benzofurans and cuprous-chloride

The secondary formation of dibenzo-p-dioxin and dibenzofurans (PCDD/Fs) in the flue gas and ash from the municipal solid waste incinerator (MSWI) systems has attracted considerable public concern. The objective of our research was thus to examine reactions in fly ash from an MSWI operated with different precursors with similar chemical compositions, such as dibenzofurans (DFs), and metal chlorides, such as copper chloride (CuCl(2)). We observed that the concentrations of PCDD/Fs in CuCl(2) and in a mixture of CuCl(2) and DFs were 369.5 and 5307.8 ng/g, respectively, and thus significantly higher in the latter. Due to the catalytic effect of copper ions and the similar structure of dibenzofurans for PCDFs, the effect of the additive in forming PCDD/Fs were obvious. The concentrations of PCDD/Fs in CuCl(2) and copper oxide (CuO) were 369.5 and 97.05 ng/g, respectively. The results also show that the PCDD/Fs concentration when copper chloride was added was four times higher than when copper oxide was added. In addition, the level of activity of the chlorine atoms is greater than that of the oxygen atoms during the formation of PCDD/Fs. This study suggests that the use of metal-containing substances (such as Cu, Cl, Zn) or chlorination precursors (such as DF, chlorobenzene) should be avoided in the combustion process.

Topics: Air Pollution; Benzofurans; Carbon; Coal Ash; Copper; Dioxins; Incineration; Oxides; Particulate Matter; Refuse Disposal

Chlorination and thermal degradation of 2-chlorodibenzodioxin and dibenzofuran were investigated using sealed tubes at 350 degrees C in the presence of CuCl(2) or CuCl. Twelve organic species, including polychlorobenzenes, were identified and quantified as a function of residence time. Time behaviours of PCDDs and PCDFs regarding destruction processes were compared. The formation of polychlorobenzenes from the thermal heterogeneous degradation of PCDDs was only a minor pathway but it could contribute to the good linear correlation observed between the concentration of polychlorobenzenes and those of PCDD/Fs in the emissions of municipal solid waste incinerators.

Topics: Benzofurans; Carbon Dioxide; Chlorobenzenes; Copper; Dibenzofurans, Polychlorinated; Dioxins; Halogenation; Hot Temperature; Polychlorinated Dibenzodioxins

Combustion experiments in a laboratory-scale fluidized-bed reactor have been performed to clarify the effects of copper chloride as a catalyst on polychlorinated dibenzofurans (PCDFs) formation in municipal waste incineration. We used model wastes with and without copper chloride (CuCl2 x 2H2O) as a catalyst, both of which contained polyvinyl chloride (PVC) as a chlorine source. Combustion temperature was set to 900 degrees C, and the amount of air supplied was twice as much as the theoretical amount. The experimental setup had been carefully planned to ensure avoidance of the influences of previous experiments. Results of these present experiments revealed that copper chloride in the waste increased the amount of PCDFs formed and made the homologue profile shifted towards the highly chlorinated species. Copper chloride contributes to PCDFs formation by promoting chlorination via catalytic reactions, whereby the reaction could be important in that organic matters are chlorinated directly by chlorinated compounds related to Deacon reaction such as copper chloride. It was elucidated that characteristic isomer distribution patterns appeared in case the waste contained copper chloride. It is probable in our experiment with copper chloride that PCDFs are mainly formed via catalytic reactions of copper compounds and carbon.

Topics: Benzofurans; Copper; Dibenzofurans, Polychlorinated; Incineration; Polyvinyl Chloride

Conversion of residue beta Tyr-297 of the Escherichia coli F1-ATPase (ECF1) to a Cys in the mutant beta Y297C led to impaired oxidative phosphorylation based on growth curves. The ATPase activity of ECF1 isolated from the mutant beta Y297C was only 1% of wild-type activity, but the residual activity involves cooperative multi-site enzyme turnover based on inhibition by DCCD and azide. ATPase activity could be increased to 8%, and 13% of wild-type by reaction of the introduced Cys with N-ethyl maleimide (NEM), and 7-chloro-4-nitrobenzofurazan (NbfCl), respectively, suggesting that enzymatic function is improved by an increased hydrophobicity of residue beta Cys-297. The mutation beta Tyr-297-->Cys had no effect on nucleotide binding in studies with the fluorescent analog lin-benzo-ADP. The asymmetry of ECF1 was investigated in the mutants beta Y297C and beta Y297C:E381C/epsilon S108C by examining the relative reactivity of Cys-297 in the three copies of the beta subunit under different nucleotide binding conditions. In agreement with a previous study (Haughton, M.A. and Capaldi, R.A. (1995) J. Biol. Chem., 270, 20568-20574), the asymmetry was maintained under all nucleotide conditions. The NbfCl reaction site was found to be beta free, which is also the site most reactive to NEM, beta epsilon is the second site which reacts with NbfCl or NEM, while the third site, beta gamma, is poorly reactive to either reagent.

Topics: Benzofurans; Binding Sites; Copper; Cross-Linking Reagents; Cysteine; Escherichia coli; Ethylmaleimide; Mutation; Nucleotides; Oxidative Phosphorylation; Protein Conformation; Proton-Translocating ATPases; Sulfhydryl Reagents