ASTM D2035-1980(2003) Standard Practice for Coagulation-Flocculation Jar Test of Water《水的凝聚絮凝瓶试验》.pdf

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1、Designation: D 2035 80 (Reapproved 2003)Standard Practice forCoagulation-Flocculation Jar Test of Water1This standard is issued under the fixed designation D 2035; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last re

2、vision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.1. Scope1.1 This practice covers a general procedure for the evalu-ation of a treatment to reduce dissolved, suspended, colloidal,and no

3、nsettleable matter from water by chemical coagulation-flocculation, followed by gravity settling. The procedure maybe used to evaluate color, turbidity, and hardness reduction.1.2 The practice provides a systematic evaluation of thevariables normally encountered in the coagulation-flocculationproces

4、s.1.3 This standard does not purport to address the safetyconcerns, if any, associated with its use. It is the responsibilityof the user of this standard to establish appropriate safety andhealth practices and determine the applicability of regulatorylimitations prior to use.2. Referenced Documents2

5、.1 ASTM Standards:2D 1129 Terminology Relating to WaterD 1192 Specification for Equipment for Sampling Waterand Steam in Closed Conduits3D 1193 Specification for Reagent WaterD 1293 Test Methods for pH of WaterD 1889 Test Method for Turbidity of WaterD 3370 Practices for Sampling Water from Closed C

6、onduits3. Terminology3.1 DefinitionsFor definitions of terms used in this prac-tice, refer to Terminology D 1129.4. Summary of Practice4.1 The coagulation-flocculation test is carried out to deter-mine the chemicals, dosages, and conditions required toachieve optimum results. The primary variables t

7、o be investi-gated using the recommended practice include, but are notlimited to:4.1.1 Chemical additives,4.1.2 pH,4.1.3 Temperature, and4.1.4 Order of addition and mixing conditions.5. Significance and Use5.1 This practice permits the evaluation of various coagu-lants and coagulant aids used in the

8、 treatment of water andwaste water for the same water and the same experimentalconditions.5.2 The effects of concentration of the coagulants andcoagulant aids and their order of addition can also be evaluatedby this practice.6. Interferences6.1 There are some possible interferences that may make the

9、determination of optimum jar test conditions difficult. Theseinclude the following:6.1.1 Temperature Change (During Test)Thermal or con-vection currents may occur, interfering with the settling ofcoagulated particles. This can be prevented by temperaturecontrol.6.1.2 Gas Release (During Test)Flotati

10、on of coagulatedfloc may occur due to gas bubble formation caused bymechanical agitator, temperature increase or chemical reaction.1This practice is under the jurisdiction of ASTM Committee D19 on Water andis the direct responsibility of Subcommittee D19.03 on Sampling of Water andWater-Formed Depos

11、its, Analysis of Water for Power Generation and Process Use,On-Line Water Analysis, and Surveillance of Water.Current edition approved July 3, 1980. Published October 1980. Originallyapproved in 1964. Last previous edition approved in 1980 as D 203580.2For referenced ASTM standards, visit the ASTM w

12、ebsite, 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, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-295

13、9, United States.6.1.3 Testing-Period Biological activity or other factorsmay alter the coagulation characteristics of water upon pro-longed standing. For this reason the period between samplingand testing should be kept to a minimum, with the time beingrecorded.7. Apparatus7.1 Multiple Stirrer A mu

14、ltiposition stirrer with continu-ous speed variation from about 20 to 150 rpm should be used.The stirring paddles should be of light gage corrosion-resistantmaterial all of the same configuration and size. An illuminatedbase is useful to observe the floc formation. Precautionarymeasures should be ta

15、ken to avoid heat being imparted by theillumination system which may counteract normal settling.7.2 Jars (or Beakers), all of the same size and shape;1500-mL Griffin beakers may be used (1000-mL recommendedminimum size).7.3 Reagent Racks A means of introducing each testsolution to all jars simultane

16、ously. There should be at least onerack for each test solution or suspension. The racks should besimilar to that shown in Fig. 1.8. Reagents8.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall conform to the specif

17、ications of the Commit-tee on Analytical Reagents of the American Chemical Society,where such specifications are available.4Other 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.8.

18、2 Purity of Water Unless otherwise indicated, referenceto water for reagent preparation shall be understood to meanType IV reagent water conforming to Specification D 1193.8.3 The following chemicals and additives are typical ofthose used for test solutions and suspensions. The latter, withthe excep

19、tion of coagulant aids, may be prepared daily bymixing chemicals with water to a concentration of 10 (60.1)g/L (1.0 mL of test solution or suspension when added to 1 Lof sample is equivalent to 10 mg/L):Prime CoagulantsAlumAl2(SO4)318H2OFerric sulfate Fe2(SO4)3xH2OFerric chloride (FeCl36H2O)Ferrous

20、sulfate (FeSO47H2O)Magnesium carbonate (MgCO33H2O)Sodium aluminate (NaAlO2)Coagulant AidsActivated silicaAnionic (polyelectrolyte)Cationic (polyelectrolyte)Nonionic PolymerOxidizing AgentsChlorine (Cl2)Chlorine dioxide (ClO2)Potassium permanganate (KMnO4)Calcium hypochlorite CaCl(ClO)4H2OSodium hypo

