跳到主要內容

臺灣博碩士論文加值系統

(44.212.96.86) 您好!臺灣時間:2023/12/10 06:09
字體大小: 字級放大   字級縮小   預設字形  
回查詢結果 :::

詳目顯示

: 
twitterline
研究生:王承洋
研究生(外文):Cheng-Yang Wang
論文名稱:二甲基甲醯胺之特殊潤濕行為: 擴散、收縮、移動
論文名稱(外文):Peculiar wetting behavior of N,N-dimethylformamide: expansion, contraction, and running
指導教授:曹恆光
指導教授(外文):Heng-Kwong Tsao
學位類別:碩士
校院名稱:國立中央大學
系所名稱:化學工程與材料工程學系
學門:工程學門
學類:化學工程學類
論文種類:學術論文
論文出版年:2019
畢業學年度:107
語文別:英文
論文頁數:41
中文關鍵詞:二甲基甲醯胺潤濕現象接觸角親水性自體移動
外文關鍵詞:NN-dimethylformamidewetting behaviorcontact anglehydrophilicself-propulsion
相關次數:
  • 被引用被引用:0
  • 點閱點閱:98
  • 評分評分:
  • 下載下載:6
  • 收藏至我的研究室書目清單書目收藏:0
二甲基甲醯胺為非揮發性溶液,其液滴在某些表面可表現非典型潤濕行
為,如: poly(methyl methacrylate)、經燃燒處理過的黃銅和藍寶石基材。類
似於水液滴擴散於完全潤濕性質基材,二甲基甲醯胺液滴展現一自發性擴
散,其擴散係數大於Tanner’s law。 液滴在擴散時,液滴的外圍厚度高於其
中心。與典型擴散不同,液滴在擴張到一定程度後會停止並開始向內收縮。
最終,液滴在五分鐘內會縮成球帽形狀並有著相當低的接觸角角度。有趣的
是,若在二甲基甲醯胺中添加界面活性劑,液滴會在擴張並收縮後表現一自
發性移動。其移動軌跡為隨機路線,擴散係數為0.005~0.01 mm2/s。有別於
大多數自發移動為反應性移動,二甲基甲醯胺液滴可重複跨越其經過的軌
跡。這種自發性移動可以被歸功於無接觸角遲滯的基材和Marangoni stress。
基於這些結果,我們提出了一種有關液滴的擴散、收縮和移動機制。
The nonvolatile N,N-dimethylformamide (DMF) droplet can display peculiar
wetting behavior on some substrates such as poly(methyl methacrylate), flametreated
brass, and sapphire. Similar to the expansion of a water drop on a total
wetting surface, the DMF droplet shows a spontaneous spreading initially but its
spreading dynamics is beyond Tanner’s law. The spreading droplet exhibits a
ridge near the rim whose height is greater than that of the center. Contrary to
typical spreading, the DMF droplet stops its outward expansion at some point and
begins inward contraction. Eventually, the droplet shrinks to a spherical cap with
a low contact angle within 5 min. It is interesting to find that upon addition of
surface-active agents, the droplet performs the self-propelled motion after
spreading-contraction. The trajectory is random and can be described as the
diffusive motion with the diffusivity ~0.005- ~0.01 mm2/s. Unlike self-propulsion
driven by reactive wetting, the DMF droplet can cross the trail left by itself. This
self-propulsion can be attributed to the effects of the hysteresis-free surface and
Marangoni stress. Based on those results, a mechanism explaining the contraction
and self-propelled droplet motion is proposed.
摘要 .................................................................................................................... i
ABSTRACT ....................................................................................................... ii
誌謝 ................................................................................................................... iii
LIST OF CONTENTS ...................................................................................... iv
LIST OF FIGURES ........................................................................................... v
CHAPTER 1 INTRODUCTION ....................................................................... 1
CHAPTER 2 EXPERIMENT ............................................................................ 4
2-1 Materials ................................................................................................... 4
2-2 Fabrication of Flamed Brass ..................................................................... 4
2-3 Observation of Shape Dynamics and Droplet Motion ............................. 4
2-4 Wettability Characterization ..................................................................... 5
2-5 Relative Humidity Control ....................................................................... 5
CHAPTER 3 RESULT AND DICUSSION ....................................................... 6
3-1 Expansion and contraction of DMF on various surfaces ......................... 6
3-2 Effect of additives and self-running droplets ......................................... 12
3-3 Humidity and Mechanism....................................................................... 18
