Electrostatically excited liquid marble as a micromixer
文献情報
Nhat-Khuong Nguyen, Pradip Singha, Hongjie An, Hoang-Phuong Phan, Nam-Trung Nguyen, Chin Hong Ooi
Liquid marble is a promising microfluidic platform for microreactor applications. However, the lack of contactless and on-demand mixing strategies significantly hinders its potential. This paper reports the use of electrostatic force as an actuation scheme to induce vibration and deformation in a liquid marble, thus enhancing the internal flow and promoting mixing in this platform. The effect of a uniform AC electric field on liquid marbles with different volumes was investigated. The results show significant improvement in mixing performance when the liquid marbles were actuated. Increasing electric field strengths also substantially enhances the mixing process. These results show the potential of using a liquid marble as a high-performance micromixer by exploiting the mechanisms of vibration and deformation.
関連文献
Viral capsids as templates for the production of monodisperse Prussian blue nanoparticles
Andrés de la Escosura, Martijn Verwegen, Friso D. Sikkema, Marta Comellas-Aragonès, Andrei Kirilyuk, Theo Rasing, Roeland J. M. Nolte, Jeroen J. L. M. Cornelissen
DOI: 10.1039/B800936H
Lewis acid-catalyzed hydrogenation: B(C6F5)3-mediated reduction of imines and nitriles with H2‡
Preston A. Chase, Titel Jurca, Douglas W. Stephan
DOI: 10.1039/B718598G
TNTadsorption on Au(111): electrochemistry and adlayer structure
Rui Wen, Hong-Xia Zhang, Cun-Ji Yan, Hui-Juan Yan, Ge-Bo Pan, Li-Jun Wan
DOI: 10.1039/B719888D
Inhibition and dispersion of proteobacterial biofilms
Justin J. Richards, Robert W. Huigens III, T. Eric Ballard, Anne Basso, John Cavanagh, Christian Melander
DOI: 10.1039/B719802G
Role and substrate specificity of the Streptomyces coelicolor RedH enzyme in undecylprodiginine biosynthesis
Stuart W. Haynes, Paulina K. Sydor, Anna E. Stanley, Lijiang Song, Gregory L. Challis
DOI: 10.1039/B801677A
Chemical modifications of AFM tips for the study of molecular recognition events
Régis Barattin, Normand Voyer
DOI: 10.1039/B614328H
Fast energy transfer within a self-assembled cyclic porphyrin tetramer
DOI: 10.1039/B718628B
Stabilization of cobalt oxyhydrate superconductor
Zhi Ren, Cao Wang, Xiang-fan Xu, Guang-han Cao, Zhu-an Xu, Yu-heng Zhang
DOI: 10.1039/B800378E
Cobalt promoted copper manganese oxide catalysts for ambient temperature carbon monoxide oxidation
Christopher Jones, Stuart H. Taylor, Andrew Burrows, Mandy J. Crudace, Christopher J. Kiely, Graham J. Hutchings
DOI: 10.1039/B800052M
A unique heterobimetallic benzyl calciate—an organometallic mixed-metal species involving a heavy alkaline-earth metal
Marites A. Guino-o, Charles F. Campana, Karin Ruhlandt-Senge
DOI: 10.1039/B715701K
こちらもおすすめ
3-イチチルビフェニルはどのように合成されますか?
3-イチチルビフェニルは、ビフェニルとイチプロピオニトリルを回収率約90%で反応させて合成されます。触媒は通常、亜リチウムホウ素を用います。
8-溴-5-三氟甲基喹啉はどのように合成されますか?
8-溴-5-三氟甲基喹啉は、5-トリフルオロメチル-2-メチル-1,3-ベンゼンジオールをブロモエタノールと反応させて生成します。この反応は塩基性条件下で行われ...
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品はありますか?
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品としては、4-...
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向や研究トレンドはどのようなものでしょうか?
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向は、主に産業用途での需要により影響を受けます。研究トレンドとし...
イソステアロイルグリセリルは安全ですか?
イソステアロイルグリセリルは一般的に安全性が高いとされていますが、過度な使用や個人差により皮�owsん炎などの反応が起こる可能性があります。使用前に医師に相談す...
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向や研究トレンドはどうですか?
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向は、医薬品や合成化学の研究分野で注目を集めています。新興研究は、該当化合物の合成改良と生体内での作用メカニズ...
3-チオフェンスチオールの物理化学的性質は何ですか?
3-チオフェンスチオールのCAS番号は7774-73-4です。結晶性の白色粉末で、分子量は122.17です。この化合物は水に微溶解し、エタノールやジクロロメタン...
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは安全ですか?
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは一定の安全性基準を満たしていま...
CAS番号1316822-90-8の化合物は安全ですか?
CAS番号1316822-90-8の化合物は安全性に関しては評価が不足していますが、一般的には生物学的に活性な物質であり、取り扱いには適切な安全防護措置が必要で...
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸はどのように保存すればよいですか?
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸は、冷暗所で保存し、直射日光から遠ざけてください。容器は密閉し、高湿度や高温を避けて保管してください。
掲載誌
Reaction Chemistry & Engineering

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.










![1,10-bis(3,5-dimethylphenyl)-12-hydroxy-4,5,6,7-tetrahydroiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocine 12-oxide structure 1,10-bis(3,5-dimethylphenyl)-12-hydroxy-4,5,6,7-tetrahydroiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocine 12-oxide structure](https://static.chemtradehub.com/structs/141/1412439-82-7-b9a9.webp)

![5'-Fluoro-[2,3'-biindolinylidene]-2',3-dione structure 5'-Fluoro-[2,3'-biindolinylidene]-2',3-dione structure](https://static.chemtradehub.com/structs/251/251903-00-1-9cb1.webp)

