CA2320828A1 - Method for the determination of hexavalent chromium using ultrasonication and strong anion exchange solid phase extraction - Google Patents

Abstract

A method for the determination of hexavalent chromium (CrVI) in environmental and industrial hygiene samples is provided. Based on the chemical properties of chromium species in aqueous solutions, a simple, fast, sensitive, and economical field method has been developed and evaluated for the determination of hexavalent chromium (CrVI). By means of ultrasonic extraction in combination with a strong anion exchange solid phase extraction (SAE-SPE) technique, the filtration, preconcentration, and isolation of CrVI in the presence of other chromium species and interferents was achieved. The method generally involves: (1) ultrasonication in basic buffer solution to extract CrVI from environmental matrices; (2) strong anion exchange solid phase extraction to separate CrVI from other chromium species and potential interferents; (3) acidification of the eluate containing the CrVI ions; (4) complexation of CrVI with a complexing agent to form a soluble, colored CrVI-complex; and (5) spectrophotometric determination of the colored CrVI-complex.
Preferably, the ultrasonication step is carried out in the presence of a slightly basic ammonium buffer and the complexing agent is 1,5-diphenylcarbazide.

Description

METHOD FOR THE DETERMINATION OF HEXAVALElI'T
CHROMTUM USL~TG ULTRAS011'ICATION AND
STROr'G AI\'IOl1' EXCHANGE SOLID PHASE EXTRACTIOl~
Field of the Invention S This invention relates to a method for the determination of hexavalent chromium (Cr"). More specifically, the present invention relates to a simple, fast, sensitive, and economical method for the determination of Cr'~ which is especially adapted for environmental and work place samples (including solid and air samples).
The present method can be used in both laboratory and field analysis.
Backsround of the Invention Chromium exists primarily in two valence states, trivalent (Crm) and hexavalent (Cr"). 'The trivalent state is relatively non-toxic, and is an essential nutrient in the human diet. On the other hand, Cr''' has been shown to be a human respiratory carcinogen in epidemiological studies of workplace exposures, and has been classified 1 S by the L'.S. Environmental Protection Agency (EPA) as a Group A inhalation carcinogen. Hence. analv~tical methods are desired which can be used to easily speciate chromium so that human exposures to Cr" can be monitored and, thus.
better controlled.
Workplace exposure to Cr'~ has been associated with a number of industrial sources, such as metal plating, spray painting, welding, tanning, and abrasive blasting operations. Environmental sources of Cr" include, for example, deteriorated or disturbed chromate-containing paint, combustion sources such as automobiles and incinerators. and fugitive dusts from contaminated soils. Because of the desire to accurately measure Cr''' at low levels, the development of analytical methods for the determination of Cr" has been a subject of significant interest in occupational and environmental health.

Chromium has been detected using atomic absorption spectrometry (Mehra et al., Talanta, 1989, 36(9), 889; Fong et al., Spectrosc. Lett., 1991, 24, 931), atomic absorption spectrometry (Jawis et al., Analyst, 1987, 122, 19; Arar et al., Environ.
Sci. Technol., 1992, 29, 1944), atomic emission spectrometry (Boumans, Line Coincidence Tables for Inductively Coupled Plasma Atomic Emission Spectrometry, Oxford University Press, Oxford, 2nd ed., 1984;. Ciglio et al., Anal. Chim.
Acta, 1991, 254, 109; Roychowdhury et al., Anal. Chem., 1990, 62, 484), X-ray fluorescence (Artier et al., Analyst, 1988, I 13, 779), charged-particle X-ray emission spectrometry and neutron activation analysis. National Institute for Occupational Safety and Health (N10SH) Methods 7024 and 7300 (IVIOSH Manual of Analytical Methods, Eller &
Cassinelli (gds.), National Institute for Occupational Safety and Health, Cincinnati, Ohio, 4'~ ed, 1994) use atomic absorption spectrometry and atomic absorption spectrometry, respectively, for the determination of chromium in workplace air samples. These methods, however, generally determine only total. Moreover, these methods generally involve expensive and complex instrumentation and are not, therefore, generally suitable for monitoring directly in the field.
Spectrophotometric and colorirrietric methods have been developed for the determination of Cr'~'. See. for example, Alvarez et al., ?alanta, 1989, 36(9), 919;
Haukka, analyst, 1991, 116, 1055; Abel et al., Am. Ind. Hyg. Assoc. J., 1974, 35, 229.
~- 20 The most~prevalent colorimetric method uses the selective reaction of Cr''' with 1,5-diphenylcarbzide (DPC) under acidic conditions to yield a red-violet Cr'''-diphenylcarbazone complex. A variation of this colorimetric method is used in NIOSH
method 7600 (1\T10SH Manual of Analytical Methods, Eller & Cassinelli (gds.), l~'ational Institute for Occupational Safety and Health, Cincinnati, Ohio, 4'"
ed, 1994) where alkaline extraction is used to help stabilize the Cr''' species.
Stripping voltammetry (Vfang et al., Analyst, 1992, 117, 1913; Elleouet et al., Anal.
Chim. Acta, 1992, 257, 301 ) and ion chromatographic assays (Powell et al., Anal. Chem., 1995, 67, 2474: Vercoutere et al., Mikrochim. Acta., 1996, I23, I09; Molina et al., Am. Ind.
Hyg. Associ. J., 1987, 48, 830; ASTM D 5281-92, "Standard Test Method for Collection and Anal~~sis of Hexavalent Chromium," in Annual Book of ASTM

-2-Standards, American Society for Testing and Materials, vol. 11.01, Philadelphia. PA, 1992; U.S. Environmental Agency, Method 218.6. Determination ofDissolved Hexavalent Chromium in Drinking Water, Groundwater and industrial Waste Vfater Effects by Ion Chromatography, EPA Office of Research and Development, Cincinnati, OH, 1990; U.S. Environmental Agency, Method 306UA, "Alkaline Digestion for Hexavalent Chromium" in Test Methods for Evaluating Solid Wastes, EPA, Washington, DC, 1995) have also been used to determine Cr"' in various samples. Many of these techniques are limited to laboratory-based analysis and cannot, therefore, be used in field monitoring and/or real-time evaluations.
Over the past decade, solid phase extraction (SPE) has been established in the analytical chemistry laboratory and has become increasingly popular. The use of SPE
for the separation and preconcentration of trace polar or non-polar target anaiytes has been widely investigated, and the advantages of such a technique over a conventional liquid-liquid extraction, coprecipitation, electrochemical deposition and evaporation have been well documented. See, for example, Masque et al:, Analyst, 1997, 132, 425-428: Corcla et al., Environ. Sci. Technol., 1994, 28, 850-858; Shahteri et al., J.
Chromatogr., 1995, 697, 131-136. Some ofthe advantages of SPE over classical analytical methods include: (l) efficiency and simplicity; (2) solvent minimization and enhanced safety with respect to hazardous samples; (3) high preconcentration factors;
(4) good recoveries; (5) flexibility; and (6) low cost.
Both off line and on-line SPE methodologies have been employed for the preseparation and preconcentration of a variety of analytes. Off line SPE
methodologies involve the use of packing materials that may contain functional groups of different polarity such as C8 or C" bonded silica phases (Falco et al., Analyst, I 997, 122, 673-677). 1~'ith on-line SPE, followed by high pressure liquid chromatography, a critical parameter is the selection of an adequate precolumn in order to avoid band broadening of the first eluded peaks, and to allow for the percolation of large sample volumes (Kiss et al., J. Chromatogr., 1996, 725, 261-272). Numerous solid-phase extractants, such as pure or modified silica, alumina. magnesia, activated carbon,

