ASTM D4025-2008a(2013) Standard Practice for Reporting Results of Examination and Analysis of Deposits Formed from Water for Subsurface Injection《报告地下喷射的水中沉积物的检验和分析结果的标准操作规程》.pdf

《ASTM D4025-2008a(2013) Standard Practice for Reporting Results of Examination and Analysis of Deposits Formed from Water for Subsurface Injection《报告地下喷射的水中沉积物的检验和分析结果的标准操作规程》.pdf》由会员分享，可在线阅读，更多相关《ASTM D4025-2008a(2013) Standard Practice for Reporting Results of Examination and Analysis of Deposits Formed from Water for Subsurface Injection《报告地下喷射的水中沉积物的检验和分析结果的标准操作规程》.pdf（4页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D4025 08a (Reapproved 2013)Standard Practice forReporting Results of Examination and Analysis of DepositsFormed from Water for Subsurface Injection1This standard is issued under the fixed designation D4025; the number immediately following the designation indicates the year oforiginal a

2、doption 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 manner in which the variousresults of examin

3、ation and analysis to determine the composi-tion of deposits formed from water for subsurface injection areto be reported.1.2 All analyses shall be made in accordance with the testmethods of ASTM, unless otherwise specified.NOTE 1While reporting of inorganic constituents in water-formeddeposits as s

4、pecified in Test Methods D4412 is sufficient for certainindustries, this practice provides for the reporting of organic and biologi-cal materials as well as inorganic constituents.NOTE 2Consistent with practices in industries where subsurfaceinjection of water is practiced, reporting includes specif

5、ying of inorganicconstituents as probable molecular combinations of the species for whichanalyses are performed.1.3 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.4 This standard does not purport to address all of thesafety c

6、oncerns, 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 limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D887 Practices for Sampling Water-Fo

7、rmed DepositsD932 Test Method for Iron Bacteria in Water and Water-Formed DepositsD933 Practice for Reporting Results of Examination andAnalysis of Water-Formed DepositsD1129 Terminology Relating to WaterD4412 Test Methods for Sulfate-Reducing Bacteria in Waterand Water-Formed DepositsE29 Practice f

8、or Using Significant Digits in Test Data toDetermine Conformance with Specifications3. Terminology3.1 DefinitionsFor definitions of terms used in thispractice, reference should be made to Terminology D1129 andPractice D887.4. History of Sample4.1 Information regarding the source and history of thesa

9、mple shall be included in the report of the analysis. Thisinformation should be that supplied by the individual submit-ting the sample as follows:4.1.1 Name of company supplying the sample,4.1.2 Name of location of plant, facility, and well,4.1.3 Date and time of sampling,4.1.4 Number of sample,4.1.

10、5 Name and other designation of equipment from whichsample was removed,4.1.6 Precise location from which sample was removed,4.1.7 Operating temperature and pressure of water or brineat location of deposit,4.1.8 Type of treatment applied to the water that formed thedeposit,4.1.9 An account of system

11、operating conditions that mayhave contributed to deposition (for example, filter channeling,chemical pump outage, or increased system temperature),4.1.10 Appearance and extent of deposit prior to removal,4.1.11 Exact method that was used in removing the sampleand notes concerning any contamination t

12、hat might haveoccurred during the process,4.1.12 Specific methods used for preservation of sampleprior to and subsequent to removal,4.1.13 Results of field tests made on the sample or relatedequipment,4.1.14 An analysis of the water from which the deposit wasformed, and4.1.15 Identity of sampler.1Th

13、is practice is under the jurisdiction of ASTM Committee D19 on Water andis the direct responsibility of Subcommittee D19.05 on Inorganic Constituents inWater.Current edition approved June 1, 2013. Published July 2013. Originally approvedin 1981. Last previous edition approved in 2008 as D4025 08a. D

14、OI: 10.1520/D4025-08AR13.2For 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.Copyright ASTM International, 100 Ba

15、rr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States15. Significance and Use5.1 This practice sets down the manner in which dataobtained from other test methods should be reported. This isdone in an effort to standardize the report form used.6. Physical Characteristics6.1 Th

16、e macroscopic characteristics of the sample, as ascer-tained by the analyst, including any peculiarities that may bepertinent to the results of the examination, shall be included inthe report.NOTE 3Characteristics such as the following may be recorded: color,form (scaly, slimy, etc.), texture (oily,

17、 smooth, friable, gritty, etc.),magnetic properties (as determined by test with magnet), and apparentstructure (amorphous, crystalline, columnar crystals).NOTE 4Any discrepancies between the physical characteristics ob-served by the analyst and those reported by the sampler should be noted.6.2 Chara

