ASTM E634-2012 red 3750 Standard Practice for Sampling of Zinc and Zinc Alloys by Spark Atomic Emission Spectrometry 《通过火花原子发射光谱法对锌和锌合金取样的标准操作规程》.pdf

《ASTM E634-2012 red 3750 Standard Practice for Sampling of Zinc and Zinc Alloys by Spark Atomic Emission Spectrometry 《通过火花原子发射光谱法对锌和锌合金取样的标准操作规程》.pdf》由会员分享，可在线阅读，更多相关《ASTM E634-2012 red 3750 Standard Practice for Sampling of Zinc and Zinc Alloys by Spark Atomic Emission Spectrometry 《通过火花原子发射光谱法对锌和锌合金取样的标准操作规程》.pdf（4页珍藏版）》请在麦多课文档分享上搜索。

1、Designation:E63405 Designation: E634 12Standard Practice forSampling of Zinc and Zinc Alloys for Optical EmissionSpectrometric AnalysisSampling of Zinc and Zinc Alloys bySpark Atomic Emission Spectrometry1This standard is issued under the fixed designation E634; the number immediately following the

2、designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This practice covers the s

3、ampling of zinc and zinc alloys to obtain a sample suitable for quantitative opticalspark atomicemission spectrochemical analysis. Included are procedures for obtaining representative samples from molten metal, fromfabricated or cast products that can be melted, and from other forms that cannot be m

4、elted.1.2 The values stated in SI units are to be regarded as 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 responsibilityof the user of this standard to establis

5、h appropriate safety and health practices and determine the applicability of regulatorylimitations prior to use.2. Summary of Practice2.1 Molten metal representative of the furnace melt is poured into a mold to produce a chill-cast sample. The sample, whichmust represent the average composition, is

6、machined to a specified shape to produce an acceptable surface for excitation.2.2 Fabricated or cast products are remelted and cast into molds or are excited directly without remelting.3. Significance and Use3.1 This practice, used in conjunction with an appropriate quantitative opticalspark atomic

7、emission spectrochemical method,is suitable for use in manufacturing control, material or product acceptance, and development and research.4. Apparatus4.1 Ladle, of steel, designed to hold sufficient molten metal to completely fill the sample mold, with a handle of sufficient lengthto reach into a f

8、urnace, trough, pot, or crucible.NOTE 1Pure zinc metal (Special High Grade) is sampled using a ceramic or graphite ladle, as the solubility of iron in Special High Grade Zinc issufficient to cause a measurable contamination.4.2 Sample Molds, designed to produce homogeneous chill-cast specimens havin

9、g smooth surfaces, free from surface pocketsand pores. The specimens shall be representative (in the region to be excited) of the product metal. The samples shall have aspectrochemical response similar to the standards used in preparing the analytical curves. This is ensured by casting standards and

10、specimens in the same manner. Also, the specimens shall have a repeatability of measurement for major elements fromexcitation-to-excitation with a relative error of no more than 2 %. Several types of molds have been found acceptable.4.2.1 Type A, Pin Mold (Fig. 1)This mold produces two diagonally ca

11、st pins with sprues at the top of the specimens. The molddimensions are such as to produce pins approximately 100 mm (3.9 in.) in length by 11 mm (0.4 in.) in diameter. The mold is madeof steel or cast iron and weighs approximately 4.5 to 5.5 kg (10 to 12 lb). Pin specimens have been found to be ver

12、y homogeneous.If properly prepared, these specimens provide very reliable results with only one burn. However, pin specimens must be reshapedfor each additional burn.4.2.2 Type B, Book Mold (Fig. 2)This mold produces a vertically cast disk with a sprue on the edge of the specimen. The molddimensions

13、 are such as to produce a disk of approximately 64 mm (2.5 in.) in diameter by 6 to 8 mm (0.2 to 0.3 in.) in thickness.A circular central recess, 15 to 25 mm (0.6 to 1.0 in.) in diameter, on one side of the specimen facilitates machining of that sidein preparation for excitation. It also promotes mo

14、re uniform freezing of the raised peripheral area. The mold is made of steel orcast iron and weighs approximately 2 to 3 kg (4 to 7 lb). This mold works well for high purity zinc grades, but with alloys may1This practice is under the jurisdiction of ASTM Committee E01 on Analytical Chemistry for Met

