CHROMIUM (3500-Cr)/Colorimetric Method

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3500-Cr CHROMIUM* 3500-Cr A. Introduction

Chromium (Cr) is the rst element in Group VIB in the periodic table; it has an atomic number of 24, an atomic weight of 51.99, and valences of 0 and 2 through 6. The average abundance of Cr in the earths crust is 122 ppm; in soils Cr ranges from 11 to 22 ppm; in streams it averages about 1 g/L, and in groundwaters it is generally 100 g/L. Chromium is found chiey in chrome-iron ore (FeO Cr2O3). Chromium is used in alloys, in electroplating, and in pigments. Chromate compounds frequently are added to cooling water for corrosion control. In natural waters trivalent chromium exists as Cr3 , Cr(OH)2 , Cr(OH)2 , and Cr(OH)4 ; in the hexavalent form chromium exists as CrO42 and as Cr2O72 . Cr3 would be expected to form strong complexes with amines, and would be adsorbed by clay minerals. Chromium is considered nonessential for plants, but an essential trace element for animals. Hexavalent compounds have been shown to be carcinogenic by inhalation and are corrosive to tissue. The chromium guidelines for natural water are linked to the hardness or alkalinity of the water (i.e., the softer the water, the lower the permitted level for chromium). The United Nations Food and Agriculture Organization recommended maximum level for irrigation waters is 100 g/L. The U.S. EPA primary drinking water standard MCL is 100 g/L for total chromium.
* Approved by Standard Methods Committee, 2001. Joint Task Group: Rock J. Vitale (chair), C. Ellen Gonter, Timothy S. Oostdyk; 20th EditionSee 3500-Al.

The colorimetric method (B) is useful for the determination of hexavalent chromium in a natural or treated water in the range from 100 to 1000 g/L. This range can be extended by appropriate sample dilution or concentration and/or use of longer cell paths. The ion chromatographic method with photometric detection (C) is suitable for determining dissolved hexavalent chromium in drinking water, groundwater, and industrial wastewater efuents from 0.5 to 5000 g/L. The electrothermal atomic absorption spectrometric method (3113B) is suitable for determining low levels of total chromium ( 50 g/L) in water and wastewater, and the ame atomic absorption spectrometric methods (3111B and C) and the inductively coupled plasma methods (3120 and 3125) are appropriate for measuring total chromium concentrations up to milligram-per-liter levels.
3. Sample Handling

If only the dissolved chromium content is desired, lter sample immediately through a 0.45- m membrane lter at time of collection, and acidify ltrate with conc nitric acid (HNO3) to pH 2. If only dissolved hexavalent chromium is desired, adjust pH of ltrate to 9 with 1N sodium hydroxide solution and refrigerate to 4 2C. If the total chromium content is desired, acidify unltered sample at time of collection with conc HNO3 to pH 2. If total hexavalent chromium is desired, adjust pH of unltered sample to 9 with 1N sodium hydroxide and refrigerate to 4 2C.

3500-Cr B. Colorimetric Method

a. Principle: This procedure measures only hexavalent chromium, Cr(VI). For total chromium determination, acid-digest the sample (see Section 3030) and follow with a suitable instrumental analysis technique. The hexavalent chromium is determined colorimetrically by reaction with diphenylcarbazide in acid solution. A red-violet colored complex of unknown composition is produced. The reaction is very sensitive, the molar absorptivity based on chromium being about 40 000 L g 1 cm 1 at 530 or 540 nm. NOTE: Validation data for Method 3500-Cr.B were developed at 540 nm. Validation data for Method 3500-Cr.C were developed at 530 nm. b. Interferences: The reaction with diphenylcarbazide is nearly specic for chromium. Hexavalent molybdenum and mercury salts will react to form color with the reagent but the intensities are much lower than that for chromium at the specied pH. Concentrations of Mo or Hg as high as 200 mg/L can be tolerated. Vanadium interferes strongly but concentrations up to

10 times that of chromium will not result in signicant analytical error. Iron in concentrations greater than 1 mg/L may produce a yellow color but the ferric ion (Fe3 ) color is not strong and no difculty is encountered normally if the absorbance is measured photometrically at the appropriate wavelength.
2. Apparatus

a. Colorimetric equipment: One of the following is required: 1) Spectrophotometer, for use at 530 or 540 nm, with a light path of 1 cm or longer. 2) Filter photometer, providing a light path of 1 cm or longer and equipped with a greenish yellow lter having maximum transmittance at 530 or 540 nm. b. Laboratory ware: Soak all reusable items (glass, plastic, etc.), including sample containers, overnight in laboratory-grade detergent, rinse, and soak for 4 h in a mixture of nitric acid (1 part), hydrochloric acid (2 parts), and reagent water (9 parts). Rinse with tap water and reagent water. NOTE: Never use chromic acid cleaning solution.

