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ASTM E3375-23

(Practice)

Standard Practice for Cone Beam Computed Tomographic (CT) Examination

Standard Practice for Cone Beam Computed Tomographic (CT) Examination

SIGNIFICANCE AND USE
4.1 The purpose of this practice is to establish instruction, procedures, and equipment qualification to inspect a component for specified discontinuities. This practice is written so it can be specified on the engineering drawing, specification, or contract. This practice requires a detailed procedure delineating the technique or procedure requirements and shall be approved by the Cognizant Engineering Organization (CEO).  
4.2 The requirements in this practice shall be used when placing a CT system into NDT service and establishing a baseline of system performance measures. Monitoring the system performance over time shall be performed, including detector correction procedures, performance measurements, and system maintenance.  
4.3 For CT examinations where specified discontinuities are not known/identified/requested/available (that is, engineering analysis, engineering information only), portions of Section 7 – 9 requirements do not necessarily apply. For these types of examinations, the purchase order or contract shall specify the development of a specific procedure, approved by purchaser and supplier, to specify the requirements of this practice to be incorporated into the examination.
SCOPE
1.1 This practice establishes the minimum requirements for computed tomography (CT) examination of components using cone beam systems. The purpose of this practice is to establish instruction, procedures, and equipment qualification to inspect a component for specified discontinuities.  
1.2 This practice applies to systems with a Digital Detector Array (DDA) and an X-ray source. It does not cover the use of isotope sources.  
1.3 There are sections in this practice that may require agreement between the purchaser and the supplier, or specific direction from the cognizant engineering organization (CEO). These items should be addressed in the purchase order or the contract. Generally, the items are application-specific, performance related, or both.  
1.4 Applications for cone-beam CT are diverse. This practice is not intended to be limiting or restrictive. Refer to Guide E1441 for guidance on CT fundamentals and Guide E1672 for tradeoffs in selection of a CT system.  
1.5 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns 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. NCRP 144 or NIST Handbook 114, or both, may be used as guides to ensure that radiographic procedures are performed so that personnel shall not receive a radiation dosage exceeding the maximum permitted by the city, state, or national codes.  
1.7 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.