15、als, Ores, and Related Materials and is the direct responsibility ofSubcommittee E01.05 on Cu, Pb, Zn, Cd, Sn, Be, their Alloys, and Related Metals.Current edition approved Oct.April 1, 2005.2012. Published November 2005.May 2012. Originally approved in 1978. Last previous edition approved in 200120

16、05 asE63496(2001).E634 05. DOI: 10.1520/E0634-05.10.1520/E0634-12.1This document is not an ASTM standard and is intended only to provide the user of an ASTM standard an indication of what changes have been made to the previous version. Becauseit may not be technically possible to adequately depict a

17、ll changes accurately, ASTM recommends that users consult prior editions as appropriate. In all cases only the current versionof the standard as published by ASTM is to be considered the official document.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2

18、959, United States.cause segregation due to solidification phenomena. Specimens should be excited only in the areas indicated in Fig. 3, and it maybe necessary to make several burns and report an average. The user is strongly cautioned to thoroughly investigate specimenhomogeneity for each alloy sys

19、tem to be analyzed.4.2.3 Type C, Center Pour Mold (Fig. 4)This mold produces a horizontally cast disk with a sprue over the center on the backside. The mold dimensions are such as to produce a disk approximately 64 mm (2.5 in.) in diameter by 8 mm (0.3 in.) in thickness.A circular central recess, 10

20、 to 20 mm (0.4 to 0.8 in.) in diameter, on one side of the specimen facilitates machining of that sidein preparation for excitation. It also promotes more uniform freezing of the raised peripheral area, but the corresponding raisedportion of the mold shall not be so large as to restrict the throat f

21、or the sprue. A slight taper, 1 to 2 deg, on the hinged portion ofthe mold facilitates opening when a specimen has been cast. The mold is made of steel or cast iron and weighs approximately 3.5to 4.5 kg (8 to 10 lb). The advantage of this mold is that the specimen obtained may be excited around the

22、entire annular area.However, as with the vertically cast disk specimens, although not as severe, segregation can be a problem. Therefore, it may benecessary to make several burns and report an average.FIG. 1 Type A Mold and SpecimenFIG. 2 Type B Mold and SpecimenE634 1224.2.4 Other MoldsMolds of dif

23、ferent types, materials, and dimensions may be used provided that the uniformity of thespecimens obtained is comparable to the uniformity of specimens obtained from Type A, B, or C molds. Further, the specimensshall have a spectrochemical response similar to the standards used for preparing the anal

24、ytical curves.4.3 Lathe or Milling Machine, capable of machining a smooth flat surface.NOTE 2When using pin specimens, reproducibility of the exact pin shape is very important. To maintain the integrity of the pin shapes it may benecessary to equip a micrometer cross-fed lathe with a special pin-sha

25、ping tool.4.4 Cutting ToolsEither alloy steel or cemented carbide is recommended.5. Sampling5.1 Molten MetalWhen molten metal is sampled, the temperature shall be well above the point at which any solid phase canbe present. Using a clean ladle, push any dross away from the sampling area. Then dip th

26、e ladle sideways into the clear area, wellbelow the surface, and stir momentarily. Turn the ladle upright and quickly withdraw. Heating the ladle prevents metal freezing,while obtaining metal well beneath the surface minimizes the danger of inclusion of oxide. Unless the mold is already hot, castand

27、 discard a preliminary specimen. Remove any excess metal from the ladle, dip it into the molten metal as before, and fill themold using an even rate of pour so as to allow for the escape of air. Do not dump the metal into the mold. Avoid overfilling thesprue or the mold may be difficult to open. All

28、ow the metal to freeze without jarring. The cast surfaces of the specimen, uponremoval from the mold, shall be free from shrinkage, inclusions, cracks, or roughness.NOTE 1Shaded areas are acceptable for analysis.FIG. 3 Specimens from Type A, B, and C MoldsFIG. 4 Type C Mold and SpecimenE634 123NOTE

29、3A change in the temperature profile of the mold, caused by a significant change in the sampling rate, may result in different chill-castcharacteristics and poor repeatability. Therefore, it is recommended that the sampling schedule be considered when an analysis program is beingdeveloped. Also, exp

