SAE AMS 2315G-2013 Determination of Delta Ferrite Content《铁素体含量测定》.pdf
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1、_ SAE Technical Standards Board Rules provide that: “This report is published by SAE to advance the state of technical and engineering sciences. The use of this report is entirely voluntary, and its applicability and suitability for any particular use, including any patent infringement arising there
2、from, is the sole responsibility of the user.” SAE reviews each technical report at least every five years at which time it may be reaffirmed, revised, or cancelled. SAE invites your written comments and suggestions. Copyright 2012 SAE International All rights reserved. No part of this publication m
3、ay be reproduced, stored in a retrieval system or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise, without the prior written permission of SAE. TO PLACE A DOCUMENT ORDER: Tel: 877-606-7323 (inside USA and Canada) Tel: +1 724-776-4970 (outside U
4、SA) Fax: 724-776-0790 Email: CustomerServicesae.org SAE WEB ADDRESS: http:/www.sae.org SAE values your input. To provide feedback on this Technical Report, please visit http:/www.sae.org/technical/standards/AMS2315G AEROSPACE MATERIAL SPECIFICATION AMS2315 REV. G Issued 1963-01 Revised 2013-02 Super
5、seding AMS2315F Determination of Delta Ferrite Content RATIONALE AMS2315G revises the requirement for heat treatment of the specimen used to evaluate delta ferrite (3.1.4.1) and introduces alternative etching procedures (3.1.6, 8.4), and is a Five Year Review and update of this specification. 1. SCO
6、PE This specification covers two methods for determining the percentage of delta ferrite in steels and other iron alloys. When applicable, this specification will be invoked by the material specification. 2. APPLICABLE DOCUMENTS The issue of the following documents in effect on the date of the purch
7、ase order forms a part of this specification to the extent specified herein. The supplier may work to a subsequent revision of a document unless a specific document issue is specified. When the referenced document has been cancelled and no superseding document has been specified, the last published
8、issue of that document shall apply. 2.1 ASTM Publications Available from ASTM International, 100 Barr Harbor Drive, P.O. Box C700, West Conshohocken, PA 19428-2959, Tel: 610-832-9585, www.astm.org. ASTM E 3 Preparation of Metallographic Specimens 3. TECHNICAL REQUIREMENTS 3.1 Specimen Preparation 3.
9、1.1 Heat Qualification Sampling shall be in accordance with 4.3.1. Samples shall be converted into test specimens in accordance with 3.1.3. 3.1.2 Product Qualification Product from a heat not qualified, based on sampling as in 4.3.1, shall be sampled in accordance with 4.3.2. Samples shall be conver
10、ted into test specimens in accordance with 3.1.3. SAE AMS2315G Page 2 of 7 3.1.3 Specimen Selection Samples of sufficient size to provide specimens having approximately 0.25 to 0.5 square inch (161 to 323 mm2) prepared surface area or of an area sufficient to randomly select the required number of f
11、ields to accurately examine the sample, shall be cut from the product as in 3.1.3.1, 3.1.3.2, or 3.1.3.3, as applicable. Each specimen shall be marked in such a manner that its orientation with respect to the direction of rolling, drawing, or extruding is easily identifiable. 3.1.3.1 Round, Hexagona
12、l, or Square Product Specimens shall be selected from an area midway between the edge and the center of the sample. 3.1.3.2 Rectangular Product Specimens shall be selected from an area midway between the longitudinal edge and the center of the sample. 3.1.3.3 Tubing and Other Hollow Shapes Specimens
13、 shall be selected from samples which include the full wall thickness of the product. 3.1.4 Heat Treatment Specimens, except as specified in 3.1.4.1, shall be austenitized at the normal recommended temperature for the grade of steel being examined and adequately quenched. The quenched specimens shal
14、l be tempered at a sufficiently high temperature to develop good metallographic contrast. 3.1.4.1 Solution and precipitation hardenable steels shall be solution heat treated and may be precipitation heat treated to develop good metallographic contrast. 3.1.5 Polishing After heat treatment as in 3.1.
15、4, a face of each specimen, perpendicular to the direction of maximum deformation, shall be ground and polished, using standard metallographic polishing techniques in accordance with ASTM E 3 to produce a surface suitable for microscopic examination. 3.1.6 Etching The polished surface of each specim
16、en shall be suitably etched to reveal delta ferrite (See 8.4). 3.2 Procedure for limited delta ferrite criterion Inspect the specimen surface at a magnification appropriate to observe the relative amount and distribution of delta ferrite present. If it is evident that many fields to be measured will
17、 have zero value, and no single field will have a value exceeding the material specification maximum, then measure a set number of fields defined in a laboratory procedure sufficient to ensure that the upper control limit of the mean is less than 50% of the material specification maximum at the 95%
18、confidence level as in 3.2.1 or 3.2.2. A 10% relative accuracy level is not required. In case of dispute over the percentage of delta ferrite, the value determined as in 3.2.1 shall govern. 3.2.1 Point Count Method 3.2.1.1 Field Measurement Project the image of the microstructure of each specimen on
19、to the ground-glass screen of a reflection-type microscope or metallograph. Place a transparent point-counting grid template either in front of or behind the ground glass. The template should consist of either 100 or 500 systematically spaced grid points, either in the form of fine crosses or a grid
20、 lattice. The magnification chosen should be high enough to clearly resolve the delta ferrite grains but not so high that the number of grid points falling in the ferrite grains exceeds one, on the average. For each specimen, count the number of grid points (i.e., the intersection point of the cross
21、es or grid blocks) that fall within the ferrite grains as one and those that fall on the phase boundaries as one-half. SAE AMS2315G Page 3 of 7 3.2.1.2 Field Selection Select the fields to be measured randomly, that is, without looking at the image, by moving the stage controls. Do not alter the pos
22、ition so that grid points fall on or miss ferrite grains. Space the fields selected around the specimen surface in a systematic pattern. Measure a sufficient number of fields so that the relative accuracy (See 3.2.1.3.5) is 10% or less. The relative accuracy of the measurement is influenced by the v
23、olume fraction of the ferrite, the magnification, the grid point density, the number of fields measured, and the field-to-field variation of the ferrite phase. 3.2.1.3 Calculation 3.2.1.3.1 Ferrite per Field Calculate the volume fraction of ferrite using Equation 1 for each field measured. V i,P i,P
24、t-100=(Eq. 1) where: V,i= Volume fraction of ferrite in % of each field P,i = Number of grid points in the ferrite phase or on the phase boundaries Pt= Number of grid points 3.2.1.3.2 Ferrite per Specimen Determine the mean value of the volume fraction of ferrite using Equation 2. VV i,n-=(Eq. 2) wh
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