USEPA/paper industry cooperative dioxin study: The 104 mill study

This paper summarizes the distribution of concentrations of 2378 substituted dibenzo-p-dioxins and dibenzofurans in bleached kraft and sulfite mill pulps, wastewater sludges, and treated effluents in the U.S. in mid-1988.     

Influence of real and synthetic municipal solid waste leachates on consolidation and shear strength behaviour of bentonites

Environmental Science and Pollution Research - For safe disposal of wastes in landfills, compacted bentonite is recommended as bottom liners due to their significant cation exchange (CEC) and...     

Ferrate(VI): green chemistry oxidant for degradation of cationic surfactant

Iron in its familiar form exists in the +2 and +3 oxidation states, however, higher oxidation state of iron +6, ferrate(VI) (Fe(VI)O(4)(2-)) can be obtained. The high oxidation power of ferrate(VI) can be utilized in developing cleaner ("greener") technology for remediation processes. This paper demonstrates the unique property of ferrate(VI) to degrade almost completely the cationic surfactant, cetylpyridinium chloride (C(5)H(5)N(+)(CH(2))(15)CH(3).H(2)O Cl(-), CPC). The Rate law for the oxidation of CPC by ferrate(VI) at pH 9.2 was found to be: -d[Fe(VI)]/dt = k[Fe(VI)][CPC](2). Ferrate(VI) oxidizes CPC within minutes and molar consumption of ferrate(VI) was nearly equal to the oxidized CPC. The decrease in total organic carbon (TOC) from CPC was more than 95%; suggesting mineralization of CPC to carbon dioxide. Ammonium ion was the other product of the oxidation. This is the first report in which Fe(VI)O(4)(2-) ion opens the pyridine ring and mineralizes the aliphatic chain of the organic molecule giving inorganic ions.     

Bromate analysis in groundwater and wastewater samples

Bromate (BrO(3)(-)) is a disinfection by-product formed during ozonation of potable water supplies containing bromide (Br(-)). Bromate has been classed by the World Health Organisation as a 'possible human carcinogen', leading to implementation of 10-25 microg L(-1)(as BrO(3)(-)) drinking water limits in legislative areas including the United States and European Union. Techniques have been developed for bromate analysis at and below regulatory limits, with Ion Chromatography (IC) coupled with conductivity detection (IC-CD), post-column reaction and ultra-violet (UV) detection (IC-PCR), or inductively coupled plasma-mass spectrometry detection (IC-ICPMS) in widespread use. The recent discovery of bromate groundwater contamination in a UK aquifer has led to a requirement for analysis of bromate in a groundwater matrix, for environmental monitoring and development of remediation strategies. The possibility of bromate-contaminated water discharge into sewage treatment processes, whether accidental or as a pump-and-treat strategy, also required bromate analysis of wastewater sources. This paper summarises techniques currently available for trace bromate analysis in potable water systems and details studies to identify a methodology for routine analysis of groundwater and wastewater samples. Strategies compared were high performance liquid chromatography (HPLC) with direct UV or PCR/UV detection, IC-CD, IC-PCR, and a simple spectrophotometric technique. IC-CD was the most cost-effective solution for simultaneous analysis of bromate and bromide within groundwater samples, having a 5 microg L(-1) detection limit of both anions with limited interference from closely-eluting species. Wastewater samples were successfully analysed for bromate only using HPLC with PCR/UV detection, with detection limits below 20 microg L(-1)(as BrO(3)(-)) and low interference. HPLC with direct UV detection was unsuitable for bromate analysis within the concentration range 50-5000 microg L(-1) which was required for this project, but column choice was shown to be a major factor in determining limits of detection. Spectrophotometry could not reproducibly determine bromate concentration, although the technique showed promise as a quick field method for high-level groundwater bromate analysis.     

Developments in forward osmosis and membrane distillation for desalination of waters

Membrane technology has become a common separation technology over the past decennia. Membranes are used more and more for the production of drinkable water from groundwater, surface water and wastewater. Membranes are now competitive versus conventional techniques. Desalination is predominantly used to eradicate the problem of water scarcity. The sustainability of all desalination processes depends mainly on the reduction of energy costs (production cost) and the increase in water recovery. Forward osmosis and membrane distillation are emerging technologies for sustainable desalination. Here we review membrane processes of forward osmosis and membrane distillation and the advancements in membrane material and modules. We also discuss the capability of membrane distillation in treating highly concentrated aqueous solutions derived from other desalination processes. Furthermore, the advancements in fabrication of high-performance membrane is reviewed and the performance of different membranes and optimization of membrane distillation process are summarized.     

