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Decay during sampling time

To measure the volume of the blood in an animal s circulatory system, the following experiment was performed. A 5.0-mL sample of an aqueous solution containing 1.7 X 105 counts per minute (cpm) of tritium was injected into the bloodstream. After an adequate period of time to allow for the complete circulation of the tritium, a 5.0-mL sample of blood was withdrawn and found to have 1.3 X 103 cpm on the scintillation counter. Assuming that only a negligible amount of tritium has decayed during the experiment, what is the volume of the animals circulatory system ... [Pg.532]

There are certain unique features to the chemical separations used in radiochemistry compared to those in ordinary analytical chemistry that are worth noting. First of all, high yields are not necessarily needed, provided the yields of the separations can be measured. Emphasis is placed on radioactive purity, expressed as decontamination factors rather than chemical purity. Chemical purity is usually expressed as the ratio of the number of moles (molecules) of interest in the sample after separation to the number of all the moles (molecules) in the sample. Radioactive purity is usually expressed as the ratio of the activity of interest to that of all the activities in the sample. The decontamination factor is defined as the ratio of the radioactive purity after the separation to that prior to the separation. Decontamination factors of 105-107 are routinely achieved with higher values possible. In the event that the radionuclide(s) of interest are short-lived, then the time required for the separation is of paramount importance, as it does no good to have a very pure sample in which most of the desired activity has decayed during the separation. [Pg.583]


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Decay time

Sample-time

Sampling time

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