CHAPTER 4 CONCLUSION ......................................................................... 23
CHAPTER 5 SUPPORTING INFORMATION .............................................. 25
CHPATER 6 REFERENCE ............................................................................. 27
[1] Sharma, J.; Mahima, S; Kakade, B. A.; Pasricha, R.; Mandale, A. B.;
Vijayamohanan, K. Solvent-Assisted One-Pot Synthesis and Self-Assembly of
4-Aminothiophenol-Capped Gold Nanoparticles. J. Phys. Chem. B 2004, 108,
13280–13286.
[2] Osakada, K.; Taniguchi, A.; Kubota, E.; Dev, S.; Tanaka, K.; Kubota, K.;
Yamamoto, T. New Organosols of Copper(II) Sulfide, Cadmium Sulfide, Zinc
Sulfide, Mercury(II) Sulfide, Nickel(II) Sulfide and Mixed Metal Sulfides in
N,N-Dimethylformamide and Dimethyl Sulfoxide. Preparation,
characterization, and physical properties. Chem. Mater. 1992, 4, 562–570.
[3] Durmaz, H.; Dag, A.; Altintas, O.; Erdogan, T.; Hizal, G.; Tunca, U. One-Pot
Synthesis of ABC Type Triblock Copolymers via in situ Click [3+2] and
Diels−Alder [4+2] Reactions. Macromolecules 2007, 40, 191–198.
[4] Goals, P. L.; Tsarevsky, N. V.; Sumerlin, B. S.; Matyjaszewski, K. Catalyst
Performance in “Click” Coupling Reactions of Polymers Prepared by ATRP:
Ligand and Metal Effects. Macromolecules 2006, 39, 6451–6457.
[5] Hsu, C.-M.; Shivkumar, S. N,N-Dimethylformamide Additions to the Solution
for the Electrospinning of Poly(e-caprolactone) Nanofibers. Mater. Eng. 2004,
289, 334–340.
[6] Lei, D.; Ying, X.; Zou, Z. Electrospinning of Polycaprolatone Nanofibers with
DMF Additive: The Effect of Solution Proprieties on Jet Perturbation and Fiber
Morphologies. Fiber Polym 2016, 17, 751–759.
[7] Yamamoto, H.; Yano, H.; Kouchi, H.; Obora, Y.; Arakawa, R.; Kawasaki, H.
N,N-Dimethylformamide-Stabilized Gold Nanoclusters as a Catalyst for the
Reduction of 4-nitrophenol. Nanoscale 2012, 4, 4148–4154.
28
[8] Tyagi, R.; Kaur, N.; Singh, B.; Kishore, D. Noteworthy Mechanistic
Precedence in the Exclusive Formation of One Regioisomer in the Beckmann
Rearrangement of Ketoximes of 4-Piperidones Annulated to Pyrazoloindole
Nucleus by Organocatalyst Derived from TCT and DMF. Synth. Commun.
2013, 43, 16–25.
[9] Semsarzadeh, M. A.; Amiri, S.; Azadeh, M. Controlled Radical Polymerization
of Vinyl Acetate in Presence of Mesoporous Silica Supported TiCl4
Heterogeneous Catalyst. Bull. Mater. Sci. 2012, 35, 867–874.
[10] Mohammad, B. T.; Ahmad, T. N,N-Dimethylformamide-Promoted Reaction
of Isocyanides and Barbituric Acids: an Easy Synthesis of 5-[(Alkyl or
Arylamino) Methylene]Barbituric Acids. J. Chem. Res. 2010, 34, 140–144.
[11] Kumar, R.; Wadhwa, D.; Prakash, O. Beckmann Rearrangement of 2-
Hydroxy-5-Methylacetophenone Oxime using Vilsmeier-Haack Reagent
(POCI3/ DMF): Synthesis of Some New Heterocycles. Heterocycl. Commun.
2010, 16, 201–205.
[12] Majid, M. H.; Mahdieh, G.; Leyla, M. Beyond a Solvent: Triple Roles of
Dimethylformamide in Organic Chemistry. RSC Adv. 2018, 8, 27832–27862.
[13] Liu, Y.; He, G.; Chen, K.; Jin, Y.; Li, Y.; Zhu, H. DMF-Catalyzed Direct and
Regioselective C–H Functionalization: Electrophilic/Nucleophilic 4-
Halogenation of 3-Oxypyrazoles. Eur. J. Org. Chem. 2011, 2011, 5323–5330.
[14] Rai, A.; Rai, V. K.; Singh, A. K.; Yadav, L. D. S. [2 + 2] Annulation of
Aldimines with Sulfonic Acids: A Novel One-Pot cis-Selective Route to β-
Sultams. Eur. J. Org. Chem. 2011, 2011, 4302–4306.
[15] Kawasaki, H.; Yamamoto, H.; Fujimori, H.; Arakawa, R.; Inada, M.; Iwasaki,
S. Surfactant-Free Solution Synthesis of Fluorescent Platinum
Subnanoclusters. Chem. Commun. 2010, 46, 3759–3761.
[16] Hyotanishi, M.; Isomura, Y.; Yamamoto, H.; Kawasaki, H.; Obora, Y.
Surfactant-Free Synthesis of Palladium Nanoclusters for Their Use in Catalytic
Cross-Coupling Reaction. Chem. Commun. 2011, 47, 5750–5752.
29
[17] Isomura, Y.; Narushima, T.; Kawasaki, H.; Yonezawa, T.; Obora, Y.