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METALS (3000)

3. Reagents

Use reagent water (see Section 1080) for reagent preparation and analytical procedure. a. Stock chromium solution: Dissolve 141.4 mg K2Cr2O7 in water and dilute to 100 mL; 1.00 mL 500 g Cr. CAUTION: Hexavalent chromium is toxic and a suspected carcinogen. Handle with care. b. Standard chromium solution: Dilute 1.00 mL stock chromium solution to 100 mL; 1.00 mL 5.00 g Cr. Prepare calibration standards at time of analysis. c. Nitric acid, HNO3, conc. d. Sulfuric acid, H2SO4, conc, 18N, and 6N. e. Sulfuric acid, H2SO4, 0.2N: Dilute 17 mL 6N H2SO4 to 500 mL with water. f. Phosphoric acid, H3PO4, conc. g. Diphenylcarbazide solution: Dissolve 250 mg 1,5-diphenylcarbazide (1,5-diphenylcarbohydrazide) in 50 mL acetone. Store in a brown bottle. Prepare weekly. Discard if the solution becomes discolored. h. Sodium hydroxide, 1N: Dissolve 40 g NaOH in 1 L water. Store in plastic bottle.

NOTE: If the solution is turbid after dilution to 100 mL in c above, take an absorbance reading before adding carbazide reagent and correct absorbance reading of nal colored solution by subtracting the absorbance measured previously.
5. Calculation
mg Cr/L g Cr (in 102 mL final volume) A

where:
A mL original sample.

6. Precision and Bias

Collaborative test data from 16 laboratories were obtained on reagent water, tap water, 10% NaCl solution, treated water from synthetic organic industrial waste, EPA extraction leachate, process water, lake water, and efuent from a steel pickle liquor treatment plant.3 The test data yielded the following relationships: Reagent water:
St So St So 0.037x 0.022x 0.006 0.004

Drinking or wastewater:
4. Procedure
0.067x 0.037x 0.004 0.002

a. Preparation of calibration curve: To compensate for possible slight losses of chromium during analytical operations, treat standards and samples with the same procedure. Accordingly, pipet measured volumes of standard chromium solution (5 g/ mL) ranging from 2.00 to 20.0 mL, to give standards for 10 to 100 g Cr, into 250-mL beakers or conical asks. Depending on pretreatment used in b below, proceed with subsequent treatment of standards as if they were samples. Develop color as for samples, transfer a suitable portion of each colored solution to a 1-cm absorption cell, and measure absorbance at 540 nm, using reagent water as reference. Correct absorbance readings of standards by subtracting absorbance of a reagent blank carried through the method. Construct a calibration curve by plotting corrected absorbance values against micrograms chromium in 102 mL nal volume. b. Treatment of sample: If sample has been ltered and/or only hexavalent chromium is desired, start analysis within 24 h of collection and proceed to 4c. NOTE: Recent evidence suggests that preserved samples can be held for 30 d without substantial changes to Cr (VI) concentrations.1,2 c. Color development and measurement: Add 0.25 mL (5 drops) H3PO4. Use 0.2N H2SO4 and a pH meter to adjust solution to pH 2.0 0.5. Transfer solution to a 100-mL volumetric ask, dilute to 100 mL, and mix. Add 2.0 mL diphenylcarbazide solution, mix, and let stand 5 to 10 min for full color development. Transfer an appropriate portion to a 1-cm absorption cell and measure its absorbance at 530 or 540 nm, using reagent water as reference. Correct absorbance reading of sample by subtracting absorbance of a blank carried through the method (see also note below). From the corrected absorbance, determine micrograms chromium present by reference to the calibration curve.

Leachate:
St So 0.032x 0.017x 0.007 0.004

where:
St So x overall precision, single-operator precision, and chromium concentration, mg/L.

