Neutron activation process, instrumental

Chemically pure reagents were used. Cadmium was added as its sulfate salt in concentrations of about 50 ppm. Lanthanides were added as nitrates. For the experiments with other metal ions so-called "black acid from a Nissan-H process was used. In this acid a large number of metal ions were present. To achieve calcium sulfate precipitation two solutions, one consisting of calcium phosphate in phosphoric acid and the other of a phosphoric acid/sulfuric acid mixture, were fed simultaneously in the 1 liter MSMPR crystallizer. The power input by the turbine stirrer was 1 kW/m. The solid content was about 10%. Each experiment was conducted for at least 8 residence times to obtain a steady state. During the experiments lic iid and solid samples were taken for analysis by ICP (Inductively Coupled Plasma spectrometry, based on atomic emission) and/or INAA (Instrumental Neutron Activation Analysis). The solid samples were washed with saturated gypsum solution (3x) and with acetone (3x), and subsequently dried at 30 C. The details of the continuous crystallization experiments are given in ref. [5]. 

Table I. Instrumental Neutron Activation Analysis (n,y) Process"...

GINAA Cyclic instrumental neutron activation analysis is used to determine very short lived isotopes. The sample is irradiated for a short time, rapidly transferred to a detector for counting the entire process repeated for a number of cycles with the gamma-ray spectrum recorded from each cycle accumulated to yield a cumulative spectrum. 

Several investigators have used neutron activation analysis (NAA) to determine the aluminium content of biological specimens both with and without some chemical processing. Instrumental neutron activation analysis involves the bombardment of a sample with neutrons and the measurement of the radioactivity induced by nuclear reactions. No chemical processing is required. Upon activation Al (100% isotopic abundance) forms the radioactive AI nuclide by a (n,y) reaction. There are a number of attractive features in this technique which include excellent sensitivity with relative independence from matrix effects and interferences. Also, there is relative freedom from contamination since the sample is analyzed directly with minimal handling. One major problem is the need to... 

Linekin, D.M. (1973) Multielement instrumental neutron activation analysis of biological tissue using a single comparator standard and data processing by computers. Int. J. Appl. Rad. Isotopes, 24,343-351. 

Other major shale constituents such as C, H, N, and S are determined by thermal decomposition and instrumental detection methods. Oxygen is determined by 14 MeV neutron activation analysis. Parr or Leco BTU bomb combustion and subsequent ion chromatographic determination is used for halogens, sulfate and nitrate. Ion chromatography is also suitable for anionic characterization of shale process waters. Two analytical procedures for oil shales should be used with caution. Kjeldahl nitrogen procedure has been found to give reproducible but considerably low results for certain oil... 

See also Activation Analysis Neutron Activation. Atomic Absorption Spectrometry Principles and Instrumentation. Atomic Emission Spectrometry Principles and Instrumentation. Chromatography Overview Principles. Gas Chromatography Pyrolysis Mass Spectrometry. Headspace Analysis Static Purge and Trap. Infrared Spectroscopy Near-Infrared Industrial Applications. Liquid Chromatography Normal Phase Reversed Phase Size-Exclusion. Microscopy Techniques Scanning Electron Microscopy. Polymers Natural Rubber Synthetic. Process Analysis Chromatography. Sample Dissolution for Elemental Analysis Dry... 

The safe and verifiable disposition, either by incineration or chemical neutralization of chemical warfare (CW) agents requires correct a priori identification of each munition or container to be processed. A variety of NDE techniques have been used or tested for the examination and characterization of munitions.[l,2] In the U.S., three widely used techniques are X-ray radiography, acoustic resonance spectroscopy (ARS), and prompt gamma ray neutron activation analysis (PINS). The technical bases, instrumental implementations, and applications of the U.S. versions of these methods are briefly discussed. 

The interaction of hydrogen chloride with alumina was also investigated with the same instruments. Changes in the surface hydroxyl groups 29b) were observed that were directly correlated with the active sites. The combination of information from the TOSCA and MARI neutron scattering spectrometers to solve problems in surface chemistry is a powerful method that will undoubtedly be exploited further. It is through an improved awareness of reactant-catalyst interactions that increased efficiencies of industrial chemical processes can be recognized and realized. 

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