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E Designation: D 6855 ~ 03 Standard Test Method for Determination of Turbidity Below 5 NTU in Static Mode’ "hss ne ire lege SS he marine loving ition indies yur gas oa ee tia eves nn You tt po Siang pon) nace ns eget at ven or apo I Scope "1 This test method covers the static determination of bidity in water (see 4.1) | 12 This test method is applicable to the rieasurement of Iubidites under 5.0 nepkelometric turbidity units (NTU). 13 This test method was tested on municipal drinking eer, ulira-pure water and low turbidity samples. It is the [bar's responsibility to ensure the validity of this test method fac waters of untested matrices. 14 This standard does nor purport 10 address all of the ‘wiry concerns, if any, associated with its use. It 1s the responsibility of the user of this standard to establish anpro- rate safety and health practices and determine the applica- Bity of regulatory limitations prior to use. Refer to the MSDSs for all chemicals used in this procedure 2 Referenced Documents 2) “STM Standards: ® LE _) Terminology Relating to Water 1.1192 Guide for Equipment for Sampling Water and Steam in Closed Conduits 1D 1193 Specification for Reagent Water 2777 Practice for Determination of Precision and Bias of Applicable Methods of Committee D19 on Water 3370 Practices for Sampling Water from Closed Conduits, D847 Practice for Writing Quality Control Specifications for Standard Test Methods for Water Analysis, E691 Practice for Conducting an Interlaboratory Study t0 Determine the Precision of a Test Method 22. Other Referenced Standards: USEPA Method 180.1 Methods for Chemical Analysis of Water and Wastes, Turbidity? "This ex meth ie under the jurcton of ASTM Comite DI9 on Wate ‘ads de duet responsibly of Subcommtce DI907 on Sediments, Goma logy, sa Open. Chanel Re. Creat eon approved Jn. 10, 2003. Pbtised Api 208, For rferennd ASTM standart, vis the ASTM weit, Wa ase. ot {Bhs ASTM Castner Service at service @asn.rg, For Ana! Book of AST Sandra votuse infermatn, eet he stands Document Summary page 00 Or ASTAC web * avaible fom Unie Stats Envieonmental Proection Ascclaton (EPA), nal Rios Bl, 1200 Peansylvania Ave, NW, Washington, DC 20460. ISO 7027 (The International Organization for Standardiza- tion) Water Quality—for the Determination of Turbdity* 3. Terminology 3.1 Definitions—For definitions of terms used in this ‘method refer to Terminology D 1129. 3.2 Definitions: 3.2.1 calibration turbidity standard—a wrbidity standard that is traceable and equivalent to the reference turbidity standard to within statistical errors, including commercially prepared 4000 NTU Formazin, stabilized formazin (see 9.2.3), and styrenedivinylbenzene (SDVB) (see 9.2.4). These stan- dards may be used to calibrate the instrument. None 1~Calietion standards may be instrument speci. 3.22 calibration verification standards—defined standards ‘used to verity the accuracy of a calibration in the measurement range of interest. These standards may not be used to perform calibrations, only calibration verification. Included standards ane opto-mechanical ight scatter devices, gel-like standards, or any other type of stable liquid standard, Noe 2—Calibaton verifcation standards maybe instrament pei 3.23 nephelometric turbidity measurement—the measure- ament of light seater from a sample ina direction tha is at 0° with respect to the centerline ofthe incident light path. Units are NTU (Nephelometric Turbidity Units); when SO 7027 technology is employed units are in FNU (Formazin Nepelo- metric Units). 3.24 ratio urbidity measurement—the measurement de- rived through the use of a nephelometric detector that serves as the primary detector and one or more other detectors used to compensate for variation in incident light fuctuaion, stray light, instrament noise, or sample color. 3.2.5 reference turbidity standard—a standard that is syn- thesized reproducibly from traceable raw materials by a skilled analyst, Al other standards are traced back to this standard The reference standard for turbidity is formazin (see 9.2.2) 3.2.6 seasoning—the process of conditioning laboratory slassware with the standard to be diluted to alower value. The * avaiable frm American National tandars Inte (ANSI), 25 W rt, » 050% er Standard Deion (5) Boise — areas irs © vas acness © aerse © Daas Grate Sanda Ovation of Cal AvEaG05(Syoun)® oct Extreme Val ‘10853 0.0883 oases oze887 4.15009 ea199 oasee7 228887 Salo Operator Standard Oovaton (5, 01547 oat7e 08 oss a0kr7 0088 00s at fralytRatative Deviation, 8° 42% 2.657% 750% 2H 1am «TSN aE TS Lacon Standard Deion ($9 Ore ogrsz = 190 onaae Goats ose ouatr’—.tsae Laboraey Reve Deion, 8% 109% 80% tose 28% tame oem base <2 She abort standard ovation and was calsuatod sing te Paves E 691 atta package Thisis be candid ceva oh rears Fon Woloae is, le nat aga oy Practice 0.277, tomaton may sl be ull tba ers ls thor, Tis ase Sanda devavon ef he means of oles ons among sx boro wes canted as the podled witiniabratoy standar deviation rom tipate observations aeng sik Sborloles. clsuted in sccortance withthe 'y; measure of Practco E 601 This lth exact squvaln! of singe opera preciso as dined Practca 2777 wien Youdoh pa aol uta, £¢ Ta aowatensviaes oy mean recover (XB, 28, nas cae "accordance wh Ie Tepredusbity