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ASTM E2446-23

(Practice)

Standard Practice for Manufacturing Characterization of Computed Radiography Systems

Standard Practice for Manufacturing Characterization of Computed Radiography Systems

SIGNIFICANCE AND USE
4.1 There are several factors affecting the quality of a CR image including the basic spatial resolution of the IP system, geometrical unsharpness, scatter and contrast sensitivity. There are several additional factors (for example, software and scanning parameters) that affect the accurate reading of images on exposed IPs using an optical scanner.  
4.2 This practice is to be used to establish a characterization of CR system by performance levels on the basis of a normalized SNR, interpolated basic spatial detector resolution and EPS. The CR system performance levels in this practice do not refer to any particular manufacturers’ imaging plates. A CR system performance level results from the use of a particular imaging plate together with the exposure conditions, standardized phantom, the scanner type, and software and the scanning parameters. This characterization system provides a means to compare differing CR technologies, as is common practice with film systems, which guides the user to the appropriate configuration, IP, and technique for the application at hand. The performance level selected may not match the imaging performance of a corresponding film class because of the difference in the spatial resolution and scatter sensitivity. Therefore, the user should always use IQIs for proof of contrast sensitivity and basic spatial resolution.  
4.3 The measured performance parameters are presented in a characterization chart. This enables users to select specific CR systems by the different characterization data to find the best system for his specific application.  
4.4 The quality factors can be determined most accurately by the tests described in this practice. Some of the system tests require special tools, which may not be available in user laboratories. Simpler tests are described for quality assurance and long term stability tests in Practice E2445.  
4.5 Manufacturers of industrial CR systems or certification agencies will use this practice. Users of i...
SCOPE
1.1 This practice covers the manufacturing characterization of computed radiography (CR) systems, consisting of a particular phosphor imaging plate (IP), scanner, software, scanner operational parameters, and an image display monitor, in combination with specified metal screens for industrial radiography.  
1.2 The practice defines system tests to be used to characterize the systems of different suppliers and make them comparable for users.  
1.3 This practice is intended for use by manufacturers of CR systems or certification agencies to provide quantitative results of CR system characteristics for nondestructive testing (NDT) user or purchaser consumption. Some of these tests require specialized test phantoms to ensure consistency of results among suppliers or manufacturers. These tests are not intended for users to complete, nor are they intended for long term stability tracking and lifetime measurements. However, they may be used for this purpose, if so desired. Practice E2445 describes tests which are intended for users to observe the CR performance and test the long term stability.  
1.4 The CR system performance is described by the basic spatial resolution, contrast, signal and noise parameters, and the equivalent penetrameter sensitivity (EPS). Some of these parameters are used to compare with DDA characterization and film characterization data (see Practice E2597 and Test Method E1815).
Note 1: For film system characterization, the signal is represented by the optical density of 2 (above fog and base) and the noise as granularity. The signal-to-noise ratio is normalized by the aperture (similar to the basic spatial resolution) of the system and is part of characterization. This normalization is given by the scanning circular aperture of 100 µm of the micro-photometer, which is defined in Test Method E1815 for film system characterization.  
1.5 The measurement of CR systems in this practice is restricted ...