21、chlorite (NaClO)AlkalisCalcium carbonate (CaCO3)Dolomitic lime(58 % CaO, 40 % MgO)Lime, hydrated Ca(OH)2Magnesium oxide (MgO)Sodium carbonate (Na2CO3)Sodium hydroxide (NaOH)Weighting AgentsBentoniteKaolinOther clays and mineralsMiscellaneousActivated carbon (powdered)4Reagent Chemicals, American Che

22、mical 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 Pharmacopeiaand National Formulary, U.S. P

23、harmacopeial Convention, Inc. (USPC), Rockville,MD.FIG. 1 Reagent Rack for Multiple Stirrer Jar Test ApparatusD 2035 80 (2003)28.4 Coagulant Aids There are numerous commerciallyavailable coagulant aids or polyelectrolytes. All polyelectro-lytes are classified anionic, cationic or nonionic, depending

24、upon their composition. These aids may have the ability toproduce large, tough, easily-settled floc when used alone or inconjunction with inorganic coagulants. A small dosage (under1 mg/L) may permit a reduction in the dosage of, or completeelimination of, the coagulant. In the latter case, the poly

25、elec-trolyte would be considered the prime coagulant rather than acoagulant aid. Aids come in powdered and liquid form.Powdered aids should be prepared as 0.1 % solutions withappropriate aliquots to provide proper dosage. Always addpowdered aids to the dissolving water rather than the reverse,and ad

26、d slowly to the shoulder of a vortex created by stirring.If a vortex is not formed, the dry powder will merely collect onthe surface of the water in gummy masses and become verydifficult to dissolve. Dissolving time may vary from severalminutes to several hours. Suggested manufacturers proceduresfor

27、 wetting, dissolving, and storing should be followed whenavailable. Liquid forms can be readily prepared to the abovestrength without difficulty.59. Sampling9.1 Collect the water sample under test in accordance withthe applicable Specification D 1192 and Practices D 3370.10. Procedure10.1 Measure eq

28、ual volumes (1000 mL) of sample intoeach of the jars or 1500-mL Griffin beakers. As many sampleportions may be used as there are positions on the multiplestirrer. Locate beakers so that the paddles are off-center, butclear the beaker wall by about 6.4 mm (14 in.). Record thesample temperature at the

29、 start of the test.10.2 Load the test chemicals in the reagent racks. Use onerack for each series of chemical additions. Make up each tubein the rack to a final volume of 10 mL, with water, beforeusing. There may be a situation where a larger volume ofreagent will be required. Should this condition

30、prevail, fill alltubes with water to a volume equal to the largest volume ofreagent in the reagent rack. When adding slurries, it may benecessary to shake the rack to produce a swirling motion justprior to transfer.10.3 Start the multiple stirrer operating at the “flash mix”speed of approximately 12

31、0 rpm. Add the test solution orsuspensions, at predetermined dosage levels and sequence.Flash mix for approximately 1 min after the additions ofchemicals. Record the flash mix time and speed (rpm).10.4 Reduce the speed as necessary to the minimum re-quired to keep floc particles uniformly suspended

32、throughoutthe “slow mix” period. Slow mix for 20 min. Record the timefor the first visible floc formation. Every 5 min (during theslow mix period), record relative floc size and mixer speed(rpm). If coagulant aids are used, mixing speed is criticalbecause excessive stirring tends to break up early f

33、loc forma-tion and may redisperse the aid.10.5 After the slow mix period, withdraw the paddles andobserve settling of floc particles. Record the time required forthe bulk of the particles to settle. In most cases this time willbe that required for the particles to settle to the bottom of thebeaker;

34、however, in some cases there may be interferingconvection currents. If so, the recorded settling time should bethat at which the unsettled or residual particles appear to bemoving equally upward and downward.10.6 After 15 min of settling, record the appearance of flocon the beaker bottom. Record the

35、 sample temperature. Bymeans of a pipet or siphon, withdraw an adequate samplevolume of supernatant liquor from the jar at a point one half ofthe depth of the sample, to conduct color,6turbidity, pH andother required analyses, (Note 1) determined in accordancewith Test Methods D 1889 and D 1293. A s

36、uggested form forrecording results is appended (see Fig. 2).NOTE 1Tests for residual chemicals should be included, for example,alum; residual Al2O3; copperas; residual Fe2O3; etc.10.7 Repeat steps 10.1-10.6 until all pertinent variableshave been evaluated.10.8 The times given in 10.3, 10.4, and 10.6

37、 are onlysuggestions.11. Reproducibility11.1 It is recognized that reproducibility of results is impor-tant. To demonstrate reproducibility, the so-called 3 and 3procedure is suggested. In this procedure, duplicate sets of 3jars each are treated simultaneously with the same chemicaldosages in jars 1

38、 and 4, 2 and 5, and 3 and 6.12. Keywords12.1 coagulation; flocculation; jar tests5A periodically updated “Report on Coagulant Aids for Water Treatment” ispublished by the Environmental Protection Agency Office of Water Supply,Cincinnati, Ohio 45268, listing coagulant aids that may be used in water

39、treatmentwithout adverse physiological effects on those using the water, based on informationsubmitted by the manufacturers or distributors, or both.6For the color determination, reference is made to Standard Methods for theExamination of Water and Waste Water, Fourteenth edition,American Public Hea

40、lthAssociation, Inc., New York, NY, 1975, pp. 6471.D 2035 80 (2003)3ASTM 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

41、 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. Your comments are in

42、vited 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 comments have not receive

43、d 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 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).FIG. 2 Jar Test DataD 2035 80 (2003)4