ImageVerifierCode 换一换
格式:PDF , 页数:4 ,大小:69.05KB ,
资源ID:508851      下载积分:10000 积分
快捷下载
登录下载
邮箱/手机:
温馨提示:
如需开发票,请勿充值!快捷下载时,用户名和密码都是您填写的邮箱或者手机号,方便查询和重复下载(系统自动生成)。
如填写123,账号就是123,密码也是123。
特别说明:
请自助下载,系统不会自动发送文件的哦; 如果您已付费,想二次下载,请登录后访问:我的下载记录
支付方式: 支付宝扫码支付 微信扫码支付   
注意:如需开发票,请勿充值!
验证码:   换一换

加入VIP,免费下载
 

温馨提示:由于个人手机设置不同,如果发现不能下载,请复制以下地址【http://www.mydoc123.com/d-508851.html】到电脑端继续下载(重复下载不扣费)。

已注册用户请登录:
账号:
密码:
验证码:   换一换
  忘记密码?
三方登录: 微信登录  

下载须知

1: 本站所有资源如无特殊说明,都需要本地电脑安装OFFICE2007和PDF阅读器。
2: 试题试卷类文档,如果标题没有明确说明有答案则都视为没有答案,请知晓。
3: 文件的所有权益归上传用户所有。
4. 未经权益所有人同意不得将文件中的内容挪作商业或盈利用途。
5. 本站仅提供交流平台,并不能对任何下载内容负责。
6. 下载文件中如有侵权或不适当内容,请与我们联系,我们立即纠正。
7. 本站不保证下载资源的准确性、安全性和完整性, 同时也不承担用户因使用这些下载资源对自己和他人造成任何形式的伤害或损失。

版权提示 | 免责声明

本文(ASTM C927-1980(2014) Standard Test Method for Lead and Cadmium Extracted from the Lip and Rim Area of Glass Tumblers Externally Decorated with Ceramic Glass Enamels《外部采用陶瓷玻璃釉装饰的玻璃酒.pdf)为本站会员(吴艺期)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 C927-1980(2014) Standard Test Method for Lead and Cadmium Extracted from the Lip and Rim Area of Glass Tumblers Externally Decorated with Ceramic Glass Enamels《外部采用陶瓷玻璃釉装饰的玻璃酒.pdf

1、Designation: C927 80 (Reapproved 2014)Standard Test Method forLead and Cadmium Extracted from the Lip and Rim Area ofGlass Tumblers Externally Decorated with Ceramic GlassEnamels1This standard is issued under the fixed designation C927; the number immediately following the designation indicates the

2、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 test method covers the determination of lead an

3、dcadmium extracted by acetic acid from the lip and rim area ofglassware used for drinking and which is exteriorly decoratedwith ceramic glass enamels. The procedure of extraction maybe expected to accelerate the release of lead and cadmium fromthe decorated area and to serve, therefore, as a severe

4、test thatis unlikely to be matched under the actual conditions of usageof such glassware. This test method is specific for lead andcadmium.NOTE 1For additional information see Test Method C738.1.2 The values stated in SI units are to be regarded asstandard. No other units of measurement are included

5、 in thisstandard.1.3 This standard may involve hazardous materials,operations, and equipment. This standard does not purport toaddress all of the safety concerns associated with its use. It isthe responsibility of the user of this standard to establishappropriate safety and health practices and dete

6、rmine theapplicability of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2C738 Test Method for Lead and Cadmium Extracted fromGlazed Ceramic Surfaces3. Terminology3.1 Definitions:3.1.1 ceramic glass decorationsceramic glass enamelsfused to glassware at temperatures abo

7、ve 425C (800F) toproduce a decoration.3.1.2 ceramic glass enamels (also ceramic enamels or glassenamels)predominately colored, silicate glass fluxes used todecorate glassware.3.1.3 lip and rim areathat part of a drinking vessel whichextends 20 mm below the rim on the outside of the specimen.4. Summa

8、ry of Test Method4.1 Lead and cadmium are extracted from the lip and rimarea of the article under test by leaching with a 4 % acetic acidsolution at 20 to 24C (68 to 75F) for 24 h and are measuredby atomic absorption spectrophotometry using specific hollowcathode or electrodeless discharge lamps for

9、 lead and cadmiumrespectively. Results are reported as micrograms per millilitre(ppm) extracted relative to the internal volume of the glassarticle.5. Significance and Use5.1 The heavy metals, lead and cadmium, are known tocause serious health effects in man if consumed in excess. It is,therefore, i

10、mportant to measure the amount that may beextracted from an area of the glass drinking vessel in contactwith the lip. Even though the amount of lead and cadmiumextracted by this test method is in no way representative of theamount of the metals extracted by actual lip contact, therelative magnitude

