With the advent of more stringent controls on wastewater treatment, sewage sludge production in Europe and many parts of the world is increasing. With this increase comes the problem of sludge disposal, and recycling to land arguably offers an economically and environmentally sustainable option. However, a major limitation of sewage sludge reuse is the potential release of heavy metals from the sludge and heavy metal accumulation to toxic levels in topsoils. The properties of the sludge play a crucial role in determining the initial release and subsequent availability of heavy metals in amended soils. Bioavailable forms of heavy metals in recently amended soils are most likely to be those that are bioavailable in the sewage sludge. In this paper, published research on the importance of sewage sludge characteristics on metal release and bioavailability will be reviewed and contrasted with original research. A selection of sludges from around Australia has been collected for this purpose. Through the use of incubation studies, isotope dilution techniques, ion-selective electrode measurements and 13C-NMR spectroscopy, the importance of a range of sludge properties on heavy metal behaviour in sludges and sludge-amended soils is addressed. 相似文献
Long-term copper smelting in the Anaconda and Deer Lodge Valley area of Montana has resulted in an extensive area of trace element contamination. Aerial extent of contamination is generally established, but total analysis of soils does not correlate to relative degree of impact on vegetation growth. Three pedons (Beaverell, Cetrack and Judco) were analyzed by routine soil characterization methods, aqua regia microwave digestion, sequential chemical extraction, and X-ray diffraction analysis with the objective of providing a better understanding of chemical forms and potential reactivity of selected trace elements (Cd, Co, Cr, Cu, Hg, Mn, Ni, P, Pb). Surface horizons of soils are more acidic than subsoils, with pH for all horizons ranging from 4.0 to 8.7. Beaverell is the most contaminated in the upper 20 cm with the sum of total extractable (SUMTE) trace elements by microwave digestion ranging from 1836 to 3605 mg kg−1, largest H2O-soluble (WS) and exchangeable (EX) fractions (e.g. 1.6 and 9.3%, respectively), and smallest residual (RES) fraction (e.g. 14.3%). Cetrack has greater SUMTE elements than Judco, though a lower WS+EX fraction due to the effects of alkaline pH, carbonates and high P. Oxide (OX), organic matter/sulfide (OM/S), and RES fractions predominate over WS, EX, and specially-sorbed/carbonate-bound fractions (SS/CAR) for all horizons. Copper, Zn, Pb and Cd are elevated in surface over subsurface horizons in these latter fractions, indicating these elements were anthropogenic additions. X-ray data indicate that Pb, Cu, Cr and Cd partially exists as both OX and sulfide mineral forms. 相似文献
Determination of triazines herbicides (atrazine and simazine) by high performance liquid chromatography (HPLC) in samples of trophic chain were worked out. Determination limits of 0.5 μg g−1 for atrazine, 0.8 μg g−1 for simazine with pesticides recovery of 70–77% in trophic chain samples were obtained. The content of simazine in soils was in range 1.72–57.89 μg g−1, in grass 5–88 μg g−1, in milk 2.32–15.29 μg g−1, in cereals 10.98–387 μg g−1, in eggs 30.14–59.48 μg g−1, for fruits: 2.45–6.19 μg g−1. The content of atrazine in soils was in range 0.69–19.59 μg g−1, in grass 7.85–23.85 μg g−1, in cereals 1.88–43.08 μg g−1. Cadmium, lead and zinc were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES) in the same samples as atrazine and simazine. Determination limits for cadmium 5 × 10−3 μg g−1, for lead 1 × 10−2 μg g−1, and for zinc 0.2 × 10−3 μg g−1, were obtained. The content of cadmium in soil was in range 0.13–5.89 μg g−1, in grass 114–627.72 × 10−3 μg g−1, in milk 8.88–61.88 × 10−3 μg g−1, in cereals 0.20–0.31 μg g−1, in eggs 0.11–0.15 μg g−1, in fruits 0.23–0.59 μg g−1. The content of lead in soils was in range 0.57–151.50 μg g−1, in grass 0.16–136.57 μg g−1, in milk 1.16–3.74 μg g−1, in cereals 1.05–5.47 μg g−1, in eggs 5.79–55.87 μg g−1, in fruits 21.00–87.36 μg g−1. Zinc content in soil was in range 9.15–424.5 μg g−1, in grass 35.20–55.87 μg g−1, in milk 20.00–34.38 μg g−1, in cereals 14.94–28.78 μg g−1, in eggs 15.67–32.01 μg g−1, in fruits 14.94–18.88 μg g−1.
