Convection inside condensing and evaporating droplets of aqueous solution

Soft Matter ◽  
2018 ◽  
Vol 14 (21) ◽  
pp. 4335-4343 ◽  
Author(s):  
Tapan Kumar Pradhan ◽  
Pradipta Kumar Panigrahi
Keyword(s):  
Aqueous Solution ◽  
Natural Convection

Buoyancy driven natural convection inside an evaporating and a condensing droplet.

scholarly journals Investigation of the Use of an Inorganic Aqueous Solution in Aluminum-Made Phase-Change Heat Transfer Devices

2017 ◽  
Vol 139 (12) ◽  
Author(s):  
Qi Yao ◽  
Michael J. Stubblebine ◽  
Ivan Catton
Keyword(s):  
Heat Transfer ◽  
Aqueous Solution ◽  
Natural Convection ◽  
Phase Change ◽  
Aluminum Surface ◽  
Back Flow ◽  
Convection Cooling ◽  
Phase Change Heat Transfer ◽  
Aluminum Passivation ◽  
Inorganic Aqueous Solution

An inorganic aqueous solution, known as IAS, has shown its compatibility with aluminum phase-change heat transfer devices. When using IAS in aluminum devices, aluminum prefers to react with the two oxidizers, permanganate and chromate, rather than water to generate a thin and compact layer of aluminum oxide, which protects the aluminum surface and prevents further reactions. In addition, an electrochemical theory of aluminum passivation is introduced, and the existence of an electrochemical cycle is demonstrated by an aluminum thermosiphon test. The electrochemistry cycle, built up by liquid back flow and tube wall, allows the oxidizers to passivate the aluminum surface inside the device without being directly in contact with it. However, failure was detected while using IAS in thermosiphons with air natural convection cooling. The importance of a continuous liquid back flow to aluminum passivation in phase-change heat transfer devices is pointed out, and a vertical thermosiphon test with natural convection cooling is used to demonstrate that a discontinuous liquid back flow is the main reason of the failures.

scholarly journals Voltammetric demonstration of thermally induced natural convection in aqueous solution

2019 ◽  
Vol 21 (19) ◽  
pp. 9969-9974 ◽  
Author(s):  
Danlei Li ◽  
Christopher Batchelor-McAuley ◽  
Lifu Chen ◽  
Richard G. Compton
Keyword(s):  
Aqueous Solution ◽  
Natural Convection ◽  
Thermally Induced ◽  
Convective Flows ◽  
Electrochemical Systems

In electrochemical systems imperfect thermostating inevitably leads to the presence of bulk convective flows.

Structures Formed by Cryoprotective Agents Used in Freezc-Etching

1971 ◽  
Vol 29 ◽  
pp. 448-449
Author(s):  
G. G. Cocks ◽  
C. E. Cluthe
Keyword(s):  
Aqueous Solution ◽  
Polyethylene Oxide ◽  
Liquid Nitrogen Temperature ◽  
Ice Crystals ◽  
Etching Technique ◽  
Structural Constituent ◽  
Cryoprotective Agents ◽  
Quick Freezing ◽  
Freeze Etching ◽  
Fractured Surface

The freeze etching technique is potentially useful for examining dilute solutions or suspensions of macromolecular materials. Quick freezing of aqueous solutions in Freon or propane at or near liquid nitrogen temperature produces relatively large ice crystals and these crystals may damage the structures to be examined. Cryoprotective agents may reduce damage to the specimem, hut their use often results in the formation of a different set of specimem artifacts.In a study of the structure of polyethylene oxide gels glycerol and sucrose were used as cryoprotective agents. The experiments reported here show some of the structures which can appear when these cryoprotective agents are used.Figure 1 shows a fractured surface of a frozen 25% aqueous solution of sucrose. The branches of dendritic ice crystals surrounded hy ice-sucrose eutectic can be seen. When this fractured surface is etched the ice in the dendrites sublimes giving the type of structure shown in Figure 2. The ice-sucrose eutectic etches much more slowly. It is the smooth continuous structural constituent surrounding the branches of the dendrites.

Preparation and characterisation of vanadium pentoxide supported rhodium catalyst

1988 ◽  
Vol 46 ◽  
pp. 946-947
Author(s):  
A. Legrouri
Keyword(s):  
Aqueous Solution ◽  
Thermal Decomposition ◽  
Physicochemical Properties ◽  
Surface Area ◽  
Vanadium Pentoxide ◽  
High Purity ◽  
Gas Adsorption ◽  
Rhodium Catalyst ◽  
Optical Methods ◽  
Reducible Oxides

The industrial importance of metal catalysts supported on reducible oxides has stimulated considerable interest during the last few years. This presentation reports on the study of the physicochemical properties of metallic rhodium supported on vanadium pentoxide (Rh/V2O5). Electron optical methods, in conjunction with other techniques, were used to characterise the catalyst before its use in the hydrogenolysis of butane; a reaction for which Rh metal is known to be among the most active catalysts.V2O5 powder was prepared by thermal decomposition of high purity ammonium metavanadate in air at 400 °C for 2 hours. Previous studies of the microstructure of this compound, by HREM, SEM and gas adsorption, showed it to be non— porous with a very low surface area of 6m2/g3. The metal loading of the catalyst used was lwt%Rh on V2Q5. It was prepared by wet impregnating the support with an aqueous solution of RhCI3.3H2O.

TEM observation of iron oxide pillars in montmorillonite

1990 ◽  
Vol 48 (4) ◽  
pp. 882-883
Author(s):  
H. Mori ◽  
Y. Murata ◽  
H. Yoneyama ◽  
H. Fujita
Keyword(s):  
Aqueous Solution ◽  
Iron Oxide ◽  
Fine Particles ◽  
Aqueous Suspension ◽  
Volume Ratio ◽  
Exchange Capacity ◽  
Nano Composites ◽  
Pillared Montmorillonite ◽  
Topographic Features ◽  
Transmission Electron

Recently, a new sort of nano-composites has been prepared by incorporating such fine particles as metal oxide microcrystallites and organic polymers into the interlayer space of montmorillonite. Owing to their extremely large specific surface area, the nano-composites are finding wide application[1∼3]. However, the topographic features of the microstructures have not been elucidated as yet In the present work, the microstructures of iron oxide-pillared montmorillonite have been investigated by high-resolution transmission electron microscopy.Iron oxide-pillared montmorillonite was prepared through the procedure essentially the same as that reported by Yamanaka et al. Firstly, 0.125 M aqueous solution of trinuclear acetato-hydroxo iron(III) nitrate, [Fe3(OCOCH3)7 OH.2H2O]NO3, was prepared and then the solution was mixed with an aqueous suspension of 1 wt% clay by continuously stirring at 308 K. The final volume ratio of the latter aqueous solution to the former was 0.4. The clay used was sodium montmorillonite (Kunimine Industrial Co.), having a cation exchange capacity of 100 mequiv/100g. The montmorillonite in the mixed suspension was then centrifuged, followed by washing with deionized water. The washed samples were spread on glass plates, air dried, and then annealed at 673 K for 72 ks in air. The resultant film products were approximately 20 μm in thickness and brown in color.

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