ImageVerifierCode 换一换
格式:PDF , 页数:10 ,大小:145.22KB ,
资源ID:522692      下载积分:5000 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-522692.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 D6501-2009 5000 Standard Test Method for Phosphonate in Brines《海水中磷酸酯的试验方法》.pdf)为本站会员(orderah291)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 D6501-2009 5000 Standard Test Method for Phosphonate in Brines《海水中磷酸酯的试验方法》.pdf

1、Designation: D6501 09Standard Test Method forPhosphonate in Brines1This standard is issued under the fixed designation D6501; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A number in parentheses indica

2、tes the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope*1.1 This test method covers the colorimetric determinationof phosphonate (PNA) in brines from gas and oil productionoperations in the range from 0.1 to 5 mg/L.1.2 Thi

3、s phosphonate method is intended for use to analyzelow concentration of phosphonate in brine containing interfer-ing elements. This test method is most useful for analyzingphosphonate at 0.1 to 1 mg/L range in brines with interferingelements; however, it requires personnel with good analyticalskill.

4、1.3 This test method has been used successfully withreagent water and both field and synthetic brine. It is the usersresponsibility to ensure the validity of this test method forwaters of untested matrices.1.4 The values stated in SI units are to be regarded asstandard. No other units of measurement

5、 are included in thisstandard.1.5 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitation

6、s prior to use. For specific hazardstatements, see 9.1.3.2. Referenced Documents2.1 ASTM Standards:2D1129 Terminology Relating to WaterD1193 Specification for Reagent WaterD2777 Practice for Determination of Precision and Bias ofApplicable Test Methods of Committee D19 on WaterD3370 Practices for Sa

7、mpling Water from Closed ConduitsD3856 Guide for Good Laboratory Practices in Laborato-ries Engaged in Sampling and Analysis of WaterD4375 Practice for Basic Statistics in Committee D19 onWaterD5810 Guide for Spiking into Aqueous SamplesD5847 Practice for Writing Quality Control Specificationsfor St

8、andard Test Methods for Water AnalysisE275 Practice for Describing and Measuring Performanceof Ultraviolet and Visible Spectrophotometers3. Terminology3.1 DefinitionsFor definitions of terms used in this testmethod, refer to Terminology D1129.3.2 Definitions of Terms Specific to This Standard:3.2.1

9、phosphonate, na group of organophosphorus com-pounds typically used for mineral scale and corrosion control,as cleaning agents, dispersants, and chelants.3.2.1.1 DiscussionTypical phosphonate compounds in-clude, but are not limited to, the following phosphonic acid andtheir neutralized salts: Aminot

10、ri(methylenephosphonic acid),1-hydroxyethylidene-1,1-diphosphonic acid, ethylenediamine-tetra (methylenephosphonic acid), hexamethylenediaminetetra(methylenephosphonic acid), and diethylenetriaminepenta(methylenephosphonic acid).4. Summary of Test Method4.1 Phosphonate materials are converted to ort

11、hophosphateby potassium persulfate digestion. The orthophosphate is thenreacted with ammonium molybdate to form a phosphomolyb-date complex. The complex is extracted with a methyl isobutylketone/cyclohexane mixture and measured colorimetrically.5. Significance and Use5.1 This test method is useful f

12、or the determination of tracelevel phosphonate residues in brines. Chemical treatmentwhich contain phosphonates are used as mineral scale andcorrosion inhibitors in gas and oil drilling and productionoperations; and other industrial applications. Often, the deci-sion for treatment is based on the ab

13、ility to measure lowphosphonate concentration and not upon performance criteria.Phosphonate concentrations as low as 0.16 mg/L have been1This test method is under the jurisdiction of ASTM Committee D19 on Waterand is the direct responsibility of Subcommittee D19.05 on Inorganic Constituentsin Water.

