J. F. López-Sánchez

Improvement of the BCR three step sequential extraction procedure prior to the certification of new sediment and soil reference materials

The Standards, Measurements and Testing Programme (formerly BCR) of the European Commission proposed a three-step sequential extraction procedure for sediment analysis, following extensive expert consultations and two interlaboratory studies. This scheme was recently used to certify the extractable trace element contents of a sediment reference material (CRM 601). Although this procedure offers a means to ensure the comparability of data in this field, some difficulties concerning the interlaboratory reproducibility still remain, and a new project is currently being conducted to determine the causes of poor reproducibility in the extraction scheme. The final objective of the project is the certification of new sediment and soil reference materials for their extractable contents of Cd, Cr, Cu, Ni, Pb and Zn. This paper presents the results of a small-scale interlaboratory study, which aimed to test a revised version of the extraction schemes by comparing the original and the modified protocols using the CRM 601 sample. This work offers an improvement to the BCR sequential extraction procedure through intercomparison exercises. This improved procedure will allow the obtaining of CRMs to validate analytical data in the analysis of soils and sediments, and it will also facilitate comparability of data in the European Union.

Use of a certified reference material for extractable trace metals to assess sources of uncertainty in the BCR three-stage sequential extraction procedure

Various potential sources of irreproducibility in the BCR three-stage sequential extraction procedure have been investigated using the lake sediment CRM 601. Of the variables considered, the pH of the hydroxylamine hydrochloride in Step 2 proved most important. Factors such as the type of acid used in pH adjustment, the temperature and duration of extraction, and working under nitrogen did not affect precision, although they did alter the amounts of metals extracted. Improved precision was obtained when the hydroxylamine hydrochloride concentration was increased from 0.1 to 0.5 mol l(-1) and when the speed of the centrifugation was increased from 1500 to 3000 x g. The addition of a MgCl2 wash between the steps of the extraction procedure gave rise to increased uncertainty. Although it did not adversely affect reproducibility, the use of filtration to separate solid and liquid phases was not recommended since it promoted dissolution of non-target phases. Neither ammonium hydrogen oxalate nor oxalic acid proved suitable alternatives in Step 2 owing to precipitation of insoluble lead salts, particularly in the presence of calcium

Certification of trace metal extractable contents in a sediment reference material (CRM 601) following a three-step sequential extraction procedure

Abstract Sequential extraction schemes have been developed in the past 20 years for the determination of binding forms of trace metals in sediment. The lack of uniformity of these schemes, however, did not allow the results so far to be compared worldwide nor the procedures to be validated. Indeed, the results obtained by sequential extraction are operationally defined, i.e. the ‘forms’ of metals are defined by the determination of extractable elements using a given procedure. Therefore the significance of the analytical results is related to the extraction scheme used. Another problem which hampered a good comparability of data was the lack of suitable reference materials which did not enable the quality of measurements to be controlled. Owing to this lack of comparability and quality control, the Community Bureau of Reference (BCR, now Standards, Measurements and Testing Programme) has launched a programme of which one of the aims was to harmonize sequential extraction schemes for the determination of extractable trace metals in sediment. This programme involved the comparison of existing procedures tested in two interlaboratory exercises, and it developed into a certification campaign of extractable trace element contents in a sediment reference material, following a three-step sequential extraction procedure duly tested and adopted by a group of 18 EU laboratories. This paper briefly describes the results of the interlaboratory studies and gives all details on the preparation of the sediment reference material, CRM 601, the homogeneity and stability studies and the analytical work performed for the certification of the extractable contents of some trace elements, following a standardized sequential (three-step) extraction procedure.

Evaluation of a sequential extraction procedure for the determination of extractable trace metal contents in sediments

The determination of extractable trace metals in sediments using sequential extraction procedures has been performed in many laboratories within the last ten years in order to study environmental pathways (e.g. mobility of metals, bounding states). However, the results obtained by different laboratories could hardly be compared due to lack of harmonized schemes. Owing to the need for standardization and subsequent validation of extraction schemes for sediment analysis, the Measurements and Testing Programme (formerly BCR Programme) of the European Commission has organized a project to adopt a sequential extraction procedure that could be used as a mean of comparison of data of extractable trace metals in sediments. A scheme was designed after a series of investigations on existing schemes and tested in interlaboratory studies. This paper presents the results of two round-robin exercises on extractable trace metals using this sequential extraction protocol and describes the final version of the extraction procedure amended according to the most recent improvements.

Selection and evaluation of sequential extraction procedures for the determination of phosphorus forms in lake sediment

In order to achieve comparable measurements in the determination of phosphate forms in freshwater sediments, the Standards, Measurements and Testing Programme (formerly BCR) of the European Commission has launched a project the first step of which was to select and evaluate collaboratively existing extraction procedures. This was carried out through expert consultations and a literature survey, and was followed by the organisation of a first interlaboratory study for the evaluation of four sequential extraction schemes, one of which was selected as the most promising method for achieving comparability. This scheme, a modified version of the Williams protocol, was further tested in a second interlaboratory study. The so-called SMT extraction scheme seems promising and will provide, in the near future, a valuable tool for water managers in the field of lake restoration. It will be particularly helpful in estimating the stock of P potentially available, hence the risk of eutrophication due to internal P release.

