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ASTM E2445/E2445M-14

(Practice)

Standard Practice for Performance Evaluation and Long-Term Stability of Computed Radiography Systems

Standard Practice for Performance Evaluation and Long-Term Stability of Computed Radiography Systems

SIGNIFICANCE AND USE
4.1 This practice is intended to be used by the NDT using organization to measure baseline performance of the CR system and to monitor its performance throughout its service as an NDT imaging system. For purposes of this document, the CR System is defined as:  
4.1.1 Storage phosphor imaging plate (IP) type and manufacturer,  
4.1.2 Read out unit (scanner or reader) manufacturer and model, including applicable scanner settings (e.g., sampling resolution, PMT gain, pixel value (PV) look up table, etc.),  
4.1.3 Image acquisition and processing software, and  
4.1.4 Image display monitor.  
4.2 It is to be understood that the CR system has already been selected and purchased by the user from a manufacturer based on the inspection needs at hand. The user shall accept the CR scanner based on manufacturer’s results of Practice E2446 on the specific CR scanner as provided in a data sheet for that serialized CR scanner or other acceptance test agreed to between the user and manufacturer (not covered in this practice). This practice is not intended to be used as an “acceptance test” of the CR system, but rather to establish a performance baseline that will enable tracking while in-service.  
4.3 Although many of the properties listed in this standard have similar metrics to those found in E2446, data collection methods are not identical, and comparisons among values acquired with each standard should not be made.  
4.4 This practice defines the tests to be performed and required intervals. Also defined are the methods of tabulating results that CR users will complete following the baseline of the CR system. These tests will also be performed periodically at the stated required intervals to evaluate the CR system to determine if the system remains within acceptable operational limits as established in this practice.  
4.5 There are several factors that affect the image quality of a CR image. Factors which are dependent on the CR system performance include basic spati...
SCOPE
1.1 This practice describes the evaluation of Computed Radiology (CR) systems for industrial radiology. It is intended to ensure that the evaluation of image quality, as far as this is influenced by the CR system, meets the needs of users of this standard, and their customers, and enables process control and long-term stability of the CR system.  
1.2 This practice specifies the fundamental parameters of CR systems to be measured to determine baseline performance, and to track the long term stability of the system. These tests are for applications up to 320kV. When greater than 320kV or when a gamma source is used, these tests may still be used to characterize a system, but may need to be modified as agreed between the user and cognizant engineering organization (CEO).  
1.3 The CR system performance tests specified in this practice shall be completed upon acceptance of the system from the manufacturer and at intervals specified in this practice to monitor long term stability of the system. The intent of these tests is to monitor the system performance degradation and to identify when an action needs to be taken when the system degrades by a certain level.  
1.4 The use of gauges2 provided in this standard is mandatory for each test. In the event these tests or gauges are not sufficient, the user, in coordination with the CEO shall develop additional or modified tests, test objects, gauges, or image quality indicators to evaluate the CR system. Acceptance levels for these ALTERNATE tests shall be determined by agreement between the user and CEO.  
1.5 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard.  
1.6 This standard does not purport to address all of t...

