Algae, Tree, Herbs, Bush, Shrub, Grasses, Vines, Fern, Moss, Spermatophyta, Bryophyta, Fern Ally, Flower, Photosynthesis, Eukaryote, Prokaryote, carbohydrate, vitamins, amino acids, botany, lipids, proteins, cell, cell wall, biotechnology, metabolities, enzymes, agriculture, horticulture, agronomy, bryology, plaleobotany, phytochemistry, enthnobotany, anatomy, ecology, plant breeding, ecology, genetics, chlorophyll, chloroplast, gymnosperms, sporophytes, spores, seed, pollination, pollen, agriculture, horticulture, taxanomy, fungi, molecular biology, biochemistry, bioinfomatics, microbiology, fertilizers, insecticides, pesticides, herbicides, plant growth regulators, medicinal plants, herbal medicines, chemistry, cytogenetics, bryology, ethnobotany, plant pathology, methodolgy, research institutes, scientific journals, companies, farmer, scientists, plant nutrition
Select Language:
 
 
 
 
Main Menu
Please click the main subject to get the list of sub-categories
 
Services offered
 
 
 
 
  Section: Practical Skills in Chemistry » Instrumental techniques
 
 
Please share with your friends:  
 
 

Radioactive decay

 
     
 
Content
Instrumental techniques
  Basic spectroscopy
    Introduction to spectroscopy
    UV Ivisible spectrophotometry
    Fluorescence
    Fluorescence spectrophotometry
    Phosphorescence and luminescence
    Atomic spectroscopy
  Atomic spectroscopy
    Atomic Absorption Spectroscopy
    Atomic Emission Spectroscopy
    Inductively coupled plasma
    Decomposition techniques for solid inorganic samples
  Infrared spectroscopy
  Nuclear magnetic resonance spectrometry
    1H-NMR spectra
    13C-NMR spectra
  Mass spectrometry
    Interfacing mass spectrometry
  Chromatography ~ introduction
    The chromatogram
    Resolution
    Detectors
  Gas and liquid chromatography
    Gas chromatography
    Liquid chromatography
    High-performance liquid chromatography
    Interpreting chromatograms
    Optimizing chromatographic separations
    Quantitative analysis
  Electrophoresis
    The supporting medium
    Capillary electrophoresis
    Capillary zone electrophoresis (CZE)
    Micellar electrokinetic chromatography (MEKC)
  Electroanalytical techniques
    Potentiometry and ion-selective electrodes
    Voltammetric methods
    Oxygen electrodes
    Coulometric methods
    Cyclic voltammetry
  Radioactive isotopes and their uses
    Radioactive decay
    Measuring radioactivity
    Chemical applications for radioactive isotopes
    Working practices when using radioactive isotopes
  Thermal analysis
    Thermogravimetry
    Applications

There are three forms of radioactivity (Table 35.1) arising from three main types of nuclear decay:

Types of radioactivity and their properties
Table 35.1 Types of radioactivity and their properties
*Note that 1MeV = 1.6 × 10−13 J.
**Distance at which radiation intensity is reduced to half.
  • Alpha decay involves t
    he loss of a particle equivalent to a helium nucleus. Alpha (α) particles, being large and positively charged, do not penetrate far in living tissue, but they do cause ionization damage and this makes them generally unsuitable for tracer studies.
  • Beta decay involves the loss or gain of an electron or its positive counterpart, the positron. There are three sub-types:
    1. Negatron (β) emission: loss of an electron from the nucleus when a neutron transforms into a proton. Examples of negatron-emitting isotopes are: 3H, 14C, 32P, 45Ca and 60Co.
    2. Positron (β) emission: loss of a positron when a proton transforms into a neutron. This only occurs when sufficient energy is available from the transition and may involve the production of gamma rays when the positron is later annihilated by collision with an electron.
    3. Electron capture (EC): when a proton 'captures' an electron and transforms into a neutron. This may involve the production of x-rays as electrons 'shuffle' about in the atom (as with 125I) and it frequently involves electron emission.
  • Internal transition involves the emission of electromagnetic radiation in the form of gamma (γ) rays from a nucleus in a met astable state and always follows initial alpha or beta decay. Emission of gamma radiation leads to no further change in atomic number or mass.
Note from the above that more than one type of radiation may be emitted when a radioisotope decays. The main radioisotopes used in chemistry and their properties are listed in Table 35.2.

Each radioactive particle or ray carries energy, usually measured in electron volts (eV). The particles or rays emitted by a particular radioisotope exhibit a range of energies, termed an energy spectrum, characterized by the maximum energy of the radiation produced, Emax (Table 35.2).

Properties of selected isotopes
Table 35.2 Properties of selected isotopes

The energy spectrum of a particular radioisotope is relevant to the following:
  • Safety: isotopes with the highest maximum energies will have the greatest penetrating power, requiring appropriate shielding (Table 35.1).
  • Detection: different instruments vary in their ability to detect isotopes with different energies.
  • Discrimination: some instruments can distinguish between isotopes, based on the energy spectrum of the radiation produced.
The decay of an individual atom (a 'disintegration') occurs at random, but that of a population of atoms occurs in a predictable manner. The radioactivity decays exponentially, having a characteristic half-life (t½). This is the time taken for the radioactivity to fall from a given value to half that value (Fig. 35.1). The tuz values of different radioisotopes range from fractions of a second to more than 1019 years (see also Table 35.2). If t½ is very short, as with 15O (t½ ≈ 2min), then it is generally impractical to use the isotope in experiments because you would need to account for the decay during the experiment and counting period.
 
Fig. 35. 1 Decay of a radioactive isotope with
time. The time taken for the radioactivity to
decline from × to 0.5× is the same as the time taken for the radioactivity to decline from 0.5× to 0.25×, and so on. This time is the half-life (t½) of the isotope.

To calculate the fraction (f) of the original radioactivity left after a particular time (t), use the following relationship:
⇒ Equation [35.1] f = ex, where x = −0.693t/t½
Note that the same units must be used for t and t½ in the above equation.

 
     
 
 
     



     
 
Copyrights 2012 © Biocyclopedia.com | Disclaimer