ASTM E2824-2011 Standard Test Method for Determination of Beryllium in Copper-Beryllium Alloys by Phosphate Gravimetric Method《用磷酸盐重量法测定铜铍合金中铍的标准试验方法》.pdf

《ASTM E2824-2011 Standard Test Method for Determination of Beryllium in Copper-Beryllium Alloys by Phosphate Gravimetric Method《用磷酸盐重量法测定铜铍合金中铍的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM E2824-2011 Standard Test Method for Determination of Beryllium in Copper-Beryllium Alloys by Phosphate Gravimetric Method《用磷酸盐重量法测定铜铍合金中铍的标准试验方法》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: E2824 11Standard Test Method forDetermination of Beryllium in Copper-Beryllium Alloys byPhosphate Gravimetric Method1This standard is issued under the fixed designation E2824; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revi

2、sion, 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 test method describes the determination of beryl-lium in copper-beryllium alloys in percentages

3、 from 0.1 % to3.0 % by the phosphate gravimetric method.1.2 UnitsThe values stated in SI units are to be regardedas standard. No other units of measurement are included in thisstandard.1.3 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is the

4、responsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use. Specific hazardstatements are given in Section 9.2. Referenced Documents2.1 ASTM Standards:2E29 Practice for Using Significant Di

5、gits in Test Data toDetermine Conformance with SpecificationsE50 Practices for Apparatus, Reagents, and Safety Consid-erations for Chemical Analysis of Metals, Ores, andRelated MaterialsE135 Terminology Relating to Analytical Chemistry forMetals, Ores, and Related MaterialsE173 Practice for Conducti

6、ng Interlaboratory Studies ofMethods for Chemical Analysis of Metals3E255 Practice for Sampling Copper and Copper Alloys forthe Determination of Chemical CompositionE1601 Practice for Conducting an Interlaboratory Study toEvaluate the Performance of an Analytical Method3. Terminology3.1 For definiti

7、ons of terms used in this method, refer toTerminology E135.4. Summary of Test Method4.1 Beryllium is precipitated as the phosphate, which isfiltered, ignited, and weighed as beryllium pyrophosphate.Interfering elements, if present, may be complexed with(ethylenedinitrilo) tetraacetate solution.5. Si

8、gnificance and Use5.1 This test method for the chemical analysis of metals andalloys is primarily intended to test such materials for compli-ance with compositional specifications. It is assumed that allwho use these test methods will be trained analysts capable ofperforming common laboratory proced

9、ures skillfully andsafely. It is expected that work will be performed in a properlyequipped laboratory.6. Interferences6.1 The elements ordinarily present in beryllium-copperalloys do not interfere.7. Apparatus7.1 Electrodes for ElectroanalysisRecommended station-ary type platinum electrodes are des

10、cribed in 7.1.1 and 7.1.2.The surface of the platinum electrode should be smooth, clean,and bright to promote uniform deposition and good adherence.Deviations from the exact size and shape are allowable. Ininstances where it is desirable to decrease the time of deposi-tion and agitation of the elect

11、rolyte is permissible, a generallyavailable rotating type of electrode may be employed. Cleaningof the electrode by sandblasting is not recommended.7.1.1 CathodesPlatinum cathodes may be either open orclosed cylinders formed from sheets that are plain or perfo-rated, or from gauze. Gauze cathodes ar

12、e recommended;preferably from 50-mesh gauze woven from approximately0.21 mm diameter wire. The top and bottom of gauze cathodesshould be reinforced by doubling the gauze about 3 mm ontoitself, or by the use of platinum bands or rings. The cylindershould be approximately 30 mm in diameter and 50 mm i

13、nheight. The stem should be made from a platinum alloy wiresuch as platinum-iridium, platinum-rhodium, or platinum-ruthenium, having a diameter of approximately 1.3 mm. Itshould be flattened and welded the entire length of the gauze.The overall height of the cathode should be approximately 1301This

14、test method is under the jurisdiction of ASTM Committee E01 onAnalytical Chemistry for Metals, Ores, and Related Materials and is the directresponsibility of Subcommittee E01.05 on Cu, Pb, Zn, Cd, Sn, Be, their Alloys, andRelated Metals.Current edition approved May 1, 2011. Published July 2011. DOI:

15、 10.1520/E2824-11.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Withdrawn.1Copyright ASTM International, 1

16、00 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.mm. A cathode of these dimensions will have a surface area of135 cm2exclusive of the stem.7.1.2 AnodesPlatinum anodes may be a spiral type whenanodic deposits are not being determined, or if the deposits aresmall (as

17、in the electrolytic determination of lead when it ispresent in concentrations below 0.2 %). Spiral anodes shouldbe made from 1.0 mm or larger platinum wire formed into aspiral of seven turns having a height of approximately 130 mm.A spiral anode of these dimensions will have a surface area of9cm2. W

18、hen both cathode and anode plates are to bedetermined, the anode should be made of the same material anddesign as the electrode described in 7.1.1. The anode cylindershould be approximately 12 mm in diameter and 50 mm inheight and the overall height of the anode should be approxi-mately 130 mm. A ga

19、uze anode of these dimensions will havea surface area of 54 cm2exclusive of the stem.7.1.3 Gauze cathodes are recommended where rapid elec-trolysis is used.8. Reagents8.1 Ammonium Acetate Solution (500 g/L)Dissolve 500 gof ammonium acetate in water, and dilute to 1 L.8.2 Ammonium Acetate Wash Soluti

20、onDilute 5 mL of theammonium acetate solution to 1 L, and adjust the pH to 5.2 60.05 with acetic acid.NOTE 1Use a pH meter for all pH adjustments.8.3 Ammonium Dihydrogen Phosphate (100 g/L)Dissolve100 g of ammonium dihydrogen phosphate (NH4H2PO4)inwater and dilute to 1 L.8.4 Ammonium (Ethylenedinitr

21、ilo) Tetraacetate Solution(28 g/L)To 2.5 g of (ethylenedinitrilo) tetraacetic acid add 30mL of water and a drop of methyl red solution. Neutralize withNH4OH (1 + 1), and warm gently to dissolve the last traces ofsolid. Cool and dilute to 100 mL.8.5 Methyl Red Indicator Solution (0.5 g/L ethanol)Diss

22、olve 0.05 g of methyl red in 100 mL of ethanol.8.6 Sulfuric-Nitric Acid MixtureAdd slowly, while stir-ring in a cold water bath, 300 mLof H2SO4to 750 mLof water.Cool and add 210 mL of HNO3.9. Hazards9.1 For precautions to be observed in this method, referenceshall be made to Practices E50. Both bery

23、llium metal and itscompounds may be toxic. Care should be exercised to preventcontact of beryllium-containing materials with the skin. Theinhalation of any beryllium-containing substance, either as avolatile compound or as finely divided powder, should beespecially avoided. Beryllium-containing resi

24、dues (especiallyignited oxide) should be carefully disposed.10. Sampling10.1 Sampling shall conform to Practice E255. However,this method does not supersede any sampling requirementsspecified in a specific ASTM material specification.11. Rounding Calculated Values11.1 Calculated values shall be roun

25、ded to the desirednumber of places as directed in Practice E29.12. Preparation of Apparatus12.1 CathodeClean the cathode in hot HNO3,(1+1),rinse with distilled water, rinse in two separate baths of ethanolor acetone. Dry at a low temperature, (110 C for 3 to 5 min),and cool to room temperature in a

26、desiccator.12.2 AnodeClean in HCl, (1 + 1), rinse with distilledwater.12.3 Weigh the cathode to the nearest 0.1 mg and record theweight. The anode does not have to be weighed.13. Procedure13.1 Transfer 5.00 g of sample to a 300-mL electrolysisbeaker. Add 42 mL of the H2SO4-HNO3mixture, cover, andall

27、ow to stand a few minutes until the reaction has nearlyceased. Heat at 80 C to 90 C until dissolution is complete andbrown fumes have been expelled. Wash down the cover glassand the sides of the beaker and dilute to about 175 mL (enoughto submerge the cathode when it is inserted).13.2 Insert the ele

28、ctrodes, cover the solution with a pair ofsplit watch glasses, and electrolyze at a current density of 0.6A/dm2for about 16 h. Wash down the cover glasses, sides ofthe beaker, and electrode stems and continue electrolysis forabout 15 min. If no copper plates on the newly exposedcathode surface, copp

