Comment on ‘‘Spreading of liquid droplets on cylindrical surfaces: Accurate determination of contact angle’’ [J. Appl. Phys.70, 493 (1991)]

1991 ◽  
Vol 70 (1) ◽  
pp. 493-494 ◽  
Author(s):  
B. J. Carroll
Keyword(s):  
Contact Angle ◽  
Accurate Determination ◽  
Liquid Droplets

Spreading of Liquid Droplets on Cylindrical Surfaces: Accurate Determination of Contact Angle.

1989 ◽  
Vol 170 ◽  
Author(s):  
H. Daniel Wagner ◽  
E. Wiesel ◽  
H. E. Gallis
Keyword(s):  
Contact Angle ◽  
Liquid Droplet ◽  
Glass Fibers ◽  
Accurate Determination ◽  
High Strength ◽  
Contact Angles ◽  
Liquid Droplets ◽  
Liquid Polymers ◽  
Solid Liquid Interface ◽  
Solid Liquid

AbstractThe wetting of cylindrical monofilaments by liquid polymers is a problem of much scientific and technological importance. In particular, the characterization of the physicochemical nature of interfaces is a key problem in the field of advanced fibrous composites. The macroscopic regime contact angle, which reflects the energetics of wetting at the solid-liquid interface, is difficult to measure by usual methods in the case of very thin cylindrical fibers.In the present article a numerical method is proposed for the calculation of macroscopic regime contact angles from the shape of a liquid droplet spread onto a cylindrical monofilament. This method, which builds on earlier theoretical treatments by Yamaki and Katayama [1], and Carroll [2], very much improve the accuracy of the contact angle obtained. Experimental results with high-strength carbon, para-aramid, and glass fibers, are presented to demonstrate the high degree of accuracy of the method proposed.

Wettability Characterization from Pore-Scale Images Using Topology and Energy Balance with Implications for Recovery and Storage

2021 ◽  
Author(s):  
Martin Blunt ◽  
Luke Kearney ◽  
Abdulla Alhosani ◽  
Qingyang Lin ◽  
Branko Bijeljic
Keyword(s):  
Contact Angle ◽  
Porous Media ◽  
Energy Balance ◽  
Accurate Determination ◽  
Direct Determination ◽  
Contact Angles ◽  
Pore Scale ◽  
Three Phase ◽  
And Storage

Abstract We present two methods to measure contact angles inside porous media using high-resolution images. The direct determination of contact angle at the three-phase contact line is often ambiguous due to uncertainties with image segmentation. Instead, we propose two alternative approaches that provide an averaged assessment of wettability. The first uses fundamental principles in topology to relate the contact angle to the integral of the Gaussian curvature over the fluid-fluid meniscus. The advantage of this approach is that it replaces the uncertain determination of an angle at a point with a more accurate determination of an integral over a surface. However, in mixed-wet porous media, many interfaces are pinned with a hinging contact angle. For predictive pore-scale models, we need to determine the contact angle at which displacement occurs when the interfaces move. To address this problem we apply an energy balance, ignoring viscous dissipation, to estimate the contact angle from the meniscus curvature and changes in interfacial areas and saturation. We apply these methods to characterize wettability on pore-scale images of two- and three-phase flow. We also discuss the implications of the results for recovery and storage applications.

A quantitative approach to inner shell losses

1978 ◽  
Vol 36 (1) ◽  
pp. 526-527 ◽  
Author(s):  
R.D. Leapman ◽  
P. Rez ◽  
D.F. Mayers
Keyword(s):  
Energy Transfer ◽  
Cross Section ◽  
Cross Sections ◽  
Accurate Determination ◽  
Background Intensity ◽  
Core Excitation ◽  
Quantitative Basis ◽  
Cross Section Differential ◽  
Bound Electrons