General Information

Status
Published
Publication Date
31-Jan-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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ASTM E3375-23 - Standard Practice for Cone Beam Computed Tomographic (CT) ExaminationASTM E3375-23 - Standard Practice for Cone Beam Computed Tomographic (CT) Examination
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ASTM E3375-23 - Standard Practice for Cone Beam Computed Tomographic (CT) Examination
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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: E3375 − 23
Standard Practice for
1
Cone Beam Computed Tomographic (CT) Examination
This standard is issued under the fixed designation E3375; 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 2. Referenced Documents
2
1.1 This practice establishes the minimum requirements for 2.1 ASTM Standards:
computed tomography (CT) examination of components using E543 Specification for Agencies Performing Nondestructive
cone beam systems. The purpose of this practice is to establish Testing
instruction, procedures, and equipment qualification to inspect E1316 Terminology for Nondestructive Examinations
a component for specified discontinuities. E1441 Guide for Computed Tomography (CT)
E1672 Guide for Computed Tomography (CT) System Se-
1.2 This practice applies to systems with a Digital Detector
lection
Array (DDA) and an X-ray source. It does not cover the use of
E1695 Test Method for Measurement of Computed Tomog-
isotope sources.
raphy (CT) System Performance
1.3 There are sections in this practice that may require
E1817 Practice for Controlling Quality of Radiological Ex-
agreement between the purchaser and the supplier, or specific
amination by Using Representative Quality Indicators
direction from the cognizant engineering organization (CEO).
(RQIs)
These items should be addressed in the purchase order or the
E2002 Practice for Determining Image Unsharpness and
contract. Generally, the items are application-specific, perfor-
Basic Spatial Resolution in Radiography and Radioscopy
mance related, or both.
E2339 Practice for Digital Imaging and Communication in
1.4 Applications for cone-beam CT are diverse. This prac- Nondestructive Evaluation (DICONDE)
E2597/E2597M Practice for Manufacturing Characterization
tice is not intended to be limiting or restrictive. Refer to Guide
E1441 for guidance on CT fundamentals and Guide E1672 for of Digital Detector Arrays
E2698 Practice for Radiographic Examination Using Digital
tradeoffs in selection of a CT system.
Detector Arrays
1.5 Units—The values stated in SI units are to be regarded
E2767 Practice for Digital Imaging and Communication in
as standard. No other units of measurement are included in this
Nondestructive Evaluation (DICONDE) for X-ray Com-
standard.
puted Tomography (CT) Test Methods
1.6 This standard does not purport to address all of the
E3147 Practice for Evaluating DICONDE Interoperability of
safety concerns associated with its use. It is the responsibility
Nondestructive Testing and Inspection Systems
of the user of this standard to establish appropriate safety,
3
2.2 ANSI Standards:
health, and environmental practices and determine the appli-
ANSI/ASNT CP 189 Standard for Qualification and Certifi-
cability of regulatory limitations prior to use. NCRP 144 or
cation of Nondestructive Testing Personnel
NIST Handbook 114, or both, may be used as guides to ensure
SNT-TC-1A Recommended Practice - Personnel Qualifica-
that radiographic procedures are performed so that personnel
tion and Certification in Nondestructive Testing
shall not receive a radiation dosage exceeding the maximum
4
2.3 ISO Standards:
permitted by the city, state, or national codes.
ISO 9712 Non-destructive Testing - Qualification and Cer-
1.7 This international standard was developed in accor-
tification of NDT Personnel
dance with internationally recognized principles on standard-
ization established in the Decision on Principles for the
Development of International Standards, Guides and Recom-
2
mendations issued by the World Trade Organization Technical For referenced ASTM standards, visit the ASTM website, www.astm.org, or
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
Barriers to Trade (TBT) Committee.
Standards volume information, refer to the standard’s Document Summary page on
the ASTM website.
1 3
This practice is under the jurisdiction of ASTM Committee E07 on Nonde- Available from American National Standards Institute (ANSI), 25 W. 43rd St.,
structive Testing and is the direct responsibility of Subcommittee E07.01 on 4th Floor, New York, NY 10036, http://www.ansi.org.
4
Radiology (X and Gamma) Method. Available from International Organization for Standardization (ISO), ISO
Current edition approved Feb. 1, 2023. Published February 2023. DOI: 10.1520/ Central Secretariat, Chemin de Blandonnet 8, CP 401, 1214 Vernier, Geneva,
E3375-23. Switzerland, https://www.iso.org.
Copyright © AST
...

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ASTM E1316-23b(Terminology)
Standard Terminology for Nondestructive Examinations

SIGNIFICANCE AND USE
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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1.1 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:
(a) Nondestructive testing methods are used extensively for the examination or inspection of materials and components.
(b) The E07 Committee on Nondestructive Testing has prepared many documents to promote uniform usage of the nondestructive testing methods that are applied to examine or inspect materials and components.  
(c) Radiologic Testing (RT) is often used to inspect material to detect internal discontinuities.
(d) Magnetic Particle Testing (MT), Liquid Penetrant Testing (PT), and Visual Testing (VT) are often used to examine the surface of a component.
(e) The Bubble Leak Testing (BLT) method is sometimes used to leak test a pressure containing component to detect leaks.
(f) A guide for Nondestructive Testing of additively manufactured materials will describe several methods but a practice will focus on a single inspection method.  
1.3 Section A defines terms that are common to multiple NDT methods, whereas the subsequent sections define terms pertaining to specific NDT methods.  
1.4 As shown on the chart below, when a nondestructive examination or inspection produces an indication, the indication is subject to interpretation as false, nonrelevant, or relevant. If it has been interpreted as relevant, the necessary subsequent evaluation will result in the decision to accept or reject the material. With the exception of accept and reject, which retain the meaning found in most dictionaries, all the words used in the chart are defined in Section A.    
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 E1901-23(Guide)
Standard Guide for Detection and Evaluation of Discontinuities by Contact Pulse-Echo Straight-Beam Ultrasonic Methods