General Information

Status
Published
Publication Date
14-Jun-2023
ICS
19.100 - Non-destructive testing
Technical Committee
E07 - Nondestructive Testing
Drafting Committee
E07.01 - Radiology (X and Gamma) Method
Current Stage
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This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the
Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
Designation: E2446 − 23
Standard Practice for
Manufacturing Characterization of Computed Radiography
1
Systems
This standard is issued under the fixed designation E2446; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope 1.5 The measurement of CR systems in this practice is
restricted to a selected radiation quality to simplify the proce-
1.1 This practice covers the manufacturing characterization
dure. The properties of CR systems will change with radiation
of computed radiography (CR) systems, consisting of a par-
energy but not the ranking of CR system performance. Users of
ticular phosphor imaging plate (IP), scanner, software, scanner
this practice may carry out the tests at different or additional
operational parameters, and an image display monitor, in
radiation qualities (X-ray or gamma ray) if required.
combination with specified metal screens for industrial radiog-
1.6 The values stated in SI are to be regarded as the
raphy.
standard.
1.2 The practice defines system tests to be used to charac-
1.7 This standard does not purport to address all of the
terize the systems of different suppliers and make them
safety concerns, if any, associated with its use. It is the
comparable for users.
responsibility of the user of this standard to establish appro-
1.3 This practice is intended for use by manufacturers of CR
priate safety, health, and environmental practices and deter-
systems or certification agencies to provide quantitative results
mine the applicability of regulatory limitations prior to use.
of CR system characteristics for nondestructive testing (NDT)
1.8 This international standard was developed in accor-
user or purchaser consumption. Some of these tests require
dance with internationally recognized principles on standard-
specialized test phantoms to ensure consistency of results
ization established in the Decision on Principles for the
among suppliers or manufacturers. These tests are not intended
Development of International Standards, Guides and Recom-
for users to complete, nor are they intended for long term
mendations issued by the World Trade Organization Technical
stability tracking and lifetime measurements. However, they
Barriers to Trade (TBT) Committee.
may be used for this purpose, if so desired. Practice E2445
2. Referenced Documents
describes tests which are intended for users to observe the CR
2
performance and test the long term stability.
2.1 ASTM Standards:
E746 Practice for Determining Relative Image Quality Re-
1.4 The CR system performance is described by the basic
sponse of Industrial Radiographic Imaging Systems
spatial resolution, contrast, signal and noise parameters, and
E1165 Test Method for Measurement of Focal Spots of
the equivalent penetrameter sensitivity (EPS). Some of these
Industrial X-Ray Tubes by Pinhole Imaging
parameters are used to compare with DDA characterization and
E1316 Terminology for Nondestructive Examinations
film characterization data (see Practice E2597 and Test Method
E1815 Test Method for Classification of Film Systems for
E1815).
Industrial Radiography
NOTE 1—For film system characterization, the signal is represented by
E2002 Practice for Determining Image Unsharpness and
the optical density of 2 (above fog and base) and the noise as granularity.
Basic Spatial Resolution in Radiography and Radioscopy
The signal-to-noise ratio is normalized by the aperture (similar to the basic
E2007 Guide for Computed Radiography
spatial resolution) of the system and is part of characterization. This
E2033 Practice for Radiographic Examination Using Com-
normalization is given by the scanning circular aperture of 100 μm of the
micro-photometer, which is defined in Test Method E1815 for film system puted Radiography (Photostimulable Luminescence
characterization.
Method)
E2445 Practice for Performance Evaluation and Long-Term
Stability of Computed Radiography Systems
1
This practice is under the jurisdiction of ASTM Committee E07 on Nonde-
structive Testing and is the direct responsibility of Subcommittee E07.01 on
2
Radiology (X and Gamma) Method. For referenced ASTM standards, visit the ASTM website, www.astm.org, or
Current edition approved June 15, 2023. Published August 2023. Originally contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
approved in 2005. Last previous edition approved in 2016 as E2446 – 16. DOI: Standards volume information, refer to the standard’
...