General Information

Status
Historical
Publication Date
30-Sep-2014
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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ASTM E2445/E2445M-14 - Standard Practice for Performance Evaluation and Long-Term Stability of Computed Radiography SystemsASTM E2445/E2445M-14 - Standard Practice for Performance Evaluation and Long-Term Stability of Computed Radiography Systems
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ASTM E2445/E2445M-14 - Standard Practice for Performance Evaluation and Long-Term Stability of Computed Radiography Systems
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REDLINE ASTM E2445/E2445M-14 - Standard Practice for Performance Evaluation and Long-Term Stability of Computed Radiography SystemsREDLINE ASTM E2445/E2445M-14 - Standard Practice for Performance Evaluation and Long-Term Stability of Computed Radiography Systems
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NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.
Contact ASTM International (www.astm.org) for the latest information
Designation: E2445/E2445M − 14
Standard Practice for
Performance Evaluation and Long-Term Stability of
1
Computed Radiography Systems
ThisstandardisissuedunderthefixeddesignationE2445/E2445M;thenumberimmediatelyfollowingthedesignationindicatestheyear
of original adoption or, in the case of revision, the year of last revision.Anumber 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 values stated in either SI units or inch-pound units
are to be regarded separately as standard. The values stated in
1.1 This practice describes the evaluation of Computed
each system may not be exact equivalents; therefore, each
Radiology (CR) systems for industrial radiology. It is intended
system shall be used independently of the other. Combining
to ensure that the evaluation of image quality, as far as this is
values from the two systems may result in non-conformance
influenced by the CR system, meets the needs of users of this
with the standard.
standard, and their customers, and enables process control and
1.6 This standard does not purport to address all of the
long-term stability of the CR system.
safety concerns, if any, associated with its use. It is the
1.2 This practice specifies the fundamental parameters of
responsibility of the user of this standard to establish appro-
CRsystemstobemeasuredtodeterminebaselineperformance,
priate safety and health practices and determine the applica-
and to track the long term stability of the system. These tests
bility of regulatory limitations prior to use.
are for applications up to 320kV. When greater than 320kV or
when a gamma source is used, these tests may still be used to
2. Referenced Documents
characterize a system, but may need to be modified as agreed
3
2.1 ASTM Standards:
between the user and cognizant engineering organization
E746Practice for Determining Relative Image Quality Re-
(CEO).
sponse of Industrial Radiographic Imaging Systems
1.3 The CR system performance tests specified in this
E1316Terminology for Nondestructive Examinations
practice shall be completed upon acceptance of the system
E1647Practice for Determining Contrast Sensitivity in Ra-
fromthemanufacturerandatintervalsspecifiedinthispractice
diology
tomonitorlongtermstabilityofthesystem.Theintentofthese
E2002PracticeforDeterminingTotalImageUnsharpnessin
tests is to monitor the system performance degradation and to
Radiology
identify when an action needs to be taken when the system
E2007Guide for Computed Radiography
degrades by a certain level.
E2033Practice for Computed Radiology (Photostimulable
2
1.4 The use of gauges provided in this standard is manda-
Luminescence Method)
tory for each test. In the event these tests or gauges are not
E2446Practice for Classification of Computed Radiology
sufficient,theuser,incoordinationwiththeCEOshalldevelop
Systems
additional or modified tests, test objects, gauges, or image
qualityindicatorstoevaluatetheCRsystem.Acceptancelevels
3. Terminology
for theseALTERNATE tests shall be determined by agreement
3.1 Definitions—The definition of terms relating to gamma-
between the user and CEO.
and X-radiology, which appear in Terminology E1316, Guide
E2007,andPracticeE2033shallapplytothetermsusedinthis
1
This practice is under the jurisdiction of ASTM Committee E07 on Nonde-
practice.
structive Testing and is the direct responsibility of Subcommittee E07.01 on
Radiology (X and Gamma) Method. 3.2 Definitions of Terms Specific to This Standard:
Current edition approved Oct. 1, 2014. Published October 2014. Originally
3.2.1 aliasing—artifacts that appear in an image when the
approved in 2005. Last previous edition approved in 2010 as E2445/E2445M-
spatial frequency of the input is higher than the output is
05(2010). DOI:10.1520/E2445_E2445M-14.
2
capable of reproducing.
ThesolesourceofsupplyoftheapparatusshowninAppendixX2knowntothe
committee at this time is Rockwell Collins’ARINC, 1300 Thomas Drive, Panama
City Beach, FL 32408, Phone: 405-605-7095, ARINC part number A0295224002
(USAF design) or A0295224003 (NAVAIR design). The NAVAIR design includes
3
two additional test targets that are not used in this test standard. If you are aware of For referenced ASTM standards, visit the ASTM website, www.astm.org, or
alternative suppliers, please provide this information to ASTM International contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
Headquarters.Your comments will receive careful consideration at a meeting of the Standards volume information, refer to the standard’s Document Summary page on
1
responsible technical committee, which you may attend. the ASTM website.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
1

----
...

