scholarly journals X-ray microtomography analysis of isothermal densification of new snow under external mechanical stress

2013 ◽  
Vol 59 (214) ◽  
pp. 233-243 ◽  
Author(s):  
Stefan Schleef ◽  
Henning Löwe

AbstractWe have investigated the isothermal densification of new snow under an external mechanical stress. New snow samples that mimic natural snow were made in the laboratory by sieving ice crystals grown in a snowmaker. This allowed us to assemble homogeneous initial samples with reproducible values of low density and high specific surface area (SSA). Laboratory creep experiments were conducted in an X-ray microtomograph at −20°C for 2 days. We focused on the evolution of density and SSA as a function of constant stress at a single temperature. External mechanical stresses resembled natural overburden stresses of a snow sample at depths of ∼0–30 cm of new snow. We demonstrate that densification increases with higher external stress and lower initial densities. We find that the evolution of the SSA is independent of the density and follows a unique decay for all measurements of the present type of new snow. The results suggest that details of the SSA decrease can be investigated using carefully designed experiments of short duration which are convenient to conduct. Additionally, we calculated the strain evolution and identify transient creep behavior that does not follow the Andrade creep law of denser snow or polycrystalline ice.

Author(s):  
W. Matysiak ◽  
T. Tański ◽  
W. Smok

Purpose: The aim of this study was to present the influence of used reinforcement phase – graphene oxide (GO) and the electrospinning process parameters (the distance between the nozzle and collector) on the morphology and the structure of the obtained composite PAN-GO nanofibres. Design/methodology/approach: To produce pure polymer nanofibers, a 10% (wt.) electrospinning solution the polyacrylonitrile (PAN) was dissolved in N, N-dimethylformamide (DMF). The spinning solution used for electrospinning PAN-GO composite fibres was made by dissolving the PAN in a mixture of GO and DMF. By changing the configuration of the distance between the nozzle and collector (10 and 20 cm) and maintaining the remaining parameters (solution flow rate and potential difference between the electrodes), four samples in the form of nanofibrous mats were made. In order to identify the structure and morphology of the reinforcing phase, X-ray microanalysis (EDX) and scanning electron microscopy (SEM) were performed. In addition, the structure of graphene oxide microparticles was investigated by a Raman spectrometer. In order to determine the influence of the distance between the nozzle and the collector used in the electrospinning process and the addition of the reinforcing phase to the morphology and structure of the obtained PAN polymer nanofibres and PAN-GO composite nanofibres, they were examined using SEM. The analysis of the chemical composition of PAN and PAN-GO fibres was carried out using X-ray microanalysis. Findings: The morphology and structure analysis indicated that polymer nanofibres PAN for both the distances between the nozzle and the collector show no structural defects and presented same diameter over the entire length of the fibre. Nanofibres with the addition of GO obtained at both distances between the electrodes, showed defects in the form of beads. In addition, it was observed that with increasing distance between the nozzle and collector the diameter of obtained nanofibres is smaller for both pure PAN and composite PAN-GO samples. Research limitations/implications: The paper is the basis for further research in the field of the use of PAN-GO composite nanofibres as water purification materials. Originality/value: The electrospinning method can be an alternative to conventional methods for the production of filtering membranes due to the ease of carrying out the process and the fact that a material with a high specific surface area is obtained.


2014 ◽  
Vol 60 (219) ◽  
pp. 94-102 ◽  
Author(s):  
Stefan Schleef ◽  
Matthias Jaggi ◽  
Henning Löwe ◽  
Martin Schneebeli

AbstractWe present an improved machine to produce nature-identical snow in a cold laboratory for reproducible experiments. The machine is based on the common supersaturation principle of blowing cold air over a heated water basin. The moist airstream is directed into a chamber, where it cools and the nucleation of ice crystals is promoted on stretched nylon wires. Snow crystals grow on the wires and are harvested regularly by a new automatic brush rack. Depending on the settings, different snow crystals can be produced, which are shown to be consistent with the Nakaya diagram. The main snow types are dendrites and needles. We prepared specimens from the snow produced by the snowmaker and analyzed them using microcomputer tomography. For dendrites we show that there are natural snow samples that have the same crystal shape and similar microstructural parameters, namely density and specific surface area. The machine can produce suitable amounts of snow for laboratory experiments in an efficient way. As an advantage over previous designs, uniform and reproducible snow samples can be generated under well-defined conditions.


Author(s):  
J.M. Titchmarsh

The advances in recent years in the microanalytical capabilities of conventional TEM's fitted with probe forming lenses allow much more detailed investigations to be made of the microstructures of complex alloys, such as ferritic steels, than have been possible previously. In particular, the identification of individual precipitate particles with dimensions of a few tens of nanometers in alloys containing high densities of several chemically and crystallographically different precipitate types is feasible. The aim of the investigation described in this paper was to establish a method which allowed individual particle identification to be made in a few seconds so that large numbers of particles could be examined in a few hours.A Philips EM400 microscope, fitted with the scanning transmission (STEM) objective lens pole-pieces and an EDAX energy dispersive X-ray analyser, was used at 120 kV with a thermal W hairpin filament. The precipitates examined were extracted using a standard C replica technique from specimens of a 2¼Cr-lMo ferritic steel in a quenched and tempered condition.