This document is not an ASTM standard and is intended only to provide the user of an ASTM standard an indication of what changes have been made to the previous version. Because
it may not be technically possible to adequately depict all changes accurately, ASTM recommends that users consult prior editions as appropriate. In all cases only the current version
of the standard as published by ASTM is to be considered the official document.
Designation: E2446 − 16 E2446 − 23
Standard Practice for
Manufacturing Characterization of Computed Radiography
1
Systems
This standard is issued under the fixed designation E2446; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope
1.1 This practice describescovers the manufacturing characterization of computed radiography (CR) systems, consisting of a
particular phosphor imaging plate (IP), scanner, software, scanner operational parameters, and an image display monitor, in
combination with specified metal screens for industrial radiography.
1.2 The practice defines system tests to be used to characterize the systems of different suppliers and make them comparable for
users.
1.3 This practice is intended for use by manufacturers of CR systems or certification agencies to provide quantitative results of
CR system characteristics for nondestructive testing (NDT) user or purchaser consumption. Some of these tests require specialized
test phantoms to ensure consistency of results among suppliers or manufacturers. These tests are not intended for users to complete,
nor are they intended for long term stability tracking and lifetime measurements. However, they may be used for this purpose, if
so desired. Practice E2445 describes tests which are intended for users to observe the CR performance and test the long term
stability.
1.4 The CR system performance is described by the basic spatial resolution, contrast, signal and noise parameters, and the
equivalent penetrameter sensitivity (EPS). Some of these parameters are used to compare with DDA characterization and film
characterization data (see Practice E2597 and Test Method E1815).
NOTE 1—For film system characterization, the signal is represented by the optical density of 2 (above fog and base) and the noise as granularity. The
signal-to-noise ratio is normalized by the aperture (similar to the basic spatial resolution) of the system and is part of characterization. This normalization
is given by the scanning circular aperture of 100 μm of the micro-photometer, which is defined in Test Method E1815 for film system characterization.
1.5 The measurement of CR systems in this practice is restricted to a selected radiation quality to simplify the procedure. The
properties of CR systems will change with radiation energy but not the ranking of CR system performance. Users of this practice
may carry out the tests at different or additional radiation qualities (X-ray or gamma ray) if required.
1.6 The values stated in SI are to be regarded as the standard.
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility
of the user of this standard to establish appropriate safety and health practices and to safety, health, and environmental practices
and determine the applicability of regulatory limitations prior to use.
1
This practice is under the jurisdiction of ASTM Committee E07 on Nondestructive Testing and is the direct responsibility of Subcommittee E07.01 on Radiology (X and
Gamma) Method.
Current edition approved June 1, 2016June 15, 2023. Published June 2016August 2023. Originally approved in 2005. Last previous edition approved in 20152016 as
E2446 – 15.E2446 – 16. DOI: 10.1520/E2446-16.10.1520/E2446-23.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
1

---------------------- Page: 1 ----------------------
E2446 − 23
1.8 This international standard was developed in accordance with internationally recognized principles on standardization
established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued
by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
2. Referenced Documents
2
2.1 ASTM Standards:
E746 Practice for Determining Relative Image Quality Response of Industrial Radiographic Imaging Systems
E1165 Test Method for Measurement of Focal Spots of Industrial X-Ray Tubes by Pinhole Imaging
E1316 Terminology for Nondestructive Examinations
E1815 Test Method for Classification of Film Systems for Industrial Radiography
E2002 Practice for Determining Image Unsharpness and Basic Spatial Resolution in Radiography and Radioscopy
E2007 Guide for Computed Radiograp
...

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3.1 The terms found in this standard are intended to be used uniformly and consistently in all nondestructive testing standards. The purpose of this standard is to promote a clear understanding and interpretation of the NDT standards in which they are used.
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1.2.3 For use in the organization of facilities and personnel concerned with liquid penetrant testing.  
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5.1 The POD analysis method described herein is based on a well-known and well established statistical regression method. It shall be used to quantify the demonstrated POD for a specific set of examination parameters and known range of discontinuity sizes under the following conditions.  
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5.1.3 A relationship between discontinuity size and POD exists and is best described by a generalized linear model with the appropriate link function for binary outcomes.  
5.2 This practice does not limit the use of a generalized linear model with more than one predictor variable or other types of statistical models if justified as more appropriate for the hit/miss data.  
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5.4 Prior to performing the analysis it is assumed that the discontinuity of interest is clearly defined; the number and distribution of induced discontinuity sizes in the POD specimen set is known and well-documented; discontinuities in the POD specimen set are unobstructed; and the POD examination administration procedure (including data collection method) is well-designed, well-defined, under control, and unbiased. The analysis results are only valid if convergence is achieved and the model adequately represents the data.  
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1.3 This practice does not specify:  
1.3.1 A testing or validation procedure to assess an implementation's conformance to the standard,  
1.3.2 The implementation details of any features of the standard on a device claiming conformance, or  
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Standard Practice for Determining Image Unsharpness and Basic Spatial Resolution in Radiography and Radioscopy for High Energy Applications

