Assessment of environmental tobacco smoke exposure: urinary cotinine concentrations in children are strongly associated with the house dust concentrations of nicotine at home

In the present study the possibility of using nicotine in house dust as an index of environmental tobacco smoke (ETS) exposure was evaluated in an environmental investigation of 23 children with asthma. A standardized procedure for house dust sampling of nicotine with a filter holder connected to a vacuum cleaner, for a defined time and area was developed (F-nicotine). Also, house dust sampling was carried out from the vacuum cleaner bags of the homes (VC-nicotine). There was a larger variation in VC-nicotine (13-655, median 66 microg/g) compared with F-nicotine (15-393 median 156 microg/g). There were statistically significant associations between an inquiry data based ETS exposure index on the one hand, and urinary cotinine concentrations in children (U-cotinine), F-nicotine and VC-nicotine of their homes, on the other. The strong correlation between U-cotinine and F-nicotine (rs = 0.93; P < 0.0001) indicates that the new standardized house dust sampling method should be useful in ETS exposure assessment. However, further validation by a larger sample size with repeated measurements in the same homes is needed.     

Seasonality of diffusive exchange of polychlorinated biphenyls and hexachlorobenzene across the air-sea interface of Kaohsiung Harbor, Taiwan

Gaseous and dissolved concentrations of polychlorinated biphenyls (PCBs) and hexachlorobenzene (HCB) were measured in the ambient air and water of Kaohsiung Harbor lagoon, Taiwan, from December 2003 to January 2005. During the rainy season (April to September), gaseous PCB and HCB concentrations were low due to both scavenging by precipitation and dilution by prevailing southwesterly winds blown from the atmosphere of the South China Sea. In contrast, trace precipitation and prevailing northeasterly winds during the dry season (October to March) resulted in higher gaseous PCB and HCB concentrations. Instantaneous air-water exchange fluxes of PCB homologues and HCB were calculated from 22 pairs of air and water samples from Kaohsiung Harbor lagoon. All net fluxes of PCB homologues and HCB in this study are from water to air (net volatilization). The highest net volatile flux observed was + 172 ng m^− 2 day^− 1 (dichlorobiphenyls) in December, 2003 due to the high wind speed and high dissolved concentration. The PCB homologues and HCB fluxes were significantly governed by dissolved concentrations in Kaohsiung Harbor lagoon. For low molecular weight PCBs (LMW PCBs), their fluxes were also significantly correlated with wind speed. The net PCB and HCB fluxes suggest that the annual sums of 69 PCBs and HCB measured in this study were mainly volatile (57.4 × 10³ and 28.3 × 10³ ng m^− 2 yr^− 1, respectively) and estimated yearly, 1.5 kg and 0.76 kg of PCBs and HCB were emitted from the harbor lagoon surface waters to the ambient atmosphere. The average tPCB flux in this study was about one-tenth of tPCB fluxes seen in New York Harbor and in the Delaware River, which are reported to be greatly impacted by PCBs.     

Back-analysis of rock mass strength parameters using AE monitoring data

Most back-analyses in geotechnical engineering are based on methods that utilize field displacement monitoring data. In the present study, a novel method is developed to back-calculate rock mass strength parameters from AE (acoustic emission) monitoring data in combination with FEM stress analysis. The method is based on the important concept of generalized AE initiation threshold of rock masses, established from comprehensive data analysis of laboratory test and underground monitoring programs using AE and microseismic (MS) techniques. An easy-to-use Wizard is developed in Microsoft Excel™ to assist site engineers to perform the back-analysis. The efficient solver in Excel is utilized to reach the optimization solution of an objective function with constraints. The Wizard allows the user to complete the analysis process in an interactive fashion. One example is given to demonstrate the back-analysis process using AE monitoring data recorded from a cavern site. The rock mass strength parameters identified from this approach compare well with field test data, suggesting that the tool can be used effectively to back-calculate rock mass strength parameters from AE monitoring data.     

