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本文(ASTM D5258-2002(2013) Standard Practice for Acid-Extraction of Elements from Sediments Using Closed Vessel Microwave Heating《使用封闭式容器微波加热法从沉淀物中酸萃取元素的标准实施规程》.pdf)为本站会员(tireattitude366)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM D5258-2002(2013) Standard Practice for Acid-Extraction of Elements from Sediments Using Closed Vessel Microwave Heating《使用封闭式容器微波加热法从沉淀物中酸萃取元素的标准实施规程》.pdf

1、Designation: D5258 02 (Reapproved 2013)Standard Practice forAcid-Extraction of Elements from Sediments Using ClosedVessel Microwave Heating1This standard is issued under the fixed designation D5258; the number immediately following the designation indicates the year oforiginal adoption or, in the ca

2、se 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 digestion of soils and sedimentsfor subsequent determination of a

3、cid-extractable concentra-tions of certain elements by such techniques as atomic absorp-tion and atomic emission spectroscopy.1.1.1 Concentrations of arsenic, cadmium, copper, lead,magnesium, manganese, nickel, and zinc can be extracted fromthe preceding materials. Other elements may be determinedus

4、ing this practice.1.2 The analytical sample is arbitrarily defined as that whichpasses a 10-mesh (approximately 2-mm openings) screen andis prepared according to Practice D3974.1.3 Actual element quantitation can be accomplished byfollowing the various test methods under other appropriateASTM standa

5、rds for element(s) of interest.1.4 The detection limit and linear concentration range foreach element is dependent on the atomic absorption or emis-sion spectrophotometric technique employed and may be foundin the manual accompanying the instrument used.1.5 Before selecting a digestion technique, th

6、e user shouldconsult the appropriate quantitation standard(s) for any specialanalytical considerations, and Practice D3974 for any specialpreparatory considerations.1.6 The extent of extraction of elements from soils andsediments by this method is dependent upon the physical andmineralogic character

7、istics of the prepared sample.1.7 The values stated in both inch-pound and SI units are tobe regarded separately as the standard. The values given inparentheses are for information only.1.8 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is th

8、eresponsibility 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. For specific hazardstatements, see Section 8.2. Referenced Documents2.1 ASTM Standards:2D1193 Specification for Reagent WaterD39

9、74 Practices for Extraction of Trace Elements fromSediments2.2 Code of Federal Regulations:3CFR Title 21, Part 1030, and Title 47, Part 183. Summary of Practice3.1 The chemical portion of this practice involves aciddigestion to dissociate the elements not interstitially bound insilicate lattices.3.2

10、 The sample is digested with nitric acid in a closedfluoropolymer vessel using microwave heating to an internalpressure of 100 psi (6.89 106dynes/cm2).3.3 This practice provides a sample suitable for analysis byatomic absorption or emission spectrophotometry.4. Significance and Use4.1 Partial extrac

11、tion of soils and sediments can provideinformation on the availability of elements to leeching, waterquality changes, or other site conditions.4.2 Rapid heating, in combination with temperatures inexcess of the atmospheric boiling point of nitric acid, reducessample preparation or reaction times.4.3

12、 Little or no acids are lost to boiling or evaporation in theclosed digestion vessel so additional portions of acid may notbe required. Increased blank corrections from trace impuritiesin acid are minimized.1This practice is under the jurisdiction of ASTM Committee D19 on Water andis the direct resp

13、onsibility of Subcommittee D19.07 on Sediments, Geomorphology,and Open-Channel Flow.Current edition approved Jan. 1, 2013. Published January 2013. Originallyapproved in 1992. Last previous edition approved in 2007 as D5258 02(2007).DOI: 10.1520/D5258-02R13.2For referenced ASTM standards, visit the A

14、STM 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.3Available from Standardization Documents Order Desk, DODSSP, Bldg. 4,Section D, 700 Robbins Ave., Phila

15、delphia, PA 19111-5098, http:/www.dodssp.daps.mil.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States15. Interferences5.1 No interferences to the digestion of soils and sedimentsusing microwave heating have been observed.5.2 Precautions s

16、hould be exercised to avoid those interfer-ences normally associated with the final determination ofelements using atomic absorption or emission spectroscopy.6. Apparatus6.1 Microwave Heating SystemA laboratory microwaveheating system capable of delivering a minimum of 570 W ofmicrowave energy. The