SIGNIFICANCE AND USE
5.1 The gauge is intended to provide a means for measuring image or detector unsharpness and basic spatial image or detector resolution as independently as practicable from the imaging system and contrast sensitivity limitations. When the duplex plate gauge is positioned directly on the film or the digital detector instead on the test object, then the determined image unsharpness UIm corresponds to the inherent film or detector unsharpness (Udetector) and the determined basic spatial image resolution SRbimage corresponds to the basic spatial detector resolution SRbdetector. SRbimage provides a value which depends on the combined effect of detector unsharpness and geometric unsharpness.  
5.2 Basis of Application:  
5.2.1 The following items are subject to contractual agreement between the parties using or referencing this standard.
5.2.1.1 Personnel Qualification—Personnel performing examinations to this practice shall be qualified in accordance with NAS410, EN 4179, ANSI/ASNT CP 189, ISO 9712, or SNT-TC-1A and certified by the employer or certifying agency as applicable. Other equivalent qualification documents may be used when specified on the contract or purchase order. The applicable revision shall be the latest unless otherwise specified in the contractual agreement between parties.
5.2.1.2 If specified in the contractual agreement, NDT agencies shall be qualified and evaluated as described in Specification E543. The applicable edition of Specification E543 shall be specified in the contract.
SCOPE
1.1 This practice covers the design and basic use of a gauge used to determine the image unsharpness and the basic spatial resolution of film radiographs or of digital images taken with CR imaging plates, digital detector arrays (DDA), or radioscopic systems (for example, with X-ray image intensifiers) for applications with Se-75, Ir-192, Co-60 and high energy sources with tube potentials ≥ 300 kV. The IQI may be used at lower tube potentials too, if the expected unsharpness is > 200 µm (SRbimage or SRbdetector > 100 µm). For the measurement of lower unsharpness values, the usage of the gauge described in Practice E2002 is recommended.  
1.2 This practice is applicable to radiographic and radioscopic imaging systems utilizing X-ray and gamma ray radiation sources.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 The gauge described can be used effectively if the duplex wire IQI of Practice E2002 does not provide sufficient contrast resolution.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM
ASTM E2663-23(Practice)
Standard Practice for Digital Imaging and Communication in Nondestructive Evaluation (DICONDE) for Ultrasonic Test Methods

