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5.1 The purpose of this practice is to describe a procedure for in-line-eddy-current examination of hot cylindrical bars in the range of diameters listed in 1.2 for large and repetitive discontinuities that may form during processing.5.2 The discontinuities in bar product capable of being detected by the electromagnetic method are listed in 1.3.1. The method is capable of detecting surface and some subsurface discontinuities that are typically in the order of 0.030 in. (0.75 mm) and deeper, but some shallower discontinuities might also be found.5.3 Discontinuities that are narrow and deep, but short in length, are readily detectable by both probe and encircling coils because they cause abrupt flux changes. Surface and subsurface discontinuities (if the electromagnetic frequency provides sufficient effective depth of penetration) can be detected by this method.5.3.1 Discontinuities such as scratches or seams that are continuous and uniform for the full length of cut length bars or extend for extensive linear distances in coiled product may not always be detected when encircling coils are used. These are more detectable with probe coils by intercepting the discontinuity in their rotation around the circumference.5.3.2 The orientation and type of coil are important parameters in coil design because they influence the detectability of discontinuities.5.4 The eddy current method is sensitive to metallurgical variations that occur as a result of processing, thus all received signals above the alarm level are not necessarily indicative of defective product.1.1 This practice covers procedures for eddy current examination of hot ferromagnetic bars above the Curie temperature where the product is essentially nonmagnetic, but below 2100 °F (1149 °C).1.2 This practice is intended for use on bar products having diameters of 1/2 in. (12.7 mm) to 8 in. (203 mm) at linear throughput speeds up to 24 000 ft/min (122 m/sec). Larger or smaller diameters may be examined by agreement between the using parties.1.3 The purpose of this practice is to provide a procedure for in-line eddy current examination of bars during processing for the detection of major or gross surface discontinuities.1.3.1 The types of discontinuities capable of being detected are commonly referred to as: slivers, laps, seams, roll-ins (scale, dross, and so forth), and mechanical damage such as scratches, scores, or indentations.1.4 This practice does not establish acceptance criteria. They must be specified by agreement between the using parties.1.5 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.1.6 This practice 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 practice to establish appropriate safety, health, environmental practices and determine the applicability of regulatory limitations prior to use.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.

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4.1 The reason for preserving military sampling standards is that many organizations throughout the world still use these standards in their current form. MIL-STD-1235B is no longer supported by the U.S. Department of Defense as of the mid-1990s and is out of print, but does exist in the public domain. This practice represents a conversion of MIL-STD-1235B to an ASTM-supported standard.4.2 This practice provides the tables and procedures for applying five different types of continuous sampling plans for inspection by attributes. These continuous sampling plans are discussed in Sections 6 – 10 of this practice and each section includes information on:(1) Initiation of 100 % inspection in use.(2) Requirements on when to switch to sampling inspection.(3) Conditions warranting a return to 100 % inspection.(4) When a change in Code Letter, if desired, can be made.(5) What to do when the checking inspector finds a defect that was originally found conforming by the screening inspector(s), that is, ineffective screening.(6) Situations where a defect is found before the switch to 100 % inspection causing excessive periods of 100 % inspection so action must be taken, that is, long periods of screening.4.2.1 Section 6 (Section 2 in MIL-STD-1235B) describes specific procedures and applications of the CSP-1 sampling plans – a single-level continuous sampling procedure which provides for alternating between sequences of 100 % inspection and sampling inspection.4.2.2 Section 7 (Section 3 in MIL-STD-1235B) describes specific procedures and applications of the CSP-F sampling plans – a variation of the CSP-1 plans in that CSP-F plans are applied to a relatively short run of product, thereby permitting smaller clearance numbers to be used.4.2.3 Section 8 (Section 4 in MIL-STD-1235B) describes specific procedures and applications of the CSP-2 sampling plans – a modification of CSP-1 in that 100 % inspection resumes only after a prescribed number of defect-free units separate any two defective sample units.4.2.4 Section 9 (Section 5 in MIL-STD-1235B) describes specific