JP2017511820A5 - - Google Patents
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- Publication number
- JP2017511820A5 JP2017511820A5 JP2016549773A JP2016549773A JP2017511820A5 JP 2017511820 A5 JP2017511820 A5 JP 2017511820A5 JP 2016549773 A JP2016549773 A JP 2016549773A JP 2016549773 A JP2016549773 A JP 2016549773A JP 2017511820 A5 JP2017511820 A5 JP 2017511820A5
- Authority
- JP
- Japan
- Prior art keywords
- nanoparticle
- iii
- range
- discontinuous phase
- aggregates
- 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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- 239000002105 nanoparticle Substances 0.000 claims description 34
- 239000000203 mixture Substances 0.000 claims description 20
- 239000003381 stabilizer Substances 0.000 claims description 10
- 239000000725 suspension Substances 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 5
- 239000012989 trithiocarbonate Substances 0.000 claims description 5
- HIZCIEIDIFGZSS-UHFFFAOYSA-L trithiocarbonate Chemical compound [S-]C([S-])=S HIZCIEIDIFGZSS-UHFFFAOYSA-L 0.000 claims description 5
- 229920001400 block copolymer Polymers 0.000 claims description 4
- -1 heterocyclic amines Chemical class 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 239000002243 precursor Substances 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 3
- 125000000524 functional group Chemical group 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 2
- 239000012988 Dithioester Substances 0.000 claims description 2
- 150000001491 aromatic compounds Chemical class 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims description 2
- 239000003638 chemical reducing agent Substances 0.000 claims description 2
- 239000004020 conductor Substances 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- 239000012990 dithiocarbamate Substances 0.000 claims description 2
- 125000005022 dithioester group Chemical group 0.000 claims description 2
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 claims description 2
- 238000013467 fragmentation Methods 0.000 claims description 2
- 238000006062 fragmentation reaction Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 150000003222 pyridines Chemical class 0.000 claims description 2
- 230000002441 reversible effect Effects 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- 239000004332 silver Substances 0.000 claims description 2
- 239000000758 substrate Substances 0.000 claims description 2
- 238000003786 synthesis reaction Methods 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- 239000012991 xanthate Substances 0.000 claims description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461935108P | 2014-02-03 | 2014-02-03 | |
| US61/935,108 | 2014-02-03 | ||
| US201461944088P | 2014-02-25 | 2014-02-25 | |
| US61/944,088 | 2014-02-25 | ||
| PCT/US2015/013830 WO2015116960A1 (en) | 2014-02-03 | 2015-01-30 | Compositions for high speed printing of conductive materials for electronic circuitry type applications, and methods relating |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2017511820A JP2017511820A (ja) | 2017-04-27 |
| JP2017511820A5 true JP2017511820A5 (https=) | 2018-03-15 |
Family
ID=52463228
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016549773A Pending JP2017511820A (ja) | 2014-02-03 | 2015-01-30 | 電子回路部品タイプの適用のための導電材料の高速印刷用の組成物、および関連する方法 |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JP2017511820A (https=) |
| CN (1) | CN105960440A (https=) |
| DE (1) | DE112015000622B4 (https=) |
| WO (1) | WO2015116960A1 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105679649B (zh) * | 2016-01-14 | 2018-08-17 | 上海大学 | 降低溶液法成膜退火温度的方法 |
| EP3321332B1 (en) * | 2016-11-10 | 2019-07-31 | Agfa-Gevaert | Method for manufacturing an electronic device, such as printed circuit board |
| US10800938B2 (en) * | 2017-09-16 | 2020-10-13 | Xerox Corporation | Molecular organic reactive inks for conductive metal printing using photoinitiators |