Kinetics and mechanisms of DMSO (dimethylsulfoxide) degradation by UV/H(2)O(2) process

The objective of this study was to elucidate the degradation pathways of dimethylsulfoxide (DMSO) during its mineralization caused by UV/H(2)O(2) treatment. In order to accomplish this, we measured the concentration time-profiles of DMSO and its degradation intermediates during the UV/H(2)O(2) treatment. In addition, we proposed a kinetic model that could account for the degradation pathways of DMSO during its UV/H(2)O(2) treatment. The results show that the degradation of DMSO by the UV/H(2)O(2) treatment can be classified into two major pathways, and this is supported by both the analysis of the intermediates and total organic carbon (TOC) measurements. Firstly, DMSO was degraded into sulfate (SO(4)(2-)) through the formation of methansulfinate (CH(3)SO(2)(-)) and methansulfonate (CH(3)SO(3)(-)) as sulfur-containing intermediates. One of the two carbon constituents of DMSO was highly resistant to mineralization, due to the formation of methansulfonate, which reacted very slowly with (.-)OH k = 0.8 x 10(7) M(-1)s(-1)). Secondly, the other carbon constituent of DMSO was relatively easily mineralized through the formation of formaldehyde (HCHO) and formate (HCO(2)(-)) as non-sulfur-containing intermediates. The kinetic model proposed in this study for the degradation of DMSO by (.-)OH in the UV/H(2)O(2) process was able to successfully predict the patterns of concentration time-profiles of all components during the UV/H(2)O(2) treatment of DMSO.     

Characteristics of emissions of air pollutants from burning of incense in temples, Hong Kong

Field investigations of target air pollutants at two of the most famous temples in Hong Kong were conducted. The air pollution problems in these two temples during peak and non-peak periods were characterized. The target air pollutants included particulate matters (PM(10), PM(2.5)), volatile organic compounds (VOCs), carbonyl compounds, carbon monoxide (CO), nitrogen oxides (NO(x)), methane (CH(4)), non-methane hydrocarbons (NMHC), organic carbon (OC), elemental carbon (EC), and inorganic ions (Cl(-), NO(3)(-), SO(4)(2-), Na(+), NH(4)(+), and K(+)). The pollutant levels of the two temples during peak period were shown to be significantly higher than those during non-peak period. The highest average CO level was obtained at Temple 1 during peak period, which exceeded IAQO 8-h Good Class criteria. In general, the average PM(2.5)/PM(10) ratios were approximately 82%. The results revealed that the fine particulates (PM(2.5)) constituted the majority of suspended particulates at both temples. It was noted that formaldehyde was the most abundant carbonyl compounds, followed by acetaldehyde. At Temple 1 during peak period, the average benzene concentration exceeded almost 8 times more than Indoor Air Quality Objectives for Office Buildings and Public Places (IAQO) [HKEPD, 2003. Guidance notes for the management of indoor air quality in offices and public places. Indoor air quality management group, The Government of the Hong Kong Special Administrative Region.] Good Class criteria. The average OC/EC ratios ranged from 2.6 to 17 in PM(10) and from 4.2 to 18 in PM(2.5) at two temples, which suggested that OC measured in these two temple areas may be due to both direct emission from incense burning and secondary formation by chemical reactions. The total mass of inorganic ions, organic carbon, and elemental carbon accounted for about 71% in PM(2.5) and 72% in PM(10).     

Fate of trace organics during rapid infiltration of primary wastewater at Fort Devens, Massachusetts

