JP7145868B2 - 粘着剤組成物及び粘着シート - Google Patents
粘着剤組成物及び粘着シート Download PDFInfo
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- JP7145868B2 JP7145868B2 JP2019546642A JP2019546642A JP7145868B2 JP 7145868 B2 JP7145868 B2 JP 7145868B2 JP 2019546642 A JP2019546642 A JP 2019546642A JP 2019546642 A JP2019546642 A JP 2019546642A JP 7145868 B2 JP7145868 B2 JP 7145868B2
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- Prior art keywords
- polyurethane
- meth
- pressure
- sensitive adhesive
- adhesive composition
- Prior art date
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- 239000000853 adhesive Substances 0.000 title description 69
- 230000001070 adhesive effect Effects 0.000 title description 69
- 239000004814 polyurethane Substances 0.000 claims description 130
- 229920002635 polyurethane Polymers 0.000 claims description 130
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 96
- 239000000178 monomer Substances 0.000 claims description 64
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims description 56
- 229920005862 polyol Polymers 0.000 claims description 31
- 150000003077 polyols Chemical class 0.000 claims description 31
- 150000001875 compounds Chemical class 0.000 claims description 26
- 239000003999 initiator Substances 0.000 claims description 22
- 239000005056 polyisocyanate Substances 0.000 claims description 17
- 229920001228 polyisocyanate Polymers 0.000 claims description 17
- 239000000758 substrate Substances 0.000 claims description 15
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- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 5
- 125000005442 diisocyanate group Chemical group 0.000 claims description 5
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- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
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- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
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- HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 3
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- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 3
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 3
- 238000000016 photochemical curing Methods 0.000 description 3
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- 238000006116 polymerization reaction Methods 0.000 description 3
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- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 3
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 2
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 2
- XLPJNCYCZORXHG-UHFFFAOYSA-N 1-morpholin-4-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCOCC1 XLPJNCYCZORXHG-UHFFFAOYSA-N 0.000 description 2
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- DPNXHTDWGGVXID-UHFFFAOYSA-N 2-isocyanatoethyl prop-2-enoate Chemical compound C=CC(=O)OCCN=C=O DPNXHTDWGGVXID-UHFFFAOYSA-N 0.000 description 2
- YHFGMFYKZBWPRW-UHFFFAOYSA-N 3-methylpentane-1,1-diol Chemical compound CCC(C)CC(O)O YHFGMFYKZBWPRW-UHFFFAOYSA-N 0.000 description 2
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 2
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 2
- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 description 2
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- 239000004698 Polyethylene Substances 0.000 description 2
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- 239000004793 Polystyrene Substances 0.000 description 2
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- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- XQBCVRSTVUHIGH-UHFFFAOYSA-L [dodecanoyloxy(dioctyl)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCCCCCCC XQBCVRSTVUHIGH-UHFFFAOYSA-L 0.000 description 2
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- 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 description 2
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- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 2
- GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 2
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- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 2
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- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- DZZAHLOABNWIFA-UHFFFAOYSA-N 2-butoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCCCC)C(=O)C1=CC=CC=C1 DZZAHLOABNWIFA-UHFFFAOYSA-N 0.000 description 1
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- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- 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
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- 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
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- 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
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