7. References
1. U.S. ENVIRONMENTAL PROTECTION AGENCY. 1996. Determination of hexavalent chromium by ion chromatography. Method 1636. EPA 821-R-96-003, U.S. Environmental Protection Agency, Washington, D.C. 2. EATON, A., A. HAGHANI & L. RAMIREZ. 2001. The Erin Brockovich factor. In Proc. Water Quality Technology Conf. (Nashville, Tenn., November 1115, 2001). American Water Works Assoc., Denver, Colo. 3. AMERICAN SOCIETY FOR TESTING AND MATERIALS. 1996. Chromium, total. D1687-92, Annual Book of ASTM Standards, Vol. 11.01. American Soc. Testing & Materials, Philadelphia, Pa.

8. Bibliography
ROWLAND, G.P., JR. 1939. Photoelectric colorimetryOptical study of permanganate ion and of chromium-diphenylcarbazide system. Anal. Chem. 11:442. URONE, P.F. 1955. Stability of colorimetric reagent for chromium, 5-diphenylcarbazide, in various solvents. Anal. Chem. 27:1354. ALLEN, T.L. 1958. Microdetermination of chromium with 1,5-diphenylcarbohydrazide. Anal. Chem. 30:447. ONISHI, H. 1979. Colorimetric Determination of Traces of Metals, 4th ed. Interscience Publishers, New York, N.Y.

CHROMIUM (3500-Cr)/Ion Chromatographic Method

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3500-Cr C. Ion Chromatographic Method

a. Principle: This method is applicable to determination of dissolved hexavalent chromium in drinking water, groundwater, and industrial wastewater efuents. An aqueous sample is ltered and its pH adjusted to 9 to 9.5 with a concentrated buffer. This pH adjustment reduces the solubility of trivalent chromium and preserves the hexavalent chromium oxidation state. The sample is introduced into the instruments eluent stream of ammonium sulfate and ammonium hydroxide. Trivalent chromium in solution is separated from the hexavalent chromium by the column. After separation, hexavalent chromium reacts with an azide dye to produce a chromogen that is measured at 530 or 540 nm. NOTE: Validation data for 3500-Cr.C were developed at 530 nm. Hexavalent chromium is identied on the basis of retention time. Although this method was developed using specic commercial equipment, use of another manufacturers equipment should be acceptable if appropriate adjustments are made. b. Interferences: Interferences may come from several sources. Use analytical grade salts for the buffer because trace amounts of chromium may be included. Several soluble species of trivalent chromium in the sample may be oxidized to the hexavalent form in an alkaline medium in the presence of such oxidants as hydrogen peroxide, ozone, and manganese dioxide. The hexavalent form can be reduced to the trivalent in the presence of reducing species in an acid medium. High ionic concentration may cause column overload. Samples high in chloride and/or sulfate might show this phenomenon, which is characterized by a change in peak geometry. Interfering organic compounds are removed by the guard column. c. Minimum detectable concentrations: The method detection levels obtained in a single laboratory with a 250- L loop were as follows:
Reagent water Drinking water Groundwater Primary wastewater efuent Electroplating waste 0.4 0.3 0.3 0.3 0.3 g/L g/L g/L g/L g/L

plastic pressurized containers to deliver eluent and post-column reagent. Use high-purity helium (99.995%) to pressurize the eluent and post-column reagent vessel. b. Guard column, to be placed before the separator column, containing an adsorbent capable of adsorbing organic compounds and particulates that would damage or interfere with the analysis or equipment.* c. Separator column, packed with a high-capacity anion-exchange resin capable of resolving chromate from other sample constituents. d. Recorder, integrator, or computer for receiving signals from the detector as a function of time. e. Laboratory ware: Soak all reusable items (glass, plastic, etc.) including sample containers, overnight in laboratory-grade detergent, rinse, and soak for 4 h in a mixture of nitric acid (1 part), hydrochloric acid (2 parts), and reagent water (9 parts). Rinse with tap water and reagent water. NOTE: Never use chromic acid cleaning solution. f. Syringe, equipped with male luer-type tting and a capacity of at least 3 mL.
3. Reagents

d. Sample preservation and holding time: Filter sample through a 0.45- m lter. Use a portion of sample to rinse syringe lter unit and lter, then collect the required volume of ltrate. Adjust pH to 9 to 9.5 by adding buffer solution dropwise while checking pH with a pH meter. Ship and store sample at 4C. Bring to room temperature before analysis. Analyze samples within 24 h of collection.
2. Apparatus

