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Nation divided cell

Figure 1-2 Transmission electron micrograph of a dividing cell of Escherichia coli 0157 H7 attached to the intestinal epithelium of a neonatal calf. These bacteria, which are able to efface the intestinal microvilli, form characteristic attachments, and secrete shiga toxins, are responsible for -73,000 illnesses and 60 deaths per year in the U. S.10a After embedding, the glutaraldehyde-fixed tissue section was immuno-stained with goat anti-0157 IgG followed by protein A conjugated to 10-nm gold particles. These are seen around the periphery of the cell bound to the O-antigen (see Fig. 8-28). Notice the two microvilli of the epithelium. Courtesy of Evelyn A. Dean-Nystrom, National Animal Disease Center, USD A, Agricultural Research Service, Ames, IA. Figure 1-2 Transmission electron micrograph of a dividing cell of Escherichia coli 0157 H7 attached to the intestinal epithelium of a neonatal calf. These bacteria, which are able to efface the intestinal microvilli, form characteristic attachments, and secrete shiga toxins, are responsible for -73,000 illnesses and 60 deaths per year in the U. S.10a After embedding, the glutaraldehyde-fixed tissue section was immuno-stained with goat anti-0157 IgG followed by protein A conjugated to 10-nm gold particles. These are seen around the periphery of the cell bound to the O-antigen (see Fig. 8-28). Notice the two microvilli of the epithelium. Courtesy of Evelyn A. Dean-Nystrom, National Animal Disease Center, USD A, Agricultural Research Service, Ames, IA.
Own experiments in divided cells using Nation membrane separators and hypochlorite solutions in the ppm range of concentration resulted in current efficiency values for active chlorine reduction of a few percent. Shifting the pH to higher values complicated the experiments. A buffer stabilised the pH but the relatively high concentration of buffer ions hindered the electrochemical reaction. Thus, quantification is difficult. Kuhn et al. (1980) showed reduction inhibition when calcareous deposits were precipitated on the cathode, but practical experiments showed the decrease of chlorine production in this case. [Pg.174]

This section is devoted to discuss the main results obtained for the treatment of organics in wastewaters by electro-Fenton using a divided cell usually with a cationic membrane (e.g., of Nation) to separate the anolyte and catholyte. Although the anode reactions do not affect the degradation of pollutants under these conditions, it is interesting to know the characteristics of their homogeneous oxidation with OH when this radical is uniquely formed in the medium from Fenton s reaction (19.12). [Pg.525]

Despite very limited resources, things were going pretty well until 1985, when bureaucratic wars started to destroy the institute. After a couple of years, the situation became unbearable and I decided to leave. However, it was very difficult to find a new position. Only in 1989 was I able to join the National Scientific Center of Hematology, where I hoped to apply our results on resonance in dividing cells to the treatment of leukemia. [Pg.445]