Surfactant-Free Single-Nano-Sized Colloidal Cu Nanoparticles for Use as An
Active Catalyst in Ullmann-Coupling Reaction. Chem. Commun. 2012, 48,
3784–3786.
[18] Gascoyne, P. R. C.; Vykoukal, J. V.; Schwartz, A. A.; Anderson, T. J;
Vykoukal, D. M.; Wayne K.; McConaghy, C. C.; Becker, F. F.; Andrews, C.
Dielectrophoresis-Based Programmable Fluidic Processors. Lab Chip 2004, 4,
299-309.
[19] Lee, M.-Y.; Srinivasan, A.; Ku, B.; Dordick, J. S. Multienzyme Catalysis in
Microfluidic Biochips. Biotechnol Bioeng. 2003, 83, 20-8.
[20] Wu, C.-J.; Huang, C.-J.; Jiang, S.; Sheng, Y.-J.; Tsao, H.-K.
Superhydrophilicity and Spontaneous Spreading on Zwitterionic Surfaces:
Carboxybetaine and Sulfobetaine. RSC Adv. 2016, 6, 24827-24834.
[21] Singh, V.; Huang, C.-J.; Sheng, Y.-J.; Tsao, H.-K. Smart Zwitterionic
Sulfobetaine Silane Surfaces with Switchable Wettability for
Aqueous/Nonaqueous Drops. J. Mater. Chem. A 2018, 6, 2279–2288
[22] Tanner, L. H. The Spreading of Silicone Oil Drops on Horizontal Surfaces. J.
Phys. D: Appl. Phys. 1979, 12, 1473–1484.
[23] Singh, V.; Wu, C.-J.; Sheng, Y.-J.; Tsao, H.-K. Self-Propulsion and Shape
Restoration of Aqueous Drops on Sulfobetaine Silane Surfaces. Langmur 2017,
33, 6182-6191.
[24] Li, S.; Liu, J.; Hou, J.; Zhang, G. Meniscus-Induced Motion of Oil Droplets.
Coll. Surf. A: Physicochem. Eng. Aspects 2016, 469, 252-255.
[25] Izri, Z.; van der Linden, M. N.; Michelin, S.; Dauchot, O. Self-Propulsion of
Pure Water Droplets by Spontaneous Marangoni-Stress-Driven Motion. Phys.
Rev. Lett. 2014, 113, 248302.
[26] Schmitt M.; Stark, H. Marangoni Flow at Droplet Interfaces: Three-
Dimensional Solution and Applications. Phys. Fluids 2016, 28, 012106.
30
[27] Myers D. Surfaces, Interfaces, and Colloids: Principles and Applications;
Wiley-VCH: New York, 1999; pp 415-420.
[28] Cira, N. J.; Benusiglio, A.; Prakash, M. Vapour-Mediated Sensing and
Motility in Two-Component Droplets. Nature 2015, 519, 446-450.
[29] Malvadkar, N. A.; Hancock, M. J.; Sekeroglu, K.; Dressick, W. J.; Demirel,
M. C. An Engineered Anisotropic Nanofilm with Unidirectional Wetting
Properties. Nat. Mater. 2010, 9, 1023−1028.
[30] Varagnolo, S.; Schiocchet, V.; Ferraro, D.; Pierno, M.; Mistura, G.; Sbragaglia,
M.; Gupta, A.; Amati, G. Tuning Drop Motion by Chemical Patterning of
Surfaces. Langmuir 2014, 30, 2401−2409.
[31] Yao, X.; Bai, H.; Ju, J.; Zhou, D.; Li, J.; Zhang, H.; Yang, B.; Jiang, L.
Running Droplet of Interfacial Chemical Reaction Flow. Soft Matter 2012, 8,
5988-5991.
[32] Wei, H.-H. Marangoni-Enhanced Capillary Wetting in Surfactant-Driven
Superspreading. J. Fluid Mech. 2018, 855, 181-2.
[33] Theodorakis, P. A.; Muller, E. A.; Craster, R. V.; Matar, O. K. Superspreading:
Mechanism and Molecular Design. Langmuir 2015, 31, 2304-2309.
[34] Rafai, S.; Sarker, D.; Bergeron, V.; Meunier, J.; Bonn, D. Superspreading:
Aqueous surfactant Drops Spreading on Hydrophobic Surfaces. Langmuir
2002, 18, 10486-10488.
[35] Dominguez, H.; Pizio, O. On the Composition Dependence of the
Microscopic Structure, Thermodynamic, Dynamic and Dielectric Properties of
Water-Dimethyl formamide Model Mixtures. Molecular dynamics simulation
results, J. Phys. Condens. Matter. 2017, 20, 43602:1-15.
[36] Weng, Y.-H.; Wu, C.-J.; Tsao, H.-K.; Sheng, Y.-J. Spreading Dynamics of a
Precursor Film of Nanodrops on Total Wetting Surfaces. Phys. CHem. Chem.
Phys. 2017, 19, 27786.
連結至畢業學校之論文網頁點我開啟連結
註: 此連結為研究生畢業學校所提供,不一定有電子全文可供下載,若連結有誤,請點選上方之〝勘誤回報〞功能,我們會盡快修正,謝謝!
QRCODE
 
 
 
 
 
                                                                                                                                                                                                                                                                                                                                                                                                               
第一頁 上一頁 下一頁 最後一頁 top
無相關期刊