30、erience has shown that pin specimens are much less sensitive than disk samples to temperature profile changes in the mold.5.2 Fabricated and Cast ProductsWhen the metal is in the wrought or cast form and a destructive test is practical, remelt arepresentative portion of the metal at a temperature we

31、ll above the liquidus line on the phase diagram of the metal. The sampleis placed in a graphite or other inert crucible and heated in a laboratory electric furnace. The melt is then cast in the mold asoutlined in 5.1. If the sample is in the form of thin sheet, turnings, or other finely divided mate

32、rial, remove any coatings or greasewith an appropriate solvent and press into a briquet before melting. Details of briquet size and formation are not critical to thesuccessful preparation of a melt. It is imperative that the specimen and the standards used in preparing the analytical curvesundergo t

33、he same sampling procedure, that is, remelting, to ensure valid analyses. However, when possible, it is recommended thatanalytical methods involving dissolution of the metal be used in preference to the remelting of samples.6. Preparation of Specimens6.1 Chill-Cast Pins from Type A MoldCut off the s

34、prues from the pins and machine the sprue ends of both pins to the sameshape. Each time the pins are reshaped, about 3 mm (0.1 in.) of metal should be removed from the end of the pins. Then makea second cut to produce a surface at an angle of about 60 deg to the axis of the pin. Continue this cut un

35、til the flat end of the pinmeasures exactly 3 mm (0.1 in.) in diameter. The completed pin tip is a truncated cone with a 120-deg apex angle and a 3-mm(0.1-in.) diameter (Fig. 3). The machined surface shall be smooth and free from scuffs, pits, or inclusions. The ideal surface isneither polished nor

36、visibly grooved, but should show a very fine tool pattern. More specifically, the ideal surface may be definedas approximately a 1.6 by 103-mm (63-in.) standard machine finish. A surface much finer or coarser may result in an analyticaldifference. Further, it is important that both specimens and sta

37、ndards have the same machine finish. Pin specimens have been foundto be very homogeneous and can be excited over the entire length of the pin. However, it is recommended that the lower 13 mm(0.5 in.) of the pin specimen (Fig. 3) not be excited because of potential solidification effects.6.2 Chill-Ca

38、st Disk from Type B or C MoldsCut off the sprue and machine the raised peripheral area surrounding the recessto a depth of 1 to 1.5 mm (0.04 to 0.06 in.) below the original surface. This depth is important because it corresponds to thecomposition on the phase diagram which represents the average com

39、position of the entire disk and, in turn, the actual compositionof the melt. Any other depth may result in an invalid analysis. The machined surface shall be smooth, and free from scuffs, pits,or inclusions. The ideal surface is neither polished nor visibly grooved, but should show a very fine tool

40、pattern. The ideal surfacemay be defined as approximately a 1.6 by 103-mm (63-in.) standard machine finish. A surface much finer or much coarser mayresult in an analytical difference. It is also important that both specimens and standards have the same machine finish. A type Bdisk may be excited onl

41、y in certain areas (Fig. 3), while a Type C disk may be excited around the entire annular area. For bothtypes, the outer 5 mm (0.2 in.) to the edge and the inner region up to about a 12-mm (0.48-in.) radius should not be excited (Fig.3).6.3 Chill-Cast Specimens from Other Acceptable MoldsSince a mol

42、d of different dimensions may result in a different freezingpattern, each type of mold shall be evaluated to determine the proper area and depth to machine the specimen to represent the truecomposition of the melt.6.4 Direct Excitation Without Casting a Specimen If the procedure outlined in Section

43、5 cannot be followed, onlyapproximate analyses can be made. The specimen shall be massive enough to prevent undue heating and shall have a flat surfacesuitable for excitation. Further, standards having a similar spectrochemical response shall be available. On sheet or platespecimens, machine off abo

44、ut 0.8 mm (0.03 in.) or one-fourth of the thickness, whichever is smaller. On thicker specimens,machine at least 1.3 mm (0.05 in.) below the original surface. Choose the location, depth, and number of areas to be analyzed toprovide a representative analysis of the product.7. Keywords7.1 optical emis

45、sion; sampling; spark atomic emission; spectrochemical analysis; zinc and zinc alloysASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of th

46、e validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. You

47、r comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive careful consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments

48、 have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or mult

49、iple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).E634 124