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ASTM E801-06

(Practice)

Standard Practice for Controlling Quality of Radiological Examination of Electronic Devices

Standard Practice for Controlling Quality of Radiological Examination of Electronic Devices

ABSTRACT
This practice is intended to control the quality and repeatability of the radiological examination of electronic devices for internal discontinuities, extraneous material, missing components, crimped or broken wires, and defective solder joints in cavities, in the encapsulating materials, or the boards. However, this practice is not intended to control the acceptability or quality of the electronic devices imaged. The quality of the radiological examination shall be determined by image quality indicators (IQIs), which shall be manufactured from clear acrylic plastic with steel covers serving as shims, lead spheres, gold or tungsten wires, and lead numbers, and shall be permanently identified with the appropriate IQI number. The IQI shall simulate as closely as possible the device being examined. For example, the IQI shall have a radiographic density or grey level nearest to that of the device being examined. Two IQIs shall be used for each radiograph, with each IQI located at diagonally opposite corners of the film, and the radiographic image free of blemishes. To identify the image, in both radiography and radioscopy, a system of positive identification of the image shall be provided, which may include any or all of the following: the name of examining laboratory, the date, the part number, the serial number, the data code, the view, and whether original or subsequent exposure.
SCOPE
1.1 This practice relates to the radiological examination of electronic devices for internal discontinuities, extraneous material, missing components, crimped or broken wires, and defective solder joints in cavities, in the encapsulating materials, or the boards. Requirements expressed in this practice are intended to control the quality and repeatability of the radiological images and are not intended for controlling the acceptability or quality of the electronic devices imaged. Note 1 - Refer to the following publications for pertinent information on methodology and safety and protection: Guides E 94 and E 1000, and "General Safety Standard for Installation Using Non-Medical X Ray and Sealed Gamma Ray Sources, Energies Up to 10 MeV Equipment Design and Use," Handbook No. 114.
1.2 If a nondestructive testing agency as described in Practice E 543 is used to perform the examination, the testing agency should meet the requirements of Practice E 543.
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.

General Information

Status
Historical
Publication Date
30-Nov-2006
ICS
19.100 - Non-destructive testing
Technical Committee
E07 - Nondestructive Testing
Drafting Committee
E07.01 - Radiology (X and Gamma) Method
Current Stage
Ref Project

Relations

Replaces
ASTM E801-01 - Standard Practice for Controlling Quality of Radiological Examination of Electronic Devices
Effective Date
01-Dec-2006
Replaced By
ASTM E801-06(2011) - Standard Practice for Controlling Quality of Radiological Examination of Electronic Devices
Effective Date
01-Dec-2011
Referred By
ASTM E94/E94M-22 - Standard Guide for Radiographic Examination Using Industrial Radiographic Film
Effective Date
01-Dec-2006
Referred By
ASTM E1742/E1742M-18 - Standard Practice for Radiographic Examination
Effective Date
01-Dec-2006
Referred By
ASTM E1161-21 - Standard Practice for Radiographic Examination of Semiconductors and Electronic Components
Effective Date
01-Dec-2006
Referred By
ASTM E543-21 - Standard Specification for Agencies Performing Nondestructive Testing
Effective Date
01-Dec-2006
Referred By
ASTM E431-96(2022) - Standard Guide to Interpretation of Radiographs of Semiconductors and Related Devices
Effective Date
01-Dec-2006