Author(s):  
Imre Pozsgai ◽  
Klara Erdöhalmi-Torok

The paintings by the great Hungarian master Mihaly Munkacsy (1844-1900) made in an 8-9 years period of his activity are deteriorating. The most conspicuous sign of the deterioration is an intensive darkening. We have made an attempt by electron beam microanalysis to clarify the causes of the darkening. The importance of a study like this is increased by the fact that a similar darkening can be observed on the paintings by Munkacsy’s contemporaries e.g Courbet and Makart. A thick brown mass the so called bitumen used by Munkacsy for grounding and also as a paint is believed by the art historians to cause the darkening.For this study, paint specimens were taken from the following paintings: “Studio”, “Farewell” and the “Portrait of the Master’s Wife”, all of them are the property of the Hungarian National Gallery. The paint samples were embedded in a polyester resin “Poly-Pol PS-230” and after grinding and polishing their cross section was used for x-ray mapping.


Author(s):  
Judith M. Brock ◽  
Max T. Otten

A knowledge of the distribution of chemical elements in a specimen is often highly useful. In materials science specimens features such as grain boundaries and precipitates generally force a certain order on mental distribution, so that a single profile away from the boundary or precipitate gives a full description of all relevant data. No such simplicity can be assumed in life science specimens, where elements can occur various combinations and in different concentrations in tissue. In the latter case a two-dimensional elemental-distribution image is required to describe the material adequately. X-ray mapping provides such of the distribution of elements.The big disadvantage of x-ray mapping hitherto has been one requirement: the transmission electron microscope must have the scanning function. In cases where the STEM functionality – to record scanning images using a variety of STEM detectors – is not used, but only x-ray mapping is intended, a significant investment must still be made in the scanning system: electronics that drive the beam, detectors for generating the scanning images, and monitors for displaying and recording the images.


2021 ◽  
Vol 11 (7) ◽  
pp. 2971
Author(s):  
Siwei Tao ◽  
Congxiao He ◽  
Xiang Hao ◽  
Cuifang Kuang ◽  
Xu Liu

Numerous advances have been made in X-ray technology in recent years. X-ray imaging plays an important role in the nondestructive exploration of the internal structures of objects. However, the contrast of X-ray absorption images remains low, especially for materials with low atomic numbers, such as biological samples. X-ray phase-contrast images have an intrinsically higher contrast than absorption images. In this review, the principles, milestones, and recent progress of X-ray phase-contrast imaging methods are demonstrated. In addition, prospective applications are presented.


2021 ◽  
Vol 13 (5) ◽  
Author(s):  
Viktória Mozgai ◽  
Bernadett Bajnóczi ◽  
Zoltán May ◽  
Zsolt Mráv

AbstractThis study details the non-destructive chemical analysis of composite silver objects (ewers, situlas, amphora and casket) from one of the most significant late Roman finds, the Seuso Treasure. The Seuso Treasure consists of fourteen large silver vessels that were made in the fourth–early fifth centuries AD and used for dining during festive banquets and for washing and beautification. The measurements were systematically performed along a pre-designed grid at several points using handheld X-ray fluorescence analysis. The results demonstrate that all the objects were made from high-quality silver (above 90 wt% Ag), with the exception of the base of the Geometric Ewer B. Copper was added intentionally to improve the mechanical properties of soft silver. The gold and lead content of the objects shows constant values (less than 1 wt% Au and Pb). The chemical composition as well as the Bi/Pb ratio suggests that the parts of the composite objects were manufactured from different silver ingots. The ewers were constructed in two ways: (i) the base and the body were made separately, or (ii) the ewer was raised from a single silver sheet. The composite objects were assembled using three methods: (i) mechanical attachment; (ii) low-temperature, lead-tin soft solders; or (iii) high-temperature, copper-silver hard solders. Additionally, two types of gilding were revealed by the XRF analysis, one with remnants of mercury, i.e. fire-gilding, and another type without remnants of mercury, presumably diffusion bonding.


1998 ◽  
Vol 29 ◽  
pp. S323-S324 ◽  
Author(s):  
S.H. Ehrman ◽  
M. Schwikowski ◽  
U. Baltensperger ◽  
H.W. Ga¨ggeler

2011 ◽  
Vol 11 (3) ◽  
pp. 184-188
Author(s):  
Syed F. Akber ◽  
Than S. Kehwar

AbstractThe partial volume (spatial) response of four ionization chambers (Keithley) in kilovoltage X-ray beams, generated by the Philips Super 80CP X-ray unit, was assessed. The volume of the ionization chambers were of 10 cm3, 15 cm3, 150 cm3, and 600 cm3 used with Keithley electrometer Model 35040. The beam output was measured using a monitor chamber (Radcal 6.0 cm3) placed close to the collimator. The source to chamber distance was kept constant at 1 m. For the measurement of the response of ionization chambers of 15 cm3, 150 cm3, and 600 cm3, a slit of 2.0 mm width was made in a lead sheet of 3.2 mm thick and size of 30 × 30 cm2 and was placed on the ionization chamber. The measurements were made for 81 kVp, 400 mA, and 0.25 s and the slit was moved at an increment of 2.0 mm over the entire length of the chamber. For the measurements of the ionization chamber of 10 cm3 (CT chamber), the beams of 120 kVp, 200 mA and 0.2 s were generated, and a slit of 5 mm width was made in a similar lead sheet that was moved at an increment of 5.0 mm. From the result it appears that the sensitive volumes of the ionization chambers affect the response of the ionization chamber to incident radiation.


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