Etsuro Shibata

Vapor pressures and enthalpies of sublimation of 17 polychlorinated dibenzo‐p‐dioxins and five polychlorinated dibenzofurans

An apparatus for vapor pressure measurement with a very small cell by the mass-loss Knudsen effusion technique was tested with solid benzoic acid and anthracene. The vapor pressure and enthalpy of sublimation results of the two reference compounds were in good agreement with accepted literature data. The vapor pressures at different temperatures of 17 polychlorinated dibenzo-p-dioxins (including dibenzo-p-dioxin) and five polychlorinated dibenzofurans (including dibenzofuran) were measured with the apparatus, and the enthalpies of sublimation of the 22 dioxins and furans were derived from the temperature dependence of vapor pressure. The results were systematically compared with the literature data.

Measurement of temperature dependence for the vapor pressures of twenty‐six polychlorinated biphenyl congeners in commercial Kanechlor mixtures by the Knudsen effusion method

The vapor pressures of the major congeners in commercial polychlorinated biphenyl (PCB) mixtures (Kanechlors; Kanebuchi Chemical Industry, Tokyo, Japan) have been experimentally determined by Knudsen mass loss effusion. We obtained vapor pressures for the individual PCBs in the crystalline solid, liquid, and subcooled liquid forms as a function of temperature. We derived the thermodynamic parameters, such as the enthalpies of sublimation and vaporization, from the temperature dependence of the vapor pressure by the Clausius-Clapeyron equation. To decide whether the commercial PCB mixtures were ideal solutions, we obtained the activity coefficients by comparing our experimental vapor pressures for pure PCB congeners with those calculated from Kanechlor molar compositional data and vapor pressure values. In many cases, we found that, at 298 K, the values of the activity coefficients of major PCBs in Kanechlor 300 and 500 ranged from 1 to 2. Thus, we suggested that the commercial PCB mixtures show slight positive deviations from ideal solution (Raoults Law) behavior at ambient temperatures.

Formation behavior of PCDD/Fs in PVC pyrolysis with copper oxide.

Formation and decomposition behaviors of PCDD/Fs during pyrolysis of polyvinyl chloride (PVC) with CuO have been investigated. These reactions proceed simultaneously, and the rate of decomposition exceeds that of formation with further retention. More 2,3,7,8-TCDD is formed when the dechlorination of PCDD/Fs proceeds significantly. Homologue profile patterns of PCDD/Fs show that the fractions of O8CDD and H6CDFs are relatively larger within PCDDs and PCDFs, respectively. Extremely large amounts of PCDD/Fs are obtained with the long retention time at 200 degrees C. The formation of PCDD/Fs decreases drastically with increase in the molar ratio of CuO/PVC. The acceptability of thermodynamic calculations on the formation of PCDD/Fs is also investigated. The thermodynamic calculated tendency of the effect of oxygen on the formation of PCDD/Fs agrees well with the experimental results, although absolute values of the amount of PCDD/Fs are much different.

Vaporization of zinc during thermal treatment of ZnO with tetrabromobisphenol A (TBBPA)

In the present work we investigate the vaporization of zinc or its compounds during thermal treatment of ZnO with tetrabromobisphenol A. Samples of 2g of ZnO:TBBPA (3.34:1) were isothermally heated in a laboratory-scale furnace at temperatures from 490 °C to 950 °C, and the solid, condensed and gaseous products formed were analyzed by X-ray diffraction analysis, electron probe microanalysis, inductively coupled plasma analysis, ion chromatography, and gas chromatography coupled with mass spectrometry. The results obtained indicate that the vaporization of ZnBr(2) formed strongly depends on heating time and temperature, yet is restrained by char, if formed with sufficient yield (above 15 wt%). Starting from 850 °C, this char commences carbothermic reduction of any remaining ZnO, which from then begins to evaporate as zinc metal vapor. Volatilization of zinc is completed at 950 °C. The presence of 5 vol.% of oxygen has no significant effect on the vaporization of formed ZnBr(2), the carbothermic reduction or the volatilization of metallic zinc. Strongly oxidizing conditions (20 vol.% of oxygen), however, boost the oxidation of char and thus the vaporization of ZnBr(2), but prevent carbothermic reduction of any un-reacted ZnO by depleting this char.

Distribution of copper, silver and gold during thermal treatment with brominated flame retardants