SIGNIFICANCE AND USE
6.1 This guide provides procedures for the application of contact straight-beam examination for the detection and quantitative evaluation of discontinuities in materials.  
6.2 Although not all requirements of this guide can be applied universally to all examinations, situations, and materials, it does provide basis for establishing contractual criteria between the users, and may be used as a general guide for preparing detailed specifications for a particular application.  
6.3 This guide is directed towards the evaluation of discontinuities detectable with the beam normal to the entry surface. If discontinuities or other orientations are of concern, alternate scanning techniques are required.
SCOPE
1.1 This guide covers procedures for the contact ultrasonic examination of bulk materials or parts by transmitting pulsed ultrasonic waves into the material and observing the indications of reflected waves. This guide covers only examinations in which one search unit is used as both transmitter and receiver (pulse-echo). This guide includes general requirements and procedures that may be used for detecting discontinuities, locating depth and distance from a point of reference and for making a relative or approximate evaluation of the size of discontinuities as compared to a reference standard.  
1.2 This guide complements Practice E114 by providing more detailed procedures for the selection and standardization of the examination system and for evaluation of the indications obtained.  
1.3 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.  
1.4 This guide 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 guide to establish the 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 E2862-23(Practice)
Standard Practice for Probability of Detection Analysis for Hit/Miss Data

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.  
5.1.1 The initial response from a nondestructive evaluation inspection system is ultimately binary in nature (that is, hit or miss).  
5.1.2 Discontinuity size is the predictor variable and can be accurately quantified.  
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.  
5.3 If the initial response from a nondestructive evaluation inspection system is measurable and can be classified as a continuous variable (for example, data collected from an Eddy Current inspection system), then Practice E3023 may be more appropriate.  
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.  
5.5 The POD analysis method described herein is consistent with the analysis method for binary data described in MIL-HDBK-1823A, and is included in several widely utilized POD software packages to perform a POD analysis on hit/miss data. It is also found in statistical software packages that have generalized line...
SCOPE
1.1 This practice covers the procedure for performing a statistical analysis on nondestructive testing hit/miss data to determine the demonstrated probability of detection (POD) for a specific set of examination parameters. Topics covered include the standard hit/miss POD curve formulation, validation techniques, and correct interpretation of results.  
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.  
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ASTM E3370-23(Practice)
Standard Practice for Matrix Array Ultrasonic Testing of Composites, Sandwich Core Constructions, and Metals

SIGNIFICANCE AND USE
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.  
5.2 This practice provides guidelines for the application of longitudinal wave examination to the detection and quantitative evaluation of damage, discontinuities, and thickness variations in materials.  
5.3 This practice is intended primarily for the testing of parts to acceptance criteria most typically specified in a purchase order or other contractual document, and for testing of parts in-service to detect and evaluate damage.  
5.4 MAUT search units provide near-surface resolution and detection of small discontinuities comparable to phased array transducers. They may or may not be capable of beam steering. The advantage of MAUT for straight-beam longitudinal wave inspections is the ability to provide real-time C-scan data, which facilitates data interpretation and shortens inspection time. Depending on inspection needs, data can be displayed as A-, B- or C-scans, or three-dimensional renderings. Toggling between pulse-echo and through transmission ultrasonic (TTU) modes without having to use another system or changing transducers is also possible.  
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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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1.4 This practice provides two ultrasonic test procedures. Each has its own merits and requirements for inspection and shall be selected as agreed upon in a contractual document.  
1.4.1 Test Procedure A, Pulse Echo (non-contacting and contacting) is at a minimum a single matrix array transducer transmitting and receiving longitudinal waves in the range of 0.5 MHz to 20 MHz (see Fig. 1). Th...

