Joint chemical flushing of soils contaminated with petroleum hydrocarbons

How to increase the efficiency of chemical flushing and decrease the remediation expenses of contaminated soils are two key scientific and technological issues to be solved. Joint chemical flushing was tested and compared with the water-flushing. The joint acid-flushing could effectively remove petroleum hydrocarbons in contaminated aquorizem and the dosage of washing powder as a flushing agent was greatly reduced, thereby, saving approximately 1200 US dollars of expenses relative to the water-flushing. The joint salt-flushing could be an optimal method for the cleanup of meadow burozem contaminated with petroleum hydrocarbons under the experimental conditions. Moreover, the amount of surfactant remained in the two washed soils after the joint acid-flushing and the joint-salt-flushing was minimal.     

Inputs and fates of petroleum hydrocarbons in a subtropical marine estuary

Inputs and fates of petroleum from a higly urbanized area to a subtropical marine estuary were investigated by measuring hydrocarbon concentrations in municipal wastewater treatment plants, urban stormwater drains, sediments, and benthic organisms in and around Tampa Bay, FL. The concentrations of petroleum hydrocarbons discharged from secondary and tertiary treatment plants in this area were lower than concentrations previously reported for other treatment plants in temperate regions. Samples collected from urban storm drains under base flow conditions were also low. The generally low levels of petroleum hydrocarbons in the sediments and organisms throughout Tampa Bay suggest that the bay is relatively pristine with respect to petroleum hydrocarbon contamination. Since it is unlikely that the anthropogenic input of hydrocarbons to this estuary is significantly lower than in other urbanized areas, we suggest that elevated annual temperatures in this subtropical system result in increased metabolic rates of microorganisms and more rapid degradation or metabolism of the petroleum hydrocarbons.     

Trace and major element pollution originating from coal ash suspension and transport processes

Coal ash obtained by coal combustion in the "Nikola Tesla A" power plant in Obrenovac, near Belgrade, Yugoslavia, is mixed with water of the Sava river and transported to the dump. In order to assess pollution caused by leaching of some minor and major elements during ash transport through the pipeline, two sets of samples (six samples each) were subjected to a modified sequential extraction. The first set consisted of coal ash samples taken immediately after combustion, while the second set was obtained by extraction with river water, imitating the processes that occur in the pipeline. Samples were extracted consecutively with distilled water and a 1 M solution of KCl, pH 7, and the differences in extractability were compared in order to predict potential pollution. Considering concentrations of seven trace elements as well as five major elements in extracts from a total of 12 samples, it can be concluded that lead and cadmium do not present an environmental threat during and immediately after ash transport to the dump. Portions of zinc, nickel and chromium are released during the ash transport, and arsenic and manganese are released continuously. Copper and iron do not present an environmental threat due to element leaching during and immediately after the coal ash suspension and transport. On the contrary, these elements, as well as chromium, become concentrated during coal ash transport. Adsorbed portions of calcium, magnesium and potassium are also leached during coal ash transport.     

Assessment of contamination by heavy metals and petroleum hydrocarbons in sediments of Montevideo Harbour (Uruguay)

As part of the first environmental assessment within Montevideo Harbour, in summer and winter of 1998, sediments samples were collected at eight locations to determine the spatial distribution of anthropogenic pollutants. Muddy sediments with high organic matter content dominate the study area. Heavy metal levels indicated that sediments were highly polluted with Zn (overall mean: 312+/-102 microg g(-1) dry sediment), Pb (85+/-31), Cu (89+/-25), Cr (162+/-62), and Hg (0.63+/-0.3) and moderately with Ni (30+/-2) and Ag (1.2+/-0.4). Depending on location and season, aliphatic hydrocarbons reached from 21 to 120 microg g(-1), while the unresolved complex mixture represented up to 76% of the total aliphatic fraction. Total PAH concentrations ranged from 1.56 to 90.44 microg g(-1); except at one location, petroleum derivatives were identified as main local source. The results pointed out that almost all the harbour area presented some substances that can cause adverse biological effects, especially in the inner region where all metals are above PEL levels. Principal components analysis confirmed that the inner harbour region is most severely affected by the pollutants and it was possible to differentiate three regions according to their environmental quality.     

