scholarly journals Casimir effect modified surface energy of a nanocavity in homogeneous media

2015 ◽  
Vol 527 (7-8) ◽  
pp. 499-506
Author(s):  
Yi Zheng ◽  
Arvind Narayanaswamy
Keyword(s):  
Surface Energy ◽  
Casimir Effect ◽  
Modified Surface ◽  
Homogeneous Media

Filler-Elastomer Interactions. Part V. Investigation of the Surface Energies of Silane-Modified Silicas

1992 ◽  
Vol 65 (4) ◽  
pp. 715-735 ◽  
Author(s):  
Meng-Jiao Wang ◽  
Siegfried Wolff
Keyword(s):  
Surface Energy ◽  
Energy Distribution ◽  
Strong Dependence ◽  
Free Energies ◽  
Specific Component ◽  
Dispersive Component ◽  
Initial Silica ◽  
Finite Concentration ◽  
Modified Surface ◽  
High Degree

Abstract As shown in previous papers of this series, the main feature of silicas with regard to surface energy, which distinguishes them from carbon blacks, is a low dispersive component, γsd, and a high specific component, γssp, of surface energy. The low γsd, would result in a lack of interaction between filler and hydrocarbon rubbers, while the high γssp would suggest a high degree of agglomeration of the filler particles in the polymer matrix. In this study, the surface free energies and the energy distribution on the surfaces of precipitated silicas which had been modified with octadecyltrimethoxy silane, 3-thiocyanatopropyltriethoxy silane and bis(3-trimethoxysilylpropyl)-tetrasulfane, respectively, were investigated by chromatography at infinite dilution and at finite concentration. A comparison with the initial silica suggests a drastic decrease in surface energy, especially of the specific component, as a result of the modification and a strong dependence of surface energy on the chemical nature of the grafts and the ratio of these grafts. The energy distribution function shows that, while the surface of the ungrafted silica is heterogeneous, the heterogeneity of the fully modified surface is drastically reduced, particularly when the product was modified with octadecyltrimethoxy silane.

scholarly journals Surface modification of polycarbonate (bisphenol A) by low pressure rf plasma

1970 ◽  
Vol 1 (2) ◽  
pp. 115-118 ◽  
Author(s):  
Deepak P Subedi ◽  
Lenka Zajickova ◽  
Vilma Bursikova ◽  
Jan Janca
Keyword(s):  
Free Energy ◽  
Surface Modification ◽  
Surface Energy ◽  
Surface Free Energy ◽  
Photoelectron Spectroscopy ◽  
Peel Test ◽  
Low Pressure ◽  
Rf Plasma ◽  
Modified Surface ◽  
The Stability

Effects of low pressure radio frequency (rf) plasma treatment on the surface properties of polycarbonate are presented in this paper. Results obtained from the surface energy measurement after different conditions of treatment are compared. After treatment the surface free energy increased from the original value of 35 mJ/m2 to 63-74 mJ/m2. X-ray photoelectron spectroscopy measurements showed an increase in oxygen to carbon ratio after the treatment indicating an increase of oxygen-containing functional groups on the polycarbonate surface. A study of the stability of the modified surface property has been made on the basis of surface free energy. To study the improvement of adhesion between the polycarbonate and thin coatings, organosilicon thin films were deposited on the untreated and plasma treated polycarbonate. The adhesion of film to substrate was quantitatively analysed by ‘cross-hatch peel test’. Key words: Polycarbonate, surface modification, rf plasma, ageing, surface energy Himalayan Journal of Sciences 1(2): 115-118, 2003

The annealed (0001) α-alumina surface and its influence on thin-film growth

1995 ◽  
Vol 53 ◽  
pp. 336-337
Author(s):  
Michael W. Bench ◽  
Paul G. Kotula ◽  
C. Barry Carter
Keyword(s):  
Electron Microscopy ◽  
Surface Energy ◽  
Film Growth ◽  
Thin Film Growth ◽  
Energy Calculations ◽  
Transmission Electron ◽  
Reflection Electron Microscopy ◽  
Low Energy Electron ◽  
Surface Nature

