Ultrasonic dispersion and attenuation near the liquid-gas critical point of4He

1974 ◽  
Vol 16 (1-2) ◽  
pp. 51-72 ◽  
Author(s):  
David B. Roe ◽  
Barnie A. Wallace ◽  
Horst Meyer
2020 ◽  
Author(s):  
Dimitrios Aggelis ◽  
Gerlinde Lefever ◽  
Dorian Serafin ◽  
Danny Van Hemelrijck

Materials ◽  
2020 ◽  
Vol 13 (20) ◽  
pp. 4528
Author(s):  
Gerlinde Lefever ◽  
Nicolas Ospitia ◽  
Dorian Serafin ◽  
Danny Van Hemelrijck ◽  
Dimitrios G. Aggelis

This study aims to experimentally investigate the ultrasonic behavior of fresh cement focusing on the contribution of the entrapped air bubbles. Frequency dispersion and attenuation carry delicate information that is not possible to gather by traditional ultrasonic pulse velocity. This is measured by simple indicators that quantify the frequency dependence of propagation velocity of longitudinal waves through fresh cementitious media. It seems that dispersion shows much stronger sensitivity to the microstructural processes, since the presence of superabsorbent polymers in mortar induces a large difference in dispersion parameters when compared to reference cement mortar, while only marginal difference in threshold-based pulse velocity. To reach this aim, references are taken from, and comparisons are made to other liquids in order first in order to validate the reliability of the methodology and to better understand the contribution of the cavities in the obtained dispersion and attenuation curves. Ultrasonic dispersion assessment of cementitious media has the potential to bring a lot of information on the microstructure of materials, as well as the ongoing processes.


Author(s):  
Charles TurnbiLL ◽  
Delbert E. Philpott

The advent of the scanning electron microscope (SCEM) has renewed interest in preparing specimens by avoiding the forces of surface tension. The present method of freeze drying by Boyde and Barger (1969) and Small and Marszalek (1969) does prevent surface tension but ice crystal formation and time required for pumping out the specimen to dryness has discouraged us. We believe an attractive alternative to freeze drying is the critical point method originated by Anderson (1951; for electron microscopy. He avoided surface tension effects during drying by first exchanging the specimen water with alcohol, amy L acetate and then with carbon dioxide. He then selected a specific temperature (36.5°C) and pressure (72 Atm.) at which carbon dioxide would pass from the liquid to the gaseous phase without the effect of surface tension This combination of temperature and, pressure is known as the "critical point" of the Liquid.


Author(s):  
B. K. Kirchoff ◽  
L.F. Allard ◽  
W.C. Bigelow

In attempting to use the SEM to investigate the transition from the vegetative to the floral state in oat (Avena sativa L.) it was discovered that the procedures of fixation and critical point drying (CPD), and fresh tissue examination of the specimens gave unsatisfactory results. In most cases, by using these techniques, cells of the tissue were collapsed or otherwise visibly distorted. Figure 1 shows the results of fixation with 4.5% formaldehyde-gluteraldehyde followed by CPD. Almost all cellular detail has been obscured by the resulting shrinkage distortions. The larger cracks seen on the left of the picture may be due to dissection damage, rather than CPD. The results of observation of fresh tissue are seen in Fig. 2. Although there is a substantial improvement over CPD, some cell collapse still occurs.Due to these difficulties, it was decided to experiment with cold stage techniques. The specimens to be observed were dissected out and attached to the sample stub using a carbon based conductive paint in acetone.


Author(s):  
T. G. Naymik

Three techniques were incorporated for drying clay-rich specimens: air-drying, freeze-drying and critical point drying. In air-drying, the specimens were set out for several days to dry or were placed in an oven (80°F) for several hours. The freeze-dried specimens were frozen by immersion in liquid nitrogen or in isopentane at near liquid nitrogen temperature and then were immediately placed in the freeze-dry vacuum chamber. The critical point specimens were molded in agar immediately after sampling. When the agar had set up the dehydration series, water-alcohol-amyl acetate-CO2 was carried out. The objectives were to compare the fabric plasmas (clays and precipitates), fabricskeletons (quartz grains) and the relationship between them for each drying technique. The three drying methods are not only applicable to the study of treated soils, but can be incorporated into all SEM clay soil studies.


Author(s):  
Linda M. Sicko ◽  
Thomas E. Jensen

The use of critical point drying is rapidly becoming a popular method of preparing biological samples for scanning electron microscopy. The procedure is rapid, and produces consistent results with a variety of samples. The preservation of surface details is much greater than that of air drying, and the procedure is less complicated than that of freeze drying. This paper will present results comparing conventional air-drying of plant specimens to critical point drying, both of fixed and unfixed material. The preservation of delicate structures which are easily damaged in processing and the use of filter paper as a vehicle for drying will be discussed.


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