-3-polyurethane, and cellulose and its derivatives, have been used in SPD
techniques.
Consequently. solid phase extraction has largely replaced classical Liquid-liquid extraction in the analytical laboratory.
More recently, innovative new cartridges for SPE, such as reversed-phase and ion-exchange of target analytes in a single resin, are being developed and many are commercially available. These resins cartridges allow for sorption of the analyte of interest while removing non-sorbed interferents, with fast, quantitative adsorption and high elution capacities. These cartridges can improve the overall specificity and sensiti~7tS~ of trace analysis. Furthermore, the use of commercially available, low cost vacuum manifolds for SPE allows for up to, and even greater than, 24 samples to be processed simultaneous)}~. Complete automation of procedures based on SPE are also available v~~ith commercial instrumentation. Despite these advantages. there have been relatively feva~ applications of SPE to inorganic materials, including heavy metals.
Ultrasonic extraction {UE) for the purpose of dissolving target heavy metal 1 ~ anal~~tes in environmental samples is also a technique that has not been used extensively. although it of~'ers great promise {Lugue de Castro et al., Trends Anal.
Chem.. 1997. 16. 16-24). LrE has been demonstrated to perform well for the quantitative dissolution of several heavy metals in a variety of environmental matrices (Narper et al.. Anal. Chem., 1983, 55, 1553-1557; Sanchez et al., Analusis, 1994. 22.
222-225: Ashley. Electroanalysis, 1995, 7, 1189-1192z), including hexavalent chromium (James et al., Environ. Sci. Technol., 1995, 29, 2377-2381).
Nonetheless. there remains a need for a simple, reliable, fast, inexpensive.
and field-based method for the detection of Cr'' in environmental and workplace samples.
This invention. combining the use of ultrasonic extraction and strong anion exchange 2> solid phase extraction, provides such a method. This method provides a novel and effective approach for the on-site determination of Cr" in environmental and workplace samples.

-4-Summary of the Invention 7"his invention relates to a method for the determination of hexavalent chromium (Cr"). Based on the chemical properties of chromium species in aqueous solutions, a simple, fast, sensitive. and economical field method has been developed and evaluated for the determination of hexavalent chromium (Cr''') in environmental and workplace air samples. By means of ultrasonic extraction in combination with a strong anion exchange solid phase extraction (SAE-SPE) technique, the filtration, preconcentration, and isolation of Cr" in the presence of other chromium species and interferents was achieved. ?'he method generally involves: (1) ultrasonication in basic buffer solution to extract Cr" from environmental matrices; (2) strong anion exchange solid phase extraction to separate Cr" from other chromium species and potential interferents; (3) acidification of the eluate containing the Cr" ions: (4) complexation of Cr" with a complexin~ agent to form a soluble, colored Cr"-complex: and (5}
spectrophotometric determination of the colored Cr"-complex. Preferably. the 1 ~ ultrasonication step is carried out in the presence of a slightly basic ammonium buffer and the complexing agent is I,5-diphenylcarbazide. This present method can effect the extraction of both soluble (K.CrO,) and insoluble (KzCrO,) forms of Cr"
without inducing Crm (Cr:03) oxidation or Cr" reduction. ?he method allows for the dissolution and purification of Cr''' from environmental and workplace air sample ?0 ... mat.rices for up to 24 samples (or even higher numbers) simultaneously in less than about 20 minutes (excluding the ultrasonic extraction time). the present method is simple, fast, quantitative, and sufficiently sensitive for the determination of occupational exposures of Cr". The method is especially applicable for on-site monitoring of Cr" in em~ironmental and industrial hygiene samples, including both 2~ solid samples {e.g., soil. paint chips, dust, solid residues, and the like) and air samples.
One objective of the present invention is to provide a method for the detection of Cr" in a sample, said method comprising:

-5-

6 PGTNS99/04200 ( 1 ) ultrasonic extraction of Cr" from the sample utilizing a first buffer solution (i. e.. the ultrasonic buffer) having a slightly basic pH, whereby the pN of the first buffer solution is such that neither significant Crm oxidation nor Cr"
reduction occurs;
(2) separation of the Cr" in the ultrasonic extractant from step ( 1 ) from any Cri° or other interferents that might be present in the sample by passage of the ultrasonic ea~tractant through a strong anion exchange solid phase extraction media;
(3) elution of the Cr'~' from the media with a second buffer solution (i.e., the elution buffer) having a slightly basic pH;
(4) acidification of the eluate containing the Cr''; and (5) addition of a complexing agent to the acidified eluate to form a colored Cr"-complex if Cr" is present in the sample. The ultrasonication step employed to liberate Cr'~' from the sample matrix is preferably carried out using a slightly basic ammonium buffer and the complexing agent is preferably 1,5-diphenylcarbazide.
Preferably. the amount of Cr" present in the sample is determined using any l 5 appropriate technique. A9ore preferably, the amount of Cr" present in the sample is determined using a simple and direct spectrophotometric procedure which can be used in the field or on-site.
Another objective of the present invention is to provide a method for the quantitative detection of Cr'~' in a sample suspected of containing Cr", said method comprising:
( 1 ) ultrasonic extraction of Cr" from the sample utilizing a first ammonium buffer solution (i.e., the ultrasonic buffer) having a slightly basic pH, whereby the pH
of the ammonium buffer solution is such that neither significant Crm oxidation nor Cr"
reduction occurs:
(2) separation ofthe Cr" in the ultrasonic extractant from step (1) from any Cra' or other interferents that might be present in the sample by passage of the ultrasonic extractant through a strong anion exchange solid phase extraction media;
(3) elution ofthe Cr''' from the media with a second ammonium buffer solution (i.e.. the eultion buffer);
s0 (4) acidification of the eluate containing Cr'~';

(5) addition of 1,5-diphenvlcarbazide to the acidified eluate to form a colored Cr"-1.5-diphenylcarbazone complex if Cr" is present in the sample; and (6) subjecting the Cr"-1,5-diphenylcarbazone complex, ifpresent, from step (5) to a spectrophotometric analysis in order to determine the amount of Cr'~' present in the sample.
?here and other objectives and advantages of the present invention will be apparem to those of ordinary skill in the art upon consideration of the present specif canon.
Brief Description of the Drawings 1 U Figure 1 is a flowchart illustrating the general procedures utilized in the present method.
Figure ? is a flowchart illustr ating one preferred embodiment of t he present invention.
Figure 3 illustrates the breakthrough of Cr" using a strong anion exchange solid phase extraction column. Curve 1 uses an elution solution of 0.02 M
ammonia sulfate and fl.02 M ammonia hydroxide buffer; Curve 2 uses an elution solution of 0.05 1~9 ammonia sulfate and 0.05 M ammonia hydroxide buffer; Curve 3 uses an elution solution of 0.5 M ammonia sulfate and 0.5 M ammonia hydroxide buffer; Curve 4 uses an elution solution of l .0 M ammonia sulfate and 1.0 M ammonia hydroxide buffer.
Figure 4 illustrates the elution of varying concentration of Cr" using a strong anion exchange solid phase extraction column with varying. Curve 1 uses an elution solution of 0.5 M ammonia sulfate and 0.5 M ammonia hydroxide buffer; Curve ?
uses an elution solution of 1.0 h~s ammonia sulfate and 1.0 M ammonia hydroxide buffer:
Cuwe ~ uses an elution solution of 2.0 M ammonia sulfate and '.0 M ammonia 2~ hydroxide buffer.

