2 edition of Spectrographic analysis utilizing a spark ray source. found in the catalog.
Spectrographic analysis utilizing a spark ray source.
Gerald Thomas Cameron
Written in English
|The Physical Object|
|Pagination||iv, 46 leaves ;|
|Number of Pages||46|
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The possibility of using the characteristic X-ray spectra for chemical analysis is as old as X-ray spectroscopy itself. In SIEGBAHN'S laboratory a number of demountable X-ray tubes and spectrographs were developed and some of these were used for chemical analysis by direct emission, notably by HADDING[I], GOLDSCHMIDT , and VON HEVESYfS].Cited by: EPA-R INSTRUMENTATION FOR MONITORING SPECIFIC PARTICULATE SUBSTANCES IN STATIONARY SOURCE EMISSIONS by John V.
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The. U.S. PATENT AND TRADEMARK OFFICE Information Products Division: Index to the U.S. Patent Classification System Entries as of J The spark generation mechanism for generating ions for spark-source mass spectrometry (SSMS) is well described in the literature Sharkey et al.,Carter et al.,Carter et al., In this method, the spark is produced by ignition between two conductors in a vacuum with a pulsed high frequency potential of 50 by: Spectrographic Analysis of Trace Elements in Aluminum Oxide Matrices, by J.
Fitzgerald, document AFCRL, January, Anisotropic Plasma-Covered Magnetic Line Source, by R. Shore and G. Meltz, document AFCRL, February, Unfortunately, this book can't be printed from the OpenBook.
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This banner text can have markup. web; books; video; audio; software; images; Toggle navigation. Paulsen, R. Alvarez, and C. Mueller, Spark source mass spectrographic analysis of ingot iron for Ag, Cu, Mo, and Ni by isotope dilution and for Co by an internal standard technique, Anal. Chem.
42, – (). CrossRef Google ScholarCited by: 1. under the title Spectrographic Analysis of Plants and Soils. Mitchell has spent short periods in the spectrochemical labora tories of Dr. Mannkopff in Gottingen and Professor Lundegardh in Stock holm, and has attended international conferences dealing with soils, plants, geochemistry and analytical chemistry.
In the fall of he attended. Direct spectrographic analysis for platinum, palladium and rhodium in gold beads from fire assay Applied Spectroscopy, vol 24 Application of an ion-selective electrode method to the determination of chloride in 41 international geochemical reference materials Geostandards Newsletter, vol 11 Fishman, Marvin J., and.
Computer-aided analysis of gamma-ray spectrometer data /, by P. Read, F. Tomnovec, and issuing body U.S. Naval Radiological Defense Laboratory (page images at HathiTrust) Computer-aided building design: study / ([Washington]: General Accounting Office, ), by United States General Accounting Office (page images at HathiTrust).
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For the species tested, it showed an increase in Ca of % corresponding to an equivalent decrease in K, which confirmed the correlation between the two elements. FIGURE 9 ~ Analysis of K and Ca by X-Ray.
Direct-current arc and alternating-current spark emission spectrographic field methods for the semiquantitative analysis of geologic materials Method for the quantatative spectrographic analysis of rocks, minerals, ores, and other materials by a powder d-c arc technique X-ray modal analysis of felsic rocks.
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inert gases for spark analysis, and still another a fusion tech nique and its advantages in homogenizing samples. But almost half, bearing nearly identical generic titles, "The Determination of-in-", told of the specific problems faced by the authors and went on to describe the conditions applied for their solu tions.
Over the last 25 years ICP-OES spectrometers, also known as ICP-AES or ICP plasma spectrometers, have become an indispensable tool for chemical elemental analysis. Optical emission spectrometers with inductively coupled plasma (ICP plasma) excitation sources offer ease of use, high sensitivity and precision and relative freedom from interferences.
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used a spark source. An obvious source for calibration standards is a laboratory analysis of samples from the stream to be analyzed. Not so obvious is the necessity for obtaining the samples (more than one) at the same sample point and under the same conditions with special attention to the possibility of losses or changes.
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