11、of metals extracted from one test specimenin relation to another test specimen provides an effective toolfor discrimination.6. Interferences6.1 Since specific hollow cathode lamps or electrodelessdischarge lamps for lead and cadmium are used, there are nointerferences.7. Apparatus7.1 Atomic Absorpti

12、on Spectrophotometer (AAS), equippedwith a 102-mm single slot or Boling burner head and digitalconcentration readout attachment (DCR) if available. This1This test method is under the jurisdiction of ASTM Committee C14 on Glassand Glass Products and is the direct responsibility of Subcommittee C14.10

13、 onGlass Decoration. It was developed jointly by ASTM Committee C-14 and C-21 onCeramic Whitewares and Related Products, the Society of Glass Decorators A-20Subcommittee on Ceramic Enameled Decorated Glass Tumblers, and an Inter-agency Task Force consisting of FDA, EPA, and CPSC of the U.S. Governme

14、nt.Current edition approved May 1, 2014. Published May 2014. Originallyapproved in 1980. Last previous edition approved in 2009 as C927 - 80 (2009). DOI:10.1520/C0927-80R14.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For A

15、nnual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States1instrument should have a sensitivity of about 0.5 g/mL of leadfor 1 % abso

16、rption and a sensitivity of about 0.025 g/mL ofcadmium for 1 % absorption. Use the operating conditions asspecified in the instrument manufacturers analytical methodsmanual.7.2 Hollow Cathode or Electrodeless Discharge LeadLamp, set at 283.3 nm.7.3 Hollow Cathode or Electrodeless Discharge CadmiumLa

17、mp, set at 228.8 nm.7.4 Glassware of chemically resistant borosilicate glass foruse in preparing and storing reagents and solutions, and for useas test specimen containers.7.5 Detection limits of lead and cadmium shall be deter-mined and reported for individual instruments. In this testmethod, the d

18、etection limit shall be defined as twice the meannoise level at 0 g/mL. Representative detection limits wouldbe approximately 0.01 to 0.03 g/mL for lead and 0.0005 to0.0010 g/mL for cadmium.8. Reagents8.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated

19、, it is intended thatall reagents shall conform to the specifications of the Commit-tee on Analytical Reagents of the American Chemical Society,where such specifications are available.3Other grades may beused provided it is first ascertained that the reagent is ofsufficiently high purity to permit i

20、ts use without lessening theaccuracy of the determination. Analyze each new batch ofreagents for lead and cadmium.8.2 Purity of WaterUnless otherwise indicated, referencesto water shall be understood to mean distilled or deionizedwater.8.3 Acetic Acid (4 volume %) Mix 1 volume of glacialacetic acid

21、with 24 volumes of water.8.4 Cadmium Standard Stock Solution (1000 g/mL ofcadmium)Dissolve 0.9273 g of anhydrous cadmium sulfatein 250 mL of 1 % HCl (8.6) and dilute to 500 mL with 1 %HCl. Commercially available standard cadmium solutions mayalso be used.8.5 Detergent RinseAdd 2 mL of hand dishwashi

22、ng de-tergent to 1 L of lukewarm tap water.8.6 Hydrochloric Acid (1 weight %)Mix 1 volume ofconcentrated hydrochloric acid (HCl, sp gr 1.19) with 37volumes of water.8.7 Lead Standard Stock Solution (1000 g/mL)Dissolve1.598 g of lead nitrate (Pb(NO3)2) in 4 % acetic acid and diluteto 1 L with 4 % ace

23、tic acid. Commercially available standardlead solutions may also be used.9. Sampling9.1 Continuous ProcessSince the amount of metal re-leased from a decoration can be affected by the firingconditions, which may not be uniform across the width of thelehr, a minimum of six samples should be taken repr

24、esentingboth sides and the center of the lehr.9.2 Load or PileA minimum of six samples should berandomly selected from throughout the load.10. Preparation of Standards10.1 Lead Standard Working SolutionsDilute lead nitratesolution (8.7) with acetic acid (8.3) to obtain working standardshaving final

25、lead concentrations of 0, 5, 10, 15, and 20 g/mL.10.2 Cadmium Standard Working SolutionsDilute cad-mium stock solution (8.4) with acetic acid (8.3) to obtainworking standards having final cadmium concentrations of 0.0,0.3, 0.5, 1, 1.5, and 2.0 g/mL.10.3 Fresh working solutions should be prepared dai

