Surface modification of triacetylcellulose by low-energy nitrogen ions for diaphragm of environmental cell transmission electron microscope

2018 ◽  
Vol 344 ◽  
pp. 58-61 ◽  
Author(s):  
Takaomi Matsutani ◽  
Masanori Murano ◽  
Tadahiro Kawasaki
Author(s):  
D.K. Dewald ◽  
T.C. Lee ◽  
J.A. Eades ◽  
I.M. Robertson ◽  
H.K. Bimbaum

The ability to observe directly and at high spatial resolution the interactions between environments and materials affords the material scientist new and unique opportunities. This capability is realized in the Environmental Cell Transmission Electron Microscope Facility which has been installed as part of the Center for Microanalysis of Materials at the Materials Research Laboratory of the University of Illinois at Urbana-Champaign.The Facility is based on a JEOL 4000EX equipped with a specially designed pole piece. An aperture limited, differentially pumped, environmental cell has been installed in this pole piece. The system is shown schematically in Figures 1 and 2. Figure 1 is a plan view of a section through the objective lens pole-piece, with the microscope axis perpendicular to the plane of the paper, showing the cell enclosing the sample rod, the gas handling system and the location of the magnetically levitated Turbo-Molecular pumps. Figure 2 shows a cross-sectional view of the environmental cell and the gas handling system. As shown in Figure 2 the electron beam passes through a series of five apertures which allow the column vacuum to be maintained while the cell pressure is increased. The actual cell apertures are located at the apex of cones to minimize the gas path length, allow maximum tilt and still permit high- angle diffraction data to be obtained. Differential pumping of the cell is achieved by the four turbo- molecular pumps, the location of which can be seen in the Figures. With this arrangement the environmental cell is capable of supporting 400 torr of N2 gas which has no noticeable effect on the microscope operation. This allows the microscope to be operated with a LaB6 filament. The gas handling system was designed to handle a variety of environments including corrosive ones.


1991 ◽  
Vol 62 (6) ◽  
pp. 1438-1444 ◽  
Author(s):  
T. C. Lee ◽  
D. K. Dewald ◽  
J. A. Eades ◽  
I. M. Robertson ◽  
H. K. Birnbaum

2001 ◽  
Vol 7 (6) ◽  
pp. 470-485 ◽  
Author(s):  
Tyrone L. Daulton ◽  
Brenda J. Little ◽  
Kristine Lowe ◽  
Joanne Jones-Meehan

AbstractReduction of Cr(VI) by the bacterium, Shewanella oneidensis (previously classified Shewanella putrefaciens strain MR-1), was studied by absorption spectrophotometry and in situ, environmental cell–transmission electron microscopy (EC-TEM) coupled with electron energy loss spectroscopy (EELS). Bacteria from rinsed cultures were placed directly in the environmental cell of the transmission electron microscope and examined under 100 Torr pressure. Bright field EC-TEM images show two distinct populations of S. oneidensis in incubated cultures containing Cr(VI)O42−: those that exhibit low image contrast and heavily precipitateencrusted cells exhibiting high image contrast. Several EELS techniques were applied to determine the oxidation state of Cr associated with encrusted cells. The encrusted cells are shown to contain a reduced form of Cr in oxidation state +3 or lower. These results demonstrate the capability to determine the chemistry and valence state of reduction products associated with unfixed, hydrated bacteria in an environmental cell transmission electron microscope.


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