The growth of semiconductors, superconductors, metals, and other insulators has been investigated using alumina substrates in a variety of orientations. The surface state of the alumina (for example surface reconstruction and step nature) can be expected to affect the growth nature and quality of the epilayers. As such, the surface nature has been studied using a number of techniques including low energy electron diffraction (LEED), reflection electron microscopy (REM), transmission electron microscopy (TEM), molecular dynamics computer simulations, and also by theoretical surface energy calculations. In the (0001) orientation, the bulk alumina lattice can be thought of as a layered structure with A1-A1-O stacking. This gives three possible terminations of the bulk alumina lattice, with theoretical surface energy calculations suggesting that termination should occur between the Al layers. Thus, the lattice often has been described as being made up of layers of (Al-O-Al) unit stacking sequences. There is a 180° rotation in the surface symmetry of successive layers and a total of six layers are required to form the alumina unit cell.

The nucleation of cavities at grain boundaries

1987 ◽  
Vol 45 ◽  
pp. 288-291
Author(s):  
P. J. Goodhew
Keyword(s):  
Surface Tension ◽  
Surface Energy ◽  
Grain Boundaries ◽  
Radiation Damage ◽  
Impurity Concentration ◽  
Driving Force ◽  
Nucleation And Growth ◽  
Phase Boundaries ◽  
Cavity Nucleation ◽  
Spherical Bubble

Cavity nucleation and growth at grain and phase boundaries is of concern because it can lead to failure during creep and can lead to embrittlement as a result of radiation damage. Two major types of cavity are usually distinguished: The term bubble is applied to a cavity which contains gas at a pressure which is at least sufficient to support the surface tension (2g/r for a spherical bubble of radius r and surface energy g). The term void is generally applied to any cavity which contains less gas than this, but is not necessarily empty of gas. A void would therefore tend to shrink in the absence of any imposed driving force for growth, whereas a bubble would be stable or would tend to grow. It is widely considered that cavity nucleation always requires the presence of one or more gas atoms. However since it is extremely difficult to prepare experimental materials with a gas impurity concentration lower than their eventual cavity concentration there is little to be gained by debating this point.

Influence of Fiber Surface Energy on Mechanical Properties of Sisal Fiber - Bio Based Epoxy Composites

2019 ◽  
Vol 35 (4) ◽  
pp. 485-496
Author(s):  
S. RAJKUMAR ◽  
◽  
R. JOSEPH BENSINGH ◽  
M. ABDUL KADER ◽  
SANJAY K NAYAK ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Surface Energy ◽  
Fiber Surface ◽  
Epoxy Composites ◽  
Sisal Fiber

Surface energy of cellulosic materials: The effect of particle morphology, particle size, and hydroxyl number

TAPPI Journal ◽  
2015 ◽  
Vol 14 (9) ◽  
pp. 565-576 ◽  
Author(s):  
YUCHENG PENG ◽  
DOUGLAS J. GARDNER
Keyword(s):  
Particle Size ◽  
Surface Energy ◽  
Particle Morphology ◽  
Nanofibrillated Cellulose ◽  
Particle Sizes ◽  
Hydroxyl Number ◽  
Small Individual ◽  
Dispersion Component ◽  
Commercial Applications ◽  
Lower Temperature

Understanding the surface properties of cellulose materials is important for proper commercial applications. The effect of particle size, particle morphology, and hydroxyl number on the surface energy of three microcrystalline cellulose (MCC) preparations and one nanofibrillated cellulose (NFC) preparation were investigated using inverse gas chromatography at column temperatures ranging from 30ºC to 60ºC. The mean particle sizes for the three MCC samples and the NFC sample were 120.1, 62.3, 13.9, and 9.3 μm. The corresponding dispersion components of surface energy at 30°C were 55.7 ± 0.1, 59.7 ± 1.3, 71.7 ± 1.0, and 57.4 ± 0.3 mJ/m2. MCC samples are agglomerates of small individual cellulose particles. The different particle sizes and morphologies of the three MCC samples resulted in various hydroxyl numbers, which in turn affected their dispersion component of surface energy. Cellulose samples exhibiting a higher hydroxyl number have a higher dispersion component of surface energy. The dispersion component of surface energy of all the cellulose samples decreased linearly with increasing temperature. MCC samples with larger agglomerates had a lower temperature coefficient of dispersion component of surface energy.

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.

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