26、ly.11. Procedure11.1 Preparation of SampleTake six identical units andcleanse each with a detergent rinse. Then rinse with tap waterfollowed by distilled water followed by air drying. Mark eachunit 7 mm below the rim. Record the internal volume of eacharticle in millilitres by filling from a graduat

27、ed cylinder toapproximately 6 to 7 mm (14 in.) of overflowing. Mark eacharticle, in a nondecorated area (if possible), 20 mm below therim on the outside. Invert the article in an appropriate labora-tory glassware container whose diameter is a minimum of 1.25times and a maximum of 2.0 times the diame

28、ter of the testspecimen at the rim. Carefully add 4 % acetic acid leachingsolution from a graduated cylinder to the 20-mm mark. Recordthe volume of solution used. Cover the glassware containers, ifpossible, to prevent evaporation and to protect them fromcontamination. Let stand for 24 h at room temp

29、erature (20 to24C) in the dark. Remove the article after the 24-h leachingperiod and determine the lead and cadmium by atomic absorp-tion. Record the lead and cadmium found in micrograms permillilitre.NOTE 2The possibility of a significant amount of evaporation exists.The analyst should determine wh

30、ether the acetic acid leaching is notice-ably below the 20-mm mark before removing the article. If it is, sufficientacetic acid solution should be added to restore the leaching solution to the20-mm mark.11.2 Determination of LeadSet the instrument (7.1) formaximum signal at 283.3 nm using the lead h

31、ollow cathodelamp (7.2)(Note 3) and air/acetylene (C2H2) flow ratesrecommended by the manufacturer. Stir the sample (leaching)solution and pour off a portion into a clean flask or aspiratefrom the extraction container if suitable. Flush the burner withwater and check zero point between readings. Det

32、ermine leadfrom a standard curve of absorbance against g/mL of lead orcalibrate the direct concentration reading (DCR) unit in theconcentration mode with lead working solutions (11.1) andread and record the sample concentration directly. Bracket thesample solution with the next higher and lower work

33、ing3Reagent 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 LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmac

34、opeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.C927 80 (2014)2solutions. Dilute samples containing more than 20 g/mL oflead with 4 % acetic acid and reanalyze.NOTE 3Electrodeless discharge lamps may be substituted for hollowcathode lamps.11.3 Determination of C

35、admiumProceed as in 11.2 usingthe cadmium hollow cathode lamp (7.3) and cadmium stan-dards (10.2). If the sample (leaching) solution contains morethan 2 g/mL of cadmium, dilute with 4 % acetic acid andreanalyze.12. Calculation12.1 Use the following equations to calculate the totalamount of lead or c

36、admium metal released from the lip and rimarea of the article expressed (1) in total micrograms and (2)parts per million of lead or cadmium metal leached relative tothe internal volume of the article.12.1.1 Determine lead or cadmium, A, in micrograms asfollows:A 5 C 3V1(1)12.1.2 Determine lead or ca

37、dmium, A, in parts per millionas follows:A 5C 3V1V2(2)where:C = concentration of lead or cadmium in leaching solution,g/mL;V1= volume of leaching solution, mL; andV2= internal volume of article, mL (Note 4).NOTE 4The internal volume of the article expressed in millilitres ofwater closely approximate

38、s its weight in grams. Therefore, in this instancemicrogram per millilitre equals microgram per gram which equals partsper million.13. Report13.1 A suggested report form is given in Fig. 1.14. Precision and Bias14.1 Precision for the analytical method for single ormultiple operator within a single l

39、aboratory is within thesensitivity of theAAS used and as specified is about 0.5 g/mLfor lead and 0.25 g/mL for cadmium.14.2 The accuracy and between-laboratory precision aredependent upon the ability to obtain representative samples forthe statistical universe being sampled.15. Keywords15.1 atomic a

40、bsorption; cadmium; ceramic glass enamels;glaze; heavy metals; leadLABORATORY TEST DATALead and Cadmium Released from Lip and Rim Area of Drinking Glassware Decorated Externally with Ceramic Glass EnamelsDateManufacturer LaboratoryPatternDetection Limit Lead Reagent Blank LeadCadmium CadmiumInternal

41、 Volume, mLSample Volume of Leach-ing Solution, mLConcentration, g/mLLead,Total g ppm Relative toInternal Volume123456AvgCadmium123456AvgFIG. 1 Report FormC927 80 (2014)3ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin

42、 this standard. Users of this standard 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 mus

43、t be reviewed every five years andif 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 the

44、responsible technical committee, 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

45、, West Conshohocken, PA 19428-2959,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/).C927 80 (2014)4

copyright@ 2008-2019 麦多课文库(www.mydoc123.com)网站版权所有
备案/许可证编号:苏ICP备17064731号-1