Heavy metal binding by the polymeric organic fractions of sewage sludges

Organic complexes in sewage sludge play an important role in the speciation and transformation of metals into potentially more toxic and bioavailable forms. Two organic fractions, bacterial extracellular polymer and fulvic acid, were extracted from mixed liquor and digested sewage sludge by methods established as the most appropriate. The homogeneity of the extracts was verified using gel permeation chromatography. Conditional stability constants and complexation capacities of the organic fractions from the sludges with copper, cadmium, nickel and zinc have been determined using equilibrium dialysis titration. Organic fractions extracted from digested sludge demonstrated a greater capacity to complex metals over mixed liquor extracts. Copper formed stronger complexes than nickel with the mixed liquor biomass and cadmium exhibited the greatest affinity for digested sludge organic matter.     

Analysis of volatile organic compounds in water,waste water and an industrial effluent

Three analytical methods have been evaluated for the determination of volatile organic compounds in water. These techniques have been subsequently applied to the study of a trade effluent discharge problem.     

Acclimatisation to nitrilotriacetic and in the activated sludge process

The period of acclimatisation prior to the biodegradation of nitrilotriacetic acid in an activated sludge pilot plant was studied in a series of experiments. The effects of low and high influent heavy metals concentrations upon acclimatisation are reported.     

Spatial distribution of mercury in the sediments and riparian environment of the River Yare, Norfolk, UK

Concentrations of total mercury (T-Hg) were determined in sediments and riparian (bankside) soils from the River Yare, Norfolk, UK to assess the current extent of contamination arising from a historical point source discharge. The results demonstrate that the spatial distribution pattern in surficial sediments and soils follows that of a distinct pollution plume with an initial increase 2-3 km downstream from the point source discharge at Whitlingham Sewage Treatment Works (STW) outfall. Average T-Hg concentrations in the surficial sediments ranged from 0.1 to 8.13 mg kg(-1); bankside soil concentrations ranged from 0.1 to 2.63 mg kg(-1). There has been a decline in downstream background sediment concentrations of Hg over time. This is likely to be the result of burial by fresh relatively uncontaminated sediments and possibly in the lower reach as a consequence of the influence of the freshwater-saline interface occurring near Cantley. Channel morphology was also shown to be an important factor in determining the large variations of Hg concentrations between sample points within transects. The predominant source of Hg to the soils appears to be due to dredging and the deposition of sediments during flooding.     

Depositional profiles and relationships between organotin compounds in freshwater and estuarine sediment cores

A range of organotin compounds including tributyltin (TBT), dibutyltin (DBT) and monobutyltin (MBT) were measured in sediment cores collected from contaminated freshwater and estuarine sites in Essex and Suffolk, U.K. Butyltin compounds were found in significant quantities at depths of up to 60 cm within the sediments of marina and boatyard complexes with TBT concentrations ranging from <3 ng g^–1 (the detection limit) to >3000 ng g^–1. In general sediment TBT concentrations decreased with depth, but maximum enrichment tended to occur just below the surface. It was evident from these core profiles that the accumulation of organotins in surface deposits was on the decline and coincided approximately, with the implementation in 1987 of the UK retail ban on the sale of TBT based antifouling paints for application on vessels <25 m in length. The degradation rate for TBT in sediments was found to exhibit first order kinetics with half lives ranging from 0.9–5.2 years between different sites. Estimated degradation rates have also been determined for DBT and MBT. These ranged from 1.5–3.0 years for DBT and 1.8–3.7 years for MBT.     

Factors controlling the accumulation of metals within fluvial systems

The magnitude and distribution of European Community (EC) regulated List I and List II metals and metalloids have been investigated in two lowland river systems in East Anglia, U.K. A combination of sediment and water quality data identified municipal sewage treatment work discharges as the main metal input sources to the river systems and identified two main areas of metal contamination: the Pix Brook, downstream of Letchworth STW on the River Ivel, and a 14 km enrichment zone adjacent to Whitlingham STW on the River Yare. The basement geology, flow dynamics, distance from point sources and sediment type were identified as important controls upon the magnitude and spatial distribution of metal contaminants.     

Risk assessment of antagonistic hazards

This paper considers the risk to major hazard plant from terrorists deliberately causing catastrophic industrial accidents. The United States of America Department of Justice [Assessment of the increased risk of terrorist or other criminal activity associated with posting off-site consequence analysis information on the internet, 2000] reports that “breaching a containment vessel of an industrial facility with an explosive or otherwise causing a chemical release may appear relatively simple to…a terrorist”. They concluded that the risk of such action is “real and credible”.

Analysis of terrorism is often hampered by its being described as ‘irrational’; one corollary would be that it is unpredictable. However, terrorism may usefully be treated as a rational behaviour and in doing so it becomes possible to assess the risks it causes.

We analyse the vulnerability of major hazard plant to terrorist attack and identify nine factors (access, security, visibility, opacity, secondary hazard, robustness, law enforcement response, victim profile, and political value) that might be used as a starting point for more formal risk assessment and management.     

Assessment of Human Exposure to Ambient Particulate Matter

ABSTRACT

Recent epidemiological studies have consistently shown that the acute mortality effects of high concentrations of ambient particulate matter (PM), documented in historic air pollution episodes, may also be occurring at the low to moderate concentrations of ambient PM found in modern urban areas. In London in December 1952, the unexpected deaths due to PM exposure could be identified and counted as integers by the coroners. In modern times, the PM-related deaths cannot be as readily identified, and they can only be inferred as fractional average daily increases in mortality rates using sophisticated statistical filtering and analyses of the air quality and mortality data. The causality of the relationship between exposure to ambient PM and acute mortality at these lower modern PM concentrations has been questioned because of a perception that there is little significant correlation in time between the ambient PM concentrations and measured personal exposure to PM from all sources (ambient PM plus indoor-generated PM).

This article shows that the critical factor supporting the plausibility of a linear PM mortality relationship is the expected high correlation in time of people's exposure to PM of ambient origin with measured ambient PM concentrations, as used in the epidemiological time series studies. The presence of indoor and personal sources of PM masks this underlying relationship, leading to confusion in the scientific literature about the strong underlying temporal relationship between personal exposure to PM of ambient origin and ambient PM concentration. The authors show that the sources of PM of non-ambient origin operate independently of the ambient PM concentrations, so that the mortality effect of non-ambient PM, if any, must be independent of the effects of the ambient PM exposures.     

The success of elutriate tests in extended prediction of water quality after a dredging operation under freshwater and saline conditions

Dredging simulation by elutriate tests accurately predicted concentrations of Hg, Cu, Mn and Fe released to the water column from contaminated sediment to within 1 order of magnitude. Hg and Cu concentrations increased by up to 7-fold after dredging, but declined to background concentrations within 48 h. Maximum loadings of Hg and Cu coincided with Fe and total organic carbon (TOC) water column concentrations, suggesting Hg and Cu are adsorbed onto particulates of Fe oxides and organic material. Seasonal changes in redox potential and temperature did not significantly affect metal release from sediments. Saline water did not cause significant increases in contaminant release from sediments to the water column over that observed for freshwater. Water quality standards of 1 µg l^–1 Hg and 28 µg l^–1 Cu as annual averages were not breached by dredging operations. Long-term effects of dredging on Hg and Cu availability, due to deposition of contaminated material as surficial sediments, is, however, of concern.