18、cteristics observed during microscopic examina-tion shall be reported and include a description of the grosscharacteristics and homogeneity or heterogeneity of thesample.6.3 Any distinct observable crystal morphology such asmonoclinic, rhombic, etc., shall be reported.NOTE 5Specific note of the pres

19、ence of any biological material in thesample should be made.7. Determinations to Be Reported7.1 The major headings for which determinations shall bereported in a complete analysis are as indicated in Table 1.Specific determinations which shall be reported under some ofthe major headings are listed i

20、n Tables 2-4. In certain instances,knowledge of the operating practices and water chemistry willhave suggested the need to perform additional analyses orindicated the need for a less complete analysis; consequently,results from determinations may not be reported for eachindividual item.8. Reporting

21、of Biological Components8.1 The results of examinations conducted to determine thepresence of microorganisms in the sample, such as thosedelineated by Test Method D932 and Practice D4412, shall bereported. The organisms present should be identified by phylawith the relative abundance noted.NOTE 6In

22、the absence of quantitative measurements, the microbio-logical constituents may be grouped as major, minor, and trace. Incategorizing the constituents, the qualitative nature of the examination andthe subjective appraisal of its proportion must be considered.NOTE 7The results of the examination shou

23、ld be qualified on the basisof any known or suspected effects related to sample handling prior to orduring analysis likely to influence the validity.9. Reporting of Chemical Analyses9.1 The major headings under which chemical analysisdetermination shall be reported are moisture and volatilematerial,

24、 solvent-extractable components, loss at 900C, ash,and inorganic components.9.2 All data shall be reported as weight percent both on anas-received basis and on a dry weight basis, with the exceptionof water and volatile material, which shall be reported on anas-received basis only.TABLE 1 Major Head

25、ings for Determinations to Be ReportedMicrobiological examinationMoisture and volatile materialSolvent-extractable components:Fluorocarbon-extractablesWater-solublesAcid-solublesSolvent-insolublesLoss at 900CAshInorganic componentsTABLE 2 Acid-Soluble Portion Ions to Be ReportedInorganic materials:c

26、alcium carbonatemagnesium sulfidebarium sulfateiron phosphatesodium hydroxideAoxideAOrganic materialsAThese ions are determined by difference. The specific ion reported is determinedby direct evidence or in absence of such evidence as hydroxide.TABLE 3 AshCommon Constituents to Be Reportedcalcium zi

27、ncmagnesium sodiumbarium potassiumstrontium phosphateiron sulfatealuminum chloridesiliconmanganeseTABLE 4 Common Inorganic Components Found inWater-Formed Deposits and Their KspValuesInorganicMaterialKspTemperature,CReferenceAl(OH)31.310331825ABaCO32.610925BBa3(PO4)23.410231825ABaSO41.1101025BCaCO34

28、.910925BCa(OH)24.710625BCa3(PO4)22.1103325BCaSO47.110525BFeCO33.1101125BFe2O31.1103618BFe(OH)32.6103925BFePO42H2O 9.9102925BSrCO35.6101025BSr3(PO4)24.010281825ASrSO43.410725BZnCO31.2101025BZn(OH)26.8101725BZnS 2.2 102525BNa2CO3NaClNa2SO4SSiO2Other siliceousmaterialALanges Handbook of Chemistry, Dean

29、, J. A., Ed., McGraw-Hill Book Co., 13thEdition, pp. 57 to 512.BHandbook of Chemistry and Physics, Weast, R. C., Ed., Chemical Rubber Co.,1991, pp. 839.D4025 08a (2013)29.3 The loss at 105C shall be reported as the moisture andvolatile material content of the sample.9.4 Reporting of solvent-extracta

30、ble materials shall be di-vided into organic solvent extractables, water-solubles, acid-extractables, and solvent insolubles.9.4.1 The organic solvent-extractable constituents shall bereported in terms of the generic nature of the extractedmaterial.When the extractable portion of the deposit compris

31、esgreater than 10 % on a dry weight basis of the deposit, morespecific identification of its composition is advised.NOTE 8A fluorocarbon refrigerant is the preferred organic solvent forsuch extractions. Where another solvent such as toluene, hexane,chloroform, or carbon tetrachloride is used, either

32、 in place of, or inaddition to the fluorocarbon, the solvent used in and the results of suchextractions shall be reported.NOTE 9The generic nature should identify the chemical class to whichthe material belongs, such as asphaltene, paraffin, amide, phosphate ester,etc.NOTE 10Elemental sulfur will no

