[Fine structural changes of the liver cell of rats administered with Kanechlor (chlorinated diphenyl compound)].
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Animals↗
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Results for “Chlorine Compounds”
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Poisoning by volatile compounds. II. Chlorinated aliphatic hydrocarbons.
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Adolescent↗
[Contamination of water by organic halogen compounds and chlorinated pesticides in Liguria].
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Hydrocarbons, Chlorinated↗
Chemiluminescence determination of chlorinated volatile organic compounds by conversion on nanometer TiO2.
A novel method based on conversion of chlorinated volatile organic compounds (CVOCs) to chlorine using a new type of column packed with nanometer TiO2 coupled with chemiluminescence (CL) has been developed for determination of them in workplace air. CVOCs are converted to chlorine by nanometer TiO2 at 220 degrees C. The Cl2 that is produced is selectively enriched on the column and subsequently released from the column at 600 degrees C. The Cl2 that is released is determined using a postcolumn CL detector. The CL intensity was linear with CCl4 in the range of 0.1-380 ppm, and the detection limit was 40 ppb (S/N = 3). Higher sensitivity could be acquired by using a larger volume of enrichment A similar procedure could be used for the determination of other CVOCs. CL intensities of CH2Cl2, CHCl3, and CCl4 at the same concentration increased in the order CH2Cl2 < CHCl3 < CCl4. The method has been successfully applied to the determination of CCl4 in workplace air, where 0.15-150 ppm CCl4 would be detected. The possible mechanism for the long lifetime of the column packed with nanometer TiO2 was tested using Raman spectrometer, X-ray powder diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy. The results showed that the column packed with nanometer TiO2 could be operated in the reversible mode for determination of CVOCs under the present conditions. The method would be potentially applied to the analysis of other chlorinated compounds in environment, such as persistent organic pollutants.
Journal Article↗
Standard-suspension-test: influence of bovine albumin, saline and water of standard hardness on M.E.-values.
Notwithstanding considerable international agreement upon the principle of the quantitative suspension test differences still exist between the main variants of this test, in particular on the diluent to be used in the test mixture. For this reason the influence of the main variables - i.e. bovine albumin (0.03%), NaCl (physiol. saline) and divalent ions (water of standard hardness) - on the activity of the different classes of disinfectants have been investigated. Using so-called borderline concentrations only a small protein effect of 0.03% bovine albumin was found with a phenolic product, quaternary ammonium compounds and aldehydes. A substantial protein effect was observed only with chlorine compounds. The chlorine consumption in the present Dutch Standard Suspension Test is approx. 20 ppm. In tests without a protein load as well as in the presence of 0.03% bovine albumin M.E.-values using saline as the diluent were usually higher than in tests using water of standard hardness (WSH) or distilled water (DW). M.E.-values of quaternary ammonium compounds in WSH were significantly lower than those in DW, presumably due to the antagonizing effect of divalent cations (Mg++ and Ca++). The different views regarding the aim of quantitative suspension tests are discussed. In The Netherlands the opinion prevails that these tests should have at least some relationship with practical conditions. The use of water of standard hardness as a diluent and the incorporation of a slight protein challenge are in agreement with this standpoint.
Disinfectants↗
The behavior of PCDD/Fs, PCBs, chlorobenzenes and chlorophenols in wet scrubbing system of municipal solid waste incinerator.
Though some researchers have already reported polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) concentration in flue gas at inlet and outlet of wet scrubber (WS) in municipal solid waste incinerator (MSWI), there are few investigations about scrubbing water, suspended solid (SS) in scrubbing water and sludge. In order to understand the behavior of PCDD/Fs in WS and to make clear the effect of the residence time of scrubbing water in WS on the PCDD/Fs concentrations in scrubbing water and at the outlet gas of WS, PCDD/Fs, polychlorinated biphenyls (PCBs), chlorobenzenes (CBzs) and chlorophenols (CPs) concentrations in various media around WS were investigated at two MSWIs. PCDD/Fs concentration in flue gas at outlet of WS was higher than that at inlet of WS in both MSWIs. In WS A, it was observed that the homologue profiles changed considerably and the concentration of higher chlorinated compounds such as H7CDD/Fs and O8CDD/F increased remarkably at outlet gas of WS A. Only CPs were transferred from flue gas to scrubbing water in both WSs. As for scrubbing water, a large amount of their chlorinated aromatic compounds was detected in SS particles. According to the results, it was found that not only flue gas conditions but also operational and structural conditions in WS had great influence on minimizing the memory of chlorinated aromatic compounds in WS.