-7-Description of the Preferred Embodiments This invention provides a simple. fast. sensitive, and economical field method for the determination of hexavalent chromium (Cr"), especially in environmental samples and workplace air samples. The present method combines ultrasonic extraction and a strong anion exchange solid phase extraction (SAE-SPE) technique to allov~~ the filtration, preconcentration, and isolation of Cry' in the presence of other chromium species and interferents. The present method is generally illustrated in Figure 1. In the first step. ultrasonication 10 is used to extract Cr" in the sample from its environmental matrix. After ultrasonic extraction. a strong anion exchange solid 1 C~ phase extraction (SAE-SPE) step 12. preferably using a column or cartridge system. is used to separate Cr" from other chromium species and potential interferents.
The Cr"
species retained on the column or cartridge containing the solid absorbing system to allo' separation from Cr'n species and other potential interferents in the sample. The Cr°' and other potential interferents pass through the column to ef~'ect the separation.
1 ~ The Cr" species are then eluted from the column or cartridge and collected. The eluant containing the Cr'~' species is then acidified in step 14. The acidified eluant is then treated with a complexing agem in step 16 to form a colored Cr"-complex which can be detected in step 1 s using any appropriate means (e.g., visual, spectroscopic, or similar methods).
20 An especially preferred embodiment of the present invention is illustrated in Figure 2 This preferred embodiment involves a first ultrasonication step 20 using a slightly basic ammonium buffer solution to extract Cr" from the environmental matrices at a p1-1 to avoid significant Ctl° oxidation and/or Cr'z reduction. A strong anion exchange solid phase extraction (SAE-SPE) step 22 is then used to separate Cr'~' '_'~ from other chromium species and potential interferents. Step 22 is preferably carried out using a column or cartridge containing pre-packed strong anion exchange material.
Cr" is then removed from the column or cartridge preferably using. for example. a slightly basic ammonium solution. The collected eluant containing Cr''' is then _g_ acidified in step 24. An effective amount of 1.5-diphenylcarbazide is added to the eluant containing Cr" in step 26 to form a soluble. colored Crv'-1,5-diphenylcarbazone complex. In the last step 28, the amount of Cr" is determined using a suitable spectrophotometric technique.
The ultrasonication step employed to liberate Cr" from the sample matrix should be carried out using a slightly basic aqueous buffer solution so as to reduce the levels of Crm oxidation and Cr" reduction to low (i.e., insignificant) levels.
Generally, the pH of buffered solution used in the ultrasonic extraction step is in the range of about 7.2 to 9.0, preferably in the range of about 7.5 to 8.5, and most preferably about 8Ø Preferably the ultrasonic solution is a buffered aqeuous ammonium solution containing between about 0.02 A9 to 0.2 M (1VH,),SO, and about 0.02 M to 0.2 M
NH,OH. even more preferably about 0.025 M to 0.1 M {NH4),SO, and about 0.025 M
to 0.1 M NH,OH, and most preferably about 0.05 M (NH,)2SOa and about 0.05 M
1'TI-i40H at a p' T of about 8Ø Other alkaline buffers (e.g., tris(hydroxymerhvl)aminomethane hydrochloride (Tris-HCl) where ammonium or ammonium hydroxide is used to obtain the desired basic pH; ammonium carbonate:
generall~~ basic buffers containing NH,- cations) can also be used. The ultrasonic extraction step can be carried out using any conventional ultrasonic bath.
LTltrasonification for about 15 to 60 minutes at about room temperature or slightly elevated temperatures should be sufficient to release the Cr'~' contained in the sample.
Preferably, the ultrasonification is carried out a temperatures less than about 40°C in order to minimise oxidation and reduction reactions. Routine experimentation can easily be carried out to determine the optimum uitrasonification conditions for any particular sample. After the ultrasonication step, the sample can be filtered if desired to remove solid material before application to the strong anion exchange resin.
Once the Cr" species has been liberated by ultrasonification, the sample is treated using a strong anion exchange resin to separate the Cr'' species from other chromium species as well as other potential interferents. The Cr" which is retained on the strong anion exch4nge resin can be eluted using a slightly basic aqueous buffer _9_ WO 99/44056 PCT/US99l04200 system. Suitable strong anion exchange resins include, for example, styrene-divinylbenzene polvrner resins to which tertiary ammonium groups have been hound (e.g.. Dowex 1-X8 from Fluka Chemical. Ronkonkoma, NY) and quaternary amine bonded silica with Cl' as the counter ion (Supelco. Inc., Bellefontaine, PA).
Other strong anion exchange resins can be used so long as they allow separation of Cr'~ from Crm and other potential interferents. Generally, cartridges pre-packaged with the strong anion exchange resins are much easier to use and are, therefore, preferred.
Strong anion exchange resins with a capacity of about 0.1 to about 2.0 meq/g are generally preferred. The strong anion exchange resins are conditioned or activated according to known procedures; such procedures are normally supplied by the resin manufacturer.
The general procedure for the preferred SPE-SAE procedure will now be detailed using a quaternary amine bonded silica resin (Cl- counter ion) as the strong anion exchange media. . suitable solid-phase extractor (from, for example.
Supelco, Inc., Bellefontaine, PA) can be attached to an appropriate small vacuum pump via a metering valve in order to assist passage of the sample and other reagents through the resin. A cartridge (3 ml) containing about 500 mg quaternary amine bonded silica sorbent with Cl' as the counter ion (capacity about 0.2 meg/g) is placed in the solid-phase extractor and then conditioned with about 3 m1 of deionized water to activate the functional groups in order to allow the Cr" to be absorbed on the resin.
The sample (generally about I to 5 ml) obtained from the sonification extraction step is then loaded on the cartridge and passed through the resin at a flow rate of about 1 ml!min to about 2 ml/min. The Cr'~ remains on the resin. After washing the cartridge with deionized water (generally about I to 5 ml), the Cr" is removed from the cartridge with a slightly basic buffer solution (generallyabout 4 to 10 ml in 1 to 3 portions) and the elutant containing the Cr'? is collected. Washing the column w.~ith water prior to removal of the Cr" helps to remove potentially interfering materials. Of course. as one of ordinary skill in the art will realize, larger or smaller cartridges or columns will generally required larger or smaller amounts. respectively, of the relevant s0 reagents.

