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pulses in the range of counting rates differing by more than six orders of magnitude.

Passive systems of neutron coincidence counting allow determining the mass of plutonium by logging spontaneous-fission neutrons of mostly evennumbered isotopes (238Pu, 240Pu, 242Pu). With plutonium isotope composition known, the measurement result – 240Pueff mass – can be converted to the total Pu mass in the sample.

The fissionable isotope 235U does not go into spontaneous fission readily enough to be logged by passive systems. In this case, instruments will register secondary induced neutron radiation, which arises under exposure to neutrons of an AmLi source (active systems). For low-energy incident neutrons, the induced fission of 238U in a specimen makes an insignificant contribution to the measured rate of neutron coincidences.

Neutron coincidence counting systems have detectors of two major configurations: well-type detectors in which a specimen is fully enclosed and collar-type detectors embracing a specimen from the outside. The geometry of the former detectors is preferable as it is possible in this case to register all emitted neutrons. But the alternative collar-type geometry allows measuring specimens too large to be placed in a well-type detector (e.g., a fuel assembly). In its inspection activities, the IAEA employs neutron instruments of more than 20 types, which have various design features and are usable for specimens of certain sizes and forms and various Pu and U mass ranges. Some of them are presented in Table 3.5.

Table 3.5

Neutron coincidence logging instruments in use for determining the mass of fissionable material

Instrument

Instrument name

Application and features

designation

and type

 

 

Passive neutron coincidence counters

FAAS

Fuel

Meant for checking Pu mass in non-irradiated

 

assembly/Capsul

MOX fuel assemblies.

 

e Assay System

 

HLNC

High-Level

Meant for checking Pu mass (from 20 g to 2 kg)

 

Neutron

in bulk materials (pellets, powder, scrap, etc.).

 

Coincidence

 

 

Counter

 

INVS

Inventory

Meant for checking Pu mass (from 0.1 g to 300

 

Sample Counter

g) in samples. Instrument options for checking

 

 

Pu mass in glove boxes.

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Table 3.5 (continued)

 

 

 

 

Instrument

Instrument name

Application and features

 

designation

and type

 

 

 

 

 

Active neutron coincidence counters

 

AWCC

Active Well

Meant for checking 235U content in samples with

 

 

Coincidence

highly enriched uranium.

 

 

Counter

 

 

 

 

UNCL

Uranium

Meant for checking

235U content in low-

 

 

Neutron

 

enrichment fuel assemblies.

 

 

Coincidence

 

 

 

 

Collar

 

 

 

 

WCAS

Waste

Crate

Meant for checking

waste for presence of

 

 

Assay System

nuclear material.

 

 

Non-destructive testing of irradiated nuclear material. Methods of checking irradiated nuclear fuel involve logging of neutrons and gamma– quanta, as well as the Cerenkov ultraviolet glow. Fission products found in irradiated fuel set up a very high radiation background. It is mainly this fact that determines the type of instruments employed for verification of spent fuel.

The main sources of neutrons emitted by spent fuel are spontaneously fissionable 242Cm and 244Cm. These isotopes are generated in a reactor when neutrons are successively captured by the nuclei of transuranic elements. There are several approaches to logging spent fuel neutrons under conditions of intensive gamma background. It is possible, for example, to choose such detectors that either will be insensitive to gamma radiation, or will protect a neutron detector from penetration of gamma rays, while letting in neutrons. Table 3.6 lists some measurement systems in use by the Agency for examining reactors’ spent fuel.

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Table 3.6

 

Spent fuel testing instruments

 

 

 

 

Instrument

Instrument

Application and features

 

designation

name and

 

 

 

type

 

 

 

 

 

 

FDET

Fork Detector

The detector head contains neutron detectors

 

 

Irradiated

insensitive to gamma radiation (four gas-filled

 

 

Fuel

proportional fission counters) and two gas-filled

 

 

Measuring

ionization chambers to match strong gamma

 

 

System

radiation. The ratio between neutron and gamma

 

 

 

data together with additional information of

 

 

 

another sort allows getting an idea of the fluence

 

 

 

received, of the initial content of fissionable

 

 

 

material, and of the number of in-pile irradiation

 

 

 

cycles.

 

SFAT

Spent Fuel

The instrument includes a multichannel gamma–

 

 

Attribute

radiation analyzer and a NaIor CdZnTe-based

 

 

Tester

detector. It can accurately detect irradiated fuel by

 

 

 

identifying the characteristic lines from 137Cs and

 

 

 

144Pr fission products and 60Co as an activation

 

 

 

product. The instrument is particularly helpful in

 

 

 

situations where the Cerenkov effect analyzers are

 

 

 

not easily useable.

