Chitin Systems Studied by Electron Diffraction, Diffraction-Contrast Electron Microscopy and Lattice Imaging

Author(s):  
Henri CHANZY ◽  
Francoise Gaill ◽  
Marie-Madeleine Giraud-Guille ◽  
Jan Persson ◽  
Junji Sugiyama ◽  
...  

Chitin the poly β (1-4)-N Acetyl D glucosamine is widespread in nature and occurs normally as a crystalline fibrillar substance. As opposed to most of the crystalline polysaccharides, chitin is quite resistant to the electron beam. In particular, at room temperature, accumulated doses as high as 200 elec/nm2 at 120 kV can be used to record successful images showing crystalline details. For this reason, chitin can be studied without too much difficulty by electron diffraction (ED), diffraction contrast transmission electron microscopy (DCTEM) and lattice imaging. This study presents some of the diversity of chitin morphology.Several chitin rich specimens were studied. They include : 1) cross sections of an ovipositor from an ichneumon fly Rhyssa persuosaria ; 2) cross sections of fragments of demineralized crab cuticle ; 3) cross sections of a tube from the vestimentiferan worm Tevnia jerichonana ; 4) bundles of chitin microfibrils isolated from Tevnia tube fragments after deproteinization.

2018 ◽  
Vol 90 (5) ◽  
pp. 833-844
Author(s):  
Leonid Aslanov ◽  
Valery Zakharov ◽  
Ksenia Paseshnichenko ◽  
Aleksandr Yatsenko ◽  
Andrey Orekhov ◽  
...  

AbstractA new method for synthesis of 2D nanocrystals in water was proposed. The use of perfluorothiophenolate ions as surfactant allowed us to produce 2D single-crystal nanosheets of CaS at pH=9 and flat nanocrystals of PbS at pH=9 at room temperature. Mesocrystalline nanobelts of CdS and mesocrystals of PbS were obtained at pH=3–5 and pH=10–12, respectively. Morphology, structure and chemical composition of nanoparticles were characterized by high-resolution transmission electron microscopy, electron diffraction and energy dispersive X-ray spectroscopy. A mechanism of nanoparticles formation was discussed.


2014 ◽  
Vol 215 ◽  
pp. 144-149 ◽  
Author(s):  
Sergey M. Zharkov ◽  
Roman R. Altunin ◽  
Evgeny T. Moiseenko ◽  
Galina M. Zeer ◽  
Sergey N. Varnakov ◽  
...  

Solid-state reaction processes in Fe/Si multilayer nanofilms have been studied in situ by the methods of transmission electron microscopy and electron diffraction in the process of heating from room temperature up to 900ºС at a heating rate of 8-10ºС/min. The solid-state reaction between the nanolayers of iron and silicon has been established to begin at 350-450ºС increasing with the thickness of the iron layer.


1986 ◽  
Vol 74 ◽  
Author(s):  
R. C. Birtcher ◽  
A. S. Liu

AbstractThe fluence dependence of Kr precipitation in Ni at room temperature has been studied with the aid of Transmission Electron Microscopy. As in other metals, the Kr precipitates in small cavities. Electron diffraction demonstrates that the Kr precipitates are solid, fcc crystals aligned with each other and the Ni lattice. The trends are similar to those observed for Kr precipitation in Al at room temperature. The average Kr lattice parameter, determined from the electron diffraction, increases with increasing Kr fluence from 0.515 nm to an asymptotic value of 0.545 nm. The asymptotic limit is due to the melting of the larger Kr precipitates. The mismatch between the Kr and Ni lattices is as large as 55%. Diffuse electron scattering was observed from large, liquid Kr precipitaes. This occurs for Kr fluences above 5.1020 Kr+ m-2 in Ni and above 2.5.1020 Kr+ m-2 in Al. At room temperature, the largest solid Kr precipitate observed in dark field images was 8.3 nm in diameter compared to 4.7 nm in Al. The larger precipitates are liquid or gas. The solid Kr metals at the same lattice parameter in both Ni and Al suggesting that the melting is thermodynamic in nature and independent of the host material.


1989 ◽  
Vol 159 ◽  
Author(s):  
J.M. Gibson

ABSTRACTThe kinematical approximation is valid for High-Energy Transmission Electron Diffraction from monolayers in planview. We use this fact to study quantitatively the attack of Si (111) 7×7 by 02. Oxygen is found to bind in the bridging position of the adatom backbonds and render the structure very stable during subsequent 02 exposure. Electron-beam exposure during dosing additionally creates rapid disordering which is presumed to represent SiOx formation.