In-vessel composting--bioremediation of aged coal tar soil: effect of temperature and soil/green waste amendment ratio

The biodegradation of 16 United States Environmental Protection Agency (USEPA)-listed polycyclic aromatic hydrocarbons (PAHs) present in contaminated soil from a manufactured gas plant site was investigated using laboratory-scale in-vessel composting-bioremediation reactors over 8 weeks. The influence of temperature (T, 38, 55, and 70 degrees C) and soil/green waste ratio (S:GW, 0.6:1, 0.7:1, 0.8:1, and 0.9:1) was investigated. A comparative study using a temperature profile during in-vessel composting-bioremediation to meet current regulatory requirements was also investigated. Temperature and amendment ratio were found to be important operating parameters for PAH removal for in-vessel composting-bioremediation of aged coal tar-contaminated soil. After 8 weeks of continuous treatment, the highest removal of 16 USEPA PAHs was observed at T=38 degrees C and S:GW=0.8:1 (75.2%). Lower removal of 16 USEPA PAHs was observed for temperature profile treatment (60.8%). We recommend that when conventional composting processes using temperature profiles to meet regulatory requirements for pathogen control need to be used, these should start with a prolonged mesophilic stage (6 weeks in this investigation) followed by thermophilic, cooling, and maturation stages.     

Removal of hydrocarbons from Nile water

The need to remove hydrocarbons from water supply sources raises questions on the efficiency of the present water treatment processes in removing hydrocarbons. Therefore, the effectiveness of physicochemical processes involving chlorination, chemical coagulation and sand filtration were investigated. The effect of variable filtration media was also examined. In addition, the use of an activated carbon column was considered, and the effect of different retention times was evaluated. Results of this study showed that chemical coagulation using alum and Nalco removed only 32% of the total hydrocarbons and 80% of turbidity. Use of sand and a mixture of anthracite and sand filters showed additional removal of hydrocarbons and turbidity during the continuous filtration process. Increasing the anthracite depth relative to the total effective filtration depth increases the efficiency of the filter. Adsorption on granular activated carbon was shown to be an effective means for the removal of hydrocarbons. Results obtained indicated that the carbon adsorption capacity increases linearly as the retention time increases.     

Biodegradability of hydrocarbons in the refinery wastewater from moustorod oil refinery

The present investigation deals with the study of hydrocarbon degradation present in refinery wastewater by natural microbial flora in addition to that obtained using Ps. aeruginosa under laboratory conditions. Results indicated that Ps. aeruginosa may have a significant role in the degradation of hydrocarbons. After seven days, several of the compounds in the original wastewater were completely degraded and four compounds (n-paraffins) were partially degraded. Without Ps. aerruginosa, the same picture had been obtained after 23 days.     

A survey of pollutant emission levels in wastewaters and residuals from the petroleum refining industry

This paper summarizes the data made available during the last decade on the subject of emission levels of wastewaters and solid residuals from the petroleum refininf industry. The data for both traditional and priority pollutants from a number of studies are considered. Specific organic compounds which are not traditional pollutants and are not on the priority pollutant list are presented for some cases. A discussion of accuracy, precision, variance, and some causes of variance is presented. Types of wastewater and residual samples for which data are presented include raw waste loadings from Class A through E refineries, loadings of various pollutants across several process units such as dissolved air flotation, activated sludge processes, carbon columns (powdered and granular), and clarifiers, and oily solids (tank bottoms, crude oil, bunker C, and waxy product).     

Radon emanation from NORM-contaminated pipe scale and soil at petroleum industry sites