 

ICVD,

Cerenkov

ICVD is a hand-held instrument employed for

 

DCVD

Viewing

identification of irradiated fuel assemblies from,

 

 

Device,

mostly, light water reactors by analyzing the

 

 

Digital

Cerenkov effect. DCVD is a highly sensitive

 

 

Cerenkov

digital device for analyzing the Cerenkov effect. It

 

 

Viewing

is particularly suitable for fuel of low burnup after

 

 

Device

prolonged cooling.

 

Destructive analysis techniques. Destructive measurements practiced to determine the element and isotope composition are applicable to all forms of bulk material found at nuclear fuel cycle facilities. Such measurements enable the Agency:

∙ to make sure that there were no long-term diversions of materials covered by the safeguards;

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∙to verify the quality of working standards in use for calibration of nondestructive analysis instruments;

∙to carry out periodic verification of measurement systems at the inspected facility.

In general, destructive verification measurements carried out by the Agency include the following successive stages:

1)independent sampling;

2)in-situ conditioning of samples to ensure their integrity during transportation;

3)packaging, sealing and dispatch of samples to the IAEA laboratories;

4)statistical estimation of the analysis results.

The main analytical methods of destructive testing practiced by the Agency during inspections are listed in Table 3.7. This table presents the estimated random and systematic components of errors in measurements of materials of nuclear grade or similar chemical purity. It is obvious that the sampling process itself or the presence of impurities in material can tangibly affect the data of Table 3.7.

 

 

 

 

 

Table 3.7

 

Main destructive analysis methods in use by the IAEA

 

 

 

 

 

 

 

 

 

 

Method

Measured

Type of

Error,

 

 

 

quantity

material

( % rel.), random

 

 

 

 

analyzed

and systematic

 

 

 

Element analysis

 

 

 

Potentiometric titration

 

U, U–Pu, U–Th a)

 

 

 

of U (Davis–Gray

U

0.05

0.05

 

method)

 

 

 

 

 

 

Potentiometric titration

 

Pu materialsa)

 

 

 

of Pu (McDonald-

Pu

0.1

0.1

 

Savage method)

 

 

 

 

 

Calorimetry of Pu

Pu

Pure Pu materials

0.1

0.1

 

solutions

 

 

 

 

 

Gravimetry with baking

U

Pure U oxides

0.05

0.05

 

X–K

fluorometric

Pu

Pu materialsa)

0.2

0.2

 

analysis

 

 

 

 

 

 

X-ray fluorescence

 

Pure U and Pu

 

 

 

spectrometry

Pu, U

oxides and MOXa)

0.3

0.3

 

Mass– spectrometry with

U, Pu

Starting solutions of

 

 

 

isotopic dilution

 

spent fuel, Pu and

0.1

0.1

 

 

 

 

U–Pu materials

 

 

 

79

 

 

Table 3.7 (continued)

 

 

 

 

 

 

Method

Measured

Type of

Error,

 

 

quantity

material

( % rel.), random

 

 

 

analyzed

and systematic

 

 

Isotope analysis

 

 

 

Thermal-ionization

 

All Pu and U

0.05 b)

0.05 b)

 

mass–spectrometry

U, Pu

materials, starting

 

 

isotopes

solutions of spent

 

 

 

 

 

fuel

 

 

 

Gamma–spectrometry of

Pu

Pure U and Pu

0.5–2.0

0.5–2.0

 

high resolution (Ge-

isotopes,

materials

 

 

 

based detector)

Am, Np

 

 

 

 

Gamma–spectrometry

235U

LEU materials

 

 

 

(NaI-based detector)

 

0.2–0.5

0.2–0.5

 

Alpha–spectrometry

238Pu

Pu materials

0.2

0.3

 

a)excepting INF;

b)for ratios of the main isotopes.

Safeguards-related activities of the IAEA

The inspection activities of the IAEA depend on the scale of nuclear operations carried out by a state. These operations will be small-scale in states having, e.g., one small research reactor alone, but can be quite extensive in countries with many nuclear fuel cycle facilities. The scope of inspection activities is the greater, the larger is the number of NFC facilities in a country. Table 3.8 presents rough estimates of the nuclear material quantities covered by the IAEA safeguards. It may be seen that the NM quantities under control are steadily growing, and so is the number of facilities under the IAEA safeguards.

This being so, the inspection activities, including independent measurements of nuclear materials and their control by means of containment and surveillance techniques, depend largely on the type of nuclear facilities under the safeguards. Reactors and storage facilities, where materials appear as articles, such as fuel assemblies, call for less inspection effort than do facilities with materials found in bulk, where the greater part of NM is in motion or under processing. Table 3.9 shows the numbers of various facilities covered by the IAEA Safeguards.

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