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WHAT TO DETECT

Perhaps the place to begin in a book about trace chemical sensing of explosives is to define trace and explosive. If trace is defined as a submilligram quantity, then it should be noted that there are no chemicals that are explosive at trace levels. To clarify this point we need to elaborate on what makes a chemical an explosive. An energetic material is defined as one that releases energy upon decomposition. This material could be an explosive, a propellant, a pyrotechnic, or a fruit cocktail. For an energetic material to be an explosive chemical or composition its must be capable of undergoing decomposition with extremely [Pg.35]

Trace Chemical Sensing of Explosives, Edited by Ronald L. Woodfin Copyright 2007 John Wiley Sons, Inc. [Pg.35]

With the size requirement in mind, let us consider the types of materials that may be explosive. The U.S. Department of Transportation (DoT) provides some guidance, specifying characteristics that, if met, require a material to be screened for explosive performance (see Table 2.2). [Pg.36]

Materials that typically fall in the explosive category are those where oxygen is incorporated within the molecule in nitro (NO2) groups. The presence of oxygen [Pg.36]

OR if its exothermic energy 500 J/g and onset below 500°C, then it must undergo DoT series one testing. [Pg.36]


Chapter 2 What To Detect Serving as a refresher in the chemistry of explosives, this chapter provides a basis for considering what molecules we may need to seek. [Pg.389]

Because of the large thickness x-rayed by high-current betatron (more than 1500 ram on plastic) the picture of defect situated near the front wall of the sample is too increased what makes difficult to detect in practice real dimensions of the defect. But there is a possibility of stereosurvey due to existence of two radiation beams simultaneously generated by betatron. [Pg.514]

It is not certain that all the effects of DES can be ascribed to its oestrogenic activity (that is to say, directly related to its ability to bind to the oestrogen receptor), but it would appear from experience with this compound that rodent assays are able to detect the relevant toxicological effects. What then was the... [Pg.2]

What systems can be used to detect and prevent grain dust explosions ... [Pg.522]

The measurement of efficiency is important, as it is used to monitor the quality of the column during use and to detect any deterioration that might take place. However, to measure the column efficiency, it is necessary to identify the position of the points of inflection which will be where the width is to be measured. The inflection points are not easily located on a peak, so it is necessary to know at what fraction of the peak height they occur, and the peak width can then be measured at that height. [Pg.182]

In order to detect incomplete requirements you either need experts on tap or checklists to refer to. It is often easy to comment on what has been included but difficult to imag-... [Pg.248]

What sources of information are used to detect, analyze, and eliminate potential causes of nonconformity ... [Pg.471]

Importance also applies to what may appear minor decisions in the planning or design phase. If such decisions are incorrect they could result in major problems downstream. If not detected, getting the decimal place wrong or the units of measure wrong can have severe consequences. Audits should verify that the appropriate controls are in place to detect such errors before it is too late. [Pg.516]

In practice it is usually possible to detect an indicator color change over a range of about two pH units. Consider, for example, what happens with bromthymol blue as the pH... [Pg.393]

What about the state of equilibrium for the reaction represented by equation (11)1 Let us place a strip of metallic copper in a zinc sulfate solution. No visible reaction occurs and attempts to detect the presence of cupric ion by adding H2S to produce the black color of cupric sulfide, CuS, fail. Cupric sulfide has such low solubility that this is an extremely sensitive test, yet the amount of Cu+2 formed cannot be detected. Apparently the state of equilibrium for the reaction (11) greatly favors the products over the reactants. [Pg.205]

Radiopharmaceuticals have one of two general functions (1) they may be used to detect or image biological problems such as tumors and (2) they may be used to treat an illness. Which type of radiation (a, p, or y) would be the most suitable for (a) detection and (b) therapy Justify your selections, (c) From standard literature sources, find at least two radionuclides that have been used for imaging body tissues, (d) What are the half-lives of these radionuclides ... [Pg.846]

