Hydrous Manganese Oxide Doped Gel Probe Sampler for Measuring In Situ Reductive Dissolution Rates. 2. Field Deployment

In situ rates of reductive dissolution in submerged shoreline sediments at Lake Tegel (Berlin, Germany) were measured with a novel hydrous manganese (Mn) oxide-doped gel probe sampler in concert with equilibrium gel probe and sequential extraction measurements. Rates were low in the top 8 cm, then showed a peak from 8 to 14 cm, with a maximum at 12 cm depth. This rate corresponded with a peak in dissolved porewater iron (Fe) at 11 cm depth. Below 14 cm, the reductive dissolution rate reached an intermediate steady value. Lower rates at depth corresponded with increases in operationally defined fractions of carbonate-bound and organic- and sulfide-bound Mn and Fe as detected by sequential extraction. Observed rates of reductive dissolution, which reflect a capacity for Mn reduction rather than actual rates under ambient conditions, appear to correlate with porewater chemistry and sequential extraction fractions as expected in early sediment diagenesis, and are consistent with previous measurements of in situ reductive dissolution rates. Significant downward advection in this bank filtration setting depletes the Mn and Fe oxides in the sediments and enhances the transport of dissolved Fe and Mn into the infiltrating water

Fractionation of lead in soil by isotopic dilution and sequential extraction

‘Reactivity’ or ‘lability’ of lead is difficult to measure using traditional methods. We investigated the use of isotopic dilution with 204Pb to determine metal reactivity in four soils historically contaminated with contrasting sources of Pb, including (i) petrol-derived Pb, (ii) Pb/Zn minespoil, (iii) long-term sewage sludge application and (iv) 19th century urban waste disposal; total soil Pb concentrations ranged from 217 to 13 600 mg kg–1. A post-spike equilibration period of 3 days and suspension in 5.0 × 10–4 M ethylenediaminetetraacetic acid provided reasonably robust conditions for measuring isotopically exchangeable Pb. However, in acidic organic soils a dilute Ca(NO3)2 electrolyte may be preferable to avoid mobilisation of ‘non-labile’ Pb. Results showed that the reactive pool of soil Pb can be a large proportion of the total soil lead content but varies with the original Pb source. A comparison of isotopic exchangeability with the results of a sequential extraction procedure showed that (isotopically) ‘non-labile’ Pb may be broadly equated with ‘residual’ Pb in organic soils. However, in mineral soils the ‘carbonate’ and ‘oxide-bound’ Pb fractions included non-labile forms of Pb. The individual isotopic signatures of labile and non-labile Pb pools suggested that, despite prolonged contact with soil, differences between the lability of the original contaminant and the native soil Pb may remain

Heavy metal contamination in some soils of the McMurdo Sound region, Antarctica

Soil samples from eight sites at Marble Point and Pram Point, McMurdo Sound region, contaminated by human activities were examined for heavy metal content, using sequential extraction methods. The redistribution of lead, zinc and copper arising from point sources of these metals was demonstrated. The levels found are not considered to represent serious pollution but do indicate that human activities can change the chemistry of the Antarctic environment in localized areas

Heavy metals partioning in three French forest soils by sequential extraction procedure

To know the concentration of heavy metal associated to chemical compounds is important to evaluate the environmental risks on soils, particularly regarding ion bioavailability. The relative mobility and strength of binding of heavy metals to the soil components can be studied using a sequential extraction procedure which provides a meaningful comparison between different soil profiles. The heavy metals partitioning bas been identified in three different french forest soils : one cambic podzol, one calcaric cambisol and one mollic andosol, using a new sequential extraction method. Results show that metal fractionation is metal and site specific. The water leaching phase does not contain any metals. The proportion of heavy metal leached in the exchangeable and the acid — soplhuabslee is significant for Cd. The residual phase is important for Cr, Pb, and to a lesser extend for Ni. The organic matter fraction is dominant for Zn and Cu. Thus, the considered heavy metals are mainly bounded to iron oxides, to the organic matter and to the mineral residue. The order of heavy metals availability in the three soils would be : Zn>Cd>Cu>Pb>NiL&egatd;C r.i sotopes in some extracts of the extraction procedure corroborate the anthropogenic inputs for two soils. These both infomations allow to trace the origin, the mobility and the distribution of Pb in the soil

Speciation of heavy metals in street dust samples from Sakarya I. Organized industrial district using the BCR sequential extraction procedure by ICP-OES

This paper focuses on the concentrations of heavy metals (Cd, Co, Cr, Cu, Mn, Ni, Pb and Zn) in 20 dust samples collected from the streets of the Organized Industrial District in Sakarya, Turkey using sequential extraction procedure were determined by ICP-OES. The three-step BCR sequential extraction procedure was used in order to evaluate mobility, availability and persistence of heavy elements in street dust samples. Three operationally defined fractions isolated using the BCR procedure was: acid extractable, reducible, and oxidizable. The mobility sequence based on the sum of the BCR sequential extraction stages: Cd (82.3%) > Mn (80.0%) > Zn (78.8%) > Cu (70.2%) > Ni (65.9%) > Pb (63.8%) > Cr (47.3%) > Co (32.6%). Validation of the analytical results was checked by analysis of the BCR-701 certified reference material. The concentrations of metals in the street dust samples have been shown a decrease after the each extraction stage. KEY WORDS: Heavy metals, ICP-OES, Organized industrial district, Sequential extraction, Dust, Turkey Bull. Chem. Soc. Ethiop. 2013, 27(2), 205-212.DOI: http://dx.doi.org/10.4314/bcse.v27i2.