The buffer system used to elute the Cr" from the strong anion exchange resin may be the same or different from that used in the ultrasonification step. It should, however, be slightly basic to avoid Cr" reduction. It is generally preferred that a buffered aqueous ammonium solution containing between about 0.25 M to 1.0 M
(NH,)=SO, and about 0.25 M to I .0 M I~TH40H is used as the eluting buffer.
More preferably, the eluting buffer solution contains about 0.5 M (NH,)~SO, and about 0.5 M NH,OH at a pH of about 8Ø Generally, the eluting buffer system is more concentrated (preferably by a factor of about 10) than the ultrasonic buffer system.
Other alkaline buffers (e.g., tris(hydroxymethyl)aminomethane hydrochloride (?ris-HCl) where ammonium or ammonium hydroxide is used to obtain the desired basic pH: ammonium carbonate; generally basic buffers containing NH,' canons) can also be used.
After elution from the SAE column or cartridge, the Cr"-containing eluant is acidif ed using suitable acids (e.g., ~Ifuric acid, hydrochloric acid, acetic acid, and the l 5 like). Generally the pH is not critical so long as the eluant is acidic, After acidification, the complexing agent is added to form a detectable Cr"-complex.
The complexing agent is added in excess in order to maximize the~amount of Cr"-complex formed. In other words, the amount of complexing agent should be suffcient to complex with essentially all of the Cr" present in the sample. Examples of suitable complexine agents include 1,5-diphenylcarbazide, 2-(5-bromo-2-pyridylazo-5-(diethylamino)phenol. L-penicillamine, 2-mercaptonicotinic acid, and the like.
1,5-Diphenylcarbazide is the preferred complexing agent. The Cr"-I,5-dipenylcarbazone complex is red-violet with an absorbance maxima at about 520-540 nm. Generally color formation occurs within a few seconds and is stable for several hours.
Nonetheless, it is generally preferred that the detection step be undertaken shortly after complex formation. The dynanuc range of the chromium-diphenylcarbazone complex was generally linear from about 10 pg/1 to about 5 mg/1 (RZ = 0.99997) using spectrophotometric determination. Selectivity was also excellent since typical interferences. including Cr'n , Fem. and CuD, are essentially eliminated in the SAE
procedure.

WO 99/44056 Pt:T/US99/04200 Quantitative or qualitative detection of the resulting Cr'''-complex can be by any suitable means. For example. the development of the colored Cr"-complex itself visually indicates the presence of Cr" in the sample. Preferably W/~'IS-based spectrophotometric detection methods are preferred for quantitative colorimetric measurement. A standard cataloging spectrophotometer, especially one adapted for field operation, is generally preferred so as to provide a portable, field-adapted detection method. For detection of Cr" using the 1,5-diphenylcarbazide complexing agent, a spectrophotometer operating at about 540 nm is preferred; this wavelength provides maximum sensitivity and generally eliminates interference of excess (i.e., l0 uncomplexed) 1.5-diphenylcarbazide complexing reagent.
The present method may be either manual, semi-automated. or fully automated.
Manual or semi-automated analysis and detection techniques might be used, for example, for screening or spot-checking a workplace environment to determine if Cr"
exposure is likely and if further, more extensi~ ~, sampling is necessary.
Generally.
15 automated techniques wherein multiple samples can be evaluated at the same time are preferred. For example. a flov~J injection analysis system as described in Wang et al.
(Analyst, 1997, 12, 1307-13l 2, which is hereby incorporated by reference) can be employed. Such a system. employing a pump and an autosampler operating under low pressure and computer control can be used to automate the precise r»anipulation of 20 microliter amounts of samples and deliver the products to a flow-through colormetric detector for the detection of Cr". In addition, commercially available, low cost vacuum manifolds for SPE can allow multiple samples to be run; generally, 24 samples (or more with appropriate modifications) at a time can easily be evaluated.
Commercial instrumentation is also available by which the SPE process can be 25 automated. Thus, the present method can provide a low cost, simple, fast, quantitative, and sensitive method for the determination of occupational exposure of Cr". This method is ideally suited for on-site monitoring of Cr''' in environmental arid industrial hygiene applications.