Radon-222 emanation fractions were determined for barite scale deposits associated with petroleum production tubing and soil contaminated with naturally occurring radioactive material (NORM). Samples were analyzed for 226Ra concentration, the results of which were used to calculate the 222Rn emanation fraction for the sample. An important parameter determining the overall Rn activity flux from a solid medium, 222Rn emanation fraction represents the fraction of 222Rn produced that enters the interconnected pore space within a medium contaminated with 226Ra before the 222Rn undergoes radioactive decay. The primary objective of the study was to determine whether 222Rn emanation fractions from pipe scale and soil from petroleum production sites are similar to those of uranium mill tailings. Pipe scale samples were collected at four sites representing a wide geographical area, and consisted primarily of barite scale where Ra atoms have replaced a fraction of the Ba within the crystal lattice of the scale. Soil samples were collected at five sites, from areas exhibiting elevated surface gamma exposure rates indicating the presence of NORM. For comparison, 226Ra concentrations and 222Rn emanation fraction were also determined for uranium mill tailings samples provided from a site in Utah. Although 2226Ra concentrations from pipe scale samples were similar to those found in uranium mill tailings, 222Rn emanation fractions from scale were generally lower. Emanation fractions from each data set were statistically different from those of mill tailings (p < or = 0.01). The differences are probably due to physical differences between the two media and to the method by which the Ra is deposited in the material. Radon emanation from soils was extremely variable owing not only to differences in physical and chemical soil properties, but also to the means by which NORM has entered the soil. Although additional emanation measurements from other sites are needed, the data collected at these sites indicate that regulations intended to protect human health from 222Rn inhalation should consider the type and properties of the medium in which the NORM is contained, rather than relying strictly on concentrations of the parent 226Ra.     

Exploring the fate,transport and risk of Perfluorooctane Sulfonate (PFOS) in a coastal region of China using a multimedia model

Perfluorooctane Sulfonate (PFOS) and related substances have been widely applied in both industrial processes and domestic products in China. Exploring the environmental fate and transport of PFOS using modeling methods provides an important link between emission and multimedia diffusion which forms a vital part in the human health risk assessment and chemical management for these substances. In this study, the gridded fugacity based BETR model was modified to make it more suitable to model transfer processes of PFOS in a coastal region, including changes to PFOS partition coefficients to reflect the influence of water salinity on its sorption behavior. The fate and transport of PFOS in the Bohai coastal region of China were simulated under steady state with the modified version of the model. Spatially distributed emissions of PFOS and related substances in 2010 were estimated and used in these simulations. Four different emission scenarios were investigated, in which a range of half-lives for PFOS related substances were considered. Concentrations of PFOS in air, vegetation, soil, fresh water, fresh water sediment and coastal water were derived from the model under the steady-state assumption. The median modeled PFOS concentrations in fresh water, fresh water sediment and soil were 7.20 ng/L, 0.39 ng/g and 0.21 ng/g, respectively, under Emission Scenario 2 (which assumed all PFOS related substances immediately degrade to PFOS) for the whole region, while the maximum concentrations were 47.10 ng/L, 4.98 ng/g and 2.49 ng/g, respectively. Measured concentration data for PFOS in the Bohai coastal region around the year of 2010 were collected from the literature. The reliability of the model results was evaluated by comparing the range of modeled concentrations with the measured data, which generally matched well for the main compartments. Fate and transfer fluxes were derived from the model based on the calculated inventory within the compartments, transfer fluxes between compartments and advection fluxes between sub-regions. It showed that soil and costal water were likely to be the most important sinks of PFOS in the Bohai costal region, in which more than 90% of PFOS was stored. Flows of fresh water were the driving force for spatial transport of PFOS in this region. Influences of the seasonal change of fresh water fluxes on the model results were also analyzed. When only seasonal changes of the fresh water flow rates were considered, concentrations of PFOS in winter and spring were predicted to be higher than that under annual average conditions, while the concentrations in summer and autumn were lower. For PFOS fluxes entering the sea, opposite conclusions were drawn compared to the concentrations. Environmental risks from the presence of PFOS in fresh water were assessed for this region through comparison with available water quality criteria values. The predicted concentrations of PFOS in the Bohai coastal region provided by the model were lower than the water quality criteria published by the United States Environmental Protection Agency and Chinese researchers, while the concentrations in more than 80% of the sampling locations exceeded the European Union Water Framework Directive Environmental Quality Standards values. Seasonal variations of flow rate might cause a significant increase in environmental risks.     

Occurrence and fate of pharmaceutical products and by-products,from resource to drinking water

Among all emerging substances in water, pharmaceutical products (PPs) and residues are a lot of concern. These last two years, the number of studies has increased drastically, however much less for water resources and drinking water than for wastewater. This literature review based on recent works, deals with water resources (surface or groundwater), focusing on characteristics, occurrence and fate of numerous PPs studied, and drinking water including water quality. Through this review, it appears that the pharmaceutical risk must be considered even in drinking water where concentrations are very low. Moreover, there is a lack of research for by-products (metabolites and transformation products) characterization, occurrence and fate in all water types and especially in drinking water.     