Remember that the aim is to detect amplitude in the range 10 to 10 , so values given in Eq. (37) are the low limits of what is required. From this last equation we can draw some conclusions. We have only three parameters to play with to lower the photon shot noise arm length, laser power and integration time. [Pg.320]

The yellow disulfide radical anion and the briUiant blue trisulfide radical anion often occur together for what reason some authors of the older Hterature (prior to 1975) got mixed up with their identification. Today, both species are well known by their E8R, infrared, resonance Raman, UV-Vis, and photoelectron spectra, some of which have been recorded both in solutions and in solid matrices. In solution these radical species are formed by the ho-molytic dissociation of polysulfide dianions according to Eqs. (7) and (8). 8ince these dissociation reactions are of course endothermic the radical formation is promoted by heating as well as by dilution. Furthermore, solvents of lower polarity than that of water also favor the homolytic dissociation. However, in solutions at 20 °C the equilibria at Eqs. (7) and (8) are usually on the left side (excepting extremely dilute systems) and only the very high sensitivity of E8R, UV-Vis and resonance Raman spectroscopy made it possible to detect the radical anions in liquid and solid solutions see above. [Pg.145]

Luminescence measurements on proteins occupy a large part of the biochemical literature. In what surely was one of the earliest scientific reports of protein photoluminescence uncomplicated by concurrent insect or microorganism luminescence, Beccari (64), in 1746, detected a visible blue phosphorescence from chilled hands when they were brought into a dark room after exposure to sunlight. Stokes (10) remarked that the dark (ultraviolet) portion of the solar spectrum was most efficient in generating fluorescent emission and identified fluorescence from animal matter in 1852. In general, intrinsic protein fluorescence predominantly occurs between 300 nm and 400 nm and is very difficult to detect visually. The first... [Pg.9]

Equation (8.29) provides no guarantee of stability. It is a necessary condition for stability that is imposed by the discretization scheme. Practical experience indicates that it is usually a sufficient condition as well, but exceptions exist when reaction rates (or heat-generation rates) become very high, as in regions near thermal runaway. There is a second, physical stability criterion that prevents excessively large changes in concentration or temperature. For example. An, the calculated change in the concentration of a component that is consumed by the reaction, must be smaller than a itself Thus, there are two stability conditions imposed on Az numerical stability and physical stability. Violations of either stability criterion are usually easy to detect. The calculation blows up. Example 8.8 shows what happens when the numerical stability limit is violated. [Pg.277]

Do the simple ANOVA test (Section 1.5.6) to detect variability between the group means in excess of what is expected due to chance alone. [Pg.55]

UV irradiation was used as a confirmation technique on any peak suspected of being TCDD ( 0.2 min) no TCDD could be detected at less than 1 ppb. The question then arises, what level of contamination had to be present in the original 2,4,5-T to detect 1 ppb TCDD in soil. [Pg.114]

This equation says that a nitrogen nucleus is composed of seven protons and seven neutrons. An alpha particle, which is identical to a helium ion, has two protons and two neutrons. A highly energetic collision fuses the two nuclei. The result is a rare isotope of oxygen with eight protons and nine neutrons. The leftover proton is ejected. And that proton is what Rutherford detected. [Pg.36]


See other pages where WHAT TO DETECT is mentioned: [Pg.35]    [Pg.36]    [Pg.37]    [Pg.38]    [Pg.39]    [Pg.40]    [Pg.35]    [Pg.36]    [Pg.37]    [Pg.38]    [Pg.39]    [Pg.40]    [Pg.1990]    [Pg.2479]    [Pg.358]    [Pg.8]    [Pg.108]    [Pg.442]    [Pg.52]    [Pg.23]    [Pg.29]    [Pg.549]    [Pg.230]    [Pg.400]    [Pg.178]    [Pg.59]    [Pg.253]    [Pg.453]    [Pg.381]    [Pg.98]    [Pg.457]    [Pg.152]    [Pg.89]    [Pg.139]    [Pg.663]    [Pg.479]    [Pg.4]    [Pg.90]   


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