14、Current edition approved Oct. 1, 2009. Published October 2009. Originallyapproved in 1999. Last previous edition approved in 2004 as D650104. DOI:10.1520/D6501-09.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book

15、 of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.1*A Summary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.shown effective i

16、n carbonate scale treatment. This test methodenables the measurement of sub-mg/L phosphonate concentra-tion in brines containing interfering elements.5.2 The procedure includes measuring total (see 12.3.8) andfree orthophosphate (see 12.4.3) ions and the difference inconcentration is the phosphonate

17、 concentration. The samplecould contain orthophosphate naturally, or from decompositionof the phosphonate during processing or well treatment or fromtreating compounds containing molecular dehydrated phos-phates.6. Interferences6.1 Sulfide interferes in this test method, but techniquesdescribed in t

18、he procedure (see 9.1.2) eliminate this interfer-ence. Concentrations less than 1000 mg/L copper (Cu+2) andsilica (SiO2/SiO32/Si+4); and less than 200 mg/L of iron(Fe+2/Fe+3) can be tolerated.6.2 Produced brines can contain high concentrations ofdissolved solids. Some of these dissolved solids tend

19、toprecipitate when produced brines reach new equilibria atatmospheric temperature and pressure. Phosphonate will co-precipitate or adsorb onto these newly formed solids andbecome unavailable for analysis. This problem can be mini-mized by acidifying the brine sample on-site with hydrochloricacid to

20、pH below 2.6.3 Glassware must be cleaned with phosphate free deter-gent and rinsed with 0.1 N hydrochloric acid to remove allresidual phosphate or phosphonate.6.4 The standard addition method in 12.6 is recommendedfor brine with high matrix interference.7. Apparatus7.1 Pressure Cooker or Sterilizer

21、(Autoclave)3.7.2 Spectrophotometer4, for measurement above 650 nmwith 4-cm light path cells. A longer light path will yield acorresponding higher sensitivity (see 12.5.1). Spectrophotom-eter practices prescribed in this test method shall conform toPractice E275.7.3 Bottle Top Liquid Dispenser5, 20-m

22、L capacity, 2.13E 0.88 0.76 0.84 2.48 0.82667 0.0611G 0.95 0.95 0.94 2.84 0.94667 0.00577 Yes, remove data from Lab hH 0.48 0.5 0.48 1.46 0.48667 0.01155I 0.83 0.85 0.83 2.51 0.83667 0.01155Brine sum 6.41 6.33 6.44 19.18Brine mean 0.80125 0.79125 0.805Brine std 0.14865 0.14066 0.14928Mean 0.79917Std

23、 0.13987Conclusions: All values from laboratory h were identified as outliers (outside of 95 % upper and lower confidencelimits.Anova Table Sourceof VarianceSum of SquaresDegrees ofFreedomMeanSquaresLabs 0.43965 7 0.06281Brine 0.00081 2 0.0004Error 0.00952 14 0.00068Total 0.44998F (lab) 92.315F(brin

24、e) 0.59405Critical F(lab) 92.315Critical F(brine) 0.59405Conclusion: The are no significant differences between results in different brines at the 95 % confidence level.Conclusion: The are significant differences between results from different laboratories at the 95 % confidence level.Anova: Two-Fac

25、tor Without ReplicationSummary Count Sum Average VarianceRow 1 3 2.57 0.85667 0.00083Row 2 3 2.52 0.84 0.0003Row 3 3 2.7 0.9 0Row 4 3 2.1 0.7 1.1E-16Row 5 3 2.48 0.82667 0.00373Row 6 3 2.84 0.94667 3.3E-05Row 7 3 1.46 0.48667 0.00013Row 8 3 2.51 0.83667 0.00013Column 1 8 6.41 0.80125 0.0221Column 2

26、8 6.33 0.79125 0.01978Column 3 8 6.44 0.805 0.02229AnovaSource of Variation SS df MS F P-Value F critRows 0.43965 7 0.06281 92.315 1.2E-10 2.7642Columns 0.00081 2 0.0004 0.59405 0.56542 3.73889Error 0.00952 14 0.00068Total 0.44998 23D6501 098TABLE X1.3 Statistical Details and Analysis of Variance fo

27、r 3 mg/L SamplesBrinesLaboratory 1 2 3 Lab Sum Lab Mean Lab Std Outlier mean test ? =A 1.34 0.99 1.12 3.45 1.15 0.176918 Xbar = 2.415000B 2.58 2.6 2.56 7.74 2.58 0.02 S mean = 0.5808860C 2.8 2.8 2.7 8.3 2.766667 0.057735D 333930Xbar 1.15/S mean=2.1782.13E 2.46 2.13 2.55 7.14 2.38 0.221133G 2.71 2.7

