Specific Surface Area of Snow Samples Determined by CH4Adsorption at 77 K and Estimated by Optical Microscopy and Scanning Electron Microscopy

2001 ◽  
Vol 35 (4) ◽  
pp. 771-780 ◽  
Author(s):  
Florent Dominé ◽  
Axel Cabanes ◽  
Anne-Sophie Taillandier ◽  
LoÏc Legagneux
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Specific Surface ◽  
Optical Microscopy ◽  
Surface Area ◽  
Specific Surface Area ◽  
Scanning Electron ◽  
Snow Samples

scholarly journals Selective Crystallization of Silicoalumophosphate Sapo-11 With A Micromesoporous Structure

2021 ◽  
Vol 9 (2) ◽  
pp. 109-111
Author(s):  
Zulfiya Khayrullina ◽  
Kanaan R. Ahmed ◽  
Samara Kambarova ◽  
Marat Agliullin
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Molecular Sieve ◽  
Mesoporous Structure ◽  
Selective Crystallization ◽  
Scanning Electron

ABSTRACT:The authors have proposed a method for the selective crystallization of a SAPO-11 silicoaluminophosphate molecular sieve with a micro-mesoporous structure. It has been shown that crystallization of a silicoaluminophosphate gel, in the preparation of which its isopropoxide is used as a source of aluminum, makes it possible to obtain a SAPO-11 molecular sieve with a specific surface area of ​​~ 207 m2 / g, a volume of micro- and mesopores of ~ 0.08 and 0.09 cm3 / g. , respectively. Using scanning electron microscopy, it was demonstrated that the crystals of the material are pseudospherical particles ~ 8-10 microns in size, consisting of aggregates of nanocrystals ~ 100-200 nm in size.

scholarly journals Nanomaterial identification of powders: comparing volume specific surface area, X-ray diffraction and scanning electron microscopy methods

2019 ◽  
Vol 6 (1) ◽  
pp. 152-162 ◽  
Author(s):  
Claire Dazon ◽  
Olivier Witschger ◽  
Sébastien Bau ◽  
Vanessa Fierro ◽  
Philip L. Llewellyn
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
X Ray Diffraction ◽  
Reliable Criterion ◽  
X Ray ◽  
Area X ◽  
Scanning Electron

This work shows that the volume specific surface area could be a reliable criterion for nanomaterial identification.

Rate of decay of specific surface area of snow during isothermal experiments and morphological changes studied by scanning electron microscopy

2003 ◽  
Vol 81 (1-2) ◽  
pp. 459-468 ◽  
Author(s):  
L Legagneux ◽  
T Lauzier ◽  
F Domin ◽  
W F Kuhs ◽  
T Heinrichs ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Specific Surface ◽  
Decay Rate ◽  
Surface Area ◽  
Specific Surface Area ◽  
Morphological Changes ◽  
Main Process ◽  
Snow Crystals ◽  
Scanning Electron

The quantification of the specific surface area (SSA) of snow crystals and of its variation during metamorphism are essential to understand and model the exchange of reactive gases between the snowpack and the atmosphere. Therefore, the decay rate of SSA of five fresh snow samples was studied in the laboratory at –4, –10, and –15°C under isothermal conditions in closed systems. The time-evolution of the snow SSA can in all cases be very well described by an empirical law of the form, SSA = – A log(t + Δt) + B, where A, B, and Δt are adjustable parameters. B seems to be closely related to the initial SSA of the snow, and A describes the SSA decay rate. Our preliminary findings at –15°C suggest that a linear relationship exists between A and B, so that it may be possible to predict the decay rate of snow SSA from its initial value. For the first time, images obtained from scanning electron microscopy show that crystal rounding of snow is the main process taking place during isothermal metamorphism. New grain boundaries also form. More surprising, however, was the formation of new basal, prismatic, and pyramidal crystal faces, sometimes with very sharp angles, especially at –15°C. The growth of facets with sharp angles is not fully explained by current theories of snow metamorphism and has not been observed before. PACS Nos.: 68.35Md, 68.37Hk, 81.20Ev, 81.05Rm

Structural and morphological features of MgO powders. The key role of the preparative starting compound