Examples The following examples are provided to illustrate the invention and not to limit the invention. All references cited in the present specification are hereby incorporated by reference.
Instrumentation and Reagents. Ultrasonic extraction was performed using a Sonicor 115V, 60 Hz laboratoy sonicator (Sonicor Instruments, Farningdale, NY, USA). The solid-phase extractor was obtained from Supelco, Inc.
(Bellefontaine, PA.
USA), and was attached to a small vacuum pump via a pressure metering valve.
The strong anion exchange cartridge used in the solid phase extraction contained 500 mg quaternan~ amine bonded silica sorbent with Cf as counter ion for strong anion exchange (capacity 0.2 meg/g): the tube size was 3 ml. These pre-packaged cartridges were obtained from Supelco, Inc., Bellefontaine, PA. A portable cataloging spectrophotometer (HACH DR'2010, HACH Company '~oveland, CO) was used for spectrophotometric measurement.
Hexavalent and trivalent chromium standards, ammonium sulfate, ammonium hydroxide. 1,5-diphenvlcarbazide (DPC). chromium oxide (Cr~03), potassium chromate (K:CrO,), hydrochloric acid, sulfuric acid, and nitric acid were all reagent grade from Aldrich (Milwaukee, V'1). T'ris(hydroxymethyl)aminomethane hydrochloride (Tris-HCI)) was from Sigma, Inc. (St. Louis, MO). Lead chromate PbCrOd) was from Fisher Scientific (Elizabeth, NJ). Chromium-containing reference materials v~~ere used as supplied: ( 1 ) paint chips -- US EPA Certified Reference Material (CRM) Ol3-050, Laramie, VVY; (2) coal fly ash -- National Institute of Standards and Technology (NIST) Standard Reference Material (SRM) 1633a, Gaithersburg, MD; and (3) welding dust loaded on glass fiber filters --Institute for Reference AJaterials and Measurements (IRMJ1~I) CRM 545) from the European Commission (IR~T1T. Geel, Belgium). For air samples, preloaded filter cassettes containing mixed cellulose ester membrane filters (0.8 lr pore size, .37 mm diameter) were obtained from SKC Inc. (Eighty Four, PA).
-IS-Solid-Phase Extraction Procedures. Solid-phase extraction (SPE) was performed with the aid of an extractor and a strong anion exchange (SAE) cartridge.
The SAE cartridge contained a silica sorbeni to which a quaternary amine was bound;
chloride ion functioned as the counter ion. Cartridges were conditioned with 3 ml of deionized water. which activated the functional groups on the sorbent, allowing for binding of Cr'~I onto the SAE sorbent. Subsequently, a 3 ml aliquot of sample solution was loaded on the SAE cartridge. After sample loading, the cartridge was rinsed with 3 ml of deionized water to remove potential interferents. Then, elution of the Cr"
concentrated on the SAE cartridge was performed with 9 ml of 0.5 M ammonium sulfate buffer solution in three 3 ml fractions.
Sample Collection. Workplace air samples were collected from aircraft painting operations at LT.S. Air Force bases using 0.8 micron, 37-mm cellulose ester membrane filters. Samples were obtained from different work practices including priminL. sanding. alodining, cutting, and grinding. The samples w~ -e transported to the laboraton~ immediately after collection, and stored in a refrigerator at 4°C until prepared for analysis. Environmental samples were collected using standard techniques.
General Procedure for Em~ironmental and Workplace Air Samples. Samples were placed into Z 5 ml plastic centrifuge tubes. Sample preparation consisted of ?0 adding 10 ml of 0.05 M (NH,)SO, and 0.05 M NH,OH (pH 8) buffer solution to the sample followed by sonication in an ultrasonic bath for 30 minutes at ambient temperature (<40 ° C). After ultrasonication, a 3 ml aliquot of the supernatant was loaded onto a strong anion exchange cartridge. The Cr'~ was eluted with 9 ml 0.5 M
(1v'H,)SO, and 0.1 M NH,OH (pH 8) buffer solution in three 3 ml fractions at a flow rate of 2 mllmin. After isolation and purification, the eluate was acidif ed with 100 pl 37°.-o HCl solution. This was followed by mixing with 2 ml of20 mM 1,5-diphem~lcarbazide complexing reagent. The reaction of 1,5-diphenylcarbazide va~ith Cr" is completed in a few seconds and the color of the complex can be stable for at least 8 hours. If analysis is not to be completed shortly after complex formation, it is preferred that they be stored at refrieerated temperatures.
Detection of Hexayalent Chromium. Quantification of hexavalent chromium was done by ea-ternal standard or standard addition methods with the spectrophotometer set at 540 nm. For the air samples, a standard addition calibration was used. Blank filters and quality controUquality assurance samples (standard solutions of known hexavalent chromium concentration) were analyzed at a minimum frequency of one per twenty experimental samples.
Example 1 -- Absorption Capacity Studies. Absorption capacities were l 0 determined using spiked Cr''' solutions produced by dissolving KZCrO, in 0.02 M, 0.05 M, and 0.5 M ammonium sulfate and ammonium hydroxide buffer solutions (pH 8).
Four different Cr" spiked solutions (1.0 mM, 2.0 mM, 4.0 mM, and 8.0 mM) were prepared and loaded onto the cartridge. eluted, and analyzed in triplicate to a ~ablish the reproducibility of the procedure. Breakthrough of the anaiyte was determined by analysis of the solution that passed through the SAE cartridge after loading of sample aliquots.
The results are showm in Figure 3 which shows that the initial breakthrough that was observed at various Cr''' loading volumes with the flow rate controlled at 2 ml/min. Similar results (not shown) were obtained with matrix spikes of cellulose ester filters. The adsorption capacities of SAE cartridges changed with increasing concentration of the ammonium sulfate and ammonium hydroxide buffer in the sample solutions (Figure 3). The adsorption capacity of SAE cartridges for Cr''' decreased more than threefold when the concentration of ammonium sulfate and ammonium hydroxide buffer solution was changed from 0.02 M (Figure 3, Curve 1 ) to 1.0 M
(Figure 3, Curare 4) at the same controlled flow rate of 2 mUmin. The adsorption capacities of SAE cartridges were also related to sample loading flow rates.
At a high flow rate of loading (e.g., 4-5 ml/min). the breakthrough of the Cr''' was more evident than was observed at a lower loading flow rate (e.g., 1 ml/min) under the same other - IS -WO 99/4405b PCT/US99/04200 experimental parameters. The percentage breakthrough increased with increased loading speed, and an optimum flow rate of about 2 ml/min was arrived at by trial and error. Generally. the throughput flow rate is an important function of SPE.
Loading flow rates are often more critical to optimizing recoveries than are the conditioning and rinse flow rates. In the conditioning step, there is nothing bound to the cartridge, and the flow rate can sometimes be increased without a loss of recovery. Flow rates may also be increased in the rinse step depending upon the banding mechanism and the sorbent/adsorbate chemistry. These trials (Figure 3) have demonstrated that reducing the concentrations of ammonium sulfate and ammonium hydroxide buffer in sample solution can improve the adsorption capacity and minimize cartridge breakthrough.
V1'hen air samples containing chromium were tested to study SAE cartridge breakthrough, they were treated in an identical manner as spiked Cr" solutions in order to evaluate the effects of ammonium sulfate and ammonium hydroxide buffer solution (pH 8) used in the extraction procedure. In these trials, the samples were treated with ultrasonication for 30 min at ambient temperature (<40 °C
bath temperature) in ammonium sulfate buffer solution. The results demonstrated no significant breakthrough of Cr'~' when. an ammonium sulfate and ammonium hydroxide buffer solution (< 0.05 M) was used to extract Cr" from samples via sonication.
Example 2 - Elution Studies. Ammonium sulfate and ammonium hydroxide buffer was used as the elution buffer solution. 'To obtain optimum recoveries, spiked Cr" solutions of four levels (10.0 pl, 20.0 ul, 40.0 pl, 80.0 pl) were eluted using different number of fractions of 0.5 M ammonium sulfate and ammonium hydroxide buffer solution (pH 8). Eluting power was investigated for five levels of Gr'~
solutions (50.0 lrg, 100.0 Ng, 200.0 Irg, 400.0 pg, 600.0 ug) at various flow rates. In each 2~ experiment, only one parameter was changed at a time. When elution flow rate is considered. it should not be too fast, since the analyte of interest may not have enough time to desorb from the cartridge. I~Tor should the flow rate be too slow, or sample preparation may be too time-consuming. As those skilled in the art will understand.

the optimum flowrates can be determined experimentally for a given experimental setup.
To evaluate the effect of ion exchange due to the elution power. eluting solutions of 0.5 M, 1.0 M, or 2.0 M ammonium sulfate and ammonium hydroxide buffer solutions (pH 8) were tested by eluting spiked Cr" solutions at 5 levels (50 lrg, 100 pg, 200 pg, 400 pg, 600 pg). The results are shown in Figure 4. The Cr'~
started to initially elute at various volumes of buffer solution, corresponding to different contents of Cr''' loaded the cartridges. Increasing the concentrations of the ammonium sulfate and ammonium hydroxide in elution solution from 0.5 M (Figure 4, Curve 1) to 2.0 M (Figure 4. Curve 3) did not significantly change the Cr''' eluting time. By eluting with 0.5 M ammonium sulfate and ammonium hydroxide buffer solution, the Cr" at all 5 Levels started to elute at flow rates lower than 1 ml/min, which is lower than the generally used flow rate of 2 ml/min. Therefore, by considering the adsorption capacity of SAE cartridges (Figure 4, Curve I ), 0.5 M
ammonium sulfate and ammonium hydroxide buffer solution was determined to perform best as an elution buffer solution in these experiments with the particular experimental setup employed.
Table I shows the recoveries of Cr" obtained from spiked Cr" solutions at 4 levels (10.0 lrg. 20.0 ug 40.0 pg. 80.0 pg) using varying number of eluting fractions (each fraction consisted of 3 ml of 0.5 M (''rH,),SO, and 0. I M. NH40H (pH 8) huffer).
_ 17_ TABLE I
Recovery ik (%) of Cr"
S ~ RSD
d C - -'~' p .
e Two Three Four Five r Fractions Fractions Fractions Fractions (pg) 10.0 85.3f2.7 95.3f3.3 95.52.7 96.312.4 ~ 20.0 83. l f 3.4 94. l f 3.7 94.914.1 95.0 f 2.9 40.0 83.9 ~ 4.8 93.3 f 3.6 94.5 f 3.2 94.8 t 2.8 80.0 82.5 t 4.5 93.0 f 4.2 94.1 t 3.7 94.6 t 3.4 "RSD" in the various Tables indicates the relative standard deviation of the samples (normally carried out in triplicate).
This data show that eluting with three fractions (3 ml for each fraction) of eluting solution allows for high recoveries (93.3 to 95.3%) and that no significant improvement in recoveries could be obtained by increasing the number of eluting fractions to more than three. Since a small volume of eluate is preferred to achieve a high enrichment factor, all the Cr" concentrated on the cartridge should be eluted in as small a volume as possible. Each fraction of 3 ml ammonium sulfate buffer solution (pH 8) was tested and good results were obtained. Under these optimum conditions, recoveries from duplicate spike solutions exhibited reproducible results. It was also confirmed from these experiments that the presence of Cr'° did not significantly affect Cr'~ recovery. These results indicated that the conditions used stabilized both Crz° and Cr" species.
These trials indicated tha: increasing either ammonium sulfate concentration above 0.5 M or using more than three eluting fractions did not significantly change Cr'7 retention abilities. Therefore, an ammonium sulfate buffer of 0.5 W with fractions (3 ml for each fraction) was found to give optimal elution power of Cr" from 2~ these SAE cartridees.
_l8_ As shown in Table I, relative standard deviations for the triplicate runs were between 2.4 and 4.8%. The limit of detection (LOD), estimated as the mass of analyte which gives a signal that is 3 times o above the mean blank signal (where o is the standard deviation of the blank signal), was about I .0 ng/mI for the spectrophotometric determination. A calibration curve was obtained by using a linear plot of the peak area as a function of standard concentrations of Cr" by least squares regression analysis.
Example 3 - Ultraso is Fxtrartinn of Soluble and lncnlnhlP ~"rt~ Although the soluble fractions of Cr" are useful parameters for estimating levels of Cr" that mav_ be directh~ absorbed b~~ humans, quantifying insoluble forms of Cr"' is pertinent to occupational hazards (such as PbCr04 in chromate ore processing and painting) associated with airborne respirable dust. Therefore, an effective and reliable method for extracting both soluble and insoluble forms of Cr" without inducing Crm oxidation or Cr'~ reduction is required. Thus, it is important to evaluate ultrasonic extraction for I 5 the dissolution of both soluble Cr" (KZCr04) and insoluble Cr" (PbCrO,) with basic buffer solutions. In this portion of the study, both ammonium sulfate and ammonium hydroxide buffer (pH 8) and/or Tris-HCI buffer solutions (with adjustment to pH 8 using I~'HaOH) were used as the ultrasonic ea-traction buffer.
As noted above, a slightly basic ammonium buffer solution may help stabilization of chromium species in this system. Ammonium sulfate and ammonium hydroxide buffer solutions were used to dissolve hexavalent chromium from environmental matrices. It is expected that conditions of the hot ammonium buffer sonication procedure might oxidize CrB' to Cr" under diverse redox conditions of various matrices. Hence no heating and relatively low concentration of the ammonium sulfate and ammonium hydroxide buffer solution (pH 8) were used to quantify and define operationally soluble and insoluble forms of Cr"
To maximize dissolution of all forms of Cr" while minimizing method-induced oxidation and reduction. an extraction protocol was employed using 0.05 M

ammonium sulfate and ammonium hydroxide buffer solution with uitrasonication at temperatures lower than about 40'C. These conditions should maintain a low activity of Crm, thereby minimizing oxidation of this species to Cr'''. Lead chromate {PbCrO~, Ksp = 1.8 x 10'") was used to represent insoluble Cr''i because it contained a greater percentage of its total Cr''' in an insoluble form. In initial trials, 300~cg (w/w) of PbCrO,, K,CrO,, and Cr20j were spiked into triplicate samples of the 10 ml 0.05 M
ammonium sulfate and ammonium hydroxide buffer solution. Since this method does not employ a high temperature to dissolve insoluble forms of Cr''', it was hypothesized that it would minimize method-induced oxidation and reduction while effectively dissolving Cr'~' Despite the demonstrated efficacy ofthe ammonium sulfate solution to dissolve insoluble forms of Cr" in solution while minimizing method-induced oxidation of Crm or reduction of Cr''', a second procedure employing T'ris-HCl buffer (with ammonium hydroxide adjustment to pH 8) ultrasonication dispersion was also tested in an attempt to quantiy Cr" in spiked solutions. As T'ris-HCL buffer contains ammonia, this ion can complex with Cr'~ and therefore may help stabilization of the trivalent 'chromium species.
'Table Il below shoves the results for Cr'~' recoveries from ammonium sulfate and ?ris-HCL buffer solutions.

TABLE II
Recovery (%) of Cr" ~ RSD

Ult i rason c Buffer Solution Spiked ~KZCrO, Spiked PbCrO, (300 Ng/IU ml) (300 pg/10 ml) Ultrasonication 30 min, Temp. <40C

0.02M(IVH,)ZSO,+ 94.513.5 86.513./

0.02 M NH,OH

0.05M(NH,)ZSO,+ 94.32.4 90.52.9 0.05 M NH,OH

0.02 M Tris-HCl + 93.9 ~ 3.8 82.5 t 4.3 NH,OH (pH 8) 0.05 M Tris-HCl + 93.7 t 2.5 85.9 ~ 3.6 NH,OH (pH 8) Ultrasonication 60 min, 'Temp.
<40C

0.02M(NH,)~SO,+ 94.413.8 90.413.9 0.02 M NH,OH

O.OSM(NH,):SO,+ 95.513.7 92.514.7 0.05 M NH,OH

0.05 M Tris-HC1 + 94.9 ~ 4.9 89.5 t 5.3 NH,OH (pH 8) One hour sonication in ammonium sulfate and ammonium hydroxide buffer solution dissolved slightly greater quantities of lead chromate (92.5%) than Tris-HCl buffer (89.5%) under the same ultrasonic extraction conditions; however, these values are not statistically different (t-test, 95% C.L). Based on the incomplete dissolution of lead chromate (Ksp =I .8 x 10'"), comparisons were made between lead chromate and potassium chromate both spiked into same buffer solutions. As indicated in Table II, Cr" is more difficult to extract from lead chromate (recovery 90.5%) than with potassium chromate (95.1 %) under the same ultrasonication time and temperature conditions. Similar results were observed for recoveries of soluble Cr" spiked in Tris-HCl buffer. Close evaluation of the ultrasonication process revealed that lead chromate crystals were slowly dissolved, and this is evident in the nearly quantitative recoveries obtained from insoluble Cr". In addition, it was noticed that extension of the ultrasonication period from 30 min to 60 min can enhance the dissolution of insoluble Cr''' and increase the recoveries from 90.5% to 92.6%.
S Samples spiked with both soluble and insolube Crm and Cr" were also evaluated. Ultrasonication was for 30 minutes at a temperature less than about 40 °C.
The results are shown in Table III below.

Recovery (%) of Cr" t RSD

Ul i trason c l0 Buffer SolutionSpiked K~CrO' Spiked KZCr04 Spiked PbCrO~

(300 pg/10 ml) + Cr'm (both + Cr~03 (both at 300 at pg/10 ml) 300 NgIlO ml) 0.02 M (NH,),SO,/94.5 ~ 3.5 94.0 ~ 2.6 85.2 t 3.7 0.02 M NH,OH

0.05 M (NH,).SO,/95.3 t 2.4 95.1 t 3.9 89.2 ~ 4.1 0.05 M NH,OH

15 0.02 M Tris-HCl93.9 t 3.8 93.3 t 2.8 83.0 t 4.8 +

'VH,OH (pH

8) 0.05 M Tris-HCl94.7 ~ 2.5 94.0 ~ 3.6 95.1 t 3.7 +

l~'H,OH (pH
8) 20 Neither method-induced reduction of Cr" nor oxidation of Cri° was observed under these experimental conditions. When Cts° was present in solutions containing Cr", Cr" was essentially unchanged. Thus, the conditions used appear to stabilize both Crj°
and Cr" species.
Examote 4 - Analysis of Reference materials. Three certified reference 25 materials (CRMs) were chosen to evaluate the basic isolation and determination procedure of the present invention. One certified reference material, US EPA
CRl~9 - z~ -013-050 (paint chips) contained relatively high levels ofnotal chromium (reference value 617.6 pg/g with a 95% confidence interval of 595 to 670 ~tg/g). Another hulk standard reference material, I~TIST SRM 1633a (coal fly ash) contained a much lower level of total chromium ( I 96 ~ 6 pg/g). No standard or reference data appears to be available for the Cr" content of these CRM samples. A third reference material, IRIvfM CRM 545, contained approximately 3 mg of total welding dust with about pg of hexavalent chromium per filter sample. This Last reference material has only just recently become available and appears to be the only known CRM for particulate hexavalent chromium.
In operation, 10 ml of 0.05 M anvnonium sulfate and 0.05 M ammonium hydroxide (pN 8) buffer solution was added to about 1 g EPA CRM 013-50 paint chips or about 2 g MST SRM 1633a coal fly ash to release the hexavalent chromium by sonication. For the mMM CRM 545 sample, the filters were sonicated in the same buffer solution. Follov~~ing sonication, aliquots of extraction solution were subjected to solid phase extraction, complexation with diphenylcarbazide, and spectrophotometric detection. The analysis results showed that the hexavalent chromium content was 54.4 t 2.3 pg/g for EPA CRM 0134-50 paint chips, and 0.19 +
0.01 ug/g for :v'IST SRM 1633a coal fly ash. These values are virtually identical to those found in using a flow-injection analysis procedure (see Example 6 below and Vfang et aL, Analyst. 1997, 122, 1307-1313). . -The recovery results for hexava 1 ent chromium from 1RMM CiRM 545 are shown in Table IV.

TABLE n' Cenified Experimental Value Value for Cr"
in CRM

Sample Vt'elding Crv' Cr''' . Cr" Recovery dust {pg/mg) (ug/filter)(pg/filter)(%) (~tg/filter) . 1 2.895 39.5 114.3 112.3 98.1 2 2.953 39.5 1 ]6.6 115.2 98.8 3 3.053 39.5 120.5 119.4 99.1 4 2.994 3 9. 5 I ] 8.2 117.4 99.3 5 2.939 39.5 116.1 115.5 99.5 Average 2.967 ~ 39.5 I 17.1 115.9 99.0 ~
t ~ 0.55 1.98 2.33 The recovery of hexavalent chromium from the iRMM CRM is quantitative (99%).
E.,ampie 5 - Workplace Air Samples. This example illustrates the use of the present method to monitor Cr" exposure at various aircraft painting and maintenance operations at U. S. Air Force bases. Air filters used to collect airborne particulate (including Cr") were placed in a 15 ml plastic tube to which 10 ml of 0.05 M
(NH,)~SO, and 0.051-4 I''1-i,OH (pH 8) buffer solution was added. This was followed by ultrasonication in an ultrasonic bath for 30 minutes (<40°C). After ultrasonication, a portion (about 3 ml) of the supernatant obtained (total of about 10 ml) was loaded onto a strong anion exchange cartridge. Washing of the SAE cartridge was performed by flushing it with 3 ml deionized water. The Cr" was eluted with 9 ml of 0.5 M
(:v'H,)=SO, and 0.1 M NH,OH (pH 8) buffer solution in three fractions at about ml/min. After isolation and purification by SAE-SPE, the eluate was acidified with 100 ul 37% HCl solution, followed by reaction with 2 ml of 20 mM 1,5-phenylcarbazide complexing reagent. The reaction of 1,5-diphenylcarbazide with Cr''' is completed in a feu~ seconds.

Quantification of hexavalent chromium for the air filter samples was preformed using the standard addition method. A blank filter (non exposure) was used as a blank sample and was subjected to the same procedure as all other air samples, and analyzed with the same technique to check for any influence of baseline shift, and to ensure matrix matching. The linear dynamic range was IO pg/1 to 3.0 mg/1 with a correlation coefficient (R') of 0.9991-0.9998 for all quality assurance/quality control samples (clean filters spiked with known quantities of hexavalent chromium). The calibration equation for the external standard or standard addition was calculated by linear regression.
The results obtained with these workplace air samples are shown in Table V
below.
-ZS-Sample Cr" Content Sample Location lrg/sampleAir Volumelrg/m' 1 0.664 147.1 4.51 Alodining F-16 2 0.707 72.67 9.73 Alodining spry>' F016 swipe and water rinse) 3 1.034 126. I 8.19 Cutting/grinding steel 4 0.643 117.2 5.48 Sanding C0130 beaver tail 5 0.52 I 73.01 . 7.14 Sanding F-I6 bare metal 6 2.952 191.5 I 5.41 Sanding F-16 under wing ~.
under couch 7 4.175 192.1 21.73 Sanding F-16 to bare metal under wing 8 4.523 173.1 26.12 Sanding F- I 6 landing gear

9 2.678 72.45 36.97 Sanding C-13U door edges

10 2.224 I 59.03 37.67 Sanding F-16 air intake

11 3.641 36.04 101.02 Priming F-16 vellovc spray

12 4.341 39.11 110.99 Priming C-130 door

13 6.922 67.01 103.32 Priming F-115 1 14 - 6.567 39.53 166.12 Priming F-16 S

8.535 48.91 174.51 Priming C-130 16 34.41 136.5 252.08 Priming F-I6 17 20.84 79.01 263.76 Ping C-130 cargo door 18 6.822 25.28 269.86 Priming water base I9 14.18 39.02 363.65 Priming F-16 landing gear 20 8.011 19.86 403.37 Priming small parts & panels The Cr" contents detected reasonably match those expected in the various workplace locations. The highest contents of Cr" were detected in paint priming operations (where the primers are known to contain high levels of Cr'''). and the lowest hexavalent chromium exposures were observed in alodining and cutting operations.

Sanding cave rise to Cry'' exposures that were intermediate in hexavalent chromium content.
Example 6 - Flow Infection Anah~sis. This example illustrates the use of flow injection analysis (FIA) using UV/VIS detection of the Cr-diphenylcarbazone complex.
Except as noted, the general procedures and reagents used in the previous examples were employed here. (This procedure is described in more detail in Wang et al., Analyst, 1997, 122, 1307-1312, which is hereby incorporated by reference in its entirety.) The flow injection system consisted of a Waters 600-MS system controller pump, a Waters 717 Plus autosampler (Millipore, Milford, MA), and a Model 783 programmable ultraviolet absorbance detector set at 540 nm (Applied Biosystems, Ramsey, NJ). The flow rate of the pump was I .0 mUmin for the mobile phase.
Upon initial start up, the system was allowed to equilibrate for about 15 minutes.
A sample volume of 10 pl was used for injections.
For elution, a 10 cm x I .5 cm id anion-exchange column containing 1.0 g resin ~~as used. The strong anion-exchange resin was Dowex 1-X8 (Fluka Chemical, Ronkonkoma. Nl'), a styrene-divinylbenzene polymer to which tertiary ammonium groups have been bound. The resin capacity was 1.3 mequiv/ml; the chloride form was used. The resin was cleaned prior to use by slurrying it with 3 M HCI, allowing it to stand for 10 minutes, and then decanting offthe acid. This procedure was repeated three times. After pouring offthe last portion ofacid, the resin was slurried with 1 M
HCl and dried prior to use.
This FIA-W/VIS method was used on a variety of spiked samples, certified reference materials, and workplace samples. In general, the samples (spiked filters (0.8 u. 37 mm). 1.0 g spiked sand, 0.1 g CRMs, and 1.0 g other fly ash and paint chip materials) were treated with 0.05 M (IVH4)~SO; 0.05 M NH3 (pH 8.0) in an ultrasonic bath for 30 minutes at about 40°C. The samples were then subjected to anion exchange separation (1.0 g Dowex 1-X8). The eluate was acidified and reacted with 2 _27_ ml of 20 rr~'vI 1,5-diphenylcarbazide complexing solution. Finally, the Cr"
content was determined by flov~~ injection analysis. The following results were obtained.
TABLE ~'I
Sample Cr" Recovery (p8/8 ~RSD) (%) ~ Spiked filter - 40 Ng/filter 37.9 f 3.2 95.6 Spiked sand - 25 Itg Cr"/g 23.8 t 4.5 95.2 Spiked sand - 25 pe Cr"lg + 23.3 t 7.6 93.8 250 erg Crmlg EPA 013-050 CRM (paint chip) 54.4 f 3.4 NIA

NIST 1633a CRM (coal fly ash) 0.19 t 3.9 NIA

Power company coal fly ash 0.5313.4 NIA

Gas pipe paint chips 352.6 t 4.4 NIA

Laboraton~ door paint chips bE .w detectionNIA
i imits University building paint chipsbelo.,~ detectionNIA
limits "NIA" in the Table indicates that no standard or reference data for Cr" was available for those particular samples and that Cr" recovery cannot be determined. The detection limit was estimated at 0.11 ng Cr'''. The results for the two CRM
samples are in good agreement with those reported in Example 4 above.

Claims (19)

That which is claimed is:

1. A method for the detection of Cr VI in a sample, said method comprising:

(1) ultrasonic extraction of Cr VI from the sample utilizing a first buffer solution having a slightly basic pH, whereby the pH of the first buffer solution is such that neither significant Cr III oxidation nor Cr VI reduction occurs;

(2) separation of the Cr VI in the ultrasonic extractant from step (1) from any Cr III or other interferents that might be present in the sample by passage of the ultrasonic extractant through a strong anion exchange solid phase extraction media;

(3) elution of the Cr VI from the media with a second buffer solution having a slightly basic pH;

(4) acidification of the eluate containing the Cr VI; and (5) addition of a complexing agent to the acidified eluate to form a colored Cr VI-complex if Cr VI is present in the sample.

2. The method as defined in claim 1, wherein the first buffer solution contains (NH4)2SO4 and NH4OH and the second buffer solution contains (NH4)2SO4 and NH4OH.

3. The method as defined in claim 2, wherein the first buffer solution contains about 0.02 M to 0.2 M (NH4)2SO4 and about 0.02 M to 0.2 M NH,OH and the second buffer solution contains 0.25 M to 1.0 M (NH4)2SO4 and about 0.25 M to 1.0 M
NH4OH.

4. The method as defined in claim 2, wherein the first buffer solution contains about 0.025 M to 0.1 M (NH4)2SO4 and about 0.025 M to 0.1 M NH4OH and the second buffer solution contains 0.25 M to 1.0 M (NH4)2SO4 and about 0.25 M to 1.0 M NH4OH.

5. The method as defined in claim 2, wherein the first buffer solution contains about 0.05 M (NH4)2SO4 and about 0.05 M NH4OH and the second buffer solution contains about 0.5 M (NH4)2SO4 and about 0.5 M NH4OH.

6. The method as defined in claim 1, wherein the strong anion exchange solid phase extraction media is a quaternary amine bonded silica with C1~ as the counter ion.

7. The method as defined in claim 4, wherein the strong anion exchange solid phase extraction media is a quaternary amine bonded silica with C1~ as the counter ion.

8. The method as defined in claim 1, wherein the complexing agent is 1, 5-diphenylcarbazide.

9. The method as defined in claim 7, wherein the complexing agent is 1, 5-diphenylcarbazide.

10. The method as defined in claim 1, further comprising subjecting the colored Cr VI-complex, if present, from step (5) to a spectrophotometric analysis to determine the amount of Cr VI present in the sample.

11. The method as defined in claim 9, further comprising subjecting the colored Cr VI-complex, if present, from step (5) to a spectrophotometric analysis to determine the amount of Cr VI present in the sample.

12. A method for the quantitative detection of Cr VI in a sample suspected of containing Cr VI, said method comprising:

(1) ultrasonic extraction of Cr VI from the sample utilizing a first ammonium buffer solution having a slightly basic pH, whereby the pH of the ammonium buffer solution is such that neither significant Cr III oxidation nor Cr VI reduction occurs;

(2) separation of the Cr VI in the ultrasonic extractant from step (1) from any Cr III or other interferents that might be present in the sample by passage of the ultrasonic extractant through a strong anion exchange solid phase extraction media;

(3) elution of the Cr VI from the media with a second ammonium buffer solution;

(4) acidification of the eluate containing Cr VI;

(5) addition of 1,5-diphenylcarbazide to the acidified eluate to form a colored Cr VI-1,5-diphenylcarbazone complex if Cr VI is present in the samples; and (6) subjecting the Cr VI-1,5-diphenylcarbazone complex, if present, from step (5) to a spectrophotometric analysis in order to determine the amount of Cr VI
present in the sample.

13. The method as defined in claim 2, wherein the first buffer solution contains (NH4)2SO4 and NH4OH and the second buffer solution contains (NH4)2SO4 and NH4OH.

l4. The method as defined in claim 13, wherein the first buffer solution contains about 0.02 M to 0.2 M (NH4)2SO4 and about 0.02 M to 0.2 M NH4OH and the second buffer solution contains 0.25 M to 1.0 M (NH4)2SO4 and about 0.25 M
to 1.0 M NH4OH.

15. The method as defined in claim 13, wherein the first buffer solution contains about 0.025 M to 0.1 M (NH4)2SO4 and about 0.025 M to 0.1 M NH4OH and the second buffer solution contains 0.25 M to 1.0 M (NH4)2SO4 and about 0.25 M
to 1.0 M NH4OH.

16. The method as defined in claim 13, wherein the first buffer solution contains about 0.05 M (NH4)2SO4 and about 0.05 M NH4OH and the second buffer solution contains about 0.5 M (NH4)2SO4 and about 0.5 M NH4OH.

17. The method as defined in claim l2, wherein the strong anion exchange solid phase extraction media is a quaternary amine bonded silica with C1~ as the counter ion.

18. The method as defined in claim 15, wherein the strong anion exchange solid phase extraction media is a quaternary amine bonded silica with C1~ as the counter ion.

19. The method as defined in claim 16, wherein the strong anion exchange solid phase extraction media is a quaternary amine bonded silica with C1~ as the counter ion and is contained in a pre-made cartridge.