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Beta detectors

Early measurements of " Th were on seawater samples and Th was co-precipitated from 20-30 L of seawater with iron hydroxide (Bhat et al. 1969). This procedure may not recover all of the " Th in the sample, and an alpha emitting Th isotope (e g., °Th or Th) is added as a yield monitor. Following chemical purification of the Th fraction by ion exchange chromatography, the Th is electrodeposited onto platinum or stainless steel planchets. The planchets are then counted in a low background gas-flow beta detector to measure the beta activity and subsequently with a silicon surface barrier detector to determine the alpha activity of the yield monitor. The " Th activity is thus determined as ... [Pg.462]

Droullard, R.F. and Holub, R.F., Continuous Working Level Measurements Using Alpha or Beta Detectors, BuMines, RI 8237, p 14 (1977). [Pg.378]

Sources for calibration of beta detectors as standard sources are characterised in terms of emerging P emission flux in 4ti sr solid angle, expressed in s. Intended for the... [Pg.103]

Table 4.12 Sources for calibration of beta detectors Chapter 4... [Pg.104]

Mount the filter containing the CSjPtClg on the ring and disc holder as shown in Fig. 5.44. Count the sample using a low background beta detector or by gamma spectrometry. [Pg.199]

A beta detector consisting of a small semiconducting wafer of CdTe at the outlet of the capillaiy will respond to labeled beta emitters. 1 O M solutions of compounds containing have been reported. [Pg.369]

Th itself decays with relatively weak betas (maximum beta energy 0.20 MeV) to 234mpa which is a high-energy beta emitter (maximum beta energy 2.29 MeV, half-life 1.17 min). Thus, if a filter is dried and carefully folded (possible with polycarbonate, e.g.. Nude-pore filters, not with membrane filters, which will break) to fit the beta detector holder and covered with a thin foil, the activity measured is due mainly to Pa, with some contribution from Th. [Pg.377]

Noble gas monitoring. There are a number of systems for noble gas monitoring. In the most frequently used system, the air is filtered (to remove vapour and particles) and then passed through a large volume shielded chamber with a sensitive gamma or beta detector inside. The filtered gas may also be passed directly through an ionization chamber or a proportional counter. These systems should be calibrated with known concentrations of suitable radionuclides. [Pg.64]

It was found that that in the case of soft beta and X-ray radiation the IPs behave as an ideal gas counter with the 100% absorption efficiency if they are exposed in the middle of exposure range ( 10 to 10 photons/ pixel area) and that the relative uncertainty in measured intensity is determined primarily by the quantum fluctuations of the incident radiation (1). The thermal neutron absorption efficiency of the present available Gd doped IP-Neutron Detectors (IP-NDs) was found to be 53% and 69%, depending on the thicknes of the doped phosphor layer ( 85pm and 135 pm respectively). No substantial deviation in the IP response with the spatial variation over the surface of the IP was found, when irradiated by the homogeneous field of X-rays or neutrons and deviations were dominated by the incident radiation statistics (1). [Pg.507]

The most widely used experimental method for determining surface excess quantities at the liquid-vapor interface makes use of radioactive tracers. The solute to be studied is labeled with a radioisotope that emits weak beta radiation, such as H, C, or One places a detector close to the surface of the solution and measures the intensity of beta radiation. Since the penetration range of such beta emitters is small (a ut 30 mg/cm for C, with most of the adsorption occurring in the first two-tenths of the range), the measured radioactivity corresponds to the surface region plus only a thin layer of solution (about 0.06 mm for C and even less for H). [Pg.77]

Alpha counting is done with an internal proportional counter or a scintiUation counter. Beta counting is carried out with an internal or external proportional gas-flow chamber or an end-window Geiger-MueUer tube. The operating principles and descriptions of various counting instmments are available, as are techniques for determining various radioelements in aqueous solution (20,44). A laboratory manual of radiochemical procedures has been compiled for analysis of specific radionucHdes in drinking water (45). Detector efficiency should be deterrnined with commercially available sources of known activity. [Pg.233]

A beta attenuation sampler uses a 30-mCi Krypton-85 source (with energy of 0.74 MeV) and detector to determinate the attenuation caused by deposited aerosols on a moving filter. lb improve the stability over time, a refiertticc reading is period-icallv made of a foil with attenuation similar to that of the Alter and collected aerosol. [Pg.1290]

Electron Capture Detector In the electron capture detector (ECD), a beta emitter such as tritium or 63Ni is used to ionize the carrier gas. Electrons from the ionization migrate to the anode and produce a steady current. If the GC effluent contains a compound that can capture electrons, the current is reduced because the resulting negative ions move more slowly than electrons. Thus, the signal measured is the loss of electrical current. The ECD is very sensitive to materials that readily capture electrons. These materials frequently have unsaturation and electronegative substituents. Because the ECD is sensitive to water, the carrier gas must be dry. [Pg.11]