29、er deposition may be considered com-pleted.13.3 Quickly withdraw the cathode from the electrolytewhile directing a gentle stream of water from a wash bottleover its surface.13.4 Evaporate the spent electrolyte to dense white fumesand fume for about 5 min to dehydrate the silicic acid. Cool,add about

30、 50 mL of water, and heat until all salts are insolution. Filter through a small, medium-texture paper, catch-ing the filtrate in a 250-mL volumetric flask. Wash the beakerand paper thoroughly with hot H2SO4(1 + 99), combining thewashings with the filtrate. Cool the solution in the volumetricflask,

31、dilute to the mark, and mix.13.5 Using a pipet, transfer 50 mL of the solution in 13.4 toa 400-mL beaker. Add 3 drops of HF and 10 mL of H2SO4(1+ 2), and evaporate to fumes. Cool to room temperature andadd 100 mL of water. Heat to dissolve soluble salts and againcool to room temperature.13.6 Add 10

32、mL of ammonium (ethylenedinitrilo) tetraac-etate solution, and adjust the pH to 2.0 6 0.05 (see Note 1 forall pH adjustments) with NH4OH (1 + 1). Boil 1 min and coolto room temperature. Add 10 mL of ammonium dihydrogenphosphate solution and adjust the pH to 5.2 6 0.05 withammonium acetate solution.1

33、3.7 Heat to boiling cautiously to prevent bumping, andthen maintain just below the boiling point until the precipitatebecomes granular. Remove from the source of heat and allowto stand at least 12 h.13.8 Filter using an 11-cm fine paper and wash six timeswith ammonium acetate wash solution. Discard

34、the filtrate.Dissolve the precipitate with 100 mL of hot HCl (1 + 4),collecting the solution in the original beaker.13.9 Add 2 mL of ammonium (ethylenedinitrilo) tetraac-etate solution, and adjust the pH to 2.0 6 0.05 with NH4OH(1 + 1). Cool, add 2 mL of ammonium dihydrogen phosphateE2824 112solutio

35、n, and adjust the pH to 5.2 6 0.05 with ammoniumacetate solution. Proceed as directed in 13.7.13.10 Filter using an 11-cm fine paper and wash six timeswith ammonium acetate wash solution. Transfer the paper to aweighed platinum crucible. Place the crucible in a mufflefurnace, and dry and char the pa

36、per by gradually increasing thetemperature to 500 C. When all the carbon has been removed,raise the temperature to 1000 C and maintain at this tempera-ture for 4 h. Cool in a desiccator and weigh.14. Calculation14.1 Calculate the percentage of beryllium as follows:Beryllium, % 5 A 3 0.0939/B! 3 100

37、(1)where:A = grams of beryllium pyrophosphate, andB = grams of sample used.15. Precision and Bias15.1 PrecisionEight laboratories cooperated in testingthis method and obtained the data summarized in Table 1.15.2 BiasNo certified reference materials suitable fortesting this test method were available

38、 when the interlaboratorytesting program was conducted. The user of this standard isencouraged to employ accepted reference materials, if avail-able, to determine the accuracy of this test method as appliedin a specific laboratory.15.3 This test method was evaluated in accordance withPractice E173 (

39、discontinued 1997). Practice E173 has beenreplaced by Practice E1601. The Reproducibility R2of PracticeE173 corresponds to the Reproducibility Index R of PracticeE1601. The Repeatability R1of Practice E173 corresponds tothe Repeatability Index r of Practice E1601.16. Keywords16.1 beryllium; copper-b

40、eryllium alloys; gravimetricASTM 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 the validity of any such patent rights, and the riskof infr

41、ingement 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. Your comments are invited either for revision of this standa

42、rd 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 have not received a fair hearing you shouldmake your vie

43、ws 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 multiple copies) of this standard may be obtained by contacti

44、ng 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/).TABLE 1 Statistical InformationTest SpecimenBerylliumFound,%Repeatability(R1, E173)Reproducibility(R2, E173)(1) Beryllium copper, B-7 1.744 0.026 0.042(2) Beryllium copper, C-7 0.460 0.020 0.046E2824 113