Modelling the transport of radionuclides from land to water

This paper addresses some fundamental problems related to the structure and function of catchment areas in general and for seasonal (weekly, monthly) mass balance calculations of radionuclides (and metals, organics and nutrients) in particular. A new catchment area model has been developed and critically tested. This modelling approach is based on mechanistic principles. The catchment area is differentiated into inflow ( approximately dry land) areas and outflow (=wetland) areas. The model also accounts for time-dependent fixation of substances in the catchment related to single-pulse fallouts. The model has a general structure. It is simple to use since there are only two soil type classes and three categories for the outflow areas. In critical tests, the model was put within a framework where it is intended, i.e., within a more comprehensive lake model. Radiocesium was used as a tracer in these tests. Modelled values were compared to empirical data from 23 lakes (351 data on (137)Cs in water, as well as in sediments, small fish and on suspended particles) covering a very wide limnological domain (latitudes from 42 to 61 degrees V, altitudes from 0 to 1090 m ASL, catchment areas from 0.17 to 114,700 km(2), precipitation from 430 to 1840 mm/year, lake areas from 0.042 to 1147 km(2), mean depths from 1.1 to 90 m, pH from 5.1 to 9 units, potassium concentrations from 0.23 to 27.5 mg/l, total P concentrations from 8.3 to 100 microg/l and theoretical water retention times from 0.02 to 137 years). When modelled values were compared to empirical data, the slope was almost perfect (0.99) as well as the coefficient of determination (r2 = 0.96).     

Leachability of elements from sub-bituminous coal fly ash from India

Environmental concerns regarding the potential contamination of soil, surface and ground water due to the presence of soluble metal species in the ash pond leachate is of great importance. Serial batch leaching was carried out simulating the rainwater condition of the study area to understand the behaviour of elements during leaching. The leachates were analysed for the elements Al, Ca, K, Mg, Na, P, S, Si, As, Ba, Fe, Mn, Mo, Ti, V, Pb, Zn, Co, Cr, Cu, Ni and Cd by inductively coupled plasma optical emission spectrometer (ICP-OES). It was found that Cd, Co, Cr and Ni did not leach from the ash while Cu and Pb concentrations were insignificant in the leachate regardless of liquid to solid (L/S) ratio. Most of the elements showed maximum concentrations at lower L/S ratio and then decreased with increasing L/S. The total cumulative concentrations of As, Mn and Mo were found to be higher than the World Health Organization (WHO) recommended values for drinking water while the concentrations of Fe, Mn and As exceeded the maximum allowable concentrations prescribed by the United States Environmental Protection Agency (USEPA). The pre and the post leached ash samples were analysed for morphology, specific surface area and mineralogical changes. Analysis of post-leached fly ash indicated changes in the specific surface area and morphology but no change in mineralogy.     

Concentrations, transport, fate, and releases of polybrominated diphenyl ethers in sewage treatment plants in the Pearl River Delta, South China

Wastewater has proved to be a significant source of polybrominated diphenyl ethers (PBDEs) in the environment. Seventeen congeners from tri- to deca-BDEs were determined to characterize the occurrence, fate, and transport of PBDEs in two sewage treatment plants in the Pearl River Delta, South China. The PBDE concentrations varied substantially from 13.3 to 2496.4 ng L(-1) in the raw wastewater, depending on the wastewater types and contents of the suspended particulate matter (SPM). The concentrations declined to 0.9 to 4.4 ng L(-1) in the treated effluent and were closely associated with SPM contents. BDE-209 was the predominant congener in the wastewater and sewage sludge. Most of PBDEs might have ended up in the sewage sludge, with <4.7% being discharged with the treated effluent. The results revealed that PBDEs were not significantly degraded by biological treatment and chlorination in the STPs. An annual release of PBDEs was estimated at 2280 kg/year through wastewater from the Pearl River Delta.     