17、system should be capable of 1 %power adjustments and 1 s time adjustment. The microwavecavity should be fluoropolymer coated and equipped withexhaust ventilation sufficient to provide ten chamber exchangesper minute.The cavity must have a 360 oscillating turntable toensure even sample heating, and b

18、e capable of holding diges-tion vessels. Safety interlocks, to shut off magnetron poweroutput, must be contained in the cavity door opening mecha-nism. The system must comply with Department of Health andHuman Services Standards under Code of Federal Regulations,Part 1030.10, Subparts (C) (1), (C) (

19、2), and (C) (3), formicrowave leakage. The system should have Federal Commu-nications Commission (FCC) type approval for operationsunder FCC Rule Part 18.6.2 Digestion VesselsA vessel of 100-mL capacity. Thevessel must be transparent to microwave energy and be capableof withstanding a minimum intern

20、al pressure of 120 psi(8.27 106dynes/cm2), and a temperature of 200C. Thevessel must contain a safety pressure relief valve, a rupturedisc, pressure venting system, or be connected to an externalsafety relief valve that will prevent possible vessel rupture orejection of the vessel cap.6.3 Pressure C

21、ontrol VesselA vessel of 100 mL capacity,transparent to microwave energy, with a port for connection toa pressure control device and capable of withstanding aminimum internal pressure of 120 psi and temperature of200C.6.4 Pressure Control DeviceAn externally or internallyoperated device to control t

22、he pressure within the digestionvessels. The controller must be capable of 1 psi (6.89 104 dynes/cm2) adjustments, controlling up to 100 psi and beequipped with an external pressure relief valve if a non-ventingcontrol vessel is used.6.5 Filtration ApparatusA gravity filter fitted with What-man No.

23、414filter paper, or equivalent.6.6 Volumetric Flask, 100-mL capacity.7. Reagents7.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall conform to the specifications of the commit-tee on Analytical Reagents of the Ame

24、rican Chemical Society,where such specifications are available.5Other grades may beused provided it is first ascertained that the reagent is ofsufficiently high purity to permit its use without lessening theaccuracy of the determination.7.2 Purity of Water Unless otherwise indicated, referencesto wa

25、ter shall be understood to mean reagent water conformingto Type III of Specification D1193.7.3 Cleaning SolutionMix one volume of technical gradenitric acid (sp gr 1.42) with one volume water.7.4 Nitric Acid (1+1)Mix one volume nitric acid (sp gr1.42) with one volume water.8. Hazards8.1 Operate and

26、maintain the microwave system in accor-dance with the manufacturers recommended safety precau-tions. Do not operate the microwave system in a fume hoodwhere it is surrounded by acid fumes that can cause corrosionof the equipment. Vent acid fumes generated inside the cavityfrom the cavity to a fume h

27、ood. Place the digestion vessels ina fume hood to remove vapors released when a vessel isopened.8.2 Perform the digestion in accordance with the manufac-turers recommended safety precautions.9. Sampling9.1 Collect a sediment sample using an appropriate sam-pling technique.9.2 Prepare the sediment sa

28、mple in accordance with Sec-tions 10 and 12 of Practice D3974.10. Vessel Cleaning10.1 The manufacturers recommended cleaning proceduremay be followed or the procedure in 10.2 through 10.4 may beused.10.2 Soak the fluoropolymer vessel parts in cleaning solu-tion at 60C for 10 min.10.3 Remove the vess

29、el parts from the cleaning solution andthoroughly rinse the parts with tap water and then with reagentwater.10.4 Allow the vessel parts to air-dry or wipe dry using aclean, soft cloth.11. Procedure11.1 Determine the power output of the microwave usingthe procedure described in the annex to ensure th

30、at the unitmeets the minimum power requirement.11.2 Obtaina1gportion of the sample prepared in 9.2,weighed to the nearest 0.1 mg, and transfer into digestionvessels. Include an empty digestion vessel in each set as amethod blank.4Whatman No. 41 filter paper, available from Whatman Specialty Products

31、, 6Just Rd., Fairfield, NJ 07004, has been found suitable for this purpose.5Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, DC. For suggestions on the testing of reagents notlisted by the American Chemical Society, see Analar Standards for Laborator