measur of Practica E he standard deat of sng meteuemen nog asst, Wh 1, Tis the equialent of the overal stndarédbiaton of Praca 82777, which er 8, Suse, 3 e roproauey 987 a Af D 6ess - 03 TABLE 2 Final Statistical Summary for Turbidity in Real World Water Samples a ‘Gompined Fite” South Acpled Soa Appied Raw Water Faw Waar = Snel fist ‘ofiter tole #2 Deleware ‘Schuytt™ —_PRECYp Te Cone, NTU NA Nx Na NA Na Wa fot Rowanes Vales e 3 ° 6 6 e ‘Mean Recovery (X84, NTU o.ea o25e1 oe) 3547 707 ce Recovery, % NA NA wa NA Na NA. eral Sertaré Devaon Sy" 0.00625 02480 oo4t70 ozsies —osm1e2 cater Standaré Deviation of Cet Avirages (Syane)* est Exrome Vas 03000 020000 1.06667 9223s saa antag ‘Single Operator Standard Deviation (5, ‘0.0050 ‘0002 tas Dosey ‘080 cos ‘Anaiet Rate Devito, rizr 3887 % heise 1s 219% ary Laboratory Strard Dewaton (5° ‘0078 ‘0028 20408 0.2669 2026 ‘oot08 Labortry Rte Deviation, 138% 100% 43% 75% 54% 1559 {5 Sterear deviation died by mean recovery (9247 obese Cane eae a pe SPCEMEY mania of Praca 31 Ts ba quale bor arc dein Pata 277 vn Gescbes he sinc sevatin ofa snglo measurement arog abrataon Where 9, «Sy ue 8 oe sence aa irogeteek the precision of sample analyses, analyze a operator and an instrament (turbidimeter). Testing was con: sample in duplicate with each batch of samples. The recom- ducted over a two day period menses frequency for detcomining precision is more than or 16.1.1 ‘The collaborative Test Data included two sr0ups of Stapicg 2% At amples detained for cash batch of spe: Staxand mebidlysanvls eeu a samples turbidity samples. Artificial Turbii surrogates in UC sad Gini of he in Ak Ra an ara ina Tae a a py agnor Sle Forma w OE 096400 St Sb at the = O01 significance ove 2 ‘Styrenedivinylbenzene (SDVB) Of 0.20, 0.50, and 2.0 NTU, 1532.1 Appendix X4 is the Table X2.1 from Practice Real world turbidity samples incladed: ‘Two siver way D 5847 for the critical values of F at the 1% significance St™ples denoted Raw Water Deleware and Raw Water (99 & confidence) level (one-sided). Also, reference Practice _ Schuykill; two settled water samples from a drinking water 1D 5847 if necessary to see an example of how the calculation Plant (DWP); ane combined filter effluent water sample from & untlizes both the single operator stendard deviation (S) and the DWP; and one tap water sample. The real-world samples have Standard deviation ofthe duplicate sample analysis values (S,). 0 aSsigned values. The true values for these samples are 15.322 The result from (S,)°/Sg)*= (standard deviation of unknown and therefore an estimate of bias cannot be made for sample reps)?/single operator standard deviation)" calculated these samples. Yue ersus © or <) critical value from table. The result will 16.1.2 Each sample was measured in triplicate over the determine if the duplicate values are acceptable. same period of time across all laboratories in an effort to se ihe Teslt exceeds the precision limit as derived minimize sample changed due to their potential lack of from the F tet, the batch must be reanalyzed or the results stability, foe rete itt tm indlontion that they do nc fll within 16.2 Rapes of this collaborative sty may nat be oral the performance criteria ofthe test procedure of ress for matics ete than hose sted 15.4 Independent Reference Material (IRM)—In order 10 : 16.3 Precision and bias was determined in accordance t0 verify the quantitative value produced by the test procedure, 5 analyze an IRM submitted asa regular sample to the laboratory YHetice D 2777 whenever possible, Final statistics for the 90 at Teast once per quarter The value ofthe IRM should be in the SOUPS of samples can be found in Tables 1 and 2. range of the determinations that the Isb normally determines 16.4 Because Youden Pair samples were not feasible in this during the analyses of samples. The value obtained must fall study, S, was calculated in accordance with the repeatability within the contol limits specified by the provider of the IRM, measure of Practice E691. This is the exact equivalent of single operator precision as defined in Practice D.2777 when 16, Precision and Bias ? Youden pairs are not utilized se ania Testmethod was tested on 7 laboratories that were 1644.1 Only a statement of single operator precise‘ ‘assembled at a common ste. Each laboratory consisted of an required. The modification of this study wes allowed aren, to section 1.3.2 in Practice D 2777, 16.4.2 The final statistical package utilized Practice D 2777 : tae ened ASTM Ineatonal Hex and nay £0 all applicable calculation with one exception, which Wat bebe msg Rona par Sc state Single Operator Standard Deviation, 988 17. Keywords 17.1 calibration; calibration turbidity standard; calibration tion; measurement; nephelometic turbidity; ratio tur- _ turbidimeter; turbidity; turbidity standards (Nonmandatory Information) | ‘Xi. CLEANING AND MAINTENANCE OF TURBIDITY SAMPLE CELLS AND CAPS XL Introduction X1.L1 Sample cells and caps must be kept scrupulously {dean both inside and outside. This level of cleanliness must be eiablished prior to cell matching process and maintained throughout the cell's working lifetime X12 Cleaning X1.2.1 Sample cells and caps must be examined prior to {leaning. All scratched, blemished, and scuffed cells should be

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