Nature and fate of Hudson Bay permafrost

Two aspects of the permafrost of the Hudson Bay region are examined. The first is the climatological conditions that support permafrost especially along the southwestern shore of Hudson Bay. The second is the fate of the permafrost using recent climate change scenarios. The continuous permafrost along the shores of southwestern Hudson Bay is examined from a climatological perspective. Two hypotheses are explored to explain the presence of continuous permafrost in this region in spite of the relatively "warm" local climate. Possible errors in the calculation of thawing degree days and the asymmetries in frozen and unfrozen soil thermal conductivities are successively examined. Only the second hypothesis is likely to explain the presence of permafrost in southwestern Hudson Bay. Sophisticated climate models are used to assess the potential change in permafrost distribution in the Hudson Bay region. Nine simulations using three different versions of the Canadian Centre of Climate Modelling and Analysis (CCCma) general circulation model are used to project permafrost distribution. Two surface temperature thresholds, –5 and –10 °C, are used to diagnose permafrost grid points. All simulations, including those that include reduction of CO₂ emissions, showed at least a 50% reduction of permafrost by 2100 using these temperature thresholds. Electronic Publication     

Soil transport and plant uptake of radio-iodine from near-surface groundwater

This paper describes a 12-month experiment designed to study the extent of upward migration of (125)I (as a surrogate for (129)I) from near-surface groundwater, through a 50-cm column of soil and into perennial ryegrass. The water table was established at a depth of 45 cm below the soil surface. By 3 months, (125)I had migrated about half way up the soil column. After this, it tended to accumulate just above this mid-point, with only very small amounts being transported to the upper 20 cm of soil. This behaviour seemed to be explained well by soil moisture and redox conditions. The experiment indicated that (125)I was mobile only within the saturated/low redox zone at the base of the soil column and accumulated in the zone of transition between anoxic and oxic soil conditions. Uptake of (125)I by the ryegrass was found to be low.     

Modelling the environmental fate of the polybrominated diphenyl ethers

In response to growing alarm over the occurrence of polybrominated diphenyl ethers (PBDEs) in remote regions, this study considers their physical chemistry, environmental partitioning and considerations regarding potential for long-range atmospheric transport (LRAT). Internally consistent physical-chemical property data are presented for five representative congeners (PBDE-15, -28, -47, -99, -153) and used in a multimedia modelling approach. Results of the Level II model indicate that PBDEs will largely partition to organic carbon in soil and sediment and that their persistence will be strongly influenced by degradation rates in these media that are not well known. TaPL3 model estimates of their characteristic travel distance (CTD) suggest limited LRAT potential. The LRAT is also evaluated qualitatively, in terms of surface-air exchange behaviour. PBDEs are shown to be sensitive to seasonally and diurnally fluctuating temperatures. When vegetation is included in the model, 50% of the total mass of PBDE-47 deposited to vegetation returns to the atmosphere, suggesting that it may migrate through a series of deposition/volatilisation hops. Key data that needs to be identified in this evaluation include a better understanding of air-surface exchange, particularly to foliage, and measurements of degradation rates in soil, sediment and vegetation.     

Effect of emissions from petroleum gas flares on the reproductive state of pine stands in the northern taiga subzone

Characteristics of the adaptive response of the female generative system of Scotch pine to air pollution caused by petroleum gas burning in flares during oil production in Western Siberia have been studied. The relationship between the individual and endogenous variations of the quantitative parameters of pine cone morphology has been analyzed in different zones of deterioration.     

Radiological hazards of TENORM in the wasted petroleum pipes

Disposal petroleum pipes containing sludge and scale as a technically enhanced natural occurring radioactive material (TENORM) leads to internal and external radiation hazards and then a significant radiation dose to the workers. In order to contribute to a future waste management policy related to the presence of TENORM in the disposal sites of wasted petroleum pipes, scale and sludge as TENORM wastes are collected form these disposal pipes for radiometric analysis. These pipes are imported from onshore oilfields at south Sinai governorate, Egypt. The highest mean ²²⁶Ra and ²²⁸Ra concentrations of 519 and 50 kBq/kg respectively, were measured in scale samples. Sludge lies within the normal range of radium concentration. The average absorbed dose caused by the exposure to the wasted pipes equal to 4.09 μGy h⁻¹ from sludge and 262 μGy h⁻¹ from scale. This is much higher than the acceptable level of 0.059 μGy h⁻¹. Due to radon inhalation, important radon related parameters are calculated which advantage in internal dose calculation. Fairly good correlation between real radium content and radon exhalation rate for sludge samples is obtained. The hazards from sludge come from its high emanation power for radon which equal to 3.83%. The obtained results demonstrate the need of screening oil residues for their radionuclide content in order to decide about their final disposal.