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ASTM E801-06 - Standard Practice for Controlling Quality of Radiological Examination of Electronic DevicesASTM E801-06 - Standard Practice for Controlling Quality of Radiological Examination of Electronic Devices
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ASTM E801-06 - Standard Practice for Controlling Quality of Radiological Examination of Electronic Devices
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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: E801 – 06
Standard Practice for
Controlling Quality of Radiological Examination of
1
Electronic Devices
This standard is issued under the fixed designation E801; 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.
This standard has been approved for use by agencies of the Department of Defense.
1. Scope E1316 Terminology for Nondestructive Examinations
1.1 This practice relates to the radiological examination of
3. Terminology
electronic devices for internal discontinuities, extraneous ma-
3.1 Definitions—Refer to Terminology E1316, Section D.
terial, missing components, crimped or broken wires, and
defective solder joints in cavities, in the encapsulating materi-
4. Direction of Radiation
als, or the boards. Requirements expressed in this practice are
4.1 When not otherwise specified, the direction of the
intended to control the quality and repeatability of the radio-
central beam of radiation shall be as perpendicular (65%)as
logical images and are not intended for controlling the accept-
possible to the surface of the film or detector.
ability or quality of the electronic devices imaged.
5. Image Quality Indicators (IQI’s)
NOTE 1—Refer to the following publications for pertinent information
on methodology and safety and protection: Guides E94 and E1000, and
5.1 The quality of all levels of radiological examination
“General Safety Standard for Installation Using Non-Medical X Ray and
shall be determined by IQI’s conforming to the following
Sealed Gamma Ray Sources, Energies Up to 10 MeV Equipment Design
2 specifications:
and Use,” Handbook No. 114.
5.1.1 The IQI’s shall be fabricated of clear acrylic plastic
1.2 If a nondestructive testing agency as described in
withsteelcovers,leadspheres,goldortungstenwires,andlead
Practice E543 is used to perform the examination, the testing
numbers. The steel covers serve as shims.
agency should meet the requirements of Practice E543.
5.1.1.1 The IQI’s shall conform to the requirements of
1.3 This standard does not purport to address all of the
Fig. 1.
safety concerns, if any, associated with its use. It is the
5.1.1.2 The IQI’s shall be permanently identified with the
responsibility of the user of this standard to establish appro-
appropriate IQI number as shown in Fig. 1. The number shall
priate safety and health practices and determine the applica-
be affixed by mounting a 0.125-in. (3.18-mm) tall lead number
bility of regulatory limitations prior to use.
on the flat bottom of a 0.250-in. (6.35-mm) diameter hole. The
identification number shall be located as shown in Fig. 1 and
2. Referenced Documents
shall be of sufficient contrast to be clearly discernible in the
3
2.1 ASTM Standards:
radiological image.
E94 Guide for Radiographic Examination
5.1.1.3 Each semiconductor IQI will have a serial number
E543 Specification for Agencies Performing Nondestruc-
permanently etched or engraved on it. Each serial number will
tive Testing
be traceable to the calibration image supplied by the manufac-
E1000 Guide for Radioscopy
turer. The manufacturer shall radiograph the IQI with lead
E1255 Practice for Radioscopy
markers identifying the serial number. See Fig. 2.
6. Application of the Image Quality Indicator (IQI)
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
6.1 The application of the IQI’s shall be made in such a
Radiology (X and Gamma) Method.
manner as to simulate as closely as possible the device being
Current edition approved Dec. 1, 2006. Published January 2007. Originally
examined. To accomplish this objective, a set of eight IQI’s is
approved in 1981. Last previous edition approved in 2001 as E801 - 01. DOI:
provided. These provide a range of cover thickness (of steel
10.1520/E0801-06.
2
Available from National Institute of Standards and Technology (NIST), 100
shim stock) that is radiologically equivalent to the range of
Bureau Dr., Stop 1070, Gaithersburg, MD 20899-1070, http://www.nist.gov.
devices from glass diodes or plastic-encapsulated circuits
3
For referenced ASTM standards, visit the ASTM website, www.astm.org, or
(number one) to large power or hybrid circuit devices (number
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
Standards volume information, refer to the standard’s Document Summary page on eight). Wire size increases with shim stock thickness because
the ASTM website.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.
1

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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 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.  
5.5 The MAUT technique has proven utility in the inspection of multi-ply carbon-fiber reinforced laminates used in primary aircraft structures.11  
5.6 For ultrasonic testing of laminate composites and sandwich core materials using conventional UT equipment consult Practice E2580. Consult Practice E114 for ultrasonic testing of materials by the pulse-echo method using straightbeam longitudinal waves introduced by a piezoelectric elemen...
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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.  
1.3 Typical test articles include monolithic composite layups such as uniaxial, cross ply and angle ply laminates, sandwich constructions, bonded structures, and filament windings, as well as forged, wrought and cast metallic parts. Two techniques can be considered based on accessibility of the inspection surface: namely, pulse echo inspection for one-sided access and through-transmission for two-sided access. As used in this practice, both require the use of a pulsed straight-beam ultrasonic longitudinal wave followed by observing indications of either the reflected (pulse-echo) or received (through transmission) wave.  
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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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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.  
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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.  
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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.  
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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.  
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Standard Practice for Liquid Penetrant Testing for General Industry

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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.  
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 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 E2446-23(Practice)
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 ...

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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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