Screening of halogenated aromatic compounds in some raw material lots for an aluminium recycling plant

Four samples of scrap raw materials for an aluminium recycling plant were screened for the occurrence of persistent halogenated aromatic compounds. The samples contained waste from handling of electric and electronic plastics, filter dust from electronic crusher, cyclone dust from electronic crusher and light fluff from car shredder. In our screening analyses, brominated flame retardants were observed in all samples. Polybrominated diphenyl ethers (PBDE) were identified in all samples in amounts of 245-67450 ng/g. The major PBDE congeners found were decabromo- and pentabromodiphenyl ethers. 1,1-bis(2,4,6-tribromophenoxy)ethane, hexabromobenzene, ethyl-pentabromobenzene, tetrabromobisphenol-A, pentabromotoluene and dimethyl tetrabromobenzene were observed in all scrap samples. The concentrations of PCBs, PCNs (polychlorinated naphthalenes) and nona- to undecachlorinated terphenyls in some of these scrap samples were remarkably high.     

Trends of organochlorine compounds in Finnish inland waters

Caged common lake mussels (Anodonta piscinalis) have been used in the monitoring of organochlorine compounds in pulp and paper mill recipient watercourses of Finland annually from 1984 to 1998. Statistically significant decreasing trends of chlorophenols and chloroguaiacols originating from chlorobleaching were observed in all recipients in parallel with the decreasing discharges from the mills. Metabolites of chlorophenols, chloroanisoles and chloroveratroles had no or slightly increasing trends. Elevated PCB concentrations were measured in four watercourses. In two areas, PCBs were found to be significantly increasing, in two other cases they showed no trend. A mill producing recycled paper was apparently responsible for an increase of PCBs and DDE in recipient watercourses. Overall decreases were observed for other chlorohydrocarbons except for DDT. Material flows of chlorohydrocarbons were positively correlated with waterflows (Q) in some cases.     

Optimisation of chemical purification conditions for direct application of solid metal salt coagulants: Treatment of peatland-derived diffuse runoff

The drainage of peatland areas for peat extraction,agriculture or bioenergy requires affordable,simple and reliable treatment methods that can purify waters rich in particulates and dissolved organic carbon.This work focused on the optimisation of chemical purification process for the direct dosage of solid metal salt coagulants.It investigated process requirements of solid coagulants and the influence of water quality,temperature and process parameters on their performance.This is the first attempt to provide information on specific process requirements of solid coagulants.Three solid inorganic coagulants were evaluated:aluminium sulphate,ferric sulphate and ferric aluminium sulphate.Pre-dissolved aluminium and ferric sulphate were also tested with the objective of identifying the effects of in-line coagulant dissolution on purification performance.It was determined that the pre-dissolution of the coagulants had a significant effect on coagulant performance and process requirements.Highest purification levels achieved by solid coagulants,even at 30% higher dosages,were generally lower(5%-30%) than those achieved by pre-dissolved coagulants.Furthermore,the mixing requirements of coagulants pre-dissolved prior to addition differed substantially from those of solid coagulants.The pH of the water samples being purified had a major influence on coagulant dosage and purification efficiency.Ferric sulphate(70 mg/L) was found to be the best performing solid coagulant achieving the following load removals:suspended solids(59%-88%),total organic carbon(56%-62%),total phosphorus(87%-90%),phosphate phosphorus(85%-92%) and total nitrogen(33%-44%).The results show that the use of solid coagulants is a viable option for the treatment of peatland-derived runoff water if solid coagulant-specific process requirements,such as mixing and settling time,are considered.     

Organic chlorine compounds in lake sediments. III. Chlorohydrocarbons, free and chemically bound chlorophenols

Chlorohydrocarbons and free and chemically bound chlorophenols, catechols and guaiacols were measured from lake sediments in Central Finland. Chlorohydrocarbons occurred at low backround levels except chlorocymenes from pulp mills and PCBs near the city of Äänekoski, where a local leakage occurrs. Free chlorophenols (hexane extractables) were found in all 18 areas studied, but the bound ones (extracted with strong alkali) only in the pulp mill reciepient lakes where they dominated. Preliminary analyses of chemically bound chlorophenols in high molecular fractions of spent bleach liquors and pulp mill effluents indicated that majority of chlorocatechols and guaiacols are bound already in the factory.     

Recent trends of biocides in pikes of the Lake Päijänne

Pikes were sampled in May 1980 from three areas of the Lake Päijänne, Finland and analyzed for their contents of total mercury, methyl mercury, hexachlorobenzene (HCB), DDE, PCB and chlorophenolic residues. An improved method for methyl mercury determination was applied and 82–84 % methylation of mercury in pikes regardless of area or biological variation was observed. Statistical analysis with previous results from the same areas gave a very significant decreasing trend of mercury levels at all three areas from 1970 to 1980. Future levels of mercury in fish to be consumed as food could be estimated from the trend regression. The very low levels of DDE and PCB showed some increasing trend when the influence of fat contents was eliminated by covariance analysis. General appearance of HCB at sub-ppb level was observed. Also pentachlorophenol occured at 10–70 ppb (fresh weight) levels at all areas, but the other chlorophenols were abundant only at Tiirinselkä which is most contaminated by pulp bleaching effluents.     

Temperature dependent properties of environmentally important synthetic musks

Environmental fate determining physical properties including their temperature dependence for five nitro musks and for seven polycyclic musks were estimated. The properties evaluated were vapor pressure in a solid and liquid state (PS and PL), solubility in water (S), Henry's law coefficient (H = PL/S) and log octanol-water partition coefficient (log KOW). Gas chromatography for starting values of vapor pressure estimation and HPLC experiments at 5-20 degrees C for comparison of the theoretical versus experimental solubilities in water were performed. The values of temperature (T) dependence coefficients (Ai and Bi) in equations: log (Property)i = Ai - Bi/T were determined. Values of properties were compared with literature-based data, and an example of their use in environmental hazard estimation by fate modeling was given.     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

Fate of chlorophenoxyacetic acids in acid soil

The relative persistence of MCPA, 2,4-D and 2,4,5-T in an acid soil was assessed under laboratory conditions with field capacity and flooded level of soil moisture. The experimental soil was incubated for 96 weeks and samples were collected at a specific interval for the determination of the residues by the gas chromatography. The decomposition was faster with MCPA than those of 2,4-D and 2,4,5-T. Soil moisture affected the degradation rate sharply.