TWI709584B - 菲涅耳透鏡及其製造方法、以及具備該菲涅耳透鏡之光學裝置及其製造方法 - Google Patents
菲涅耳透鏡及其製造方法、以及具備該菲涅耳透鏡之光學裝置及其製造方法 Download PDFInfo
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| USD903187S1 (en) * | 2019-01-25 | 2020-11-24 | Eaton Intelligent Power Limited | Optical structure |
| USD901752S1 (en) | 2019-01-25 | 2020-11-10 | Eaton Intelligent Power Limited | Optical structure |
| US11236887B2 (en) | 2019-01-25 | 2022-02-01 | Eaton Intelligent Power Limited | Optical structures for light emitting diodes (LEDs) |
| CN114269550A (zh) * | 2019-09-20 | 2022-04-01 | 三井化学株式会社 | 光学部件的制造方法及光学部件 |
| EP4149758A4 (en) * | 2020-05-14 | 2024-09-11 | 3M Innovative Properties Company | MULTILAYER OPTICAL FILMS COMPRISING AT LEAST ONE LAYER OF FLUORINATED (CO)POLYMER PREPARED USING A FLUORINATED PHOTOINITIATOR, AND METHODS OF PREPARATION AND USE THEREOF |
| CN112851600B (zh) * | 2021-01-11 | 2022-10-04 | 江苏泰特尔新材料科技股份有限公司 | 一种高耐热双环氧化物的制备方法 |
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| US6743510B2 (en) * | 2001-11-13 | 2004-06-01 | Sumitomo Chemical Company, Limited | Composition comprising a cationic polymerization compound and coating obtained from the same |
| JP2004170862A (ja) * | 2002-11-22 | 2004-06-17 | Dainippon Printing Co Ltd | フレネルレンズ |
| US7149032B2 (en) * | 2005-03-29 | 2006-12-12 | Tomoegawa Paper Co., Ltd. | Anti-glare film |
| ES2710880T3 (es) * | 2005-12-21 | 2019-04-29 | Carl Zeiss Vision Australia Holdings Ltd | Revestimientos para elementos ópticos |
| TWI427117B (zh) * | 2008-05-30 | 2014-02-21 | Nitto Denko Corp | 光學元件用樹脂組成物、使用其之光學元件及光學鏡片之製造方法 |
| WO2010004879A1 (ja) * | 2008-07-11 | 2010-01-14 | コニカミノルタオプト株式会社 | 光学素子、光学素子の製造方法、及び電子機器の製造方法 |
| WO2012081393A1 (ja) * | 2010-12-14 | 2012-06-21 | 株式会社ダイセル | 硬化性組成物、及び硬化樹脂 |
| JP2013003322A (ja) * | 2011-06-15 | 2013-01-07 | Konica Minolta Advanced Layers Inc | 光学素子の製造方法及び光学素子 |
| FR2979734B1 (fr) * | 2011-09-02 | 2014-05-23 | Arjowiggins Security | Structure de securite comportant une structure optique reflechissante, et procede associe. |
| JP5950667B2 (ja) * | 2012-04-16 | 2016-07-13 | キヤノン株式会社 | 光学用部材、その製造方法および光学用部材の光学膜 |
| CN104540868B (zh) * | 2012-08-31 | 2018-06-01 | 株式会社大赛璐 | 固化性组合物及其固化物、光学构件以及光学装置 |
| JP6170951B2 (ja) * | 2013-01-31 | 2017-07-26 | 株式会社ダイセル | ウェハレベルレンズ用硬化性組成物、ウェハレベルレンズの製造方法及びウェハレベルレンズ、並びに光学装置 |
| US9207123B2 (en) * | 2013-03-01 | 2015-12-08 | Sandia Corporation | Athermal channeled spectropolarimeter |
| JP5807139B2 (ja) * | 2013-03-26 | 2015-11-10 | 富士フイルム株式会社 | 光学レンズ及びその製造方法、並びにレンズユニット、撮像モジュール、電子機器 |
| EP3037852A4 (en) * | 2013-08-20 | 2017-03-22 | Daicel Corporation | Wafer lens, wafer lens array, wafer lens laminate, and wafer lens array laminate |
-
2015
- 2015-08-20 JP JP2015162635A patent/JP2017040791A/ja active Pending
-
2016
- 2016-08-03 WO PCT/JP2016/072817 patent/WO2017029996A1/ja not_active Ceased
- 2016-08-03 US US15/751,387 patent/US20180196167A1/en not_active Abandoned
- 2016-08-03 CN CN201680045065.5A patent/CN107850691A/zh active Pending
- 2016-08-03 CN CN202210564159.0A patent/CN114879286A/zh active Pending
- 2016-08-03 EP EP16836987.4A patent/EP3339917A4/en not_active Withdrawn
- 2016-08-18 TW TW105126326A patent/TWI709584B/zh not_active IP Right Cessation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200942894A (en) * | 2008-01-23 | 2009-10-16 | Sony Corp | Lens barrel and image pickup unit |
| WO2015098736A1 (ja) * | 2013-12-26 | 2015-07-02 | 株式会社ダイセル | レンズ用硬化性組成物、並びにレンズ及び光学装置 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN107850691A (zh) | 2018-03-27 |
| EP3339917A4 (en) | 2019-04-03 |
| JP2017040791A (ja) | 2017-02-23 |
| TW201718689A (zh) | 2017-06-01 |
| US20180196167A1 (en) | 2018-07-12 |
| CN114879286A (zh) | 2022-08-09 |
| EP3339917A1 (en) | 2018-06-27 |
| WO2017029996A1 (ja) | 2017-02-23 |
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