32、yChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmaceutical Convention, Inc. (USPC), Rockville,MD.D5258 02 (2013)2NOTE 1The pressure control vessel must contain1gofsamplematerial.11.3 Add 20 mL of HNO3(1 + 1) to each sample and blankdigest

33、ion vessel.11.4 Close each digestion vessel according to the manufac-turers recommended procedures.11.5 Place the closed digestion and pressure control vesselinto the instrument turntable and assemble following themanufacturers suggested procedure.NOTE 2The pressure control vessel is connected to th

34、e pressurecontrol device and may be assembled into the turntable differently than thestandard digestion vessels. Refer to the manufacturers suggested proce-dure.11.6 Set the pressure control device to control the digestionvessel pressure at 100 psi (6.89 106dynes/cm2).11.7 Heat the vessels to obtain

35、 an internal pressure 100 psi(6.89 106dynes/cm2) and maintain for 30 min. Refer to themanufacturers suggested procedure.11.8 Allow the vessels to cool to room temperature, andthen vent excess pressure from the vessels. Refer to themanufacturers recommended venting procedure.11.9 Remove the vessels f

36、rom the turntable, place in a fumehood, and open the vessel.11.10 Transfer the contents of the digestion vessel to afiltration device and filter. Wash the vessel and filter thoroughlywith small portions of water. Alternatively, separate the solidand liquid phases by centrifugation.11.11 Transfer the

37、 filtered solution and washes, or centrate,to a 100-mL volumetric flask and dilute to volume with water.12. Precision and Bias12.1 This practice was tested by digesting a single sampleby one laboratory. Table 1 summarizes precision and bias of thetrace element analyses conducted on six portions of N

38、ISTRiver Sediment (SRM 1645)6digested by this practice. Alltrace element concentrations were determined by flame orgraphite furnace atomic absorption techniques.13. Keywords13.1 digestion; microwave; sediments; soils; vesselANNEX(Mandatory Information)A1. PROCEDURE TO DETERMINE DELIVERED POWER OF MI

39、CROWAVE OVEN AT 100 %INSTRUMENT POWERA1.1 Remove the turntable, drive lug, and all vessels fromthe instrument cavity.A1.2 Adjust the instrument cavity exhaust to minimumairflow.A1.3 Program the instrument for 4 min time and 100 %power.A1.4 Transfer 20006 2 mL of room temperature (19 to25C) water int

40、o a 2-L polypropylene beaker.A1.5 Measure and record the initial water temperature, Ti,to the nearest 0.1C.A1.6 Place the beaker in the right front corner of theinstrument cavity.A1.7 Heat the water for the programmed time.A1.8 When the heating cycle is complete, immediatelyremove the beaker from th

41、e cavity, thoroughly stir the water toensure even heat distribution, and measure the finaltemperature, Tf, to the nearest 0.1C.A1.9 Calculate the delivered power as follows:P 5 Tf2 Ti! 3356NIST Standard Reference Materials, Office of Standard Reference Materials,U.S. Department of Commerce, Gaithers

42、burg, MD 20899.TABLE 1 Recovery Data for Six Digestions of NIST River Sediment (SRM 1645)AElement Amount Present (g/g) Amount Recovered(g/g)Number of Digestions Standard Deviation Bias (g/g)Arsenic 66 (not cert.) 72 6 4 6Cadmium 10.2 1.5 12 6 5 0Copper 109 19 121 6 2 12Lead 714 28 726 6 8 12Magnesiu

43、m 7400 200 7200 6 70 200Manganese 785 97 750 6 10 35Nickel 45.8 2.9 49 6 1 3Zinc 1720 170 1720 6 10 0ASee Footnote 7 for availability information.D5258 02 (2013)3where:P = delivered power, watts,Tf= final water temperature, C,Ti= initial water temperature, Cand:35 54.2 31.0 3 Mtwhere:4.2 = conversio

44、n factor for thermochemical calories towatts,1.0 = heat capacity of water, calories/g per C,M = mass of water, g, andt = heating time, s.ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this sta

45、ndard are expressly advised that determination of the 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 an

46、dif not revised, either reapproved or withdrawn. Your 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,

47、which you may attend. If you feel that your comments 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 19428-295

48、9,United States. Individual reprints (single or multiple 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/).D5258 02 (2013)4

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