28、2.71 8.12 2.706667 0.005774 Yes, remove data from Lab aH 2.06 2.05 2.1 6.21 2.07 0.026458I 2.7 2.5 2.8 8 2.666667 0.152753Brine sum 19.65 18.77 19.54 57.96Brine mean 2.45625 2.34625 2.4425Brine std 0.528608 0.634754 0.593795Mean 2.415Std 0.563452Conclusions: All values from laboratory a were identif

29、ied as outliers (outside of 95 % upper and lower confidence limitsand T value, extreme mean tested, that exceeds the critical value (see Practice D277798).Anova Table Source ofVarianceSum SquaresDegrees ofFreedomMeanSquaresLabs 7.086 7 1.012286 1.55E-10Brine 0.057475 2 0.028737 0.114685Error 0.15852

30、5 14 0.011323Total 7.302 23F (lab) 89.39915F(brine) 2.537928Critical F(lab) 2.764196Critical F(brine) 3.73889Conclusion: There are no significant differences between results with different brines at the 95 % confidence level.Conclusion: There are significant differences between results from differen

31、t laboratories at the 95 % confidence level.Anova: Two-Factor Without ReplicationSummary Count Sum Average VarianceRow 1 3 3.45 1.15 0.0313Row 2 3 7.74 2.58 0.0004Row 3 3 8.3 2.766667 0.003333Row4 3930Row 5 3 7.14 2.38 0.0489Row 6 3 8.12 2.706667 3.33E-05Row 7 3 6.21 2.07 0.0007Row 8 3 8 2.666667 0.

32、023333Column 1 8 19.65 2.45625 0.279427Column 2 8 18.77 2.34625 0.402913Column 3 8 19.54 2.4425 0.352593AnovaSource of Variation SS df MS F P-Value F critRows 7.086 7 1.012286 89.39915 1.55E-10 2.764196Columns 0.057475 2 0.028737 2.537928 0.114685 3.73889Error 0.158525 14 0.011323Total 7.302 23D6501

33、 099SUMMARY OF CHANGESCommittee D19 has identified the location of selected changes to this standard since the last issue (D650104)that may impact the use of this standard. (Approved October 1, 2009.)(1) The SI statement was added to Section 1.(2) D1192 was removed from Sections 2 and 10.1.(3) Reage

34、nt references were added to Sections 8, 9, 10, 11, and12.(4) Section 16.3.4 was modified.ASTM 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 o

35、f 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 andif not revised, either reapproved or withdrawn.

36、 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, which you may attend. If you feel that your comm

37、ents 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

38、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).TABLE X1.4 Statistical Details for the 0.8-mg/L Samples After the Removal of OutliersNOTE 1T

39、hese are the values at 0.8 mg/L after the removal of the outliers.BrinesLaboratory 1 2 3 Lab Sum Lab Mean Lab Std Outlier Single Value ? =A 0.84 0.84 0.89 2.57 0.8567 0.0289B 0.83 0.83 0.86 2.52 0.8400 0.0173 Xbar 0.7/S =1.902.73C 0.9 0.9 0.9 2.7 0.9000 0.0000D 0.7 0.7 0.7 2.1 0.7000 0.0000 NoE 0.88

40、 0.76 0.84 2.48 0.8267 0.0611G 0.95 0.95 0.94 2.84 0.9467 0.0058I 0.83 0.85 0.83 2.51 0.8367 0.0115Brine sum 5.93 5.83 5.96 17.72Brine mean 0.8471 0.8329 0.8514Brine std 0.0783 0.0832 0.0767Mean 0.8438 So 0.0268Std 0.0758TABLE X1.5 Statistical Details for the 3 mg/L Samples After the Removal of Outl

41、iersNOTE 1Data for 3 mg/L after outliers have been removed.BrinesLaboratory 1 2 3 Lab Sum Lab Mean Lab Std Outlier Single Value ? =B 2.58 2.6 2.56 7.74 2.5800 0.0200 Xbar 2.05/S =1.892.73C 2.8 2.8 2.7 8.3 2.7667 0.0577D 3 3 3 9 3.0000 0.0000 NoE 2.46 2.13 2.55 7.14 2.3800 0.2211G 2.71 2.7 2.71 8.12 2.7067 0.0058H 2.06 2.05 2.1 6.21 2.0700 0.0265I 2.7 2.5 2.8 8 2.6667 0.1528Brine sum 18.31 17.78 18.42 54.51Brine mean 2.6157 2.5400 2.6314Brine std 0.2978 0.3460 0.2797Mean 2.5957 So 0.1047Std 0.2889D6501 0910

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