Microanalysis by EELS has been developing rapidly and though the general form of the spectrum is now understood there is a need to put the technique on a more quantitative basis (1,2). Certain aspects important for microanalysis include: (i) accurate determination of the partial cross sections, σx(α,ΔE) for core excitation when scattering lies inside collection angle a and energy range ΔE above the edge, (ii) behavior of the background intensity due to excitation of less strongly bound electrons, necessary for extrapolation beneath the signal of interest, (iii) departures from the simple hydrogenic K-edge seen in L and M losses, effecting σx and complicating microanalysis. Such problems might be approached empirically but here we describe how computation can elucidate the spectrum shape.The inelastic cross section differential with respect to energy transfer E and momentum transfer q for electrons of energy E0 and velocity v can be written as

Fast calibration of CBED patterns for quantitative analysis

1993 ◽  
Vol 51 ◽  
pp. 674-675
Author(s):  
M.A. Gribelyuk ◽  
M. Rühle
Keyword(s):  
Reciprocal Lattice ◽  
Accurate Determination ◽  
Incident Beam ◽  
Crystal Thickness ◽  
Structure Model ◽  
Beam Direction ◽  
Transmitted Beam ◽  
Reciprocal Vector ◽  
On Line

A new method is suggested for the accurate determination of the incident beam direction K, crystal thickness t and the coordinates of the basic reciprocal lattice vectors V1 and V2 (Fig. 1) of the ZOLZ plans in pixels of the digitized 2-D CBED pattern. For a given structure model and some estimated values Vest and Kest of some point O in the CBED pattern a set of line scans AkBk is chosen so that all the scans are located within CBED disks.The points on line scans AkBk are conjugate to those on A0B0 since they are shifted by the reciprocal vector gk with respect to each other. As many conjugate scans are considered as CBED disks fall into the energy filtered region of the experimental pattern. Electron intensities of the transmitted beam I0 and diffracted beams Igk for all points on conjugate scans are found as a function of crystal thickness t on the basis of the full dynamical calculation.

Computer-Assisted High-Re Solution TEM

1990 ◽  
Vol 48 (1) ◽  
pp. 162-163
Author(s):  
F.A. Ponce ◽  
H. Hikashi
Keyword(s):  
Signal To Noise Ratio ◽  
Accurate Determination ◽  
Computer Software ◽  
Video Camera ◽  
Image Contrast ◽  
Objective Lens ◽  
Computer Assisted ◽  
Optical Parameters ◽  
Astigmatism Correction

The determination of the atomic positions from HRTEM micrographs is only possible if the optical parameters are known to a certain accuracy, and reliable through-focus series are available to match the experimental images with calculated images of possible atomic models. The main limitation in interpreting images at the atomic level is the knowledge of the optical parameters such as beam alignment, astigmatism correction and defocus value. Under ordinary conditions, the uncertainty in these values is sufficiently large to prevent the accurate determination of the atomic positions. Therefore, in order to achieve the resolution power of the microscope (under 0.2nm) it is necessary to take extraordinary measures. The use of on line computers has been proposed [e.g.: 2-5] and used with certain amount of success.We have built a system that can perform operations in the range of one frame stored and analyzed per second. A schematic diagram of the system is shown in figure 1. A JEOL 4000EX microscope equipped with an external computer interface is directly linked to a SUN-3 computer. All electrical parameters in the microscope can be changed via this interface by the use of a set of commands. The image is received from a video camera. A commercial image processor improves the signal-to-noise ratio by recursively averaging with a time constant, usually set at 0.25 sec. The computer software is based on a multi-window system and is entirely mouse-driven. All operations can be performed by clicking the mouse on the appropiate windows and buttons. This capability leads to extreme friendliness, ease of operation, and high operator speeds. Image analysis can be done in various ways. Here, we have measured the image contrast and used it to optimize certain parameters. The system is designed to have instant access to: (a) x- and y- alignment coils, (b) x- and y- astigmatism correction coils, and (c) objective lens current. The algorithm is shown in figure 2. Figure 3 shows an example taken from a thin CdTe crystal. The image contrast is displayed for changing objective lens current (defocus value). The display is calibrated in angstroms. Images are stored on the disk and are accessible by clicking the data points in the graph. Some of the frame-store images are displayed in Fig. 4.

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