Transport and fate of trace organics were studied during rapid infiltration of primary wastewater at a land application facility in Fort Devens, Massachusetts. A preliminary sampling trip was made to compare trace organic concentrations in the infiltrating wastewater and in ground water samples from three monitoring wells around the site. Trace organic concentrations were reduced by the rapid infiltration process. However, significant concentrations of specific compounds could be detected in ground water down-gradient of the site.Therefore, a field study was undertaken to determine the primary region where trace organics were removed in the system. Teflon monitoring wells were installed at a depth of 1.2 m in one of the basins at the site prior to flooding. Flooding was initiated and samples of the raw wastewater, the wastewater entering the basin, the infiltrate at 1.2-m depth and the ground water down-gradient of the site were analyzed for six compounds selected for the study.Results from replicate samples during the 6-day flooding period demonstrated that most of the removal for the six compounds occurred in the top meter of the soil, although concentrations of each compound increased substantially in the basin infiltrate from two of the sample points after the fourth day of flooding. No removal of p-dichlorobenzene, p-(I,1,3,3-tetramethylbutyl)phenol and 2-(methylthio)benzothiazole was apparent in the aquifer itself, as indicated by relatively high concentrations of these compounds in the contaminated monitoring well down-gradient of the site.These data indicate that trace organic concentrations in primary effluent can be reduced by rapid infiltration and that most of the removal occurs in the top meter of the soil during the early phase of the flooding cycle. This removal capability can rapidly diminish, however, and result in ground water contamination by trace organics above background levels.     

Études des transformations des formes du carbone, azote, phosphore, soufre et des principaux éléments minéraux au cours de la mesure de la demande totale en oxygene—III transformation des formes du soufre

Previous experiments carried out with the laboratory TOD meter Ionics 225 of the DOW Chèmical made it possible (after a high temperature catalytic action) to characterize the stable forms of organic and inorganic carbon and nitrogen (NH₄⁺, NO₂⁻, NO₃⁻), and the principal cations (Na⁺, K⁺, Ca²⁺, Mg²⁺) in the course of the total oxygen demand (TOD) measurement.The object of this study is firstly to compare the oxidation capability of different techniques of organic pollution (particularly the COD and TOD) in relation to the constituent elements of the organic matter C, N, P, S, and to calculate the possible interferences of the inorganic compounds at the time of TOD test.These investigations warrant the application of this technique to measure the amount of organic pollution in relatively mineralized conditions (Industrial wastewater, sea-water…). The present publication is concerned more with the study of the transformation of the organic and inorganic sulphur forms (S²⁻, SO₃²⁻. SO₄²⁻) in the course of the TOD measurement.The study of the oxidizability of the organic sulphur compound type C_xH_yO_zS, made it possible to establish a specific relation with a ratio of 0–50 mg of organic sulphur l⁻¹, between the oxygen demand of this element [TOD (S)] and its concentration (TOD (S) = 0.97 [S]).These tests showed a partial oxidation of the sulphur to SO₂ and SO₃ as the literature claimed. On the other hand, the oxidation of the same compounds during the COD tests varies greatly and although it is not possible to establish a correlation between these two measurements, as applies in the case of organic nitrogen, nevertheless these experiments showed a greater reliability of the TOD compared with the COD in the oxidation of organic matter in general. We then carried out experiments on the different mineral forms of sulphur in order to distinguish the possible effects and to recommend simple improvements.A relative study on sulphate ions had been carried out with standard solutions which have the same TOD (the basic TOD is obtained using potassium phthalate acid) and the same increasing concentration of the salt M₂SO₄ type. The experiments showed that the basic TOD decreases when the concentration of sulphate ions is increased (Fig. 3). Therefore, the interference is negative and taking into consideration the specific oxygen demand of the cation, we can propose an evaluation of this interference (ΔTOD (SO₄²⁻) = 0.203 [SO₄²⁻]). The same experiments have been conducted with a salt of M₂SO₃ type and similar results obtained (Fig. 5).The specific interference of the sulphite ion is negative and can be estimated by the following equation (ΔTOD (SO₃²⁻) = 0.132 [SO₃²⁻]). In both cases, we have to note that the transformation of these inorganic anions occurs between those relative to the theoretical dissociation reaction corresponding to the appearance of the oxide SO₂ and SO₃. For sulphurous on the contrary, the interference is positive and therefore corresponds to an extra oxygen demand (Fig. 8).The experiments were conducted directly with the M₂S salts (M representing K or Na) in aqueous solution.The evaluation of this interference had been made in the consideration of two concentration ranges of the sulphurous ions (0–35 mg S²⁻ l⁻¹): TOD (S²⁻) = 0.4 [S²⁻] and (35–100 mg S²⁻ l⁻¹): TOD (S²⁻) = 1.2 [S²⁻] − 30.Therefore this study confirms a better oxidation of the organic matter by TOD test in comparison with COD test.But sulphate and sulfite have a negative interference in the TOD measurement, whereas sulphurous is positive.The evaluation model of these interferences allows a correction to be made of the TOD value or to verify TOD measurement of organic pollution obtained by this technique.     