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- 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
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
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- 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
- C09J2301/00—Additional features of adhesives in the form of films or foils
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- Chemical Kinetics & Catalysis (AREA)
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP2017195411 | 2017-10-05 | ||
JP2017195411 | 2017-10-05 | ||
PCT/JP2018/035399 WO2019069746A1 (ja) | 2017-10-05 | 2018-09-25 | 粘着剤組成物及び粘着シート |
Publications (2)
Publication Number | Publication Date |
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JPWO2019069746A1 JPWO2019069746A1 (ja) | 2020-09-10 |
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KR102567177B1 (ko) * | 2018-09-26 | 2023-08-16 | 가부시끼가이샤 레조낙 | 표면 보호 시트용 점착제 조성물 및 표면 보호 시트 |
CN112673072A (zh) * | 2018-09-26 | 2021-04-16 | 昭和电工株式会社 | 表面保护片用粘着剂组合物及表面保护片 |
WO2021019868A1 (ja) * | 2019-07-29 | 2021-02-04 | 昭和電工株式会社 | 粘着シートおよび粘着剤組成物 |
JP7338299B2 (ja) | 2019-07-30 | 2023-09-05 | 株式会社レゾナック | 光硬化性粘着剤組成物および粘着シート |
CN113993663B (zh) * | 2019-09-05 | 2024-05-31 | 株式会社力森诺科 | 背面研磨带 |
JPWO2021125152A1 (ko) * | 2019-12-17 | 2021-06-24 | ||
JP6769574B1 (ja) * | 2020-06-01 | 2020-10-14 | 東洋インキScホールディングス株式会社 | 粘着シート、粘着シート付き被着体、および粘着シートの使用方法 |
KR102229884B1 (ko) * | 2020-07-01 | 2021-03-18 | 동우 화인켐 주식회사 | 점착제 조성물 및 그를 이용한 점착 시트 |
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WO2023276944A1 (ja) * | 2021-06-30 | 2023-01-05 | 昭和電工株式会社 | 粘着剤組成物及び保護シート |
JP2024531176A (ja) * | 2021-08-11 | 2024-08-29 | サムヤン コーポレイション | (メタ)アクリル変性ポリウレタン組成物及びその製造方法 |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000038547A (ja) | 1998-07-24 | 2000-02-08 | Mitsubishi Rayon Co Ltd | 光硬化型接着剤組成物およびそれを用いた光学部材 |
JP2007279234A (ja) | 2006-04-04 | 2007-10-25 | Nitto Denko Corp | 粘着剤層付光学部材の製造方法、粘着剤層付光学部材及び画像表示装置 |
JP2009084372A (ja) | 2007-09-28 | 2009-04-23 | Nippon Shokubai Co Ltd | 電子線硬化性樹脂組成物、積層体、及び、粘着シート又は粘着フィルム |
JP2010059240A (ja) | 2008-09-01 | 2010-03-18 | Dainippon Printing Co Ltd | 粘着シート |
JP2011079888A (ja) | 2009-10-02 | 2011-04-21 | Denki Kagaku Kogyo Kk | (メタ)アクリル系樹脂組成物、接着剤組成物及び仮固定・剥離方法 |
JP2012131981A (ja) | 2010-12-03 | 2012-07-12 | Nippon Synthetic Chem Ind Co Ltd:The | 粘着剤、光学部材用粘着剤、粘着剤層付き光学部材、画像表示装置、活性エネルギー線硬化性粘着剤組成物 |
JP2014210895A (ja) | 2013-04-22 | 2014-11-13 | 昭和電工株式会社 | 透明粘着シート用光硬化性組成物、それを用いた粘着シートおよびその用途 |
WO2016002387A1 (ja) | 2014-06-30 | 2016-01-07 | Dic株式会社 | 紫外線硬化型粘着剤組成物、粘着フィルム、及び、粘着フィルムの製造方法 |
WO2016001350A1 (en) | 2014-07-03 | 2016-01-07 | Laboratoire Hra-Pharma | Method for providing regular contraception |
JP2017125178A (ja) | 2016-01-07 | 2017-07-20 | デンカ株式会社 | 組成物及びそれを用いた部材の仮固定方法 |
JP2018095770A (ja) | 2016-12-15 | 2018-06-21 | 昭和電工株式会社 | 光硬化性組成物、及び粘着シート |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101993678B (zh) * | 2009-08-26 | 2013-08-07 | 比亚迪股份有限公司 | 一种紫外光固化胶及其制备方法 |
CN102898958B (zh) * | 2011-07-25 | 2016-11-02 | 汉高股份有限公司 | 一种粘合剂组合物 |
WO2014122866A1 (ja) * | 2013-02-08 | 2014-08-14 | 昭和電工株式会社 | 熱伝導性粘着剤組成物、熱伝導性粘着シート、難燃性熱伝導性粘着剤組成物、難燃性熱伝導性粘着シート、熱伝導性絶縁塗膜及び金属成形品 |
TWI601798B (zh) | 2014-06-18 | 2017-10-11 | 昭和電工股份有限公司 | 透明黏著薄片用光硬化性組成物、透明黏著薄片 |
US10662355B2 (en) * | 2015-09-10 | 2020-05-26 | Mitsui Chemicals Tohcello, Inc. | Pressure-sensitive adhesive composition, process for producing same, and pressure-sensitive adhesive film |
-
2018
- 2018-09-25 CN CN201880064352.XA patent/CN111164176B/zh active Active
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Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000038547A (ja) | 1998-07-24 | 2000-02-08 | Mitsubishi Rayon Co Ltd | 光硬化型接着剤組成物およびそれを用いた光学部材 |
JP2007279234A (ja) | 2006-04-04 | 2007-10-25 | Nitto Denko Corp | 粘着剤層付光学部材の製造方法、粘着剤層付光学部材及び画像表示装置 |
JP2009084372A (ja) | 2007-09-28 | 2009-04-23 | Nippon Shokubai Co Ltd | 電子線硬化性樹脂組成物、積層体、及び、粘着シート又は粘着フィルム |
JP2010059240A (ja) | 2008-09-01 | 2010-03-18 | Dainippon Printing Co Ltd | 粘着シート |
JP2011079888A (ja) | 2009-10-02 | 2011-04-21 | Denki Kagaku Kogyo Kk | (メタ)アクリル系樹脂組成物、接着剤組成物及び仮固定・剥離方法 |
JP2012131981A (ja) | 2010-12-03 | 2012-07-12 | Nippon Synthetic Chem Ind Co Ltd:The | 粘着剤、光学部材用粘着剤、粘着剤層付き光学部材、画像表示装置、活性エネルギー線硬化性粘着剤組成物 |
JP2014210895A (ja) | 2013-04-22 | 2014-11-13 | 昭和電工株式会社 | 透明粘着シート用光硬化性組成物、それを用いた粘着シートおよびその用途 |
WO2016002387A1 (ja) | 2014-06-30 | 2016-01-07 | Dic株式会社 | 紫外線硬化型粘着剤組成物、粘着フィルム、及び、粘着フィルムの製造方法 |
WO2016001350A1 (en) | 2014-07-03 | 2016-01-07 | Laboratoire Hra-Pharma | Method for providing regular contraception |
JP2017125178A (ja) | 2016-01-07 | 2017-07-20 | デンカ株式会社 | 組成物及びそれを用いた部材の仮固定方法 |
JP2018095770A (ja) | 2016-12-15 | 2018-06-21 | 昭和電工株式会社 | 光硬化性組成物、及び粘着シート |
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TWI695873B (zh) | 2020-06-11 |
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