SIGNIFICANCE AND USE
5.1 Personnel that are responsible for the creation, transfer, and storage of ultrasonic test results will use this standard. This practice defines a set of information modules that, along with Practice E2339 and the DICOM standard, provides a standard means to organize ultrasonic test parameters and results. The ultrasonic test results may be displayed and analyzed on any device that conforms to this standard. Personnel wishing to view any ultrasonic inspection data stored in DICONDE format may use this document to help them decode and display the data contained in the DICONDE compliant inspection record.
SCOPE
1.1 This practice covers the interoperability of ultrasonic imaging equipment by specifying image data transfer and archival storage methods in commonly accepted terms. This document is intended to be used in conjunction with Practice E2339. Practice E2339 defines an industrial adaptation of NEMA PS3 / ISO 12052 (DICOM, see http://medical.nema.org), an international standard for image data acquisition, review, transfer, and archival storage. The goal of Practice E2339, commonly referred to as DICONDE, is to provide a standard that facilitates the display and analysis of NDE test results on any system conforming to the DICONDE standard. Toward that end, Practice E2339 provides a data dictionary and set of information modules that are applicable to all NDE modalities. This practice supplements Practice E2339 by providing information object definitions, information modules, and data dictionary that are specific to ultrasonic test methods.  
1.2 This practice has been developed to overcome the issues that arise when analyzing or archiving data from ultrasonic test equipment using proprietary data transfer and storage methods. As digital technologies evolve, data must remain decipherable through the use of open, industry-wide methods for data transfer and archival storage. This practice defines a method where all the ultrasonic technique parameters and test results are communicated and stored in a standard format regardless of changes in digital technology.  
1.3 This practice does not specify:  
1.3.1 A testing or validation procedure to assess an implementation's conformance to the standard.  
1.3.2 The implementation details of any features of the standard on a device claiming conformance.  
1.3.3 The overall set of features and functions to be expected from a system implemented by integrating a group of devices each claiming DICONDE conformance.  
1.4 Although this practice contains no values that require units, it does describe methods to store and communicate data that do require units to be properly interpreted. The SI units required by this practice are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM
ASTM E1815-18(2023)(Test Method)
Standard Test Method for Classification of Film Systems for Industrial Radiography

SIGNIFICANCE AND USE
4.1 This test method provides a relative means for classification of film systems used for industrial radiography. The film system consists of the film and associated processing system (the type of processing and processing chemistry). Section 9 describes specific parameters used for this test method. In general, the classification for hard X-rays, as described in Section 9, can be transferred to other radiation energies and metallic screen types, as well as screens without films. The usage of film system parameters outside the energy ranges specified may result in changes to a film/system performance classification.  
4.1.1 The film performance is described by contrast and noise parameters. The contrast is represented by gradient and the noise by granularity.  
4.1.2 A film system is assigned a particular class if it meets the minimum performance parameters: for Gradient G at  D – D0 = 2.0 and D – D0 = 4.0, and gradient/noise ratio at D – D0 = 2.0, and the maximum performance parameter: granularity σD at  D = 2.0.  
4.2 This test method describes how the parameters shall be measured and demonstrates how a classification table can be constructed.  
4.3 Manufacturers of industrial radiographic film systems and developer chemistry will be the users of this test method. The result is a classification table as shown by the example given in Table 2. Another table also includes speed data for user information. Users of industrial radiographic film systems may also perform the tests and measurements outlined in this test method, provided that the required test equipment is used and the methodology is followed strictly. (A) Family of films ranging in speed and image quality.  
4.4 The publication of classes for industrial radiography film systems will enable specifying bodies and contracting parties to agree to particular system classes, which are capable of providing known image qualities. See 8.2.  
4.5 ISO 11699–1 and European standard EN 584-1 describe the same m...
SCOPE
1.1 This test method covers a procedure for determination of the performance of film systems used for industrial radiography. This test method establishes minimum requirements that correspond to system classes.  
1.2 This test method is to be used only for direct exposure-type film exposed with lead intensifying screens. The performance of films exposed with fluorescent (light-emitting) intensifying screens cannot be determined accurately by this test method.  
1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses are for information only.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM
ASTM E1254-13(2023)(Guide)
Standard Guide for Storage of Radiographs and Unexposed Industrial Radiographic Films

SIGNIFICANCE AND USE
3.1 The provisions of this guide are intended to control the quality of industrial radiographs and unexposed films only and are not intended for controlling the acceptability of the materials or products radiographed. It is further intended that this guide be used as an adjunct to Guide E94.  
3.2 The necessity for applying specific control procedures such as those described in this guide is dependent to a certain extent, on the degree to which a user adheres to good processing and storage practices as a matter of routine procedure.
SCOPE
1.1 This guide may be used for the control and maintenance of industrial radiographs and unexposed films used for industrial radiography.  
1.2 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.
Note 1: For information purposes, refer to Terminology E1316. The terms stated therein, however, are not specifically referenced in the text of this document.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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