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[The use of summary indices for assessing organochlorine compounds in water].

Adsorption of chlorinated organic compounds (COC) on activated charcoal and determination of ionic chlorine by gas chromatography were used for assessment of water pollution by COC. Content of adsorbing COC was the following (micrograms CI-/l): in river water 10-470, in drinking water 10-1180, in underground water 90-150; content of volatile COC was (micrograms CI-/l): in drinking water 2-117, in underground water 14-16.

Chlorine↗

Carcinogenicity of chlorinated methane and ethane compounds administered in drinking water to mice.

The chlorinated hydrocarbons chloroform (CHCl3), 1,1-dichlorethane (1,1-DCE) and 1,2-dichloroethane (1,2-DCE) have been detected in finished drinking water. When administered to B6C3F1 mice by gavage in corn oil, these compounds have been shown to induce hepatic tumors. The present study examines the effect on liver tumor incidence of continuous treatment of CHCl3 (600 mg/L and 1800 mg/L), 1,1-DCE (835 mg/L and 2500 mg/L), and 1,2-DCE (835 mg/L and 2500 mg/L) administered in drinking water to male B6C3F1 mice using a two-stage (initiation/promotion) treatment protocol. Seventy 4-week-old male B6C3F1 mice constituted each treatment group. Of these mice, 35 were initiated by treatment with diethylnitrosamine (DENA) (10 mg/L) in the drinking water for 4 weeks. The remaining 35 received deionized drinking water. Each group was subsequently treated with one of two concentrations of CHCl3, 1,1-DCE, or 1,2-DCE in drinking water for 52 weeks. An additional group received phenobarbital (PB) (500 mg/L) and served as the positive control for liver tumor promotion. Mice were sampled after 24 weeks (10 mice) and 52 weeks (25 mice). At sampling, liver and lung tumors were detected. None of the compounds increased the number or incidence of lung or liver tumors by themselves. PB promoted liver tumor formation (but not lung tumors) in the DENA-initiated mice. 1,1-DCE and 1,2-DCE did not affect the incidence or number of liver or lung tumors in the DENA-initiated animals. CHCl3, however, inhibited liver and lung tumorigenesis in the DENA-initiated mice.

Animals↗

Disinfection by-products in the chlorination of organic nitrogen compounds: by-products from kynurenine.

Volatile by-products in the chlorination of 3 humic acids as naturally-occurring substances and 37 nitrogen compounds normally found in excrement were analyzed, and as result kynurenine, a urinary metabolite of tryptophan was found a suitable model compound for dichloroacetonitrile-forming precursors. Possible pathways for the formation of chlorination by-products from kynurenine were also proposed by identification and kinetic properties of by-products decomposed further from each product.

Chromatography, Gas↗

Complete degradation of polychlorinated hydrocarbons by a two-stage biofilm reactor.

A two-stage anaerobic-aerobic biofilm reactor successfully degraded a mixture of chlorinated organic compounds to water-soluble metabolic intermediates and carbon dioxide. Reductive dechlorination of hexachlorobenzene (HCB), tetrachloroethylene (PCE), and chloroform (CF) occurred on all tested primary carbon sources such as glucose, methanol, and acetate. However, the extent of dechlorination was maximum when the anaerobic biofilm column was fed acetate as a primary carbon source. HCB, PCE, and CF were dechlorinated to the levels of tri- and dichlorinated products (99, 80, and 32%, respectively) with acetate in the feed. This is important, since these less-chlorinated compounds can be metabolized by the aerobic biofilm. The effluent from the anaerobic biofilm column was fed directly into the aerobic column. After both columns, the total amount transformed into nonvolatile intermediates and carbon dioxide was 94, 96, and 83% for [14C]HCB, [14C]trichloroethylene, and [14C]CF, respectively. This research shows the potential application of this novel two-stage bioreactor system for treating groundwaters and industrial effluents composed of highly chlorinated aliphatic and aromatic hydrocarbons.

Aerobiosis↗

Impact of bleached kraft mill effluents on drinking water quality.

Bleaching effluents from kraft pulp mills contain large quantities of chlorinated organic compounds, some of which are mutagenic. Mutagenic chloro-organic compounds are also formed as by-products in chlorination of drinking water. The work reported here was a combined field and laboratory study aimed at comparing the evidence of health risks from pulp mill contaminants in drinking water, with corresponding evidence from normal, chlorine disinfection by-products. The study was performed in a Swedish river basin with a large, public water works located downstream from a bleached kraft mill. Chemical analyses (gas chromatography and determination of adsorbable organic halogen) and bioassays for mutagenic activity (bacterial and mammalian cell bioassays) were performed on samples of river water, drinking water and laboratory produced drinking water. The study showed that the bleached kraft effluents caused a considerable, long-range transport of chloro-organic substances in the receiving waters, and a substantial increase in the total amount of organic chlorine in drinking water produced downstream from the mill. As regards Ames mutagenic compounds, however, chlorination of naturally occurring humic substances during the chlorine disinfection step in drinking water production, proved to be a far more important source. The contribution of volatile chloro-organic compounds from the kraft mill was also much smaller than the contribution from normal disinfection by-products. The chromosome aberration tests gave no clear evidence of a positive response for any of the samples tested.