Instrumentation. Traditional methods of alpha and beta spectrometry instrumentation have changed little over the past decade. Alpha spectrometric methods typically rely on semi-conductor or lithium-drifted silicon detectors (Si(Li)), or more historically gridded ion chambers, and these detection systems are still widely used in various types of uranium-series nuclide measurement for health, environmental, and... [Pg.30]

In contrast to the other ionization detectors a decrease in the detector background current is measured rather than an increase in the number of ions or electrons generated. The detector standing current results from the bombardment of the carrier gas by beta electrons forming a plasma of positive ions. [Pg.141]

Light-silver-colored element generated from a plutonium isotope (241Pu) by beta decay. Never detected in nature. Chemically similar to Europium. A few tons have been produced throughout the world through regeneration of fuel rods. Americium is a good source of alpha rays. Hence it is suitable to measure thicknesses, as a detector in smoke alarms, and for the activation analysis of the tiniest amounts of substances. [Pg.156]

Gotti et al. [42] reported an analytical study of penicillamine in pharmaceuticals by capillary zone electrophoresis. Dispersions of the drug (0.4 mg/mL for the determination of (/q-penicillaminc in water containing 0.03% of the internal standard, S -met hy I - r-cystei ne, were injected at 5 kPa for 10 seconds into the capillary (48.5 cm x 50 pm i.d., 40 cm to detector). Electrophoresis was carried out at 15 °C and 30 kV, with a pH 2.5 buffer of 50 mM potassium phosphate and detection at 200 rnn. Calibration graphs were linear for 0.2-0.6 pg/mL (detection limit = 90 pM). For a more sensitive determination of penicillamine, or for the separation of its enantiomers, a derivative was prepared. Solutions (0.5 mL, final concentration 20 pg/mL) in 10 mM phosphate buffer (pH 8) were mixed with 1 mL of methanolic 0.015% 1,1 -[ethylidenebis-(sulfonyl)]bis-benzene and, after 2 min, with 0.5 mL of pH 2.5 phosphate buffer. An internal standard (0.03% tryptophan, 0.15 mL) was added and aliquots were injected. With the same pH 2.5 buffer and detection at 220 nm, calibration graphs were linear for 9.3-37.2 pg/mL, with a detection limit of 2.5 pM. For the determination of small amounts of (L)-penicillamine impurity, the final analyte concentration was 75 pg/mL, the pH 2.5 buffer contained 5 mM beta-cyclodextrin and 30 mM (+)-camphor-10-sulfonic acid, with a voltage of 20 kV, and detection at 220 nm. Calibration graphs were linear for 0.5-2% of the toxic (L)-enantiomer, with a detection limit of 0.3%. [Pg.141]

Gas-filled detectors are used, for the most part, to measure alpha and beta particles, neutrons, and gamma rays. The detectors operate in the ionization, proportional, and G-M regions with an arrangement most sensitive to the type of radiation being measured. Neutron detectors utilize ionization chambers or proportional counters of appropriate design. Compensated ion chambers, BF3 counters, fission counters, and proton recoil counters are examples of neutron detectors. [Pg.41]

The alpha curve is higher than the beta curve from Region I to part of Region IV due to the larger number of ion pairs produced by the initial reaction of the incident radiation. Detector voltage principles are summarized below. [Pg.42]

To a limited degree, the fill-gas will determine what type of radiation the proportional counter will be able to detect. Argon and helium are the most frequently used fill gases and allow for the detection of alpha, beta, and gamma radiation. When detection of neutrons is necessary, the detectors are usually filled with boron-triflouride gas. [Pg.43]

If a radioactive source that is an emitter of beta particles is placed near the detector, the beta particles will pass between the plates and strike atoms in the air. With sufficient energy, the beta particle causes an electron to be ejected from an atom in air. A single beta particle may eject 40 to 50 electrons for each centimeter of path length traveled. The electrons ejected by the beta particle often have enough energy to eject more electrons from other atoms in air. The total number of electrons produced is dependent on the energy of the beta particle and the gas between the plates of the ionization chamber. [Pg.53]

When using an ionization chamber for detecting neutrons, beta particles can be prevented from entering the chamber by walls thick enough to shield out all of the beta particles. Gamma rays cannot be shielded from the detector therefore, they always contribute to the total current read by the ammeter. This effect is not desired because the detector responds not only to neutrons, but also to gamma rays. Several ways are available to minimize this problem. [Pg.56]


See other pages where Beta detectors is mentioned: [Pg.183]    [Pg.1585]    [Pg.183]    [Pg.77]    [Pg.82]    [Pg.183]    [Pg.1585]    [Pg.183]    [Pg.77]    [Pg.82]    [Pg.509]    [Pg.570]    [Pg.643]    [Pg.443]    [Pg.391]    [Pg.108]    [Pg.1291]    [Pg.392]    [Pg.93]    [Pg.66]    [Pg.63]    [Pg.464]    [Pg.142]    [Pg.369]    [Pg.656]    [Pg.656]    [Pg.657]    [Pg.475]    [Pg.82]    [Pg.123]    [Pg.38]    [Pg.41]    [Pg.67]   
See also in sourсe #XX -- [ Pg.82 ]




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