Described below extraction and mineralization methods for particular trophic chains allowed to determine of atrazine, simazine, cadmium, lead and zinc with good repeatability and precision. Emphasis was focused on liquid–liquid extraction and solid-phase extraction of atrazine and simazine from analysed materials, as well as, on monitoring the content of herbicides and metals in soil and along trophic chain. Higher concentration of pesticides in samples from west region of Poland in comparison to that of east region is likely related to common applying them in Western Europe in relation to East Europe. The content of metals strongly depends on samples origin (industry area, vicinity of motorways). 相似文献
‘Metal ash’ presents a waste disposal problem in most of the developing countries as the industries employ obsolete technologies.
In this paper we describe analysis of tin ash, zinc ash and aluminium ash by means of optical methods, such as X-ray diffraction
(XRD), inductively coupled plasma mass spectrometry (ICP-MS), electron probe micro analysis (EPMA), scanning electron microscopy
(SEM) and chemical methods. The results of tin ash obtained by XRD method matched well with the cassiterite, a naturally occurring
mineral of tin. ICP-MS studies reveal the presence of a large number of tracer metals, which may cause pollution by tertiary
dispersion and this aspect is discussed. Conversely, the data generated by chemical methods are limited. However, the methods
are simple and cost-effective. Then, they can easily be adopted by low-budget industries. Simple and cost-effective process
to recover tin from tin ash is described. It is based on heating tin ash with sodium cyanide to about 900°C to separate tin
component from the metal ash. The process recovers good quality tin and offers a very high yield. The process can be scaled
up to small pilot plant. 相似文献
Soil contamination with tetrabromobisphenol A(TBBPA) has caused great concerns;however, the presence of heavy metals and soil organic matter on the biodegradation of TBBPA is still unclear. We isolated Pseudomonas sp. strain CDT, a TBBPA-degrading bacterium, from activated sludge and incubated it with ~(14)C-labeled TBBPA for 87 days in the absence and presence of Cu~(2+)and humic acids(HA). TBBPA was degraded to organic-solvent extractable(59.4% ± 2.2%) and non-extractable(25.1% ± 1.3%) metabolites,mineralized to CO_2(4.8% ± 0.8%), and assimilated into cells(10.6% ± 0.9%) at the end of incubation. When Cu~(2+)was present, the transformation of extractable metabolites into non-extractable metabolites and mineralization were inhibited, possibly due to the toxicity of Cu~(2+)to cells. HA significantly inhibited both dissipation and mineralization of TBBPA and altered the fate of TBBPA in the culture by formation of HA-bound residues that amounted to 22.1% ± 3.7% of the transformed TBBPA. The inhibition from HA was attributed to adsorption of TBBPA and formation of bound residues with HA via reaction of reactive metabolites with HA molecules, which decreased bioavailability of TBBPA and metabolites in the culture. When Cu~(2+)and HA were both present, Cu~(2+)significantly promoted the HA inhibition on TBBPA dissipation but not on metabolite degradation. The results provide insights into individual and interactive effects of Cu~(2+)and soil organic matter on the biotransformation of TBBPA and indicate that soil organic matter plays an essential role in determining the fate of organic pollutants in soil and mitigating heavy metal toxicity. 相似文献