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Astm Iso 52903-2 (2020)
Astm Iso 52903-2 (2020)
Astm Iso 52903-2 (2020)
for the
Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
ISO/ASTM 52903-2:2020(E)
TABLE 1 Specifications for mechanical tension testing of material extrusion based additive manufacturing for plastics
SpecificationA,B Class I Class II Class III
Build certification A minimum of three XY or YX tension A minimum of three XY or YX tension No tension specimens needed unless
specimens, and a minimum of three specimens requested by customer
ZX or ZY tension specimens
A
For part orientation notation, see ISO/ASTM 52921.
B
For ASTM D638 or ISO 527-1, smaller tension specimens may be used for ZX or ZY samples for build heights less than 57 mm (2.25 in.).
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ISO/ASTM 52903-2:2020(E)
9.5.1 Support material shall be removed from the test 10. Qualification
specimens and parts in accordance with the material manufac- 10.1 Additive manufacturing equipment qualification—
turer’s recommendations. Equipment qualification shall comply with the OEM recom-
9.5.2 If applicable, additional post processing methods for mended performance. The customer may require additional
test specimens and parts shall comply with all customer equipment performance characteristics.
specified requirements. The following subclauses (9.5.3 to
9.5.5) describe some post processing methods. Customer 10.2 Build qualification—The part manufacturer shall use
specifications may supersede the methods listed. OEM parameters for the material being used or modified
9.5.3 Parts may be finished (e.g. drilled, holes reamed, parameters based on best practice.
deburred, or hand sanded) to remove excess material from the 10.3 Additive manufacturing equipment requalification—
part to meet requirements. A tumbler may also be used if the Systems that are not currently under an active maintenance
part geometry allows. contract shall follow OEM’s recertification process.
9.5.4 Parts may be visually examined for defects and
anomalies (e.g. curl, growth, nodules, discoloration, distortion, 11. Report
layer lines, etc.) according to the customer’s requirements and 11.1 If requested, a report shall be provided by the part
part supplier’s standard practice. Parts may be scrapped if manufacturer to the customer at the time of shipment stating
visual defects are present. that the parts were manufactured in accordance with this
9.5.5 High intensity light can be required to check internal document.
features. Light source shall be sufficient to yield penetration of
the part structure requiring inspection. Care should be taken so 12. Keywords
the light source does not damage the plastic part. 12.1 additive manufacturing; equipment; extrusion; plastics
Bibliography
(1) ISO 178 Plastics — Determination of flexural properties (10) ASTM D256 Test Methods for Determining the Izod Pendulum
(2) ISO 179-1 Plastics — Determination of Charpy impact properties Impact Resistance of Plastics
— Part 1: Non-instrumented impact test (11) ASTM D638 Test Method for Tensile Properties of Plastics
(3) ISO 179-2 Plastics — Determination of Charpy impact properties (12) ASTM D785 Test Method for Rockwell Hardness of Plastics and
— Part 2: Instrumented impact test Electrical Insulating Materials
(4) ISO 291 Plastics — Standard atmospheres for conditioning and (13) ASTM D790 Test Methods for Flexural Properties of Unreinforced
testing and Reinforced Plastics and Electrical Insulating Materials
(5) ISO 527-1 Plastics — Determination of tensile properties — Part (14) ASTM D4000 Classification System for Specifying Plastic Materi-
1: General principles als
(6) ISO 1043-1 Plastics — Symbols and abbreviated terms — Part 1:
(15) SAE AS 9100D Quality Management Systems — Requirements
Basic polymers and their special characteristics
for Aviation, Space and Defense Organizations
(7) ISO 2602 Statistical interpretation of test results — Estimation of
(16) ASQ ANSI C1 Specification of General Requirements for a Qual-
the mean — Confidence interval
(8) ISO 9001 Quality management systems — Requirements ity Program
(9) ISO 13485 Medical devices — Quality management systems —
Requirements for regulatory purposes
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