| 1. |
- Aromaa, Mikko, et al.
(författare)
-
Atmospheric synthesis of superhydrophobic TiO2 nanoparticle deposits in a single step using Liquid Flame Spray
- 2012
-
Ingår i: Journal of Aerosol Science. - : Elsevier BV. - 0021-8502. ; 52, s. 57-68
-
Tidskriftsartikel (refereegranskat)abstract
- Titanium dioxide nanoparticles are synthesised in aerosol phase using the Liquid Flame Spray method. The particles are deposited in-situ on paperboard, glass and metal surfaces. According to literature, titanium dioxide is supposed to be hydrophilic. However, hydrophobic behaviour is observed on paperboard substrates but not on metal or glass substrates. Here, the water contact angle behaviour of the deposits is studied along with XRD, XPS, BET and HR-TEM. The deposits are compared with silicon dioxide deposits having, as expected, hydrophilic properties synthesised with the same method. It seems probable that the deposition process combusts some substrate material from the paperboard substrate, which later on condenses on top of the deposit to form a carbonaceous layer causing the hydrophobic behaviour of the TiO2 deposit. The similar layer does not form when depositing the nanoparticles on a metal or glass surfaces. The observations are more than purely aerosol phenomena. However, they are quite essential in nanoparticle deposition from the aerosol phase onto a substrate which is commonly utilised. (C) 2012 Elsevier Ltd. All rights reserved.
|
|
| 2. |
- Eriksson, Mimmi, et al.
(författare)
-
Direct Observation of Gas Meniscus Formation on a Superhydrophobic Surface
- 2019
-
Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 13:2, s. 2246-2252
-
Tidskriftsartikel (refereegranskat)abstract
- The formation of a bridging gas meniscus via cavitation or nanobubbles is considered the most likely origin of the submicrometer long-range attractive forces measured between hydrophobic surfaces in aqueous solution. However, the dynamics of the formation and evolution of the gas meniscus is still under debate, in particular, in the presence of a thin air layer on a superhydrophobic surface. On superhydrophobic surfaces the range can even exceed 10 μm. Here, we report microscopic images of the formation and growth of a gas meniscus during force measurements between a superhydrophobic surface and a hydrophobic microsphere immersed in water. This is achieved by combining laser scanning confocal microscopy and colloidal probe atomic force microscopy. The configuration allows determination of the volume and shape of the meniscus, together with direct calculation of the Young-Laplace capillary pressure. The long-range attractive interactions acting on separation are due to meniscus formation and volume growth as air is transported from the surface layer.
|
|
| 3. |
- Eriksson, Mimmi, et al.
(författare)
-
Effects of Gas Layer Thickness on Capillary Interactions at Superhydrophobic Surfaces
- 2024
-
Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 40:9, s. 4801-4810
-
Tidskriftsartikel (refereegranskat)abstract
- Strongly attractive forces act between superhydrophobic surfaces across water due to the formation of a bridging gas capillary. Upon separation, the attraction can range up to tens of micrometers as the gas capillary grows, while gas molecules accumulate in the capillary. We argue that most of these molecules come from the pre-existing gaseous layer found at and within the superhydrophobic coating. In this study, we investigate how the capillary size and the resulting capillary forces are affected by the thickness of the gaseous layer. To this end, we prepared superhydrophobic coatings with different thicknesses by utilizing different numbers of coating cycles of a liquid flame spraying technique. Laser scanning confocal microscopy confirmed an increase in gas layer thickness with an increasing number of coating cycles. Force measurements between such coatings and a hydrophobic colloidal probe revealed attractive forces caused by bridging gas capillaries, and both the capillary size and the range of attraction increased with increasing thickness of the pre-existing gas layer. Hence, our data suggest that the amount of available gas at and in the superhydrophobic coating determines the force range and capillary growth.
|
|
| 4. |
- Eriksson, Mimmi, et al.
(författare)
-
Effects of liquid surface tension on gas capillaries and capillary forces at superamphiphobic surfaces
- 2023
-
Ingår i: Scientific Reports. - : Springer Nature. - 2045-2322. ; 13:1
-
Tidskriftsartikel (refereegranskat)abstract
- The formation of a bridging gas capillary between superhydrophobic surfaces in water gives rise to strongly attractive interactions ranging up to several micrometers on separation. However, most liquids used in materials research are oil-based or contain surfactants. Superamphiphobic surfaces repel both water and low-surface-tension liquids. To control the interactions between a superamphiphobic surface and a particle, it needs to be resolved whether and how gas capillaries form in non-polar and low-surface-tension liquids. Such insight will aid advanced functional materials development. Here, we combine laser scanning confocal imaging and colloidal probe atomic force microscopy to elucidate the interaction between a superamphiphobic surface and a hydrophobic microparticle in three liquids with different surface tensions: water (73 mN m−1), ethylene glycol (48 mN m−1) and hexadecane (27 mN m−1). We show that bridging gas capillaries are formed in all three liquids. Force-distance curves between the superamphiphobic surface and the particle reveal strong attractive interactions, where the range and magnitude decrease with liquid surface tension. Comparison of free energy calculations based on the capillary menisci shapes and the force measurements suggest that under our dynamic measurements the gas pressure in the capillary is slightly below ambient.
|
|
| 5. |
|
|
| 6. |
|
|
| 7. |
|
|
| 8. |
- Haapanen, Janne, et al.