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: E2445 − 05 (Reapproved 2010) E2445/E2445M − 14
Standard Practice for
Qualification Performance Evaluation and Long-Term
1
Stability of Computed RadiologyRadiography Systems
This standard is issued under the fixed designation E2445;E2445/E2445M; 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 specifies the fundamental parameters of computed radiography systems to assure satisfactory and repeatable
results for nondestructive testing.
1.1 This practice describes the evaluation of Computed Radiology (CR) systems for industrial radiography.radiology. It is
intended to ensure that the evaluation of image quality, as far as this is influenced by the scanner/IPCR system, meets the needs
of users and enables the test of long-term stability. of this standard, and their customers, and enables process control and long-term
stability of the CR system.
1.2 This practice specifies the fundamental parameters of CR systems to be measured to determine baseline performance, and
to track the long term stability of the system. These tests are for applications up to 320kV. When greater than 320kV or when a
gamma source is used, these tests may still be used to characterize a system, but may need to be modified as agreed between the
user and cognizant engineering organization (CEO).
1.3 The CR system performance tests specified in this practice shall be completed upon acceptance of the system from the
manufacturer and at intervals specified in this practice to monitor long term stability of the system. The intent of these tests is to
monitor the system performance degradation and to identify when an action needs to be taken when the system degrades by a
certain level.
1.4 Each of the tests described may be performed with individual gages specified. The user shall decide which tests shall be used
2
for system control using individual test objects or the CR test phantomThe use of gauges (providedAppendix X1). The computed
radiological tests, specified as “user tests” in this practice, may be utilized at appropriate intervals determined by the user, based
on the application of the examination operations. The in this standard is mandatory for each test. In the event these tests or gauges
are not sufficient, the user, in coordination with the CEO shall develop additional or modified tests, test objects, gauges, or image
quality indicators to evaluate the CR system. Acceptance levels for these ALTERNATE tests shall be appropriate for the materials
and range of use of the system. Fading, uniformity, and erasure tests shall also be part of the control system. All other tests for
qualification and capability are to be performed and certified by the CR equipment manufacturer. determined by agreement
between the user and CEO.
1.5 The values stated in either SI units or inch-pound units are to be regarded as the standard. Values in inch-pound units are
for information purposes.separately as standard. The values stated in each system may not be exact equivalents; therefore, each
system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the
standard.
1.6 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 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, 2010Oct. 1, 2014. Published November 2010October 2014. Originally approved in 2005. Last previous edition approved in 20052010
as E2445 - 05.E2445/E2445M-05(2010). DOI:10.1520/E2445–05R10. DOI:10.1520/E2445_E2445M-14.
2
The sole source of supply of the apparatus shown in Appendix X2 known to the committee at this time is Nuclear Associates, A Division of Cardinal Health, 120 Andrews
Road, Hicksville, NY 11801, Phone: 1-888-466-8257, Catalog Number: 07-605-2435. Rockwell Collins’ARINC, 1300 Thomas Drive, Panama City Beach, FL 32408, Phone:
405-605-7095, ARINC part number A0295224002 (USAF design) or A0295224003 (NAVAIR design). The NAV
...