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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.
SCOPE
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.  
1.2 This practice also provides a reference:  
1.2.1 By which a liquid penetrant examination process recommended or required by individual organizations can be reviewed to ascertain its applicability and completeness.  
1.2.2 For use in the preparation of process specifications and procedures dealing with the liquid penetrant testing of parts and materials. Agreement by the customer requesting penetrant testing is strongly recommended. All areas of this practice may be open to agreement between the cognizant engineering organization and the supplier, or specific direction from the cognizant engineering organization.  
1.2.3 For use in the organization of facilities and personnel concerned with liquid penetrant testing.  
1.3 This practice does not indicate or suggest criteria for evaluation of the indications obtained by penetrant testing. It should be pointed out, however, that after indications have been found, they must be interpreted or classified and then evaluated. For this purpose there must be a separate code, standard, or a specific agreement to define the type, size, location, and direction of indications considered acceptable, and those considered unacceptable.  
1.4 Units—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.  
1.5 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.  
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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 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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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
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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
ASTM E2491-23(Guide)
Standard Guide for Evaluating Performance Characteristics of Phased-Array Ultrasonic Testing Instruments and Systems

SIGNIFICANCE AND USE
5.1 This guide is intended to evaluate performance assessment of combinations of phased-array probes and instruments. It is not intended to define performance and acceptance criteria, but rather to provide data from which such criteria may be established.  
5.2 Recommended procedures described in this guide are intended to provide performance-related measurements that can be reproduced under the specified test conditions using simple targets and the phased-array test system itself. It is intended for phased-array flaw detection instruments operating in the nominal frequency range of 1 MHz to 20 MHz, but the procedures are applicable to measurements on instruments utilizing significantly higher frequency components.  
5.3 This guide is not intended for service calibration, or maintenance of circuitry for which the manufacturer’s instructions are available.  
5.4 Implementation of specific assessments may require more detailed procedural instructions in a format of the using facility.  
5.5 The measurement data obtained may be employed by users of this guide to specify, describe, or provide performance criteria for procurement and quality assurance, or service evaluation of the operating characteristics of phased-array systems.  
5.6 Not all assessments described in this guide are applicable to all systems. All or portions of the guide may be used as determined by the user.
SCOPE
1.1 This guide covers procedures for evaluating some performance characteristics of phased-array ultrasonic examination instruments and systems.  
1.2 Evaluation of these characteristics is intended to be used for either comparing instruments and systems or, by periodic repetition, for detecting long-term changes in the characteristics of a given instrument or system. Significant changes may be indicative of impending failure, and, if beyond certain limits, will require corrective maintenance. Some electronic instrument characteristics in phased-array units are similar to non-phased-array units and may be measured as described in Practice E1065 or Guide E1324.  
1.3 Ultrasonic examination systems using pulsed-wave trains and A-scan presentation (rf or video) may be evaluated.  
1.4 This guide establishes no performance limits for examination systems; if such acceptance criteria are required, these shall be specified by the using parties. Where acceptance criteria are implied herein, they are for example only and are subject to more or less restrictive limits imposed by customer’s and end user’s controlling documents.  
1.5 The specific parameters to be evaluated, conditions, frequency of test, and report data required shall be determined by the user.  
1.6 This guide may be used for the evaluation of a complete examination system, including search unit, instrument, interconnections, scanner fixtures, connected alarm, and auxiliary devices. This guide is not intended to be used as a substitute for calibration or standardization of an instrument or system to inspect any given material.  
1.7 Required test apparatus includes selected test blocks and position encoders in addition to the instrument or system to be evaluated.  
1.8 Alternate procedures, such as examples described in this document, or others, may only be used with customer approval.  
1.9 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.10 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.  
1.11 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 Recommendatio...

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