a. Reagent water: Deionized or distilled water free from interferences at the minimum detection level of each constituent, ltered through a 0.2- m membrane lter and having a conductance of less than 0.1 S/cm. Use for preparing all reagents (see Section 1080). b. Cr(VI) stock solution, 100 mg Cr6 /L: Prepare from primary standard grade potassium dichromate. Dissolve 0.1414 g K2Cr2O7 in water and dilute to 500 mL in a volumetric ask. pH adjustment is not required. Store in plastic. CAUTION: Hexavalent chromium is toxic and a suspected carcinogen; handle with care. c. Eluent: Dissolve 33 g ammonium sulfate (NH4)2SO4, in 500 mL water and add 6.5 mL conc ammonium hydroxide, NH4OH. Dilute to 1 L with water. d. Post-column reagent: Dissolve 0.5 g 1,5-diphenylcarbazide in 100 mL HPLC-grade methanol. Add with stirring to 500 mL water containing 28 mL conc H2SO4. Dilute to 1 L with water. Reagent is stable for 4 or 5 d; prepare only as needed. e. Buffer solution: Dissolve 33 g ammonium sulfate, (NH4)2SO4, in 75 mL water and add 6.5 mL conc ammonium hydroxide, NH4OH. Dilute to 100 mL with water.
4. Procedure

a. Ion chromatograph equipped with a pump capable of precisely delivering a ow of 1 to 5 mL/min. The metallic parts of the pump must not contact sample, eluent, or reagent. Sample loops should be available or the instrument should be capable of delivering from 50 to 250- L injections of sample. The visible absorption cell should not contain metallic parts that contact the eluent-sample ow. The cell must be usable at 530 nm. Use

a. Instrument setup: Establish ion chromatograph operating conditions as indicated in Table 3500-Cr:I. Set ow rate of the eluent pump at 1.5 mL/min and adjust pressure of reagent delivery module so that the system ow rate, measured after the detector, is 2.0 mL/min. Measure system ow rate using a graduated cylinder and stopwatch. Allow approximately 30 min after adjustment before measuring ow.

* IonPac NG1, Dionex, 4700 Lakeside Drive, Sunnyvale, CA 94086, or equivalent. IonPac AS7, Dionex, or equivalent.

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METALS (3000)

TABLE 3500-Cr:I. ION CHROMATOGRAPHIC CONDITIONS Variable Guard column Separator column Eluent Eluent ow rate Post-column reagent Value Dionex IonPac NG1 Dionex IonPac AS7 250 mM (NH4)2SO4 100 mM NH4OH 1.5 mL/min 2 mM diphenylcarbohydrazide 10% v/v CH3OH 1N H2SO4 0.5 mL/min Visible @ 530 nm 3.8 min

TABLE 3500-Cr:II. SINGLE-LABORATORY PRECISION Sample Type Reagent water Drinking water Groundwater Primary wastewater efuent Electroplating efuent Concentration* g/L 100 1000 100 1000 100 1000 100 1000 100 1000

AND

BIAS RPD 0.8 0.0 6.7 1.5 0.0 0.8 0.7 2.7 0.4 0.4

Mean Recovery % 100 100 105 98 98 96 100 104 99 101

Post-column reagent ow rate Detector Retention time

Use an injection loop size based on required sensitivity. A 50- L loop is sufcient, although a 250- L loop was used to determine the method detection level. b. Calibration: Before sample analysis, construct a calibration curve using a minimum of a blank and three standards that bracket the expected sample concentration range. Prepare calibration standards from the stock standard (3b) by appropriate dilution with reagent water in volumetric asks. Adjust to pH 9 to 9.5 with buffer solution (3e) before nal dilution. Injection volumes of standards should be about 10 times the injection loop volume to insure complete loop ushing. c. Sample analysis: Bring chilled, pH-adjusted sample to ambient temperature. Fill a clean syringe with sample, attach a 0.45- m syringe lter, and inject 10 times the sample loop volume into the instrument. Dilute any sample that has a concentration greater than the highest calibration standard.
5. Calculation

* Sample fortied at this concentration level. RPD - relative percent difference between fortied duplicates.