Figure 4. Optical image and two infrared images of a dividing cell (35 pm x 20 pm) obtained from IR spectromicroscopy. These chemical maps are derived from the strength of absorption bands from approximately 100 infrared transmittance spectra collected over the area of the dividing cell. The maximum in the color scale (yellow) represents the position of the maximum absorption by the cell, while the minimum (blue) represents no absorption by the cell. Strikingly, the intensity map of the amide II absorption band shows two peaks in the center of the two halves of the cell, representing the position of two separate nuclei before the cell division is complete. The intensity map of the C-H stretch absorption bands shows that lipids are concentrated at the contractil ring, where the cleavage furrow is located. [Used by permission of the National Academy of Sciences, U.S.A., from Jamin et al. (1998), Proc Natl Acad Sci, Vol. 95, Fig. 3, p. 4839.]... Figure 4. Optical image and two infrared images of a dividing cell (35 pm x 20 pm) obtained from IR spectromicroscopy. These chemical maps are derived from the strength of absorption bands from approximately 100 infrared transmittance spectra collected over the area of the dividing cell. The maximum in the color scale (yellow) represents the position of the maximum absorption by the cell, while the minimum (blue) represents no absorption by the cell. Strikingly, the intensity map of the amide II absorption band shows two peaks in the center of the two halves of the cell, representing the position of two separate nuclei before the cell division is complete. The intensity map of the C-H stretch absorption bands shows that lipids are concentrated at the contractil ring, where the cleavage furrow is located. [Used by permission of the National Academy of Sciences, U.S.A., from Jamin et al. (1998), Proc Natl Acad Sci, Vol. 95, Fig. 3, p. 4839.]...
Fig. 4. A mouse spleen cell and tumor cell fuse to form a hybridoma. As the hybridoma divides, it gives rise to a clone of identical cells, giving the name monoclonal" to the antibodies those cells produce (reprinted with permission from Olsen. 1986. p. 27. Copyright. National Academy Piessl... Fig. 4. A mouse spleen cell and tumor cell fuse to form a hybridoma. As the hybridoma divides, it gives rise to a clone of identical cells, giving the name monoclonal" to the antibodies those cells produce (reprinted with permission from Olsen. 1986. p. 27. Copyright. National Academy Piessl...
Fig. 5.14 Electrochemical carboxylation of aldehydes. Reagents and conditions divided flow cell, Nation membrane, BDD/Si electrodes, NBu4+BF4 in DMF, 20-25°C, 0.6 A dm-2, 5h, 27% yield in rac-28 at 88% conversion of 27... Fig. 5.14 Electrochemical carboxylation of aldehydes. Reagents and conditions divided flow cell, Nation membrane, BDD/Si electrodes, NBu4+BF4 in DMF, 20-25°C, 0.6 A dm-2, 5h, 27% yield in rac-28 at 88% conversion of 27...
Fig. 13.7 Linear sweep voltammograms for electrochemical HDH of pentachlorophenol (PCP) and 2,4-dichlorophenol (DCP) on a Ti mesh-supported Pd cathode (2mgPdcm-2, 4cm2). Cell H-cell divided by a Nation 117 membrane. Anode Pt mesh (lOcm2). Catholyte 0.05MNa2S04 (pH 3) solution without (blank) or with saturated PCP and DCP. Anolyte 0.05 M Na2S04 (pH 3) solution. Scan rate 5 mV s-1. Temperature 21.5 0.5°C... Fig. 13.7 Linear sweep voltammograms for electrochemical HDH of pentachlorophenol (PCP) and 2,4-dichlorophenol (DCP) on a Ti mesh-supported Pd cathode (2mgPdcm-2, 4cm2). Cell H-cell divided by a Nation 117 membrane. Anode Pt mesh (lOcm2). Catholyte 0.05MNa2S04 (pH 3) solution without (blank) or with saturated PCP and DCP. Anolyte 0.05 M Na2S04 (pH 3) solution. Scan rate 5 mV s-1. Temperature 21.5 0.5°C...
A new version of MCFC technology - the direct carbon fuel cell (DCFC) - is under development at the Lawrence Livermore National Laboratory in the USA. Instead of using gaseous fuel, a slurry of finely divided carbon particles dispersed in molten alkali metal carbonates is fed to the cell. The carbon is made by the pyrolysis of almost any waste hydrocarbon e.g., petroleum coke), a process that is already carried out industrially on a large scale to produce carbon black for use in the manufacture of tyres, inks, plastic fillers, etc. The pyrolysis reaction yields hydrogen that can itself be utilized in another fuel cell ... [Pg.216]

As we have seen elsewhere, the cell is divided into various compartments, nucleus, mitochondria, cytosol and so on, each one separated from the rest by membrane barriers. If everything could move freely across these membranes there would be no point in having them. They would be bfce national borders with no one checking passports, visas, smuggling, etc. The organelles keep certain processes inside their boundaries, e.g. the Krebs cycle, which takes place exclusively inside the mitochondria, or anaerobic glycolysis exclusively in the cytosol, etc. On the other hand, if there were no communication and traffic between compartments, there would in effect be no cell and no organism - the whole has to be more than the mere sum of its parts, and these parts are not set up to be autonomous but to carry out specialised functions as part of an overall team effort. [Pg.264]

The concept had been tested at Los Alamos National Laboratory until 2005. The cell included an ion-exchange membrane, that divided the cell into an anode chamber with an anode, and a cathode chamber with an oxygen gas diffusion cathode. The design of the cell was adjusted to reduce the formation of peroxide associated with the reduction of oxygen. ... [Pg.409]

Many fuel cell engineers prefer employment within the national laboratories and government agencies such as the Pacific Northwest National Laboratory, the National Renewable Energy Laboratory, the Ai onne National Laboratory, the National Aeronautics and Space Administration (NASA), DOE, and DARPA. Others find work in academia. Such professionals divide their time between teaching university classes on fuel cells and conducting their own research. [Pg.833]

Chlamydomonas segnis Ettl. was obtained from Dr. M. Czuba and Dr. D. Mortimer of the National Research Council, Ottawa, Ontario, Canada. The algae were cultivated in Kuhl s liquid medium, (Kuhl and Lorenzen 1964) which was autoclaved prior to use (final pH 6.8). The algal cells were induced to divide synchronously and were incubated in a growth chamber at 25° C with a photoperiod of 12 hr dark/12 hr light at 5.5 Klux from Sylvania cool white fluorescent lamps. The cultures were stirred constantly and bubbled with air... [Pg.394]


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