroperoxide carbonic acid -2- ethylhexyl, bis- (t-butyl peroxy) -3 1,1-, 3,5- trimethyls
Bis- (t-amyl peroxy) -3 hexamethylene, 1,1-, bis- (t-amyl peroxy) hexamethylenes of 3,5- trimethyl-cyclohexanes, 1,1-, 1,1- are bis-
Bis- (t-butyl peroxy) butane of (t-butyl peroxy) hexamethylene, 2,2-, peroxidating 2- ethylhexyl carbonate tert-pentyl ester, 2,5- diformazan
Base 2, one kind of bis- (benzoyl the peroxide)-hexanes of 5-, peroxidating carbonic acid tert-pentyl ester, 3,3,5 trimethylhexanoate of peroxidating
Or it is a variety of by any proportion mixing composition;The light stabilizer is hindered amine light stabilizer, by 3,5- di-t-butyl -4- hydroxyl
Base-benzoic acid cetyl ester, three (1,2,2,6,6- pentamethyl -4- piperidyl) phosphite esters, decanedioic acid double -2,2,6,6- tetra-
Methyl piperidine alcohol ester, double -1- decane oxygroups -2,2,6,6- tetramethyl piperidine -4- alcohol sebacates, succinic acid and hydroxyl -2 4-,
Bis- (2,2,6,6- tetramethyl -4- piperidyl) -1, the 6- hexamethylene diamines and 2 of polymer, the N of 2,6,6- tetramethyl -1- piperidine alcohols, N ' -,
Chloro- 6- (1,1,3, the 3- tetramethyl butyl) amino -1,3,5-triazines of 4- bis- polymer, N, bis- (2,2,6, the 6- tetramethyls-of N ' -
4- piperidyl) -1,6- hexamethylene diamine and morpholine -2, the polymer of 4,6- tri- chloro-1,3,5-triazines it is one or more by arbitrarily matching
It is formed than mixing;The tackifier are by gamma-aminopropyl-triethoxy-silane, γ-methacryloxypropyl trimethoxy silicon
Alkane, γ-(the third oxygen of 2,3- epoxy) propyl trimethoxy silicane, vinyltrimethoxysilane, N- (β-aminoethyl)-γ-ammonia third
One or more the pressing of base trimethoxy silane, γ-glycidyl ether oxygen propyl trimethyl silane, 3- propyl silane
Any proportion mixing composition.
7. ultraviolet light according to claim 1 solidifies packaging adhesive film, which is characterized in that the preparation process specifically: will
Raw material uses double screw extruder extruding pelletization after mixing.The particle made is squeezed out with single screw extrusion machine, extrudate warp
Casting film-forming, rolling after cooling obtain the glue film with a thickness of 0.5mm.
8. a kind of solar cell module for solidifying packaging adhesive film with ultraviolet light described in claim 1, which is characterized in that pass through
Following methods are prepared: solidifying packaging adhesive film, cell piece, the second ultraviolet light cure package according to lower cover plate, the first ultraviolet light
The sequence of glue film successively organizes arrangement, is put into ultraviolet irradiation room, irradiates under 100 DEG C of -100wUVA ultraviolet lamp tubes about 1 minute.It
Upper cover plate is covered on the second ultraviolet light solidification packaging adhesive film afterwards, vacuum laminator is sent into, in 130-150 DEG C of laminated about 3-5
Minute.
9. a kind of solar cell module for solidifying packaging adhesive film with ultraviolet light described in claim 1, which is characterized in that pass through
Following methods are prepared: solidifying packaging adhesive film, cell piece, the second ultraviolet light cure package according to lower cover plate, the first ultraviolet light
Glue film, upper cover plate sequence successively organize arrangement, be sent into vacuum laminator, 130-150 DEG C laminated 3-5 minutes, using
Ultraviolet irradiation device irradiates 1 minute under 100 DEG C of -100wUVA ultraviolet lamp tubes.
10. solar cell module according to claim 9, which is characterized in that the visible spectrum wave of the upper cover plate
Transmitance >=85% of section, transmitance >=60% of ultraviolet spectra wave band.
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