Concentration du virus de l'hepatite a sur des membranes de celluloseHepatitis a virus concentration on cellulose membranes

Viral hepatitis type A is the most prevalent waterborne disease in U.S.A. and the number of cases has been increasing in recent years (Melnick et al., 1978). Till now, few works were performed on Hepatitis A Virus (HAV) concentration in water (Hejkal et al., 1982, Elkana et al., 1983). In this paper the filter adsorption-elution method, widely used with other viruses (Wallis and Melnick, 1967; Fields et Metcalf, 1975; Smith and Gerba, 1982), was selected to concentrate HAV from experimentally-contaminated distilled water. Filtration was performed through two cellulose membranes (RAWP 04700 and HAWP 04700 Millipore). Eluate or filtrate viruses were precipitated by polyethylene glycol 6000. HAV is detected by solid phase radioimmunoassay according to a previously described method (Deloince et al., 1982). Figure 1 shows the results of adsorbing HAV at different pH levels. Analysis of variance pointed out that, for the pH levels between 3 and 4, the differences were not significant (P = 0.05). Table 1 shows the effects of pH and number of passages of 3% beef extract or 0.2 M glycin buffer on HAV elution. For both eluents the differences in function of pH levels and number of passages of eluent through the membrane were not significant (variance analysis P = 0.05). On the other hand, the comparison between the two eluents pointed out the higher efficiency of beef extract (t-test, P = 0.001). After this procedure, HAV replication occurred in human hepatocarcinoma cells PLC/PRF/5 (Fig. 2) inoculated according to a previously described method (Crance et al., 1983). As poliovirus (Sobsey et al., 1973), HAV adsorption is the most efficient at acid pH levels. Between pH 4.5 and 5, the remarkable adsorption decrease might be related to the inversion of the HAV electrostatic charges sign, i.e. to the occurrence of an isoelectric point. The HAV elution is different from the poliovirus one, the efficiency of which increased with pH (Wallis et al., 1972) and eluent passage numbers (Farrah et al., 1976). That might suggest that from pH 7.5, both the HAV particles and membranes have negative charges which give enough repulsive forces to allow a good elution efficiency. Improvement of HAV elution efficiency by beef extract is similar to a result obtained with poliovirus by Landry et al. (1978). This effect might be explained by the proteinous material presence in beef extract. HAV replication in cell cultures shows the biological properties preservation after this procedure.     

Radiological and legal aspects of energy production by burning peat

Peat burning is planned as one of the future sources for heat production in Sweden. At the end of 1983, results of some investigations on peat ashes indicated enhanced uranium contents. Recent measurements on peat areas have shown external gamma radiation dose rates up to 10 microGy/h and samples of dried peat have shown a radium content up to 3.3·10⁵ Bq/kg. In order to estimate the radiological impact of the use of peat as an energy source, the National Institute of Radiation Protection in Sweden has initiated some research projects. Some preliminary results will be discussed against the background of possible need for limits and protection measures. In some cases the high uranium content of the ash makes it necessary, with present regulations, to have special licenses. Both the radiological impact and legal aspects will be discussed.     

A microbial sensor for BOD

A microbial amperometric sensor for the determination of the biochemical oxygen demand (BOD) determination using Trichosporon cutaneum cells immobilized in polyvinylalcohol has been developed. This sensor allowed BOD measurement with very short response times (< 30 s), an operation stability of 48 days and a serial coefficient of variation of ±3.3% when a sample solution containing 22 mg l⁻¹ BOD was employed. A linear range was obtained up to 100 mg l⁻¹ BOD using a glucose/glutamic acid standard. The sensitivity and specificity was increased by incubation of the BOD sensor with the respective wastewater. Comparable results were obtained for BOD values estimated by the biosensor and those determined by the 5-day method.