1998 ◽  
Vol 13 (8) ◽  
pp. 2218-2223 ◽  
Author(s):  
S. Ardizzone ◽  
C. L. Bianchi ◽  
B. Vercelli
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Degree Of Crystallinity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Starting Compound ◽  
Scanning Electron

The present paper reports data concerning magnesia samples obtained by calcination of different precursor salts at different increasing temperatures (873–1253 K). The oxides are characterized by x- ray diffraction, scanning electron microscopy, and N2 adsorption at subcritical temperatures. The samples appear to be composed, at any temperature, of pure periclase with a degree of crystallinity which increases with the temperature of calcination. Morphologically, the products have the shape either of lamellas or of cubes of variable dimensions, depending on the nature and route of preparation of the precursor salts. The variation of the specific surface area and the degree of porosity with the nature of the precursors and the temperature is discussed.

Effects of dry grinding on pyrophyllite

Clay Minerals ◽  
1988 ◽  
Vol 23 (4) ◽  
pp. 399-410 ◽  
Author(s):  
J. L. Pérez-Rodríguez ◽  
L. Madrid Sánchez del Villar ◽  
P.J. Sánchez-Soto
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Grinding Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dry Grinding ◽  
Scanning Electron ◽  
Area Data

AbstractDry grinding of pyrophyllite (Hillsboro, USA) has been studied by X-ray diffraction (XRD), specific surface area measurements (BET) and scanning electron microscopy (SEM). At the beginning of the grinding process, some effects such as delamination, gliding and folding of the layers, and decrease in particle size were detected by SEM and XRD, resulting in a large increase in specific surface area, up to a maximum of ∼60 m2·g−1. Marked changes in the structure take place between 30 and 32 mins grinding. Longer grinding times increase the degree of disorder and SEM and specific surface area data suggest that aggregation occurs. XRD results indicate that some residual order persists in the degraded structure.

scholarly journals Influence of mechanical activation on synthesis of zinc metatitanate

2005 ◽  
Vol 37 (2) ◽  
pp. 115-122 ◽  
Author(s):  
Nebojsa Labus ◽  
Nina Obradovic ◽  
Tatjana Sreckovic ◽  
V. Mitic ◽  
Momcilo Ristic
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Low Temperature ◽  
Specific Surface ◽  
Mechanical Activation ◽  
Surface Area ◽  
Perovskite Structure ◽  
Mechanical Treatment ◽  
X Ray ◽  
Scanning Electron

Investigations of a ZnO-TiO2 binary oxide mixture during mechanical treatment were mainly focused on obtaining orthotitanate Zn2TiO4 with a spinel structure. Due to the specific way of energy transfer during mechanical treatment using a high-energy ball mill, the system passes through low temperature ZnTiO3 metatitanate phase formation. Mechanical activation was performed on an equimolar ratio mixture of ZnO and TiO2. The anatase phase was previously submitted to heat treatment for achieving a starting mixture rich in a rutile phase. Milling conditions were preset for observing the formation of a low temperature ZnTiO3 phase with a perovskite structure. The powder microstructure was characterized using scanning electron microscopy. A nitrogen gas sorption analyzer with the BET method was used to determine the specific surface area and porosity, indicating changes of powder sample properties during mechanical activation. Also, X ray powder diffractometry was applied to obtain the phase composition. Powders were then pressed into pellets and their compressibility was observed through density changes. According to microstructures obtained by scanning electron microscopy analysis, the system underwent a primary and secondary agglomeration process. Specific surface area measurements supported that conclusion. Compressibility investigations established the difference between compressibility of the non-activated mixture and activated powders. X-ray diffraction analysis revealed that a perovskite structure forms simultaneously with a spinel phase during the process of mechanical activation.

Digital imaging: When should one take the plunge?