33、rmally be extracted in part byorganic solvents. If sulfur is identified in the extract, specific notation ofits presence shall be made.9.4.2 The water-soluble portion of the sample shall bereported. If the water-soluble portion of the sample is in excessof 10 % on a dry weight basis, determination f

34、or sodium, Na+;potassium, K+; magnesium, Mg+2; calcium, Ca+2; sulfate,SO42; and chloride, Cl, shall also be reported.9.4.3 Reporting of the acid-soluble portion shall indicate thetotal proportion of such components. Results of analyses of theacid-soluble portion for ions and radicals in Table 2 shal

35、l alsobe reported. Where the equivalents of cations exceed theequivalents of anions, the difference shall be reported ashydroxide or oxide ion. Where there exists evidence frompetrographic examination, X-ray analysis, or other directanalyses that either is specifically present in the sample, suchevi

36、dence shall be reflected in the reported acid-soluble com-ponents. Otherwise, the difference shall be reported as hydrox-ide ion.NOTE 11It is recommended practice to use 15 % hydrochloric acid(1 + 7) in the determination of the acid-soluble content. In some cases,however, the history of the sample m

37、ay indicate a preference for use ofanother acid. In either case, the type of acid used and its concentrationshall be noted.NOTE 12Where significant discrepancies exist between the totalacid-soluble portion and the inorganic materials identified, due regardmust be given to identification of the prese

38、nce of acid-soluble organicconstituents.9.5 The loss at 900C shall be reported. This determinationis generally indicative of the decomposition of organic com-ponents; however, the determination will also include loss ofcombined water.NOTE 13Recognition should be made of the fact that the process ofh

39、eating to 900C results in the conversion of certain inorganic salts. Forexample, hydroxides, carbonates, and sulfides are converted to oxides.9.6 The total ash shall be reported with the constituentslisted in Table 3 specified.9.7 The inorganic constituents identified in an analysis shallbe reported

40、 both as their common ionic species and also interms of probable molecular combinations listed in Table 4.For convenience of calculation, the ionic species may also bereported as equivalents.9.7.1 The probable mineral composition shall be determinedby association of ions on an equivalent basis so as

41、 to form thecompound having the lowest Ksp(based on stability constant ofmetal complexes) value. After complete association of one ofthe ions in the first compound is achieved, the association iscontinued in a manner to form the compound with the nextlowest Kspand so on until all ions are associated

42、. Kspvalues forcommon minerals are also listed in Table 4. Where evidenceexists from petrographic examination, X-ray diffraction, orother direct analyses, such evidence shall override the probablecombinations of ions above.NOTE 14The use of Kspvalues in determining probable mineralcomposition of a d

43、eposit should be approached and the results of suchconsiderations regarded with caution. Conditions under which depositionoccurred may be such as to cause major changes in Kspvalues and maythen substantially alter the likelihood of a given mineral being present ina deposit.10. Completeness and Accur

44、acy of Analysis10.1 The completeness and accuracy of the analysis shouldbe carefully appraised before reporting.10.1.1 The items to be included in a complete report arespecified in Table 1. Any listed for which determinations werenot obtained should be so indicated.10.1.2 Each determination reported

45、 shall be accompaniedby indication of the established precision for the methods used.10.1.3 The summation of the determinations of moistureand volatile material, loss at 900C, and ash shall total 100 65 % on an as-received basis.10.1.4 The inorganic composition developed should accountfor 100 6 5 %

46、of the ash content of the sample.NOTE 15In appraising the relationship between ash content andinorganic composition, conversion of certain salts during the ashingprocess as indicated in Note 15 must be considered.10.1.5 Consideration should also be given to reconciling thedeterminations obtained for

47、 ions and radicals comprising thewater-soluble components and acid-extractables with the inor-ganic composition reported.10.1.6 Where the loss at 900C is in excess of 15 % of thesample on a dry weight, the determinations for fluorocarbon-extractables and acid-soluble organics should be appraised.Whe

48、re discrepancies exist between the loss at 900C and theextracted organics, additional work to identify nonextractedorganic materials in the sample is indicated.10.2 Quantitative determinations shall be reported to sig-nificant figures consistent with the precision of the methodused (Note 18). When a

49、 quantitative determination is made anda negative result is obtained, it shall be reported as “0.0” witha notation as to the amount of sample used and the method ofdetermination. When a determination has been omitted, but theheading of the determination is carried in a tabulation withdeterminations of other samples, the absence of a determina-tion for any other specific sample shall be indicated by an entry“no determination” or by a dash. The terms “nil,” “none,” and“trace” shall not be used. If a qualitative d