CERTIFICATION OF THE EXTRACTABLE CONTENTS OF CD, CR, CU, NI, PB AND ZN IN A FRESHWATER SEDIMENT FOLLOWING A COLLABORATIVELY TESTED AND OPTIMISED THREE-STEP SEQUENTIAL EXTRACTION PROCEDURE

Sequential extraction procedures have been used during the last decades to study and determine trace element mobility in aquatic sediments. However, the results obtained are operationally defined and, therefore, the significance of the analytical results is related to the extraction scheme used. So, there is a need for suitable reference materials for this type of study to enable the validation of the methodologies and to control the quality of the measurements. This paper describes the preparation of a sediment reference material, BCR-701, the homogeneity and stability studies and the analytical work performed for the certification of the extractable contents of some trace elements, following a collaboratively tested and optimised sequential (three-step) extraction procedure. The paper contains all the results and gives the methods used to certify the extractable contents (mass fractions expressed as mg kg-1 on a dry matter basis) of Cd, Cr, Cu, Ni, Pb and Zn in all steps. Moreover, indicative values are given for the aqua regia extractable contents of the six elements in the sediment and the residue obtained after sequential extraction.

Three-stage sequential extraction procedure for the determination of metals in river sediments

A three-stage sequential extraction procedure, following a protocol proposed by a European working group coordinated and supported by the Community Bureau of Reference (BCR), has been applied to two river sediments from an industrial region of East Catalonia, Spain. The extractant solutions were: Step One, acetic acid (0.11 mol l(-1)); Step Two, hydroxylammonium chloride (0.1 mol l(-1), pH 2); Step Three, hydrogen peroxide (8.8 mol l(-1)) oxidation followed by extraction with ammonium acetate (1 mol l(-1), pH 2). The six elements determined in the extracts were Cd, Cr, Cu, Ni, Pb and Zn. Analysis of the extracts was carried out by flame atomic absorption spectrometry (FAAS). There were slight differences in analyte sensitivity between calibrants prepared in the extractant matrices and acidified aqueous calibrants. No significant matrix interferences were found except for Cr in the acetic acid and hydroxylammonium chloride extracts, which required determination by the standard additions method. The other elements (plus all the elements in the ammonium acetate extracts) were determined by direct calibration against calibrant solutions prepared in the same matrices as the samples.

Determination and speciation of copper and lead in sediments of a Mediterranean river (River Tenes, Catalonia, Spain)

Abstract Total concentrations of Cu and Pb and the speciation of these metals in sediments of the River Tenes are studied in order to establish the extent to which they are polluted and their capacity of remobilization. Five samples taken along the river were analyzed, major components of the sediments were studied using XRF and total Pb and Cu content were determined by AAS. In order to test the accuracy of the digestion methods used (triacid attack with nitric, perchloric and hydrofluoric acids or diacic attack with nitric and hydrochloric acids) for the determination of total trace metal, a standard reference material was also analyzed. Triacid attack is proposed to obtain good results. The results show a highly polluted area (1556 mg kg−1 Cu and 1555 mg kg−1 Pb) in the last sampling site analyzed. For metal speciation, the sequential scheme of Tessier et al. was used. From the results obtained, it can be concluded that Cu content in non-residual fraction is bonded mainly to organic matter, whereas non-residual Pb is mainly associated to iron and manganese oxides.

Trace metal partitioning in marine sediments and sludges deposited off the coast of Barcelona (Spain)

As part of a study on the environmental impact of the sludges discharged on the littoral platform in front of Barcelona (Spain), marine sediment samples were analysed. Major components were determined and the Tessier sequential extraction procedure was applied to study Cd, Cu, Cr, Ni, Pb and Zn distribution in eleven samples taken at nine sampling sites. From the data it can be inferred that in this type of sediment with high carbonate content, Cd is the most easily extractable metal, followed by Cr, Pb and Zn, and that Cu and Ni are the most retained. The anthropogenic contribution is also evaluated from the total metal contents using the metal content of a relatively non-polluted sediment sample taken from the same area as a baseline.

Optimization of Tessier Procedure for Metal Solid Speciation in River Sediments

Abstract Optimization of Tessier procedure for trace metal partitioning in sediments is studied. Firstly simplex optimization method is applied and the results indicate that the volume of extractant solution/weight of sediment ratio (V/m) is the main variable. Optimization of V/m ratio for second, third and fourth fractions of Tessier scheme is studied on two different river sediments. The optimum values of V/m ratio obtained are applied for copper, lead, chromium and nickel partitioning. The results obtained are compared with those obtained using Tessier procedure. Some conclusions about the behaviour of each fraction are presented.