Tiêu chuẩn quốc tế
Số hiệu
Standard Number
ASTM E1210-99
Năm ban hành 1999
Publication date
Tình trạng
W - Hết hiệu lực
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Tên tiếng Anh
Title in English Standard Test Method for Fluorescent Liquid Penetrant Examination Using the Hydrophilic Post-Emulsification Process
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Chỉ số phân loại Quốc tế (ICS)
By field
19.100 - Thử không phá hủy và thiết bị
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Số trang
Page 7
Giá:
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Phạm vi áp dụng
Scope of standard 1.1 This test method covers procedures for fluorescent penetrant examination utilizing the hydrophilic post-emulsification process. It is a nondestructive testing method for detecting discontinuities that are open to the surface such as cracks, seams, laps, cold shuts, laminations, isolated porosity, through leaks, or lack of fusion and is applicable to in-process, final, and maintenance examination. It can be effectively used in the examination of nonporous, metallic materials, both ferrous and nonferrous, and of nonmetallic materials such as glazed or fully densified ceramics and certain nonporous plastics and glass. 1.2 This test method also provides a reference: 1.2.1 By which a fluorescent penetrant examination hydrophilic post-emulsification process recommended or required by individual organizations can be reviewed to ascertain their applicability and completeness. 1.2.2 For use in the preparation of process specifications dealing with the fluorescent penetrant examination of materials and parts using the hydrophilic post-emulsification process. Agreement by the purchaser and the manufacturer regarding specific techniques is strongly recommended. 1.2.3 For use in the organization of the facilities and personnel concerned with the liquid penetrant examination. 1.3 This test method does not indicate or suggest standards for evaluation of the indications obtained. It should be pointed out, however, that after indications have been produced, they must be interpreted or classified and then evaluated. For this purpose there must be a separate code or specification or a specific agreement to define the type, size, location, and direction of indications considered acceptable, and those considered unacceptable. 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 and health practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see Notes 4, 12, and 18.
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