| CN110358368A (zh) * | 2019-05-31 | 2019-10-22 | 南开大学 | 一种可拉伸微电子电路导电油墨及其合成方法 |
| GB2592557B (en) | 2019-10-22 | 2024-07-10 | Lumet Tech Ltd | Transferable composition and methods for preparing and using the same |
| CN111574885B (zh) * | 2020-05-19 | 2023-07-14 | 成都怀慈福佑电子科技有限公司 | 一种面向印刷电子技术的生物可降解电子材料 |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2166092T3 (es) | 1996-07-10 | 2002-04-01 | Du Pont | Polimerizacion con caracteristicas vivientes. |
| FR2764892B1 (fr) | 1997-06-23 | 2000-03-03 | Rhodia Chimie Sa | Procede de synthese de polymeres a blocs |
| US7138468B2 (en) * | 2002-03-27 | 2006-11-21 | University Of Southern Mississippi | Preparation of transition metal nanoparticles and surfaces modified with (CO)polymers synthesized by RAFT |
| DE10236133A1 (de) * | 2002-08-07 | 2004-02-26 | Byk-Chemie Gmbh | Verwendung von Gradientencopolymeren als Dispergiermittel zur Behandlung von Pigmenten und Feststoffen |
| KR20060056900A (ko) * | 2003-06-24 | 2006-05-25 | 폴리머스 오스트레일리아 프로프라이어터리 리미티드 | 나노복합체 중의 아크릴 분산제 |
| EP1650264A1 (en) * | 2003-07-25 | 2006-04-26 | Kaneka Corporation | Resin composition containing ultrafine particles |
| KR100740634B1 (ko) * | 2003-09-12 | 2007-07-18 | 내셔날 인스티튜트 오브 어드밴스드 인더스트리얼 사이언스 앤드 테크놀로지 | 미세한 액적(液滴)의 형상으로 분사해, 적층 도포 가능한금속 나노 입자 분산액 |
| US7632905B2 (en) | 2004-04-09 | 2009-12-15 | L'oreal S.A. | Block copolymer, composition comprising it and cosmetic treatment process |
| CN102424703B (zh) * | 2004-10-04 | 2014-03-26 | 悉尼大学 | 使用raft试剂的表面聚合方法和聚合产物 |
| JP2008527169A (ja) * | 2005-01-10 | 2008-07-24 | イシウム リサーチ デベロップメント カンパニー オブ ザ ヘブリュー ユニバーシティー オブ イエルサレム | 金属ナノ粒子の水系分散物 |
| JP2008528782A (ja) * | 2005-02-04 | 2008-07-31 | アグフア・グラフイクス・ナームローゼ・フエンノートシヤツプ | イオン性芳香族モノマーから成るブロックコポリマーを含んでなる安定な顔料分散系 |
| JP2009506173A (ja) * | 2005-08-26 | 2009-02-12 | カーネギー メロン ユニバーシティ | 導電性ポリマーおよびコントロールラジカル重合 |
| TWI312799B (en) * | 2005-12-30 | 2009-08-01 | Ind Tech Res Inst | Viscosity controllable highly conductive ink composition and method for fabricating a metal conductive pattern |
| GB0624729D0 (en) * | 2006-12-12 | 2007-01-17 | Univ Leeds | Reversible micelles and applications for their use |
| JP2009170447A (ja) * | 2008-01-10 | 2009-07-30 | Sharp Corp | 導電性パターン形成材料、導電性パターン形成方法および配線基板 |
| US20090181183A1 (en) | 2008-01-14 | 2009-07-16 | Xerox Corporation | Stabilized Metal Nanoparticles and Methods for Depositing Conductive Features Using Stabilized Metal Nanoparticles |
| EP2285881B1 (en) * | 2008-05-16 | 2014-01-22 | The University Of Sydney | Polymer microgel beads and preparative method thereof |
| EP2444462A4 (en) * | 2009-06-16 | 2014-03-05 | Bando Chemical Ind | ELECTRICALLY CONDUCTIVE INK AND METHOD OF MANUFACTURING BASE MATERIALS WITH ELECTRICALLY CONDUCTIVE COATING FILM FIXED AND USED THEREOF |
| EP2369597B1 (de) * | 2010-03-12 | 2014-06-25 | Clariant International AG | Herstellung leitfähiger Oberflächenbeschichtungen mit Dispersion mit elektrostatisch stabilisierten Silbernanopartikeln |
| US8324294B2 (en) * | 2011-03-07 | 2012-12-04 | Xerox Corporation | Solvent-based inks comprising silver nanoparticles |
| JP5798396B2 (ja) * | 2011-07-14 | 2015-10-21 | リンテック株式会社 | ブロック共重合体、その製造方法、粘着組成物及び粘着シート |
| US20130224905A1 (en) * | 2012-02-27 | 2013-08-29 | E I Du Pont De Nemours And Company | Silver paste and use thereof in the production of solar cells |
| US20140349025A1 (en) * | 2013-05-23 | 2014-11-27 | E I Du Pont De Nemours And Company | Conductive compositions and methods relating thereto |
-
2015
- 2015-01-30 CN CN201580006688.7A patent/CN105960440A/zh active Pending
- 2015-01-30 WO PCT/US2015/013830 patent/WO2015116960A1/en not_active Ceased
- 2015-01-30 DE DE112015000622.2T patent/DE112015000622B4/de not_active Expired - Fee Related
- 2015-01-30 JP JP2016549773A patent/JP2017511820A/ja active Pending
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