Air Pollutants↗
Fractionation of mutagenic compounds formed during chlorination of humic water.
Mutagenic compounds formed during chlorination of humic water were fractionated by reversed phase high performance liquid chromatography, size exclusion chromatography and thin layer chromatography, in sequence. Following each chromatographic separation the mutagenic compounds were found in one fraction predominantly. A remarkable purification of active compounds was achieved without serious losses of activity, thus enabling further purification and mass spectrometric studies of the main mutagens.
Chlorine↗
Cubic phase gel as a drug delivery system for topical application of 5-ALA, its ester derivatives and m-THPC in photodynamic therapy (PDT).
The ability of the cubic liquid-crystalline phase to incorporate and control the release of drugs of varying size and polar characteristics makes it an interesting candidate as a drug delivery system. In the present study we investigated a new potential application of the cubic phase (monoolein/water; 70:30, w/w) to deliver pro-drugs and a photosensitizer for topical application in photodynamic therapy (PDT). Therefore the pro-drug 5-aminolevulinic acid (5-ALA, a PpIX precursor), its ester derivatives (hexylester, octylester and decylester), and the chlorine compound meso-tetra(hydroxyphenyl)chlorine (m-THPC) were incorporated into the cubic phase gel of monoolein/water and their physicochemical and spectroscopic properties were investigated at 37 degrees C. Drug stability was monitored for short and long periods of time. 5-ALA and its ester derivatives as non-fluorescent probes had their properties studied after chemical reaction leading to a fluorescent derivative. For all the compounds analyzed in this study the spectroscopic properties were clearly defined with potential photodynamic activity in the gel formulation. We are currently evaluating the potential of monoolein/water as a drug delivery system in the treatment of different cutaneous diseases and other PDT applications.
Administration, Topical↗
Nonpoint sources of volatile organic compounds in urban areas-relative importance of land surfaces and air.
Volatile organic compounds (VOCs) commonly detected in urban waters across the United States include gasoline-related compounds (e.g. toluene, xylene) and chlorinated compounds (e.g. chloroform, tetrachloroethane [PCE], trichloroethene [TCE]). Statistical analysis of observational data and results of modeling the partitioning of VOCs between air and water suggest that urban land surfaces are the primary nonpoint source of most VOCs. Urban air is a secondary nonpoint source, but could be an important source of the gasoline oxygenate methyl-tert butyl ether (MTBE). Surface waters in urban areas would most effectively be protected by controlling land-surface sources.
Journal Article↗
Redox potential measurements for determining the disinfecting power of chlorinated water.
The kill of Escherichia coli within 3 min. was studied in chlorine-demand-free water using sodium hypochlorite, monochloramine, dichloramine, halazone, chloramine T, cyanuric acid + sodium hypochlorite and cyanuric acid + monochloramine. The redox potential and the available chlorine were measured. The redox potential was found to be better correlated with the disinfecting property of the water than was the amount of available chlorine. For individual pure chlorine compounds, the measuring of available chlorine showed in general a somewhat better correlation with reduction of the bacteria than the redox potential showed.
Benzoates↗
Reductive dehalogenation of chlorinated dioxins by an anaerobic bacterium.
Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDDs and PCDFs) are among the most notorious environmental pollutants. Some congeners, particularly those with lateral chlorine substitutions at positions 2, 3, 7 and 8, are extremely toxic and carcinogenic to humans. One particularly promising mechanism for the detoxification of PCDDs and PCDFs is microbial reductive dechlorination. So far only a limited number of phylogenetically diverse anaerobic bacteria have been found that couple the reductive dehalogenation of chlorinated compounds--the substitution of a chlorine for a hydrogen atom--to energy conservation and growth in a process called dehalorespiration. Microbial dechlorination of PCDDs occurs in sediments and anaerobic mixed cultures from sediments, but the responsible organisms have not yet been identified or isolated. Here we show the presence of a Dehalococcoides species in four dioxin-dechlorinating enrichment cultures from a freshwater sediment highly contaminated with PCDDs and PCDFs. We also show that the previously described chlorobenzene-dehalorespiring bacterium Dehalococcoides sp. strain CBDB1 (ref. 3) is able to reductively dechlorinate selected dioxin congeners. Reductive dechlorination of 1,2,3,7,8-pentachlorodibenzo-p-dioxin (PeCDD) demonstrates that environmentally significant dioxins are attacked by this bacterium.
Bacteria, Anaerobic↗
The micro- and ultramicro-determination of chlorine in organic compounds.
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Chlorine↗
[Efficiency of oxidant gas generator cells powered by electric or solar energy].
Diseases caused by microbial contaminants in drinking water continue to be a serious problem in countries like Mexico. Chlorination, using chlorine gas or chlorine compounds, is one of the best ways to treat drinking water. However, difficulties in handling chlorine gas and the inefficiency of hypochlorite solution dosing systems--due to sociopolitical, economic, and cultural factors--have reduced the utility of these chlorination procedures, especially in far-flung and inaccessible rural communities. These problems led to the development of appropriate technologies for the disinfection of water by means of the on-site generation of mixed oxidant gases (chlorine and ozone). This system, called MOGGOD, operates through the electrolysis of a common salt solution. Simulated system evaluation using a hydraulic model allowed partial and total costs to be calculated. When powered by electrical energy from the community power grid, the system had an efficiency of 90%, and in 10 hours it was able to generate enough gases to disinfect about 200 m3 of water at a cost of approximately N$8 (US $1.30). When the electrolytic cell was run on energy supplied through a photoelectric cell, the investment costs were higher. A system fed by photovoltaic cells could be justified in isolated communities that lack electricity but have a gravity-fed water distribution system.
Chlorine↗
Helium microwave-induced plasma mass spectrometric detection for reversed-phase high-performance liquid chromatography.
Reversed-phase high-performance liquid chromatography (HPLC) is directly coupled to helium microwave-induced plasma mass spectrometry (He MIP-MS) for the element-selective detection of halogenated organic compounds. Absolute detection limits are approximately 50 pg Br for brominated compounds, 1 pg I for iodinated compounds, and 10 ng Cl for chlorinated compounds. The linear dynamic range for Br- and I-containing compounds is 3-4 orders of magnitude. However, the linear range for chlorinated species is severely limited by high background at m/z = 35. The relative standard deviation for repetitive injections is less than 10%. The helium microwave-induced plasma is operated at moderate powers (300-350 W) and with a total helium consumption of 6-8 L/min. The effect of organic solvents on the background mass spectrum is investigated.
Bromides↗
Characterization of a mutagenic bacterial product in human feces.
Mutagens detectable with the Ames assay have been found in the feces of apparently healthy individuals and the incidence of this mutagenic activity was found to be greater in a population at high risk for colon cancer than in a population at low risk. A compound accounting for the mutagenic activity has been isolated by high performance liquid chromatography. Two closely related forms which behave identically chemically could be resolved. The compound was active on Salmonella typhimurium TA98 and TA100, had a characteristic ultraviolet absorption spectrum with maxima at about 320, 340, and 365 nm, fluoresced green in long wavelength ultraviolet light, and had the same mobility on the thin-layer chromatography as the mutagenic activity in a direct ether extract of feces. The compound was unstable in air but could be stabilized in the presence of butylated hydroxytoluene. Upon oxidation the compound lost its mutagenicity and its ultraviolet absorption spectrum underwent a blue shift so that the absorption maxima were at 295, 310, and 325 nm. Determination of the structure of the mutagen has been difficult since the compound was not volatile and production of a volatile derivative has not been successful. On thin-layer chromatography plates the compound reacted with reagents that detect chlorinated compounds. By thermal energy analysis it did not appear to contain a nitroso group. The compound increased in concentration upon anaerobic incubation of feces at 37 C and this increase was prevented by cold, air, and antimicrobial agents. This suggests to us that the fecal flora produces the compound.