Determine area or height of the Cr(VI) peak in the calibration standard chromatograms. Establish a calibration curve by performing a regression analysis of peak height or peak area against standard concentration in mg/L. If correlation coefcient is less than 0.995, do not use these data. Check analytical process. For samples, measure area (or height) of Cr(VI) peak in sample chromatogram, as determined by retention time. Calculate Cr(VI) concentration by interpolating from the calibration line. Correct data for any dilutions made. Currently available instrumentation automates the entire measurement process (peak measurement, calibration, and sample measurements and calculations). Ensure that enough quality control samples are analyzed to monitor the instrumental processes.
6. Quality Control

bration range; prepare from a source independent of the calibration standards. Use acceptance criteria for check standard recovery and calibration standard concentration based on project goals for precision and accuracy. Typical values for recovery of the check standard range from 90 to 110%. The acceptance criteria for the calibration blank are typically set at the nominal MDL. c. Reagent blank analysis: Analyze one laboratory reagent blank with each batch of samples. Signicant Cr(VI) detected in the reagent blank is a sign of contamination. Identify source and eliminate contamination. d. Laboratory-fortied matrix (also known as matrix spike) analysis: To a portion of a sample, add a known quantity of Cr(VI). After analysis, calculate percent recovery of the known addition. If the recovery falls outside the control limits (typically 75 to 125%), the matrix may be interfering with the analysis. If matrix interferences are thought to be present, use the method of standard additions, if appropriate, to minimize the effect of interferences. NOTE: There are situations where low recoveries of analyte additions can be overcome, or where the non-detected analyte results can be further validated by the application of three-point method of standard addition. The decision to apply method of standard additions should be a function of achieving desired data quality objectives. Analyze fortied matrix samples as frequently as dictated by project goals and anticipated similarity of matrices in the sample set. e. Laboratory control sample: Analyze a laboratory control sample (LCS) from an external source with every sample batch. Process LCS and samples identically, including ltering and pH adjustment. Base acceptance criteria for LCS recovery on project goals for precision and bias. Typical values for acceptable recovery range from 90 to 110%.
7. Precision and Bias

a. Initial demonstration of performance: Before sample analysis, set up instrument and analyze enough known samples to determine estimates for the method detection level and linear calibration range. Use the initial demonstration of performance to characterize instrument performance, i.e., method detection levels (MDLs) and linear calibration range. b. Initial and continuing calibration performance: Initially, after every 10 samples, and after the nal sample, analyze an independent check sample and a calibration blank. The concentration of the calibration check sample should be near the mid-cali-

The instrument operating conditions and data from a singlelaboratory test of the method are shown in Tables 3500-Cr:I and 3500-Cr:II, respectively. Multilaboratory test data are shown in Table 3500-Cr:III. Fifteen laboratories analyzed samples ranging from 1.2 to 960 g Cr/L.
The multilaboratory precision and bias data cited in this method were the result of a collaborative study carried out jointly between U.S. EPA Environmental Monitoring Systems Laboratory (Cincinnati) and Committee D-19 of ASTM.

COPPER (3500-Cu)/Introduction

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OF

TABLE 3500-Cr:III. MULTILABORATORY DETERMINATION HEXAVALENT CHROMIUM* Amount Added g/L 6.00 8.00 16.0 20.0 100 140 800 960 6.0 8.0 16.0 20.0 100 140 800 960 Amount Found g/L 6.68 8.64 17.4 21.4 101 143 819 966 5.63 7.31 15.1 19.8 98.9 138 796 944

BIAS

FOR

St

0.050x

0.559 1.04x 0.183

Mean recovery St 1.03 1.10 2.25 2.31 1.91 5.52 24.3 18.5 1.17 1.91 2.70 1.01 4.36 8.39 60.6 72.1 So 0.53 0.77 3.76 12.7 Bias % 11.3 8.0 8.8 7.0 1.0 2.1 2.4 7.3 6.2 8.6 5.6 1.0 1.1 1.4 0.5 1.7

Water Reagent

where:
So St x single-operator precision, overall precision, and added amount.

For wastewater matrix:

Waste

0.55 1.85 3.31 27.1

The eleven water samples consisted of a reagent water blank and ve Youden pairs. The nine wastewater samples consisted of a wastewater blank and four Youden pairs.
8. Bibliography
U.S. ENVIRONMENTAL PROTECTION AGENCY. 1991. Methods for the Determination of Metals in Environmental Samples. Method 218.6, EPA-600/ 4-91-010, Environmental Monitoring Systems Lab., Cincinnati, Ohio. DIONEX. 1990. Technical Note No. 26. Dionex, Sunnyvale, Calif. EDGEL, K.W., J.A. LONGBOTTOM & R.A. JOYCE. 1994. Determination of dissolved hexavalent chromium in drinking water, ground water, and industrial wastewater efuents by ion chromatography: Collaborative study. J. Assoc. Ofc. Anal. Chem. 77:994.

* Each Youden pair was used to calculate one laboratory data point (So).

For reagent water matrix: