Gradients In Thin Films Technique Research Articles

Speciation and Bioavailability Measurements of Environmental Plutonium Using Diffusion in Thin Films.

The biological uptake of plutonium (Pu) in aquatic ecosystems is of particular concern since it is an alpha-particle emitter with long half-life which can potentially contribute to the exposure of biota and humans. The diffusive gradients in thin films technique is introduced here for in-situ measurements of Pu bioavailability and speciation. A diffusion cell constructed for laboratory experiments with Pu and the newly developed protocol make it possible to simulate the environmental behavior of Pu in model solutions of various chemical compositions. Adjustment of the oxidation states to Pu(IV) and Pu(V) described in this protocol is essential in order to investigate the complex redox chemistry of plutonium in the environment. The calibration of this technique and the results obtained in the laboratory experiments enable to develop a specific DGT device for in-situ Pu measurements in freshwaters. Accelerator-based mass-spectrometry measurements of Pu accumulated by DGTs in a karst spring allowed determining the bioavailability of Pu in a mineral freshwater environment. Application of this protocol for Pu measurements using DGT devices has a large potential to improve our understanding of the speciation and the biological transfer of Pu in aquatic ecosystems.

Mercury Distribution in the Deûle River (Northern France) Measured by the Diffusive Gradients in Thin Films Technique and Conventional Methods.

The distribution of mercury in surface water and in sediment from Deûle River in Northern France was studied by application of conventional sampling methods and by diffusive gradients in thin films technique (DGT). Concentration of total dissolved mercury in surface water was 20.8 ± 0.8 ng l(-1). The particulate mercury concentration was 6.2 ± 0.6 µg g(-1). The particulate mercury was accumulated in sediment (9.9 ± 2.3 mg kg(-1)), and it was transformed by methylating bacteria to methylmercury, mainly in the first 2-cm layer of the sediment. Total dissolved concentration of mercury in sediment pore water obtained by application of centrifugation extraction was 17.6 ± 4.1 ng l(-1), and it was comparable with total dissolved pore water mercury concentration measured by DGT probe containing Duolite GT-73 resin gel (18.2 ± 4.3 ng l(-1)), taking the sediment heterogeneity and different principles of the applied methods into account. By application of two DGT probes with different resin gels specific for mercury, it was found that approximately 30% of total dissolved mercury in sediment pore water was present in labile forms easy available for biota. The resolution of mercury DGT depth profiles was 0.5 cm, which allows, unlike conventional techniques, to study the connection of the geochemical cycle of mercury with geochemical cycles of iron and manganese.

A method for measurement of free cadmium species in waters using diffusive gradients in thin films technique with an ion-imprinted sorbent

A diffusive gradients in thin films (DGT) device for the analysis of free Cd(II) species, based on Cd(II) ion-imprinted sorbent (IIS) as the binding agents and commercial polyethersulfone membrane (PES) as diffusion layer, was developed (PES/IIS-DGT). DGT time-series experiments showed that the mass of free Cd(II) species accumulated by PES/IIS-DGT was linear vs. time (R2 = 0.9953) and the concentration of free Cd(II) species by PES/IIS-DGT was in good agreement with the total dissolved concentrations of free Cd(II) species in simple synthetic solutions where free ionic species dominated. PES/IIS-DGT performance was independent in the range of pH 4.5–7.5 and ionic strength range from 1.0 × 10−3 to 0.7 mol L−1. The measurement of free Cd(II) species in synthetic solution containing different concentrations of ligands by PES/IIS-DGT showed an excellent agreement with the value measured by Cd(II) ion selective electrodes (Cd-ISE), indicating that PES/IIS-DGT method is more suitable than Cd-ISE for the measurement of low concentration of free Cd(II) species due to the enrichment of IIS for the analytes.

Spatial and temporal distribution of Au and other trace elements in an estuary using the diffusive gradients in thin films technique and grab sampling

This study reports the first surface water evaluation of the temporal and spatial variability of Au in an estuary, using recently developed modifications to the diffusive gradients in thin films (DGT) and grab sampling techniques. At the two study sites in the Swan River estuary that were more marine in character, the DGT-measured concentrations of Au (26.3 and 31.3ng/L) were within the range of total concentrations measured on individual days (13.2–30.6ng/L and 11.2–37.2ng/L, respectively). In contrast, at an upstream site, Au concentrations measured by DGT were significantly lower than totals (3.9ng/L for DGT, compared with 13.2–28.8ng/L for grab sampling), likely due to either size exclusion of colloids (>70nm) by DGT or formation of a dissolved, non-DGT-labile Au species (<0.45μm). DGT-measured concentrations of other metals (Cu, Co, Cr, U, V, Mo and As) were also lower than total concentrations, although in contrast to DGT-measured Au, this phenomenon occurred at all sites. Furthermore, daily grab samples for Au, taken over the 10-day deployment (which included a rain event), showed that Au concentrations could spike substantially (from 15.1ng/L to 37.2ng/L) over intervals as short as one day. The combination of simultaneous deployment of different DGT devices and grab sampling represents a new development in efforts to understand the transport and fate of Au together with other elements in dynamic environments such as estuaries.

In situ selective determination of methylmercury in river water by diffusive gradient in thin films technique (DGT) using baker's yeast (Saccharomyces cerevisiae) immobilized in agarose gel as binding phase

Saccharomyces cerevisiae immobilized in agarose gel as binding phase and polyacrylamide as diffusive layer in the diffusive gradient in thin films technique (DGT) was used for selective determination of methylmercury (MeHg). Deployment tests showed good linearity in mass uptake up to 48 h (3276 ng). When coupling the DGT technique with Cold Vapor Atomic Fluorescence Spectrometry, the method has a limit of detection of 0.44 ng L−1 (pre concentration factor of 11 for 48 h deployment). Diffusion coefficient of 7.03 ± 0.77 × 10−6 cm2 s−1 at 23 °C in polyacrylamide gel (pH = 5.5 and ionic strength = 0.05 mol L−1 NaCl) was obtained. Influence of ionic strength (from 0.0005 mol L−1 to 0.1 mol L−1 NaCl) and pH (from 3.5 to 8.5) on MeHg uptake were evaluated. For these range, recoveries of 84–105% and 84–98% were obtained for ionic strength and pH respectively. Potential interference due to presence of Cu, Fe, Mn, Zn was also assessed showing good recoveries (70–87%). The selectivity of the proposed approach was tested by deployments in solutions containing MeHg and Hg(II). Results obtained showed recoveries of 102–115 % for MeHg, while the uptake of Hg(II) was insignificant. The proposed approach was successfully employed for in situ measurements in the Negro River (Manaus-AM, Brazil).

Dynamics of phosphorus–iron–sulfur at the sediment–water interface influenced by algae blooms decomposition

This study addresses the previously unknown effects of algae blooms on the dynamics of phosphorus (P), iron (Fe) and sulfur (S) across a lacustrine sediment-water interface (SWI). A mesocosm experiment was conducted in-situ to investigate these effects based on two recently-developed diffusive gradients in thin-films techniques (DGT). Soluble P, Fe(II), and S(-II) exhibited similar changing trends in a water column subject to the algae addition. Peak concentrations appeared on day 7 of the 16-day experiment. The lowest Eh occurred at the experiment’s midway point indicating a strong algae degradation. A maximum increase in DGT-labile S appeared on day 8 near the SWI, while the DGT-labile P and Fe exhibited persistent increases almost to the end of experiment. Significantly positive correlations of labile P were observed switching from between labile Fe and labile S in sediments, suggesting a significant change in original Fe-coupled dynamics of P under algae decomposition. Apparent fluxes were calculated based on DGT profiles where a simultaneous release of P and S occurred from degraded algae, resulting in bidirectional diffusion fluxes from sediment to overlying water. In contrast, sediment acted as a major source of labile Fe due to added depth and apparently positive fluxes.

Sediment metal bioavailability in Lake Taihu, China: evaluation of sequential extraction, DGT, and PBET techniques.

The European "Community Bureau of Reference" (BCR) sequential extraction procedure, diffusive gradient in thin-films technique (DGT), and physiologically based extraction test were applied to assess metal bioavailability in sediments of Lake Taihu (n = 13). Findings from the three methods showed that Cd was a significant problem in the western lake whereas Cu, Zn, and Ni pollution was most severe in the northern lake. Results from the sequential extraction revealed that more than 50% of the Cu and Zn were highly mobile and defined within the extractable fraction (AS1 + FM2 + OS3) in the majority of the sediments, in contrast extractable fractions of Ni and Cd were lower than 50% in most of the sampling sites. Average Cu, Zn, Ni, and Cd bioaccessibilities were <50% in the gastric phase. Zn and Cd bioaccessibility in the intestinal phase was ∼50% lower than the gastric phase while bioaccessibilities of Cu and Ni were 47-57% greater than the gastric phase. Linear regression analysis between DGT and BCR measurements indicated that the extractable fractions (AS1 + FM2 + OS3) in the reducing environment were the main source of DGT uptake, suggesting that DGT is a good in situ evaluation tool for metal bioavailability in sediments.

Determination of mercury species by the diffusive gradient in thin film technique and liquid chromatography – atomic fluorescence spectrometry after microwave extraction

A diffusive gradient in thin films technique (DGT) was combined with liquid chromatography (LC) and cold vapor atomic fluorescence spectrometry (CV-AFS) for the simultaneous quantification of four mercury species (Hg2+, CH3Hg+, C2H5Hg+, and C6H5Hg+). After diffusion through an agarose diffusive layer, the mercury species were accumulated in resin gels containing thiol-functionalized ion-exchange resins (Duolite GT73, and Ambersep GT74). A microwave-assisted extraction (MAE) in the presence of 6M HCl and 5M HCl (55°C, 15min) was used for isolation of mercury species from Ambersep and Duolite resin gels, respectively. The extraction efficiency was higher than 95.0% (RSD 3.5%). The mercury species were separated with a mobile phase containing 6.2% methanol+0.05% 2-mercaptoethanol+0.02M ammonium acetate with a stepwise increase of methanol content up to 80% in the 16th min on a Zorbax C18 reverse phase column. The LODs of DGT–MAE–LC–CV-AFS method were 38ngL−1 for CH3Hg+, 13ngL−1 for Hg2+, 34ngL−1 for C2H5Hg+ and 30ngL−1 for C6H5Hg+ for 24h DGT accumulation at 25°C.

Evaluation of the diffusive gradients in thin films technique using a mixed binding gel for measuring iron, phosphorus and arsenic in the environment.

Simultaneous measurements of dissolved iron (Fe), phosphorus (P), and arsenic (As) were made using the diffusive gradients in thin films technique equipped with a mixed binding gel impregnated with zirconium oxide and Chelex-100 (ZrO-Chelex DGT). The ZrO-Chelex binding gel exhibited rapid binding dynamics to Fe(II), P(PO4(3-)), and As(III)/As(V) in mixed solutions of the three elements. The bound Fe, P, and As could be quantitatively recovered using an established four-step elution procedure. Simultaneous measurements of the three elements with ZrO-Chelex DGT were validated through time-series experiments, and there was no influence of pH (4.1 to 7.1) and ionic strength (0.01 to 800 mM). The DGT capacities for As(III) and As(V) were 69.0 μg and 186 μg per device, respectively, which were much greater than those of the widely used ferrihydrite DGT. Applications in synthesized freshwaters and in sediments further confirmed its feasibility in simultaneous measurements in the environment. The present study offered that the ZrO-Chelex DGT will be a useful tool in in situ monitoring of Fe-P-As and assessment of their interactions in the biogeochemical processes.

Preliminary Investigation concerning Metals Bioavailability in Waters of Aries River Catchment by Using the Diffusive Gradients in Thin Films Technique

The paper presents the metals content and bioavailability in waters of Aries River catchment, Romania. Concentration of labile dissolved metal species measured by diffusive gradients in thin films technique (DGT), metals in colloidal and in particulate phases, and also general physical-chemical indicators of water were determined. Very high total metal concentrations were found in the tributaries that drain the mining areas. However, the influence of the polluted tributaries on the Aries River water quality was moderate, as a consequence of the tributaries low flow rate compared with that of the Aries River. Using the DGT technique the bioavailable metals fractions expressed as % of total dissolved metals concentrations were found to be 28–88% for Cu, 43–72% for Zn, 73–85% for Fe, and 33–70% for Mn. Depending on the used method for dissolved metals determination the classification of waters according to quality classes may differ. Excluding the colloidal metal fractions, DGT measures only truly dissolved metal concentrations. In cases with very high metal contamination the differences between total dissolved and DGT-labile concentrations are unimportant for waters classification. However, where the metals concentration is near the thresholds values the determination method is very important.

Measurement of labile arsenic speciation in water and soil using diffusive gradients in thin films (DGT) and X-ray absorption near edge spectroscopy (XANES)

Environmental context Both inorganic and organic arsenic species are toxic to the environment when labile. The Diffusive Gradients in Thin Films technique, equipped with ferrihydrite binding gel enables measurement of labile arsenic species from water and soil solutions. This study indicated that labile arsenic species are quantitatively adsorbed to the gel, and that they are stable for up to 2 weeks following deployment. Abstract Arsenic speciation was determined in the solution extracted from a ferrihydrite binding gel layer in a DGT unit (FB-DGT) deployed in water using coupled high-performance liquid chromatography and hydride generation atomic fluorescence spectrometry (HPLC-HG-AFS). However, the extent of change in arsenic speciation during the extraction process is unknown. By identifying the arsenic species in the FB-DGT gel directly, using X-ray absorption near edge spectroscopy (XANES) fitting with model arsenic compounds, we obtain a better understanding of the ability of FB-DGT to measure labile arsenic species in solution. The results presented herein confirm that FB-DGT accumulated labile inorganic and methylated arsenic species. Arsenic species bound to the FB-DGT gel were stable for up to 2 weeks following deployment. However, caution should be applied when interpreting the proportion of As species measured by HPLC-HG-AFS in solution extracted from FB-DGT because the distribution of arsenic species in extracted solutions was found to be modified by the extraction process. Some (~20%) of arsenate was converted into arsenite, and a significant amount (~25%) of dimethylarsinic acid (DMAsV) was converted into monomethylarsonic acid (MMAsV) or arsenate (AsV). Only inorganic arsenite (iAsIII) was stable during the extraction process. These findings suggested that, based on the XANES measurement, although As species were quantitatively accumulated in the FB-DGT gel, the FB-DGT technique was still unsuitable for studying As speciation. This is because changes in arsenic speciation were observed to occur during gel extraction, prior to HPLC-HG-AFS measurement, and because the XANES technique is available for routine measurements.

Measurement of dissolved reactive phosphorus in water with polyquaternary ammonium salt as a binding agent in diffusive gradients in thin-films technique.

Diffusive gradients in thin-films (DGT) sampler with a polyquaternary ammonium salt (PQAS) aqueous solution as a binding phase and a dialysis membrane as a diffusive phase (PQAS DGT) was developed for the measurement of dissolved reactive phosphorus (DRP) in water. The performance of PQAS DGT was not dependent upon pH 3-10 and ionic strength from 1 × 10(-4) to 1 mol L(-1). The effective binding capacity of PQAS DGT containing 2.0 mL of 0.050 mol L(-1) PQAS solution was estimated as 9.9 μg cm(-2). The measurement of DRP in a synthetic solution by PQAS DGT over a 48 h deployment period demonstrated high consistency with the concentration of DRP in the synthetic solution measured directly by the ammonium molybdate spectrophotometric method. Field deployments of PQAS DGT samplers allowed for accurate measurement of the DRP concentration in situ. The advantages of PQAS DGT include no requirement of the elution steps and direct concentration measurements of the binding phase.

Diffusive gradient in thin films technique for assessment of cadmium and copper bioaccessibility to radish (Raphanus sativus)

The aim of this study was to assess cadmium and copper uptake by radish (Raphanus sativus) and to test the capability of the diffusive gradient in thin films (DGT) technique to predict bioaccessibility of the metals for this plant. Radish plants were grown in pots filled with uncontaminated control and artificially contaminated soils differing in cadmium and copper contents. Metal concentrations in plants were compared with free ion metal concentrations in soil solution, and concentrations measured by DGT. Significant correlation was found between metal fluxes to plant and metal fluxes into DGT. Pearson correlation coefficient for cadmium was 0.994 and for copper 0.998. The obtained results showed that DGT offers the possibility of simple test procedure for soils and can be used as a physical surrogate for plant uptake.

Measurements of labile Cd, Cu, Ni, Pb, and Zn levels at a northeastern Brazilian coastal area under the influence of oil production with diffusive gradients in thin films technique (DGT)

In this work, the ability of the diffusive gradients in thin films technique (DGT) was evaluated for monitoring the concentrations, and estimating the availability, of metals at a northeastern Brazilian coastal area under the influence of oil production. Three sites with an average distance between 0m (EM-1), 100m (EM-2), and 1000m (EM-3) of a submarine outfall-I (Guamaré—RN, Brazil) and another site (GA-1) with an average distance of 12000m east of Outfall I, near the city of Galinhos, were studied. DGT units were deployed at the same sites in three campaigns from July, 2010 to June, 2011.Effects on the accuracy of analytical results regarding the deployment time, gel porosity, and thickness were evaluated. There was no difference between the measurements obtained with two sets of DGT devices, those assembled with open or restrictive pore gel, respectively, showing that organic metallic species are not present near the submarine outlet. After 21day deployments in a region (near Submarine Outfall I) that receives produced waters that have been treated, there was evidence of biofilm formation on DGT membranes. However, it was demonstrated that the biofilm interference with DGT measurements was negligible.Data found in this work show that total concentrations of Cd, Cu, Pb, Ni, and Zn in seawater samples collected at sites GA-1 and EM-1 in two campaigns were below 0.33, 1.67, 0.47, 0.70, 2.86ngmL−1 respectively. For the first time, labile levels of Cd, Cu, Pb, Ni, and Zn in an area under the influence of oil production were determined. DGT measurements allowed the verification of the effects of temporal variation on levels of Zn and Ni. There were no effects of spatial variations on levels of Cd, Cu, Ni, Pb, and Zn at the four studied sites, suggesting no contamination of these metals at the northeastern Brazilian coastal area investigated in this work.

Application of the diffusive gradients in thin films technique for available potassium measurement in agricultural soils: Effects of competing cations on potassium uptake by the resin gel

The utilization of Amberlite (IRP-69 ion-exchange resin, 100–500 wet mesh) as the binding phase in the diffusive gradients in thin films (DGT) technique has shown potential to improve the assessment of plant-available K in soils. The binding phase has recently been optimized by using a mixed Amberlite and ferrihydrite (MAF) gel which results in linear K uptake over extended deployment periods and in solutions with higher K concentrations. As restriction of K uptake by Ca on the Amberlite based resin gel has been previously proposed, potential competing effects of Ca2+, Mg2+ and NH4+ on K uptake by the MAF gel were investigated. These cations had no effect on K elution efficiency which was 85%. However, K uptake by the MAF gel was restricted in the presence of competing cations in solution. Consequently, the diffusion coefficient of K decreased in the presence of cations compared to previous studies but was stable at 1.12×10−5cm2s−1 at 25°C regardless of cation concentrations. Uptake of K by the DGT device was affected by the presence of excessive Ca in more than 30% of twenty typical Australian agricultural soils. However, this problem could be circumvented by using a shorter deployment time than the normal 24h. Moderate correlation of concentrations of K extracted by DGT with Colwell K (extracted by NaHCO3, R2=0.69) and NH4OAc K (R2=0.61) indicates that DGT measures a different pool of K in soils than that measured by the standard extractants used. In addition, the MAF gel has the ability to measure Ca and Mg simultaneously.

Comparison of diffusive gradients in thin film technique with traditional methods for evaluation of zinc bioavailability in soils.

The technique of diffusive gradients in thin film (DGT) has been shown to be a promising tool to assess zinc (Zn) bioavailability in soils, but there exists considerable debate on its suitability. In this study, Zn bioavailability was systematically investigated in wheat- and maize-grown soils using this technique and seven traditional methods, including soil solution concentration and six widely used single-step extraction methods (HAc, EDTA, NaAc, NH4Ac, CaCl₂, and MgCl₂). The concentrations of Zn in the shoots and roots of these two plant species increased continuously with increasing additions of Zn to the soils, accompanied by significant decreases in shoot biomass and root biomass at Zn concentrations greater than 400 mg kg(-1) for maize and 800 mg kg(-1) for wheat. Zinc uptake and accumulation was higher in maize roots than in wheat roots. Both the concentrations of bioavailable Zn measured by DGT (CDGT) and soil solutions (Csol) increased linearly with increasing additions of Zn to the soils, while no strong linear relationships were observed for the extraction methods. Higher concentrations of extractable Zn, lower values of Csol, and larger values of R (i.e., the ratio of CDGT to Csol) were observed in maize-grown soils compared with those of wheat-grown soils, while the values of C DGT between the two plants were similar. These findings demonstrate that there likely exists a stronger resupply of Zn from the soil solid phases in maize-grown soils to satisfy a higher Zn uptake and accumulation in this plant. Linear correlation analyses showed that CDGT had the highest correlation coefficients with plant Zn concentrations compared with other traditional methods, implying that the DGT technique is more sensitive and robust in reflecting Zn bioavailability in soils to plants.

Determination of lead in soybean sauces by the diffusive gradients in thin films technique

A diffusive gradients in thin films (DGT) device with sodium poly (aspartic acid) (PASP) as a novel binding agent (PASP DGT) combined with graphite furnace atomic absorption spectrometry (GFAAS) was developed for the sampling and measurement of lead in soybean sauce samples. The performance of PASP DGT was independent of pH in the range of 3–6 and salinity in the range from 4 to 14g/L (as NaCl). There was no significant difference between PASP DGT technique and hydride generation atomic fluorescence spectrometry (HG-AFS) method for the measurement of lead in soybean sauce samples. The recoveries of lead in spiked soybean sauce samples determined by PASP DGT coupled with GFAAS were 94.3–97.2% with the relative standard deviations of 2.52–3.09%. The concentrations of Pb in twelve soybean sauce samples determined by PASP DGT coupled with GFAAS were in the range of 0.09–0.71mg/L.

Effect of aging on arsenic and lead fractionation and availability in soils: Coupling sequential extractions with diffusive gradients in thin-films technique

We coupled the diffusive gradients in thin-films (DGT) technique with two sequential extraction methods to investigate the influence of aging on As and Pb fractionation and availability in three soils spiked with As (40 or 400mgkg−1), Pb (150 or 1500mgkg−1) or As+Pb (40mgkg−1 As and 150mgkg−1 Pb). During aging, As moved from the more available (non-specifically and specifically sorbed) to less available (amorphous and crystallized Fe/Al) fractions while Pb moved from the first three fractions (exchangeable, carbonate and Fe/Mn hydroxide) to organic fraction. However, even after 33-week aging, much more As and Pb were in the least available residual fraction in spiked soils than native soils (11–59% vs. 1.2–12%). Relatively, As in spiked soils was much more available than Pb with 11–14% As and 46–59% Pb in the residual fraction. Correlation analysis indicated that As in the non-specifically and specifically sorbed fractions and Pb in the exchangeable fraction were likely sources of DGT-measured labile As and Pb. The fact that As and Pb distribution and availability in spiked soils were significantly different from native soils suggests caution needs to be exercised when using spiked soils for research.

Determination of Chromium Speciation in Tap Water Using Diffusive Gradients in Thin Film Technique

Abstract A dual diffusive gradients in thin film (DGT) device method for in situ fractionation of dissolved inorganic Cr was developed by simultaneously deploying two types of DGT devices with different binding phases in tap water. The concentration of Cr(III) in the tap water determined by a DGT device with sodium poly(aspartic acid) (PASP) solution as the binding phase (PASP DGT) was 3.18 µg L−1, and the recoveries of the spiked Cr(III) were 97.9%–105.3%; the concentration of Cr(VI) in the tap water determined by a DGT device with poly(quaternary ammonium) salt (PQAS) solution as the binding phase (PQAS DGT) was 2.92 µg L−1, and the recoveries of the spiked Cr(VI) were 98.2%–107.7%. The ratios of the total Cr measured by DGT to the total Cr measured by ICP-MS were 102.9%–105.7%.

Selective sampling and measurement of Cr (VI) in water with polyquaternary ammonium salt as a binding agent in diffusive gradients in thin-films technique

A diffusive gradients in thin films (DGT) device with polyquaternary ammonium salt (PQAS) as a novel binding agent (PQAS DGT) combined with graphite furnace atomic absorption spectrometry (GFAAS) was developed for the selective sampling and measurement of Cr (VI) in water. The performance of PQAS DGT was independent of pH 3–12 and ionic strength from 1×10−3 to 1molL−1. DGT validation experiments showed that Cr (VI) was measured accurately as well as selectively by PQAS DGT, whereas Cr (III) was not determined quantitatively. Compared with diphenylcarbazide spectrophotometric method (DPC), the measurement of Cr (VI) with PQAS DGT was agreement with that of DPC method in the industrial wastewater. PQAS-DGT device had been successfully deployed in local freshwater. The concentrations of Cr (VI) determined by PQAS DGT coupled with GFAAS in Nuer River, Ling River and North Lake were 0.73±0.09μgL−1, 0.50±0.07μgL−1 and 0.61±0.07μgL−1, respectively. The results indicate that PQAS DGT device can be used for the selective sampling and measurement Cr (VI) in water and its detection limit is lower than that of DPC method.