Bacteria↗
Catalytic reduction of chlorinated and recalcitrant compounds in contaminated water.
Catalysis dechlorination of chlorinated organic matter by palladium/iron bimetallic particles represents one of the latest innovative technologies for contaminated soil and groundwater remediation. The reaction of dechlorination is believed to take place on the surface site of the catalyst in a pseudo-first-order mode. The dechlorination rate increases with an increase of the bulk loading of palladium due to the increase of both the surface loading of palladium and the total surface area exposed. The results show that no other intermediates were generated besides Cl-, benzene and chlorobenzene during dechlorination of o-dichlorobenzene.
Catalysis↗
Association between drinking water disinfection and somatic parameters at birth.
We conducted an epidemiological study in Liguria, Italy, on the association between somatic parameters at birth and drinking water disinfection with chlorine dioxide and/or sodium hypochlorite. Over 2 years (1988-1989), 676 births at two public hospitals, one in Genoa (548 cases) and another in Chiavari (128 cases) were examined and data regarding both mother and child were obtained from hospital records. Results indicate a higher frequency of small body length (< or = 49.5 cm) and small cranial circumference (< or = 35 cm) in infants born to mothers who drank water treated with chlorine compounds. In particular, the statistical analysis (by simultaneous variance analysis and Scheffé test) indicated that there may be an association between infants with smaller body length and mothers who drank water treated with chlorine dioxide [adjusted odds radio (OR) = 2.0; 95% CI = 1.2-3.3] or sodium hypoclorite (adjusted OR = 2.3; 95% CI = 1.3-4.2) and between infants with smaller cranial circumference and mothers who drank water treated with chlorine dioxide (adjusted OR = 2.2; 95% CI = 1.4-3.9) or sodium hypochlorite (adjusted OR = 3.5; 95% CI = 2.1-8.5). The presence of neonatal jaundice is almost twice as likely (adjusted OR = 1.7; 95% CI = 1.1-3.1) in infants whose mothers drank water treated with chlorine dioxide.
Adult↗
[Anesthetic gases, the ozone layer and the greenhouse effect. How harmful are the anesthetic emissions for the global environment?].
During the last decade, world society has acknowledged the harmful effects on the environment of the greenhouse effect and of depletion of the ozone layer, caused by industrial emissions of man-made compounds. Ozone depletion is caused mainly by chlorine compounds or nitrogen oxides released by degradation in the stratosphere. The greenhouse effect is caused by increased trapping of terrestrial heat radiation. Degradation of the anaesthetic vapours halothane, enflurane and isoflurane releases chlorine, and nitrous oxide degradation produces reactive nitrogen oxides. Nitrous oxide in particular, but also the vapours, absorb terrestrial radiation. The total discharge of anaesthetic vapours contributes to less than 0.01% of the total atmospheric chlorine load, and the annual Norwegian release of approximately two tons accounts for 0.2% of the world total. It is estimated that the total amount of nitrous oxide released from anaesthetics accounts for 0.05% of the greenhouse effect, while annual Norwegian emissions of nitrous oxide (less than 160 tons) comprise 0.2-0.4% of world total. Because of their favourable clinical properties and their modest contribution to ozone depletion and the greenhouse effect, medical use of inhalational anaesthetic agents should not be banned. However, low flow anaesthetic techniques should be employed, in order to reduce their negative impacts on the atmosphere.
Air Pollutants↗