US2256171A - Method of focusing electron microscopes - Google Patents

Method of focusing electron microscopes Download PDF

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Publication number
US2256171A
US2256171A US321237A US32123740A US2256171A US 2256171 A US2256171 A US 2256171A US 321237 A US321237 A US 321237A US 32123740 A US32123740 A US 32123740A US 2256171 A US2256171 A US 2256171A
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United States
Prior art keywords
electron
conglomerate
contrasts
substance
substances
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Expired - Lifetime
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US321237A
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English (en)
Inventor
Ruska Helmut
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Fides Gesellschaft fuer die Verwaltung und Verwertung von Gewerblichen Schutzrechten mbH
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Fides Gesellschaft fuer die Verwaltung und Verwertung von Gewerblichen Schutzrechten mbH
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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00Sampling; Preparing specimens for investigation
    • G01N1/28Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/2853Shadowing samples
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J37/00Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
    • H01J37/02Details
    • H01J37/21Means for adjusting the focus

Definitions

  • the present invention relates to a method of improving or facilitating the focusing of electron microscopes.
  • the substances to be examined are provided with means contrasting therewith, so that the dinerence in contrast between the added means and the actual image of the substances can be easily determined on the fluorescent screen.
  • the strong contrasts thus appearing in the magnified image of the conglomerate permit an easy and sharp focusing of the image.
  • the substances to be examined in the electron microscope are provided with materials having a specific density considerably higher than the density of the substances. Only small particles of these materials are added to the substances to be examined, and the size of these particles must correspond substantially to the size of the substances.
  • the added materials must be of a type suitable for obtaining in the image on the fluorescent screen of the electron microscope the strong contrasts necessary for adjusting the image to be in sharp focus. It is advisable to use only such materials which do not react in any way with the substance itself, and it is easily possible, for example by tests, to determine the type of materials best suitable for a particular purpose.
  • colloids of various metals for example gold or silver colloids, have been found suitable, although colloidal metallic oxides may also be used.
  • the concentration of viri for example, may be in the amount of 10-- to 10* grams of virous protein for each cubic centimeter of solvent.
  • the concentration in gold to be added thereto may then, for example, amount to 10- to 10- grams per cubic centimeter.
  • the solvent to be used should be a volatile substance, for example, water or xylene without any contents in nonvolatile substances or salts.
  • the gold-containing solution is applied to a supporting foil as customary in electron microscopes for supporting the object to be studied. After volatilization of the solvent,
  • the dried residue left on the foil is a conglomerate of the substance to be studied and gold particles.
  • the foil is then placed into the electron microscope and the focusing is effected in the customary manner, except that the strong contrasts now appearing in the magnified image render the focusing very easy and accurate.
  • the method of electron-microscopically examining organic substances of weak electronoptical contrasts which comprises adding to the organic substance to be examined colloidal particles of an inorganic material chemically inert With respect to said organic substance and of greater density than said organic substance so as to form a conglomerate of strong electronoptical contrasts, subjecting the conglomerate thus obtained to electron-microscopical magnification, and adjusting the magnification by focusing the magnified image on the contrasts of the conglomerate.
  • the method of electron-microscopically examining substances of Weak electron-optical contrasts which comprises adding to the substance to be examined a colloid non-reactive as regards said substance and of greater specific weight than said substance so as to obtain a conglomerate with strong electron-optical contrasts, subjecting said conglomerate to electronmicroscopical magnification, and adjusting the magnification by focusing the magnified image on the contrasts of the conglomerate.
  • the method of electron-microscopically examining organic substance containing virus or other organisms of Weak electron-optical contrasts which comprises admixing to said organic substance an inorganic material non-reactive as regards said substance and of considerably greater density than said substance, said material being finely subdivided into particles of a size in the order of magnitude of the size of said organisms,' whereby a conglomerate of strong electron-optical contrasts is obtained, subjecting said conglomerate to electron-microscopical magnification, and adjusting the magnification by focusing the magnified image on the contrasts of the conglomerate.
  • the method of electron-microscopically examining substances of weak electron-optical contrasts which comprises adding to the slib stance to be examined a colloid of noble metal so as to obtain a conglomerate of strong electron-optical contrasts containing said substance and colloidal gold particles in juxtaposition and non-reactive as regards each other, subjecting said conglomerate to electron-microscopical magnification, and adjusting the magnification by focusing the magnified image on the contrast.
  • the method of electrran-microscopically examining substances of weak electron-optical I contrasts which comprises adding to the substance to be examined a colloidal metallic oxide non-reactive as regards said substance so as to obtain a conglomerate of strong electron-optical contrasts containing in juxtaposition particles of said substance and colloidal oxide particles, subjecting said conglomerate to electron-microscopical magnification, and adjusting the magnification by focusing the magnified image on the contrasts of the conglomerate.

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  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
US321237A 1938-09-16 1940-02-28 Method of focusing electron microscopes Expired - Lifetime US2256171A (en)

Applications Claiming Priority (1)

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DE2256171X 1938-09-16

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US2256171A true US2256171A (en) 1941-09-16

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US321237A Expired - Lifetime US2256171A (en) 1938-09-16 1940-02-28 Method of focusing electron microscopes

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US (1) US2256171A (en, 2012)
NL (1) NL56609C (en, 2012)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3536911A (en) * 1967-09-25 1970-10-27 Fritz Grasenick Apparatus for preparing embedded specimens for examination with an optical or electron microscope

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3536911A (en) * 1967-09-25 1970-10-27 Fritz Grasenick Apparatus for preparing embedded specimens for examination with an optical or electron microscope

Also Published As

Publication number Publication date
NL56609C (en, 2012)

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