scholarly journals Interaction of Surface Energy Components between Solid and Liquid on Wettability, and Its Application to Textile Anti-Wetting Finish

Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 498 ◽  
Author(s):  
Kwanwoo Song ◽  
Jinwook Lee ◽  
Seong-O Choi ◽  
Jooyoun Kim
Keyword(s):  
Surface Roughness ◽  
Surface Energy ◽  
Experimental Validation ◽  
Polar Component ◽  
Basic Information ◽  
Surface Energies ◽  
Energy Profiles ◽  
Silane Coating ◽  
Energy Components

With various options of anti-wetting finish methods, this study intends to provide basic information that can be applied in selecting a relevant anti-wetting chemical to grant protection from spreading of liquids with different surface energy profiles. With such an aim, the anti-wetting effectiveness of fluorinated coating and silane coating was investigated for liquids having different surface energy components, water (WA), methylene iodide (MI) and formamide (FA). The wetting thermodynamics was experimentally investigated by analyzing dispersive and polar component surface energies of solids and liquids. The role of surface roughness in wettability was examined for fibrous nonwoven substrates that have varied surface roughness. The presence of roughness enhanced the anti-wetting performance of the anti-wetting treated surfaces. While the effectiveness of different anti-wetting treatments was varied depending on the liquid polarities, the distinction of different treatments was less apparent for the roughened fibrous surfaces than the film surfaces. This study provides experimental validation of wetting thermodynamics and the practical interpretation of anti-wetting finishing.

A look into the interaction of metal oxide thin films with biological media: Albumin and Fibrinogen adsorption

2012 ◽  
Vol 1376 ◽  
Author(s):  
P. Silva-Bermudez ◽  
S. Muhl ◽  
M. Rivera ◽  
S. E. Rodil
Keyword(s):  
Surface Roughness ◽  
Surface Energy ◽  
Protein Adsorption ◽  
Photoelectron Spectroscopy ◽  
Ex Situ ◽  
Polar Component ◽  
Metal Oxide Thin Films ◽  
Adsorbed Protein ◽  
Major Chemical ◽  
Fibrinogen Adsorption

ABSTRACTIn the present work, the adsorption of albumin and fibrinogen on Ta, Nb, Ti and Zr oxidesthin films deposited on Si (100) wafers by magnetron sputtering was studied in order to get a better understanding of the correlation among the surface properties of these oxides and the protein adsorption phenomena on their surfaces. The surface energy, hydrophobicity, chemical composition, roughness and atomic order of the films were characterized. The films were immersedfor 45 minutes in single protein solutions; either albumin or fibrinogenand the adsorbed protein layer on the films was studied ex-situ in a dry ambient using bothX-ray photoelectron spectroscopy and atomic force microscopy.The adsorption of albumin and fibrinogen on the films modified the surface morphology and decreased the surface roughness for all the four different metal oxides. The XPS results confirmed the presence of the protein on the surface of the films and showed that the two proteins studied were adsorbed without undergoing a major chemical decomposition. A correlation between the surface roughness,the polar component of the surface energy of the films and the atomic percentage of nitrogen on the films after protein adsorption, an indirect signal of the amount of protein adsorbed, was found for albumin and fibrinogen adsorption on Ta, Nb and Ti oxides; the largest the roughness or the polar component the largest amount of adsorbed protein.

scholarly journals Thermodynamics of manganese oxides: Sodium, potassium, and calcium birnessite and cryptomelane

2017 ◽  
Vol 114 (7) ◽  
pp. E1046-E1053 ◽  
Author(s):  
Nancy Birkner ◽  
Alexandra Navrotsky
Keyword(s):  
Surface Energy ◽  
Surface Area ◽  
Oxidation State ◽  
Manganese Oxides ◽  
Lower Surface ◽  
Surface Energies ◽  
Surface Areas ◽  
Bulk Thermodynamics ◽  
Lower Surface Energy