1988 ◽  
Vol 58 (7) ◽  
pp. 414-417 ◽  
Author(s):  
P. Näslund ◽  
R. Vuong ◽  
H. Chanzy ◽  
J. C. Jésior

The crystalline ultrastructure of flax fibers was studied using diffraction contrast transmission electron microscopy applied to ultrathin transverse sections obtained with an experimental diamond knife with a cutting angle of only 26.6°. This technique permitted the recording of electron micrographs where individual crystalline microfibrils could be seen in the middle of their tightly packed arrangements. The microfibrils in flax had diameters ranging from 1 to 4 nm; in some instances their angular and nearly square contours were revealed.


Author(s):  
G. G. Shaw

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.


Author(s):  
R. W. Anderson ◽  
D. L. Senecal

A problem was presented to observe the packing densities of deposits of sub-micron corrosion product particles. The deposits were 5-100 mils thick and had formed on the inside surfaces of 3/8 inch diameter Zircaloy-2 heat exchanger tubes. The particles were iron oxides deposited from flowing water and consequently were only weakly bonded. Particular care was required during handling to preserve the original formations of the deposits. The specimen preparation method described below allowed direct observation of cross sections of the deposit layers by transmission electron microscopy.The specimens were short sections of the tubes (about 3 inches long) that were carefully cut from the systems. The insides of the tube sections were first coated with a thin layer of a fluid epoxy resin by dipping. This coating served to impregnate the deposit layer as well as to protect the layer if subsequent handling were required.


Author(s):  
A.J. Tousimis ◽  
T.R. Padden

The size, shape and surface morphology of human erythrocytes (RBC) were examined by scanning electron microscopy (SEM), of the fixed material directly and by transmission electron microscopy (TEM) of surface replicas to compare the relative merits of these two observational procedures for this type specimen.A sample of human blood was fixed in glutaraldehyde and washed in distilled water by centrifugation. The washed RBC's were spread on freshly cleaved mica and on aluminum coated microscope slides and then air dried at room temperature. The SEM specimens were rotary coated with 150Å of 60:40- gold:palladium alloy in a vacuum evaporator using a new combination spinning and tilting device. The TEM specimens were preshadowed with platinum and then rotary coated with carbon in the same device. After stripping the RBC-Pt-C composite film, the RBC's were dissolved in 2.5N HNO3 followed by 0.2N NaOH leaving the preshadowed surface replicas showing positive topography.


Author(s):  
S. Mahajan

The evolution of dislocation channels in irradiated metals during deformation can be envisaged to occur in three stages: (i) formation of embryonic cluster free regions, (ii) growth of these regions into microscopically observable channels and (iii) termination of their growth due to the accumulation of dislocation damage. The first two stages are particularly intriguing, and we have attempted to follow the early stages of channel formation in polycrystalline molybdenum, irradiated to 5×1019 n. cm−2 (E > 1 Mev) at the reactor ambient temperature (∼ 60°C), using transmission electron microscopy. The irradiated samples were strained, at room temperature, up to the macroscopic yield point.Figure 1 illustrates the early stages of channel formation. The observations suggest that the cluster free regions, such as A, B and C, form in isolated packets, which could subsequently link-up to evolve a channel.


Author(s):  
Joseph J. Comer ◽  
Charles Bergeron ◽  
Lester F. Lowe

Using a Van De Graaff Accelerator thinned specimens were subjected to bombardment by 3 MeV N+ ions to fluences ranging from 4x1013 to 2x1016 ions/cm2. They were then examined by transmission electron microscopy and reflection electron diffraction using a 100 KV electron beam.At the lowest fluence of 4x1013 ions/cm2 diffraction patterns of the specimens contained Kikuchi lines which appeared somewhat broader and more diffuse than those obtained on unirradiated material. No damage could be detected by transmission electron microscopy in unannealed specimens. However, Dauphiné twinning was particularly pronounced after heating to 665°C for one hour and cooling to room temperature. The twins, seen in Fig. 1, were often less than .25 μm in size, smaller than those formed in unirradiated material and present in greater number. The results are in agreement with earlier observations on the effect of electron beam damage on Dauphiné twinning.


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