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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.
SCOPE
1.1 This standard covers the terminology used in the standards prepared by the E07 Committee on Nondestructive Testing. These nondestructive testing (NDT) methods include: acoustic emission, electromagnetic testing, gamma- and X-radiology, leak testing, liquid penetrant testing, magnetic particle testing, neutron radiology and gauging, ultrasonic testing, and other technical methods.  
1.2 Committee E07 recognizes that the terms examination, testing, and inspection are commonly used as synonyms in nondestructive testing. For uniformity and consistency in E07 nondestructive testing standards, Committee E07 encourages the use of the terms examination or inspection and their derivatives when describing the application of nondestructive test methods. In a specific standard, either examination or inspection shall be used consistently throughout the document. Similarly, E07 encourages the use of the term test and its derivatives when referring to the body of knowledge of a nondestructive testing method. There are, however, appropriate exceptions when the term test and its derivatives may be used to describe the application of a nondestructive test, such as measurements which produce a numeric result (for example, when using the leak testing method to perform a leak test on a component, or an ultrasonic measurement of velocity). Additionally, the term test should be used when referring to the NDT method, that is, Radiologic Testing (RT), Ultrasonic Testing (UT), and so forth. (Example: Radiologic Testing (RT) is often used to examine material to detect internal discontinuities.)
Note 1: The following sentences clarify this policy and illustrate its use:
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SIGNIFICANCE AND USE
5.1 Liquid penetrant testing methods indicate the presence, location, and to a limited extent, the nature and magnitude of the detected discontinuities. Each of the various penetrant methods has been designed for specific uses such as critical service items, volume of parts, portability, or localized areas of examination. The method selected will depend accordingly on the design and service requirements of the parts or materials being tested.
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1.1 This practice2 covers procedures for penetrant examination of materials. Penetrant testing is a nondestructive testing method for detecting discontinuities that are open to the surface such as cracks, seams, laps, cold shuts, shrinkage, laminations, through leaks, or lack of fusion and is applicable to in-process, final, and maintenance examinations. It can be effectively used in the examination of nonporous, metallic materials, ferrous and nonferrous metals, and of nonmetallic materials such as nonporous glazed or fully densified ceramics, as well as certain nonporous plastics, and glass.  
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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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SIGNIFICANCE AND USE
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SIGNIFICANCE AND USE
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 The procedures described in this practice have proven utility in the inspecting (1) monolithic polymer matrix composites (laminates) for bulk defects, (2) metals for corrosion during the service life of the part of interest, (3) thickness checks, (4) adhesive bonding of metals, composites, and sandwich core constructions, (5) coatings, and (6) composite filament windings. Both unpressurized, and with suitable precautions, pressurized materials and components are inspected.  
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5.5 The MAUT technique has proven utility in the inspection of multi-ply carbon-fiber reinforced laminates used in primary aircraft structures.11  
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SCOPE
1.1 This practice covers procedures for matrix array ultrasonic testing (MAUT) of monolithic composites, composite sandwich constructions, and metallic test articles. These procedures can be used throughout the life cycle of a part during product and process design optimization, on line process control, post-manufacturing inspection, and in-service inspection.  
1.2 In general, ultrasonic testing is a common volumetric method for detection of embedded or subsurface discontinuities. This practice includes general requirements and procedures which may be used for detecting flaws and for making a relative or approximate evaluation of the size of discontinuities and part anomalies. The types of flaws or discontinuities detected include interply delaminations, foreign object debris (FOD), inclusions, disbond/un-bond, fiber debonding, fiber fracture, porosity, voids, impact damage, thickness variation, and corrosion.  
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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.  
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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 ...

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ASTM
ASTM E3388-23(Practice)
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 E2934-23(Practice)
Standard Practice for Digital Imaging and Communication in Nondestructive Evaluation (DICONDE) for Eddy Current (EC) Test Methods

SIGNIFICANCE AND USE
5.1 Personnel that are responsible for the creation, transfer, and storage of eddy current NDE test results will use this standard. This practice defines a set of information modules that, along with Practice E2339 and the DICOM standard, provide a standard means to organize eddy current test parameters and results. The eddy current examination results may be displayed or analyzed on any device that conforms to the standard. Personnel wishing to view any eddy current examination data stored according to Practice E2339 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 eddy current imaging and data acquisition equipment by specifying the image data transfer and archival storage in commonly accepted terms. This document is intended to be used in conjunction with Practice E2339 on Digital Imaging and Communication in Nondestructive Evaluation (DICONDE). Practice E2339 defines an industrial adaptation of NEMA PS3 / ISO 12052, an international standard for image data acquisition, review, storage, 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 results on any system conforming to the DICONDE standard. Toward that end, Practice E2339 provides a data dictionary and a set of information modules that are applicable to all NDE modalities. This practice supplements Practice E2339 by providing information object definitions, information modules, and a data dictionary that are specific to eddy current test methods.  
1.2 This practice has been developed to overcome the issues that arise when analyzing or archiving data from eddy current 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 eddy current technique parameters and inspection data are communicated and stored in a standard manner 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, or  
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 Units—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 values stated in SI units 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 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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