Manganese oxides with layer and tunnel structures occur widely in nature and inspire technological applications. Having variable compositions, these structures often are found as small particles (nanophases). This study explores, using experimental thermochemistry, the role of composition, oxidation state, structure, and surface energy in the their thermodynamic stability. The measured surface energies of cryptomelane, sodium birnessite, potassium birnessite and calcium birnessite are all significantly lower than those of binary manganese oxides (Mn3O4, Mn2O3, and MnO2), consistent with added stabilization of the layer and tunnel structures at the nanoscale. Surface energies generally decrease with decreasing average manganese oxidation state. A stabilizing enthalpy contribution arises from increasing counter-cation content. The formation of cryptomelane from birnessite in contact with aqueous solution is favored by the removal of ions from the layered phase. At large surface area, surface-energy differences make cryptomelane formation thermodynamically less favorable than birnessite formation. In contrast, at small to moderate surface areas, bulk thermodynamics and the energetics of the aqueous phase drive cryptomelane formation from birnessite, perhaps aided by oxidation-state differences. Transformation among birnessite phases of increasing surface area favors compositions with lower surface energy. These quantitative thermodynamic findings explain and support qualitative observations of phase-transformation patterns gathered from natural and synthetic manganese oxides.

Surface Energies Acting at the Interfaces of Ceramics and Glasses while in Contact with Organic and Biological Liquids

2005 ◽  
Vol 284-286 ◽  
pp. 1023-1026 ◽  
Author(s):  
Simeon Agathopoulos ◽  
M. Nedea ◽  
Brandusa Ghiban ◽  
José Maria F. Ferreira ◽  
P. Nikolopoulos
Keyword(s):  
Surface Energy ◽  
Experimental Results ◽  
Dispersion Forces ◽  
Interfacial Interactions ◽  
Polar Liquids ◽  
Surface Energies ◽  
Solid Substrates ◽  
Biological Liquids ◽  
Solid Liquid ◽  
Energy Components

The surface energy components which govern the interfacial interactions between bioinert solid substrates of partial stabilized ZrO2 (with 3 mol% Y2O3) and a glass with a composition of 55SiO2×10Na2O×35MgO in contact with organic and biological liquids under equilibrium regime, were determined. The experimental results indicated that the interfacial bonding between zirconia and the polar liquids is result of interactions due to dispersion forces. In the case of the glass, polar forces significantly contribute to solid/liquid interfacial interactions.

Role of the Shuttleworth effect in adhesion on elastic surfaces

MRS Advances ◽  
2016 ◽  
Vol 1 (10) ◽  
pp. 621-630
Author(s):  
Shayandev Sinha ◽  
Siddhartha Das
Keyword(s):  
Surface Energy ◽  
Surface Stress ◽  
Soft Lithography ◽  
Particle Surface ◽  
Elastic Solid ◽  
Adhesion Energy ◽  
Surface Energies ◽  
The Difference ◽  
The Impact

AbstractThe Shuttleworth effect ensures that at an interface, where one of the phases is an elastic solid, surface stress is not equal to the surface energy. In this paper, we provide a free energy based approach to quantify the impact of the Shuttleworth effect in the adhesion of a rigid, spherical particle on an elastic solid. Our paper has four key findings. Firstly, we demonstrate that the difference in the elastic-solid-particle surface stress and surface energies is linearly proportional to the adhesion energy. Secondly, we establish that the surface stresses being larger than the surface energies provide the sufficient condition for an energetically favorable adhesion. Thirdly, we show that for a given adhesion energy and solid-vapor surface energy increase in particle-vapor surface energy makes the adhesion, in presence of the Shuttleworth effect, more favorable. Finally, and most importantly, we identify the necessary parameter space corresponding to which the Shuttleworth effect may or may not enhance the adhesion as compared to the case that does not account for the Shuttleworth effect. We anticipate that our findings will significantly impact our understanding of a plethora of problems involving adhesion and indentation on soft surfaces, such as nanoparticle adhesion on cells, nanoindentation based characterization of soft solids, applications of adhesion-based soft lithography techniques, etc.