High CO<Subscript>2</Subscript> absorption of <Emphasis Type="Italic">O</Emphasis>-carboxymethylchitosan synthesised from chitosan

CO₂ absorption by liquid-containing amines to form carbamate and bicarbonates is an effective method of CO₂ mitigation from industrial exhausts, but this process is expensive and requires large quantities of amines. Here we modified chitosan, a naturally occurring biopolymer containing NH₂ functions, to use it for CO₂ absorption in aqueous media. Chitosan was dispersed in 40% aqueous NaOH solution then treated with monochloroacetic acid dissolved in isopropanol, to yield O-carboxymethylchitosan. Results show that the CO₂ absorption capacity of O-carboxymethylchitosan is 0.508 g/g, which is higher than the capacity of conventional amines such as 1-aminoamine, 2-methylpropanolamine and methyldiethanol amine, but lower than the capacity of monoethanolamine. A cyclic study showed that O-carboxymethylchitosan is a stable component for CO₂ absorption and regeneration.     

Estimating Population Size in a Continuous-time Removal Experiment with a Known Sub-population Size Ratio

We study a continuous-time removal model for estimating the population size for a population in which a sub-population size ratio is known. The maximum likelihood estimate and the optimal martingale estimate of the population size are obtained; these are shown to be equivalent. A comparison between the proposed estimator and the maximum likelihood estimate which ignores the information on the known size ratio is made, using a simulation study. The asymptotic variances of these two estimators are also obtained, and a comparison between them is made. The sensitivity of mis-specification of the known size ratio is examined. We also apply the corresponding discrete-time model to the proposed continuous-time setting, and study the efficiency of the corresponding discrete-time type estimator relative to the proposed estimator.     

Reduction of DNA mismatch repair protein expression in airway epithelial cells of premenopausal women chronically exposed to biomass smoke

Biomass burning is a major source of indoor air pollution in rural India. This study examined whether chronic inhalation of biomass smoke causes change in the DNA mismatch repair (MMR) pathway in the airway cells. For this, airway cells exfoliated in sputum were collected from 72 premenopausal nonsmoking rural women (median age 34 years) who cooked with biomass (wood, dung, crop residues) and 68 control women who cooked with cleaner fuel liquefied petroleum gas (LPG) for the past 5 years or more. The levels of particulate matters with diameters less than 10 and 2.5 μm (PM₁₀ and PM_2.5) in indoor air were measured by real-time aerosol monitor. Benzene exposure was monitored by measuring trans,trans-muconic acid (t,t-MA) in urine by high-performance liquid chromatography with ultraviolet detector. Generation of reactive oxygen species (ROS) and level of superoxide dismutase (SOD) in airway cells were measured by flow cytometry and spectrophotometry, respectively. Immunocytochemical assay revealed lower percentage of airway epithelial cells expressing MMR proteins mutL homolog 1 (MLH1) and mutS homolog 2 (MSH2) in biomass-using women compared to LPG-using controls. Women who cooked with biomass had 6.7 times higher level of urinary t,t-MA, twofold increase in ROS generation, and 31 % depletion of SOD. Indoor air of biomass-using households had three times more particulate matters than that of controls. ROS, urinary t,t-MA, and particulate pollution in biomass-using kitchen had negative correlation, while SOD showed positive correlation with MSH2 and MLH1 expression. It appears that chronic exposure to biomass smoke reduces MMR response in airway epithelial cells, and oxidative stress plays an important role in the process.     

Humic acids as reducing agents: the involvement of quinoid moieties in arsenate reduction

Purpose  

Dissolved humic acids abiotically reduced inorganic arsenic to varying degrees, depending on solution pH, ionic strength, and type of humate used. The functionalities of dissolved organic matter responsible for these redox reactions remained in question, but quinoid moieties undoubtedly played an important role. It is not fully understood whether the quinoids are solely responsible for arsenate reduction, and what the kinetics of the relevant processes are.