Cells, Cultured↗

Analyses of known and new types of polyhalogenated aromatic substances in oven ash from recycled aluminium production.

Persistent aromatic bromine, chlorine and mixed chlorine-bromine compounds were analysed from recycled aluminium smelter (ALS) ashes to explore the impact of brominated flame retardants (BFR) on their formation. Polybrominated diphenyl ethers (PBDE) were the most abundant original BFRs found. Induction furnace ash contained tetra- to octa-BDEs about 2000ng g(-1) in similar congener ratios as the original scrap, but contents of nona- and deca-BDEs were only 25 and 5ng g(-1) indicating their significant degradation in ALS process. In the most non-polar fraction, PCB levels and profiles were similar as earlier ALS ash samples in 1990s. The highest PCB level measured was that of deca-CB (450ng g(-1)) in the induction furnace ash. In this fraction, bromo compounds were non-detectable (<5ng g(-1)). Fraction of the most polar compounds (from reversed toluene elution of carbon column ("dioxin fraction") contained PCDDs, PCDFs and polychlorinated dibenzothiophenes (PCDTs) in similar amounts and congener profiles as earlier investigated ALS ash samples. Bromine-containing dioxin and furan congeners were not detected. From individual PCDDs and PCDFs, octaCDF was the most abundant (205ng g(-1)) in induction furnace ash. In this fraction, the original BFR, tetrabromo-bisphenol-A, was identified. Its level in the induction furnace ash was approximated to be 388ng g(-1). In addition, 12 novel brominated and chlorinated compounds were found as abundant (8-441ng g(-1) in the induction furnace ash) contaminants from the fraction. Four of them were bisphenol derivatives, five biphenylols, then octachlorofluorenone (OCFL) and octachlorobiphenylene (OCBP). Their structures or structure types were deduced from total low-resolution EI mass spectra by theoretical isotope cluster simulation (ICLU) and through known fragmentation rules.

Air Pollutants, Occupational↗

Improvement by chlorine of the intestinal absorption of inorganic and organic Mg compounds and of their protective effect against adrenergic cardiopathy.

Comparative studies on the therapeutic effects of MgSO4, MgCl2, Mg aspartate, and Mg aspartate hydrochloride were carried out in Sprague-Dawlwy rats. In general, the intestinal absorption of Mg and its uptake into bone were improved after oral or intraduodenal administration of the two compounds containing chlorine; however, in these animals, gain in body weight was reduced, especially after MgCl2. Treatment with 9-alpha-fluorocortisol plus epinephrine resulted in cardiac hypertrophy and necroses. All Mg compounds fed in amounts leading to marked hypermagnesemia prevented hypertrophy; as regards the incidence and severity of necroses, however, MgSO4 and Mg aspartate proved ineffective. Significant protective effects were observed only after MgCl2 and Mg aspartate hydrochloride, indicating the central pathogenic role of extracellular hypochloremic alkalosis in metabolic heart necroses.

Animals↗

Subchronic toxicity of chlorine dioxide and related compounds in drinking water in the nonhuman primate.

Subchronic toxicities of ClO2, NaClO2, NaClO3 and NH2Cl were studied in the African Green monkeys (Cercopithecus aethiops). The chemicals were administered in drinking water during 30-60 days subchronic rising dose protocols. The only unexpected and significant toxic effect was elicited by ClO2; this chemical inhibited thyroid metabolism in the animals at a dose of ca. 9.0 mg/kg/day. A statistically significant decrease of serum thyroxine occurred after the fourth week of exposure to 100 mg/l.concentration. The extent of thyroid suppression was dose dependent in each individual monkey, and was reversible after cessation of exposure. NaClO2 and NaClO3 failed to elicit similar effects in doses up to ca. 60 mg/kg/day. Also, NaClO4 or NH2Cl did not cause T-4 suppression in doses of 10 mg/kg/day. The selective thyroid effect of ClO2 was unexplained and it appeared to be paradoxical since ClO2 was rapidly reduced by the oral and gastric secretions to nonoxidizing species (presumably Cl-). No evidence of thyroid effects were detected in the serum of human volunteers who ingested approximately 1 mg/l. of ClO2 in drinking water as a result of routine use in the community water treatment process. Sodium chlorite induced dose-dependent oxidative stress on hematopoesis, causing decreased hemoglobin and red cell count and increased methemoglobin content. At the same time, serum transaminase (SGPT) levels showed significant subclinical elevation. The hematologic effects of NaClO2 rebounded during exposure indicating compensatory hemopoietic activity taking effect during oxidative stress. Sodium chlorate and chloramine did not induce detectable hematologic changes in the animals.

Animals↗

Effects of common ophthalmic preservatives on ocular health.

Preservatives are an important component of ophthalmic preparations, providing antimicrobial activity in the bottle and preventing decomposition of active drug. Often underrecognized, however, are the significant cytotoxic effects of preservatives associated with long-term therapy and especially use of multiple preserved drugs. The most common preservatives in ophthalmic preparations for glaucoma and surface eye disease-benzalkonium chloride (BAK), chlorobutanol, sodium perborate, and stabilized oxychloro complex (SOC)-were reviewed. Compared with other preservatives, SOC caused the least amount of damage to rabbit corneal epithelial cells. BAK has demonstrated cytotoxic effects in cell culture, as well as in animal and human studies. Physicians should consider treatment with new-generation preparations containing low-risk preservatives such as SOC, especially in patients receiving multiple ophthalmic medications.

Animals↗

Mutagenicity testing of chlorinated biphenyls and chlorinated dibenzofurans.

4 chlorinated biphenyl and 5 chlorinated dibenzofuran compounds have been evaluated in the reversion assay developed by B.N Ames using Salmonella typhimurium histidine auxotrophs. All these compounds (2,4,2'-4'-tetrachlorobiphenyl, 3,4,3',4'-tetrachlorobiphenyl, 4-chlorobiphenyl, 2,4,,6,2',4',6'-hexachlorobiphenyl, dibenzofuran, 2,9-dichlorodibenzofuran, 3,6-dichlorodibenzofuran, 2,3,7,8-tetrachlorodibenzofuran and octachlorodibenzofuran) were nonmutagenic for strains TA98 and TA100 when tested over a 3-log dose range. They were also not mutagenic whether or not varying concentrations of microsomal extracts (S9) from uninduced rats or from rats induced by several methods were included in the experimental protocol.

Animals↗

Polychlorinated naphthalenes in U.K. soils: time trends, markers of source, and equilibrium status.

Polychlorinated naphthalenes (PCNs) have been analyzed in archived soil from the U.K. to investigate historical trends. Samples were obtained from the Broadbalk experiment plots (1944-1986) and Luddington experiment station (1968-1990). Luddington samples also include a set of soils that received a one-time sludge treatment in 1968, and duplicate samples of this archived sludge were also analyzed. Peak residues of sumPCN (sum of all PCN congeners quantified) were approximately 9000 pg g(-1) dry weight in 1956, declining to approximately 300 pg g(-1) in contemporary soils. The one-time sludge application resulted in elevated soil residues that were 1.5-6 times higher than the control plot over the time series. This increase is consistent with the known application rate and the amount of sumPCN in the applied sludge (approximately 250,000 pg g(-1) dry wt). Half-lives forthe Luddington control soil and the sludge-amended soil for the period 1972-1990 were 5.3 and 9.9 years, respectively. Investigation of time trends revealed differences between homologue groups with the higher molecular weight congeners peaking earlier in the time series (pre-1950) and the lower molecular weight congeners peaking later, ca. 1970. Time trends of individual congeners were investigated in terms of their relative mass percent contribution to the sum of their homologue group. Significant (p < 0.05) increasing trends were observed for several congeners associated with combustion sources (CN-29, -51, -52/60, -54, and -66/67) suggesting that combustion related sources are more important now than they were in the past. However, no decreasing trend was observed for congeners that were thought to be susceptible to degradation by photolysis suggesting that this may not be a key elimination pathway of PCNs in the environment. A simple calculation of the fugacity status of PCNs in air and soil showed that the tri-CNs are exhibiting net outgassing, while the penta-CNs are still being deposited to soil. Interestingly, the penta-CNs associated with combustion show the largest gradient for air-to-soil transfer, supporting the notion that combustion sources are important contributors to contemporary air burdens of these congeners.

Air Pollutants↗

Square planar vs tetrahedral geometry in four coordinate iron(II) complexes.

The geometric preferences of a family of four coordinate, iron(II) d6 complexes of the general form L2FeX2 have been systematically evaluated. Treatment of Fe2(Mes)4 (Mes = 2,4,6-Me3C6H2) with monodentate phosphine and phosphite ligands furnished square planar trans-P2Fe(Mes)2 derivatives. Identification of the geometry has been accomplished by a combination of solution and solid-state magnetometry and, in two cases (P = PMe3, PEt2Ph), X-ray diffraction. In contrast, both tetrahedral and square planar coordination has been observed upon complexation of chelating phosphine ligands. A combination of crystallographic and magnetic susceptibility data for (depe)Fe(Mes)2 (depe = 1,2-bis(diethylphosphino)ethane) established a tetrahedral molecular geometry whereas SQUID magnetometry and Mössbauer spectroscopy on samples of (dppe)Fe(Mes)2 (dppe = 1,2-bis(diphenylphosphino)ethane) indicated a planar molecule. When dissolved in chlorinated solvents, the latter compound promotes chlorine atom abstraction, forming tetrahedral (dppe)Fe(Mes)Cl and (dppe)FeCl2. Ligand substitution reactions have been studied for both structural types and are rapid on the NMR time scale at ambient temperature.

Journal Article↗