A new method for quantifying the blocking of coated paperboard

TAPPI Journal ◽  
2010 ◽  
Vol 9 (5) ◽  
pp. 29-35 ◽  
Author(s):  
PAULINE SKILLINGTON ◽  
YOLANDE R. SCHOEMAN ◽  
VALESKA CLOETE ◽  
PATRICE C. HARTMANN
Keyword(s):  
Surface Roughness ◽  
Fatty Acid ◽  
Surface Energy ◽  
Film Thickness ◽  
External Factors ◽  
Additive Concentration ◽  
Pressure Surface ◽  
Fatty Acid Amides ◽  
Coated Surfaces ◽  
Definite Period

Blocking is undesired adhesion between two surfaces when subjected to pressure and temperature constraints. Blocking between two coated paperboards in contact with each other may be caused by inter-diffusion, adsorption, or electrostatic forces occurring between the respective coating surfaces. These interactions are influenced by factors such as the temperature, pressure, surface roughness, and surface energy. Blocking potentially can be reduced by adjusting these factors, or by using antiblocking additives such as talc, amorphous silica, fatty acid amides, or polymeric waxes. We developed a method of quantifying blocking using a rheometer. Coated surfaces were put in contact with each other with controlled pressure and temperature for a definite period. We then measured the work necessary to pull the two surfaces apart. This was a reproducible way to accurately quantify blocking. The method was applied to determine the effect external factors have on the blocking tendency of coated paperboards, i.e., antiblocking additive concentration, film thickness, temperature, and humidity.

scholarly journals Dynamics of Monolayer Growth in Vapor–Liquid–Solid GaAs Nanowires Based on Surface Energy Minimization

Nanomaterials ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1681
Author(s):  
Hadi Hijazi ◽  
Vladimir G. Dubrovskii
Keyword(s):  
Surface Energy ◽  
Continuous Process ◽  
Vapor Liquid Solid ◽  
Gaas Nanowires ◽  
Monolayer Growth ◽  
Surface Energetics ◽  
Monolayer Expansion ◽  
Vapor Liquid Solid Growth ◽  
Vapor Liquid

The vapor–liquid–solid growth of III-V nanowires proceeds via the mononuclear regime, where only one island nucleates in each nanowire monolayer. The expansion of the monolayer is governed by the surface energetics depending on the monolayer size. Here, we study theoretically the role of surface energy in determining the monolayer morphology at a given coverage. The optimal monolayer configuration is obtained by minimizing the surface energy at different coverages for a set of energetic constants relevant for GaAs nanowires. In contrast to what has been assumed so far in the growth modeling of III-V nanowires, we find that the monolayer expansion may not be a continuous process. Rather, some portions of the already formed monolayer may dissolve on one of its sides, with simultaneous growth proceeding on the other side. These results are important for fundamental understanding of vapor–liquid–solid growth at the atomic level and have potential impacts on the statistics within the nanowire ensembles, crystal phase, and doping properties of III-V nanowires.

scholarly journals Vertical Orientation of Liquid Crystal on 4-n-Alkyloxyphenoxymethyl-Substituted Polystyrene Containing Liquid Crystal Precursor

Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 736
Author(s):  
Kyutae Seo ◽  
Hyo Kang
Keyword(s):  
Molecular Structure ◽  
Liquid Crystal ◽  
Surface Energy ◽  
Polymer Films ◽  
Ultraviolet Irradiation ◽  
Molar Fraction ◽  
Side Chain ◽  
Polymer Modification ◽  
Vertical Orientation ◽  
Surface Energies

We synthesized a series of polystyrene derivatives that were modified with precursors of liquid crystal (LC) molecules, such as 4-ethyloxyphenol (homopolymer PEOP and copolymer PEOP#; # = 20, 40, 60, and 80, where # indicates the molar fraction of 4-ethyloxyphenoxymethyl in the side chain), 4-n-butyloxyphenol (PBOP), 4-n-hexyloxyphenol (PHOP), and 4-n-octyloxyphenol (POOP), via polymer modification reaction to investigate the orientation of LC molecules on polymer films, exhibiting part of the LC molecular structure. LC molecules showed a stable and uniform vertical orientation in LC cells fabricated with polymers that have 4-ethyloxyphenoxymethyl in the range of 40–100 mol%. In addition, similar results were obtained in LC cells fabricated with homopolymers of PEOP, PBOP, PHOP, and POOP. The vertical orientation of LC molecules in LC cells fabricated with polymer films correlated to the surface energy of polymer films. For example, vertical LC orientation was observed when the total surface energies of the polymer films were lower than approximately 43.2 mJ/m2. Good alignment stabilities were observed at 150 °C and 20 J/cm2 of ultraviolet irradiation for LC cells fabricated with PEOP film.

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