Investigating Uranium incorporation in modern carbonates by sequential extraction: Applied to the Permian - Triassic boundary in Lung Cam, Vietnam

The Uranium (U) isotopic system can be used to model the extent of global-scale ocean anoxia by utilizing the 238U/235U ratios as a paleo-redox indicator (δ238U). While recent studies have shown promise with the use of this novel proxy, variability is seen in modern carbonate sediment samples suggesting that more work is needed in order to understand elemental U uptake during early marine diagenesis. This thesis utilizes a sequential extraction methodology in order to understand the distribution of authigenic U within carbonate sediments. This thesis consists of four parts, (1) an evaluation and modification of a sequential extraction methodology for U uptake in modern carbonate sediments, (2) application of the modified sequential extraction method to the study U distribution within chemical fractions within Bahamian bulk sediments, (3) the application of the modified methodology to study the U distribution across the Permian–Triassic boundary from the Lung Cam section in Northern Vietnam, and (4) the implications of authigenic U toward the δ238U paleo-redox marker. Results show that a sequential extraction can be successful within carbonate sediments. The results of this sequential extraction shows that the majority of authigenic U is found within the exchangeable and carbonate fraction. This thesis hypothesizes that this U component is a non-crystalline U(IV) species. Furthermore, this authigenic U component was also found within the Permian–Triassic section located in Lung Cam, Vietnam, thus illustrating preservation of heavy authigenic U within the rock record

Fractionation of potentially toxic elements in urban soils from five European cities by means of a harmonised sequential extraction procedure

The revised (four-step) BCR sequential extraction procedure has been applied to fractionate the chromium, copper, iron, manganese, nickel, lead and zinc contents in urban soil samples from public-access areas in five European cities. A preliminary inter-laboratory comparison was conducted and showed that data obtained by different laboratories participating in the study were sufficiently harmonious for comparisons to be made between cities and land types (e.g. parks, roadside, riverbanks, etc.). Analyte recoveries by sequential extraction, with respect to direct aqua regia digestion, were generally acceptable (100 ± 15%). Iron, nickel and, at most sites, chromium were found mainly in association with the residual phase of the soil matrix. Copper was present in the reducible, oxidisable and residual fractions, whilst zinc was found in all four sequential extracts. Manganese was strongly associated with reducible material as, in some cities, was lead. This is of concern because high lead concentrations were present in some soils (>500 mg kg−1) and the potential exists for remobilisation under reducing conditions. As would be expected, extractable metal contents were generally highest in older, more heavily industrialised cities. Copper, lead and zinc showed marked (and often correlated) variations in concentrations between sites within the same city whereas manganese and, especially, iron, did not. No overall relationships were, however, found between analyte concentrations and land use, nor between analyte partitioning and land use

Fractionation of CIMV wheat straw lignin as an approach for promoting it interaction with isocyanates and characteristic of products obtained

The reactivity of CIMV lignin fractions with MDI has been investigated in extra dry dioxane (DOX) in argon atmosphere at 25 degrees of Celsius, using FTIR spectroscopy (absorbance band at 2273 cm^-1) for monitoring the NCO group disappearance during reaction. Five CIMV lignin fractions were obtained and investigated: 2 fractions obtained by separate extractions with DOX and methanol and 3 fractions obtained in the process of sequential extraction of CIMV lignin with dichloromethane, methanol and methanol/dichloromethane mixture. The highest second rate constants was detected for both methanol soluble lignin fractions

Comparison of sequential and single extraction in order to estimate the environmental impact of metals from fly ash

The aim of this paper is to simulate leaching of metals from fly ash in different environmental conditions using ultrasound and microwave-assisted extraction techniques. Single-agent extraction and sequential extraction procedures were used to determine the levels of different metals leaching. The concentration of metals (Al, Fe, Mn, Cd, Co, Cr, Ni, Pb, Cu, As and Be) in fly ash extracts were measured by inductively coupled plasma-atomic emission spectrometry. Single-agent extractions of metals were conducted at sonication times of 10, 20, 30, 40 and 50 min. Single-agent extraction with deionized water was also performed by exposing samples to microwave radiation at temperature of 50 degrees C. The sequential extraction was conducted according to the BCR procedure which was modified and applied to study the partitioning of metals in coal fly ash. The microwave-assisted sequential extraction was performed at different extraction temperatures: 50, 100 and 150 degrees C. The partitioning of metals between the individual fractions was investigated and discussed. The efficiency of the extraction process for each step was examined. In addition, the results of the microwave-assisted sequential extraction are compared to the results obtained by standard ASTM method. The mobility of most elements contained in the fly ash is markedly pH sensitive

Effect of different extracting solvents on antioxidant activity and phenolic compounds of a fruit and vegetable residue flour

In order to quantify antioxidant capacity in food products, several methods have been proposed over the years. Among them, DPPH radical is widely used to determine the antioxidant capacity of different substrates. However, it is known that different types of extractants, providing different responses, can extract a variety of bioactive compounds. Besides, storage time seems to interfere in the stability of these substances. Integral use of fruits and vegetables has been proposed along the years as a means of reducing environmental pollution and give a better destination to by-products from food industries. Thus, this study aimed to evaluate the antioxidant potential of a fruit and vegetables residue flour (FVR) with sequential and non-sequential extraction, in order to evaluate its antioxidant activity and phenolic compounds. And these compounds stability during storage of 180 days. It was observed that in non-sequential extraction, water was able to reduce by 74% the radical; however, at sequential extraction process, using six different extractors, each one was able to reduce at least 40% of DPPH. The total soluble phenolic contents in sequential extraction were 22.49 ± 1.59 mg GAE/g FVR on the first day and 5.35 ± 0.32 mg GAE/g FVR after 180 days