procedures and applications of the CSP-T sampling plans – a multi-level continuous sampling procedure which provides for reducing the sampling frequency upon demonstration of superior product quality.4.2.5 Section 10 (Section 6 in MIL-STD-1235B) describes specific procedures and applications of the CSP-V sampling plans – a single-level continuous sampling procedure which is an alternative to CSP-T in that these plans provide for reducing the clearance number in good quality situations where reduction of sampling frequency has no economic merit.AbstractThis practice establishes tables and procedures for applying five different types of continuous sampling plans for inspection by attributes using MIL-STD-1235B as a basis for sampling a steady stream of lots indexed by AQL. This practice represents a conversion of MIL-STD1235B to an ASTM-supported standard.1.1 This practice establishes tables and procedures for applying five different types of continuous sampling plans for inspection by attributes using MIL-STD-1235B as a basis for sampling a steady stream of lots indexed by AQL.1.2 This practice provides the sampling plans of MIL-STD-1235B in ASTM format for use by ASTM committees and others. It recognizes the continuing usage of MIL-STD-1235B in industries supported by ASTM. Most of the original text in MIL-STD-1235B is preserved in Sections 6 – 10 of this practice.1.3 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.1.4 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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4.1 This practice describes the procedures that can be used to prepare new and weathered zinc-coated surfaces on after-fabrication steel products for painting, and that can improve the bond of paint to the zinc surface.1.1 This practice describes methods of preparing surfaces of new and weathered hot-dip galvanized steel for painting with liquid paint and coating products. Preparing surfaces of new and partially weathered galvanized steel for powder coating is addressed in Practice D7803. Hot-dip galvanized steel is produced by the immersion of fabricated or unfabricated products in a bath of molten zinc, as specified in Specifications A123/A123M or A153/A153M. This practice covers surface preparation on iron and steel products and hardware that have not been painted previously. Galvanized surfaces may have been treated with protective coatings to prevent the occurrence of wet storage stain. This practice does not apply to sheet galvanized steel products nor to the coil coating or continuous roller coating processes. Sheet and coil surface preparation can be done in accordance with Practice D7396.1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.1.3 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.1.4 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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4.1 This guide contains a listing of those characterization parameters that are directly related to the functionality of hyaluronan. This guide can be used as an aid in the selection and characterization of the appropriate hyaluronan for a particular application. This guide is intended to give guidance in the methods and types of testing necessary to properly characterize, assess, and ensure consistency in the performance of a particular hyaluronan. It may have use in the regulation of these devices by appropriate authorities.4.2 The hyaluronan covered by this guide may be gelled, cross-linked, extruded, or otherwise formulated into biomedical devices for use in tissue engineered medical products or drug delivery devices for implantation as determined to be appropriate, based on supporting biocompatibility and physical test data. Recommendations in this guide should not be interpreted as a guarantee of clinical success in any tissue engineered medical product or drug delivery application.4.3 To ensure that the material supplied satisfies requirements for use in TEMPs, several general areas of characterization should be considered. These are: identity of hyaluronan, physical and chemical characterization and testing, impurities profile, and performance-related tests.1.1 This guide covers the evaluation of hyaluronan suitable for use in biomedical or pharmaceutical applications, or both, including, but not limited to, Tissue Engineered Medical Products (TEMPs).1.2 This guide addresses key parameters relevant to the characterization and purity of hyaluronan.1.3 As with any material, some characteristics of hyaluronan may be altered by processing techniques, such as cross-linking and sterilization, required for the production of a specific formulation or device. Therefore, properties of fabricated forms of this polymer should be evaluated using test methods that are appropriate to ensure safety and efficacy and are not addressed in this guide.1.4 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 and health practices and determine the applicability of regulatory requirements prior to use.

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