JP2015183179A5 - - Google Patents
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- JP2015183179A5 JP2015183179A5 JP2014063918A JP2014063918A JP2015183179A5 JP 2015183179 A5 JP2015183179 A5 JP 2015183179A5 JP 2014063918 A JP2014063918 A JP 2014063918A JP 2014063918 A JP2014063918 A JP 2014063918A JP 2015183179 A5 JP2015183179 A5 JP 2015183179A5
- Authority
- JP
- Japan
- Prior art keywords
- parts
- acrylate
- ethyl acetate
- solvent
- solution
- 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.)
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- XEKOWRVHYACXOJ-UHFFFAOYSA-N acetic acid ethyl ester Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2,2'-azo-bis-isobutyronitrile Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 2
- CUXGDKOCSSIRKK-UHFFFAOYSA-N 7-methyloctyl prop-2-enoate Chemical compound CC(C)CCCCCCOC(=O)C=C CUXGDKOCSSIRKK-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-VAWYXSNFSA-N Azobisisobutyronitrile Chemical compound N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 2
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
Description
製造例(A1)〔重合体(A)の製造〕:
撹拌機、還流冷却管、窒素導入管、温度計、滴下管を備えた反応装置に窒素雰囲気下、2−エチルヘキシルアクリレート25部、イソノニルアクリレート15部、シクロヘキシルアクリレート10部、4−ヒドロキシブチルアクリレート0.25部、重合開始剤であるアゾビスイソブチロニトリルを適量、さらに溶剤として酢酸エチルを仕込んだ。溶液温度が80℃になるまで加熱した。
次いで、滴下管に2−エチルヘキシルアクリレート25部、イソノニルアクリレート15部、シクロヘキシルアクリレート10部、4−ヒドロキシブチルアクリレート0.25部、重合開始剤であるアゾビスイソブチロニトリルを適量、さらに溶剤として酢酸エチルを仕込んだ。
前記反応装置を溶液温度が80℃になるまで加熱し、反応装置内で反応が開始したことを確認後、前記滴下管から溶液を2時間かけて滴下した。滴下終了後、反応温度を約80℃に保持し5時間反応を継続した後、冷却を開始した。次いで酢酸エチルで希釈し、不揮発分を40%に調整した。これにより重量平均分子量は90万の重合体(A1)溶液を得た。
Production Example (A1) [Production of Polymer (A)]:
A reactor equipped with a stirrer, a reflux condenser, a nitrogen inlet tube, a thermometer, and a dropping tube, under a nitrogen atmosphere, 25 parts 2-ethylhexyl acrylate, 15 parts isononyl acrylate, 10 parts cyclohexyl acrylate, 4-hydroxybutyl acrylate 0 .25 parts, an appropriate amount of azobisisobutyronitrile as a polymerization initiator, and ethyl acetate as a solvent were charged. Heated until the solution temperature reached 80 ° C.
Next, 25 parts of 2-ethylhexyl acrylate, 15 parts of isononyl acrylate, 10 parts of cyclohexyl acrylate, 0.25 part of 4-hydroxybutyl acrylate, an appropriate amount of azobisisobutyronitrile as a polymerization initiator, and a solvent as a solvent Ethyl acetate was charged.
The reactor was heated until the solution temperature reached 80 ° C., and after confirming that the reaction had started in the reactor, the solution was dropped from the dropping tube over 2 hours. After completion of dropping, the reaction temperature was kept at about 80 ° C. and the reaction was continued for 5 hours, and then cooling was started. Subsequently, it diluted with ethyl acetate and the non volatile matter was adjusted to 40%. As a result, a polymer (A1) solution having a weight average molecular weight of 900,000 was obtained.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014063918A JP6237393B2 (en) | 2014-03-26 | 2014-03-26 | Adhesive and adhesive sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014063918A JP6237393B2 (en) | 2014-03-26 | 2014-03-26 | Adhesive and adhesive sheet |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2015183179A JP2015183179A (en) | 2015-10-22 |
JP2015183179A5 true JP2015183179A5 (en) | 2016-12-08 |
JP6237393B2 JP6237393B2 (en) | 2017-11-29 |
Family
ID=54350087
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2014063918A Active JP6237393B2 (en) | 2014-03-26 | 2014-03-26 | Adhesive and adhesive sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP6237393B2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018035226A (en) * | 2016-08-30 | 2018-03-08 | リンテック株式会社 | Adhesive composition, and adhesive sheet |
KR102446328B1 (en) * | 2016-09-21 | 2022-09-21 | 동우 화인켐 주식회사 | Adhesive Composition and Adhesive Sheet Using the Same |
JP6969515B2 (en) * | 2017-07-24 | 2021-11-24 | 荒川化学工業株式会社 | UV curable adhesive, cured product, adhesive sheet |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5758647B2 (en) * | 2011-02-17 | 2015-08-05 | 日東電工株式会社 | Optical adhesive sheet |
JP2013032500A (en) * | 2011-06-30 | 2013-02-14 | Nitto Denko Corp | Adhesive agent composition, adhesive agent layer, and adhesive sheet |
JP2013129789A (en) * | 2011-12-22 | 2013-07-04 | Nitto Denko Corp | Adhesive, adhesive layer, and adhesive sheet |
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2014
- 2014-03-26 JP JP2014063918A patent/JP6237393B2/en active Active
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