1996 ◽  
Vol 54 ◽  
pp. 602-603
Author(s):  
John F. Mansfield
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Optical Microscopy ◽  
Digital Imaging ◽  
Storage Devices ◽  
Major Benefit ◽  
Transmission Electron ◽  
New Instrument ◽  
Scanning Electron

The current imaging trend in optical microscopy, scanning electron microscopy (SEM) or transmission electron microscopy (TEM) is to record all data digitally. Most manufacturers currently market digital acquisition systems with their microscope packages. The advantages of digital acquisition include: almost instant viewing of the data as a high-quaity positive image (a major benefit when compared to TEM images recorded onto film, where one must wait until after the microscope session to develop the images); the ability to readily quantify features in the images and measure intensities; and extremely compact storage (removable 5.25” storage devices which now can hold up to several gigabytes of data).The problem for many researchers, however, is that they have perfectly serviceable microscopes that they routinely use that have no digital imaging capabilities with little hope of purchasing a new instrument.

Investigation of Die Tilting of Packages with Single and Multi-chips

2018 ◽  
Author(s):  
Lo Chea Wee ◽  
Tan Sze Yee ◽  
Gan Sue Yin ◽  
Goh Cin Sheng
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Electron Beam ◽  
Optical Microscopy ◽  
Device Performance ◽  
Electronic Components ◽  
Area Of Interest ◽  
On Chip ◽  
Scanning Electron

Abstract Advanced package technology often includes multi-chips in one package to accommodate the technology demand on size & functionality. Die tilting leads to poor device performance for all kinds of multi-chip packages such as chip by chip (CbC), chip on chip (CoC), and the package with both CbC and CoC. Traditional die tilting measured by optical microscopy and scanning electron microscopy has capability issue due to wave or electron beam blocking at area of interest by electronic components nearby. In this paper, the feasibility of using profilemeter to investigate die tilting in single and multi-chips is demonstrated. Our results validate that the profilemeter is the most profound metrology for die tilting analysis especially on multi-chip packages, and can achieve an accuracy of <2μm comparable to SEM.

The External Morphology of the Eggs of Culex (Culex) saltanensis (Diptera: Culicidae) Under Scanning Electron Microscopy

2020 ◽  
Author(s):  
J R Santos-Mallet ◽  
T D Balthazar ◽  
A A Oliveira ◽  
W A Marques ◽  
A Q Bastos ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Optical Microscopy ◽  
Osmium Tetroxide ◽  
Neotropical Region ◽  
External Morphology ◽  
Metal Supports ◽  
Scanning Electron

Abstract The aim of the present study was to describe the morphology of the eggs of Culex (Culex) saltanensis Dyar that occurs in the Neotropical region. Eggs of the Cx. (Cux.) saltanensis were collected at the Mata Atlântica FIOCRUZ campus, fixed in 1% osmium tetroxide, prepared for mounting on metal supports, observed under a scanning electron microscope, and described morphologically. The eggs had a coniform shape with a length of approximately 0.5 mm (505–510 µm) and a width in the median portion of 117 µm (113–123 µm). Upper portion is lined with tubers of irregular shape and varying sizes (0.64–1.31 µm), located on a cross-linked matrix forming bands observed under optical microscopy. The micropyle is encased in a necklace of approximately 6.6-µm plates arranged in a flower-like shape. Comparing Cx. (Cux.) saltanensis eggs with several species of different genera, important divergent characteristics can be observed. However, this study points to the need for new descriptions of eggs of species belonging to the same subgenus in order to analyze if there will be differences between them. Culex (Cux.) saltanensis eggs have particular characteristics not observed in eggs of other Culicidae genera.

Damage Analysis of Heat Resistant Steels

2007 ◽  
Vol 537-538 ◽  
pp. 303-306
Author(s):  
Tamás Bíró ◽  
László Dévényi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Optical Microscopy ◽  
Damage Analysis ◽  
Resistant Steel ◽  
Heat Resistant Steel ◽  
Advantages And Disadvantages ◽  
Heat Resistant ◽  
Heat Resistant Steels ◽  
Scanning Electron

This paper shows the result of some metallographical examinations that have been carried out on low-alloyed Cr-Mo-V heat resistant steel. The aim of this research is to present and compare the advantages and disadvantages of the mainly applied metallographical methods. These techniques are optical microscopy, scanning electron microscopy, replica method and special applications of these methods. We have proved that using the investigated methods together gives much more information about the lifetime of the specimen than using these techniques particularly.

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