ultramicroscope
(ŭl'trə-mī'krə-skōp')
n.
A microscope with high-intensity illumination used to study very minute objects, such as colloidal particles that scatter the light and appear as bright spots against a dark background.
ultramicroscopy ul'tra·mi·cros'co·py (-krŏs'kə-pē) n.
A form of microscope that uses the Tyndall effect to reveal the presence of particles that cannot be seen with a normal optical microscope. Colloidal particles, smoke particles, etc., are suspended in a liquid or gas in a cell with a black background and illuminated by an intense cone of light that enters the cell from the side and has its apex in the field of view. The particles then produce diffraction-ring systems, appearing as bright specks on the dark background.
(ŭl'trə-mī'krə-skōp')
n.
A microscope with high-intensity illumination used to study very minute objects.
An ultramicroscope is a system of illumination for viewing tiny particles. When the diameter of a particle is below or near the wavelength of light (around 500 nanometers), the particle cannot be seen in a light microscope with the usual method of illumination. The ultramicroscope system is based on light scattering, not light reflection. In the system, the particles to be observed are dispersed in a liquid or gas colloid (or less often in a coarser suspension). The colloid is placed in a light-absorbing, dark enclosure, and illuminated with a convergent beam of intense light entering from one side. Light hitting the colloid particles will get scattered. In discussions about light scattering, the converging beam is called a "Tyndall cone". The scene is viewed through an ordinary microscope placed at right angles to the direction of the lightbeam. Under the microscope, the individual particles will appear as small fuzzy spots of light moving irregularly. The spots are inherently fuzzy because light scattering produces fuzzier images than light reflection. The particles are in Brownian motion in most kinds of liquid and gas colloids, which causes the movement of the spots. The ultramicroscope system can also be used to observe tiny nontransparent particles dispersed in a transparent solid or gel.
The "ultra" in "ultramicroscope" refers to the ability to see objects whose diameter is shorter than the wavelength of visible light, on the model of the "ultra" in ultraviolet.
Ultramicroscopes have been used for general observation of aerosols and colloids, and in the study of Brownian motion, and in observing ionization tracks in cloud chambers.
In 1902 the ultramicroscope was developed by Richard Adolf Zsigmondy (1865 - 1929) and Henry Siedentopf (1872 - 1940), working for Carl Zeiss AG. Applying bright sunlight for illumination they were able to determine the size of 4 nm small nanoparticles in cranberry glass. Zsigmondy further improved the ultramicroscope and presented the immersion ultramicroscope in 1912, allowing the observation of suspended nanoparticles in defined fluidic volumes. In 1925 he was awarded the Nobel Prize in Chemistry for his research on colloids and the ultramicroscope.
For a different type of microscopy that also leverages light scattering against a dark background see dark field microscopy.
In the first decade of the 21th century, the illumination mode of the ultramicroscope has been extended to fluorescence measurement, as light sheet fluorescence microscopy.
References
- Nobel lecture of R. A. Zsigmondy: Properties of colloids (including a short explanation of the ultramicroscope)
- An Introduction to Colloids, by Sumanyu Chauhan, published online at Scribd.com.
- An Introduction to Colloids by James B. Calvert
- T. Mappes et al.: The Invention of Immersion Ultramicroscopy in 1912—The Birth of Nanotechnology? Angewandte Chemie International Edition, vol. 51, pp. 11208-11212 describing the early development of ultramicroscopes and showing the use of an antique immersion ultramicroscope with a video of vividly moving silver nanoparticles of 50 nm size.
- Antique immersion ultramicroscope with optics as of the 1912 patent
Three-dimensional reconstruction and segmentation of intact Drosophila by ultramicroscopy
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