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Source materials, analyses possible

Still and so far, the analysis of the most important odorous substances in materials (unfortunately not always) by means of GC—O has revealed much useful knowledge on material odorants, possible sources and starting points for odor minimization and product improvement (Mayer and Breuer, 2004a, 2004b, 2005, 2006). [Pg.176]

Instrumental neutron activation analysis was used to determine concentrations of several major and trace elements in samples of heavily corroded residues found in crucible fragments excavated at Tel Dan, Israel. The residues were mostly hard, metallic phases admixed with nonmetallic inclusions that appeared to be ceramic material from the loose porous interior of the crucible itself The objective was to identify the metals that had been melted in these crucibles. A method is described that attempts to separate nonmetallic and metallic phase data. In comparison to previous reports on analyses of source materials thought to have been used at Dan in this period (Late Bronze II Age-Early Iron I Age 1400-1000 B.C.), high gold concentrations were found. These appear to be correlated to arsenic and antimony concentrations. This finding is discussed in relation to possible changes in the source of tin at this period. [Pg.199]

Bitumen Sources. Analyses of possible source materials are given in Table VIII. The seepages of Hit and such bitumen lakes as Abu Gir are the traditional sources for asphalts of the cities of lower Mesopotamia. Despite repeated attempts, samples could not be obtained for analysis. [Pg.165]

The intention has been to achieve a balance between sufficient mathematical analysis and as much practical material as possible. An emphasis has been put on the users point of view because the user needs to know, or be able to find out quickly, the information that is of immediate application in the design of a plant. The subjects described are those most frequently encountered by electrical engineers in the oil industry. References are frequently made to other texts, published papers and international standards for guidance and as sources of further reading material. [Pg.630]

From the perspective of radiation damage studies, it is important to characterise the effect of irradiation rather than provide a comprehensive description of all microstructural features. Consequently, for each irradiated material examined it is useful to characterise an unirradiated sample of the same material so that the difference in scattering response can be used to assess directly the effect of irradiation. Typically, samples are 10 x 10 x 2mm These are simple to fabricate from Charpy specimens (10 x 10 x 55 mm ) and are sufficiently thick to enable a statistically significant number of neutrons to scatter and be detected. Use of thinner samples will result in a smaller fraction of the incident neutrons scattering but, with modem high flux neutron sources, SANS analysis of these thinner samples is perfectly possible. [Pg.224]

Although the source of raw materials may not be at the plant site, it is an e.xtremcly important factor in the ultimate location of the plant. Process development work and economic studies will indicate the minimum standards for raw materials selection. When these standards have been determined, all possible sources of acceptable raw materials can be located and a detailed analysis can proceed. [Pg.163]

This section will deal briefly with some aspects of expls safety peculiar to neutron activation analysis expts. We are concerned here with a) the possible effect of the ionizing radiation dose on the energetic material which will cause it to be more sensitive or hazardous to normal handling as an expl, and b) the potential direct expl hazards involved in the physical and mechanical transportation of samples to and horn the irradiation source and in a nuclear counting system... [Pg.387]

One approach to the problem of matrix effects is to prevent the matrix materials reaching the electrospray source by carrying out some form of clean-up prior to analysis and/or to employ chromatographic separation. It is not always possible, however, to develop a simple procedure for sample clean-up and since this approach involves further work-up with the associated increase in analysis time and potential for sample loss it is therefore not ideal. [Pg.271]

There are also several possibilities for the temporal distribution of releases. Although some releases, such as those stemming from accidents, are best described as instantaneous release of a total amount of material (kg per event), most releases are described as rates kg/sec (point source), kg/sec-m (line source), kg/sec-m (area source). (Note here that a little dimensional analysis will often indicate whether a factor or constant in a fate model has been inadvertently omitted.) The patterns of rates over time can be quite diverse (see Figure 3). Many releases are more or less continuous and more or less uniform, such as stack emissions from a base-load power plant. Others are intermittent but fairly regular, or at least predictable, as when a coke oven is opened or a chemical vat... [Pg.10]


See other pages where Source materials, analyses possible is mentioned: [Pg.280]    [Pg.241]    [Pg.79]    [Pg.615]    [Pg.22]    [Pg.419]    [Pg.699]    [Pg.1236]    [Pg.136]    [Pg.852]    [Pg.1001]    [Pg.280]    [Pg.675]    [Pg.27]    [Pg.308]    [Pg.1167]    [Pg.63]    [Pg.187]    [Pg.225]    [Pg.517]    [Pg.477]    [Pg.208]    [Pg.259]    [Pg.745]    [Pg.271]    [Pg.253]    [Pg.253]    [Pg.178]    [Pg.130]    [Pg.208]    [Pg.66]    [Pg.91]    [Pg.422]    [Pg.934]    [Pg.410]    [Pg.412]    [Pg.516]    [Pg.22]    [Pg.49]    [Pg.153]    [Pg.611]   
See also in sourсe #XX -- [ Pg.164 , Pg.165 ]




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Source analysis

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