(författare)
-
Binary TiO2/SiO2 nanoparticle coating for controlling the wetting properties of paperboard
- 2015
-
Ingår i: Materials Chemistry and Physics. - : Elsevier BV. - 0254-0584 .- 1879-3312. ; 149, s. 230-237
-
Tidskriftsartikel (refereegranskat)abstract
- We introduce a flame based aerosol method to fabricate thin films consisting of binary TiO2/SiO2 nanoparticles deposited directly from the flame onto the paperboard. Nanocoatings were prepared with Liquid Flame Spray (LFS) in a roll-to-roll process with the line speed of 50 m/min. Surface wetting behavior of nanocoated paperboard was studied for different Ti/Si ratios in the precursor, affecting TiO2/SiO2 ratio in the coating. Wettability could be adjusted to practically any water contact angle between 10 and 160° by setting the Ti/Si ratio in the liquid precursor. Structure of the two component nanocoating was analysed with FE-SEM, TEM, EDS, XPS and XRD. The porous thin film coating was concluded to consist of ca. 10 nm sized mixed oxide nanoparticles with segregated TiO2 and SiO2 phases. Accumulation of carbonaceous compounds on the surface was seen to be almost linearly dependent on the Ti/Si ratio, indicating of each species being exposed in corresponding amount. However, wetting of the surface was observed to follow merely an S-shaped curve, caused by the roughness of the nanocoated surface. Reasons for the observed superhydrophobicity and superhydrophilicity of these binary nanocoatings on paperboard are discussed.
|
|
| 9. |
- Haapanen, Janne, et al.
(författare)
-
On the limit of superhydrophobicity : Defining the minimum amount of TiO2 nanoparticle coating
- 2019
-
Ingår i: Materials Research Express. - : IOP Publishing. - 2053-1591. ; 6:3
-
Tidskriftsartikel (refereegranskat)abstract
- Fabrication of superhydrophobic surfaces in large scale has been in high interest for several years, also titanium oxide nanostructures having been applied for the purpose. Optimizing the amount and structure of the TiO2 material in the coating will play a key role when considering upscaling. Here, we take a look at fabricating the superhydrophobic surface in a one-step roll-to-roll pilot scale process by depositing TiO2 nanoparticles from a Liquid Flame Spray onto a moving paperboard substrate. In order to find the minimum amount of nanomaterial still sufficient for creating superhydrophobicity, we varied nanoparticle production rate, flame distance from the substrate and line speed. Since the deposited amount of material sideways from the flame path was seen to decrease gradually, spatial analysis enabled us to consistently determine the minimum amount of TiO2 nanoparticles on the substrate needed to achieve superhydrophobicity. Amount as low as 20-30 mg m-2 of TiO2 nanoparticles was observed to be sufficient. The scanning electron microscopy revealed that at this amount, the surface was covered with nanoparticles only partially, but still sufficiently to create a hierarchical structure to affect wetting significantly. Based on XPS analysis, it became apparent that TiO2 gathers hydrocarbons on the surface to develop the surface chemistry towards hydrophobic, but below the critical amount of TiO2 nanoparticles, the chemistry could not enable superhydrophobicity anymore. While varying the deposited amount of TiO2, besides the local spatial variance of the coating amount, also the overall yield was studied. Within the text matrix, a yield up to 44% was achieved. In conclusion, superhydrophobicity was achieved at all tested line speeds (50 to 300 m min-1), even if the amount of TiO2 varied significantly (20 to 230 mg m-2).
|
|
| 10. |
- Harra, Juha, et al.
(författare)
-
Characteristics of nFOG, an aerosol-based wet thin film coating technique
- 2018
-
Ingår i: JCT Research. - : Springer Science and Business Media LLC. - 1547-0091 .- 2168-8028 .- 1935-3804. ; 15:3, s. 623-632
-
Tidskriftsartikel (refereegranskat)abstract
- An atmospheric pressure aerosol-based wet thin film coating technique called the nFOG is characterized and applied in polymer film coatings. In the nFOG, a fog of droplets is formed by two air-assist atomizers oriented toward each other inside a deposition chamber. The droplets settle gravitationally and deposit on a substrate, forming a wet film. In this study, the continuous deposition mode of the nFOG is explored. We determined the size distribution of water droplets inside the chamber in a wide side range of 0.1–100 µm and on the substrate using aerosol measurement instruments and optical microscopy, respectively. The droplet size distribution was found to be bimodal with droplets of approximately 30–50 µm contributing the most to the mass of the formed wet film. The complementary measurement methods allow us to estimate the role of different droplet deposition mechanisms. The obtained results suggest that the deposition velocity of the droplets is lower than the calculated terminal settling velocity, likely due to the flow fields inside the chamber. Furthermore, the mass flux of the droplets onto the substrate is determined to be in the order of 1 g/m3s, corresponding to a wet film growth rate of 1 µm/s. Finally, the nFOG technique is demonstrated by preparing polymer films with thicknesses in the range of approximately 0.1–20 µm.
|
|