The growing consumption of electric and electronic equipment results in creating an increasing amount of electronic waste. The most economically and environmentally advantageous methods for the treatment and recycling of waste electric and electronic equipment (WEEE) are the thermal techniques such as direct combustion, co-combustion with plastic wastes, pyrolysis and gasification. Nowadays, this kind of waste is mainly thermally treated in incinerators (e.g. rotary kilns) to decompose the plastics present, and to concentrate metals in bottom ash. The concentrated metals (e.g. copper, precious metals) can be supplied as a secondary raw material to metal smelters, while the pyrolysis of plastics allows the recovery of fuel gases, volatilising agents and, eventually, energy. Indeed, WEEE, such as a printed circuit boards (PCBs) usually contains brominated flame retardants (BFRs). From these materials, hydrobromic acid (HBr) is formed as a product of their thermal decomposition. In the present work, the bromination was studied of copper, silver and gold by HBr, originating from BFRs, such as Tetrabromobisphenol A (TBBPA) and Tetrabromobisphenol A-Tetrabromobisophenol A diglycidyl ether (TTDE) polymer; possible volatilization of the bromides formed was monitored using a thermo-gravimetric analyzer (TGA) and a laboratory-scale furnace for treating samples of metals and BFRs under an inert atmosphere and at a wide range of temperatures. The results obtained indicate that up to about 50% of copper and silver can evolve from sample residues in the form of volatile CuBr and AgBr above 600 and 1000°C, respectively. The reactions occur in the molten resin phase simultaneously with the decomposition of the brominated resin. Gold is resistant to HBr and remains unchanged in the residue.

Study on simultaneous recycling of EAF dust and plastic waste containing TBBPA.

In the present work we investigated the fates of zinc, lead, and iron present in electric arc furnace dust during thermal treatment of the dust with tetrabromobisphenol A (TBBPA) and tetrabromobisphenol A diglycidyl ether (TBBPADGE). Mixtures of these materials were compressed into pellets and heated in a laboratory-scale furnace at 550 °C for 80 min, under oxidizing and inert conditions. The solid, condensed, and gaseous-phase products were characterized using an array of analytical methods: scanning electron microscopy, X-ray diffraction, electron probe microscopy, inductively coupled plasma, ion chromatography, and gas chromatography. The results indicated that heating the mixtures under specific conditions enabled high separation of zinc and lead from iron-rich residues, by a bromination-evaporation process. In the case of TBBPADGE, a maximum of 85% of zinc and 81% of lead were effectively separated under the above conditions. The process is based on the reaction between the highly reactive HBr gas evolved during thermal degradation of the flame-retarded materials with zinc (ZnO and ZnFe2O4) and lead in the dust, followed by complete evaporation of the formed metallic bromides from the solid residue.

Influence of Temperature and Heating Time on Bromination of Zinc Oxide during Thermal Treatment with Tetrabromobisphenol A

Our prior research indicates that hydrogen bromide (HBr) evolved during thermal decomposition of tetrabromobisphenol A (TBBPA) can be utilized as a reagent for selective bromination and evaporation of zinc oxide. The present work investigated dependency of the bromination reaction on time at selected temperatures using a laboratory-scale furnace. The formed solid, condensed, and gaseous products were analyzed by X-ray diffraction analysis, electron probe microanalysis, inductively coupled plasma analysis, ion chromatography, and gas chromatography coupled with mass spectrometry. Results indicate that the bromination rate is strongly dependent on heating time. This dependency is a direct consequence of progress in the decomposition of TBBPA, which provides inorganic bromine suitable for the reaction. The bromination rate increases with time until the bromine source is depleted. The process is shorter at higher applied temperatures and appears instantaneous at 310 degrees C and above. However, the maximum bromination yield is independent of the applied conditions and ranges from 64 to 70%. Additionally, the influence of oxidizing conditions on the bromination reaction and the effect of ZnO on decomposition of TBBPA were investigated in this study.

Vapor pressure of ten polychlorinated biphenyl congeners and two commercial fluids as a function of temperature

The Knudsen mass-loss effusion technique was used to measure the vapor pressures of commercial Kanechlor fluids (Kanechlor 300 and Kanechlor 500) and 10 major individual polychlorinated biphenyls (PCBs) in Kanechlors as a function of temperature and ortho-chlorine substitution. From the temperature dependence of vapor pressure, the thermodynamic parameters, such as enthalpies and entropies of sublimation and vaporization, were derived using the Clausius-Clapeyron equation. The results were compared with both experimental and calculated literature values. The ortho-chlorine substitution effects on the vapor pressure of major PCB congeners in Kanechlor mixtures were studied on the same homologous series. Within this series, the greater the number of chlorine substitutions in the ortho-positions, the higher the vapor pressure, because of the ortho-effect.

Thermodynamic prediction of vapor pressures for polychlorinated dibenzo‐p‐dioxins, polychlorinated dibenzofurans, and polybrominated dibenzo‐p‐dioxins

The vapor pressures and thermal properties of nonmeasured polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and seven polybrominated dibenzo-p-dioxins (PBDDs) were predicted using a correlation method based on the experimental vapor pressures for 22 PCDD/Fs and octabrominated dibenzo-p-dioxin obtained by the Knudsen effusion method. The vapor pressures of all 59 PCDDs and 131 PCDFs predicted in the present study were more or less higher than the data predicted by Rordorf, although the calculation method was the same. For the most toxic 2,3,7,8-tetrachlorinated dibenzo-p-dioxin, the vapor pressure at 298 K predicted in the present study was 6.2 x 10(-6) Pa, which was 31-fold higher than the value provided by Rordorf (2.0 x 10(-7) Pa). The predicted vapor pressures for low-brominated PBDDs agreed with the data estimated by Rordorf. For 2,3,7,8-tetrabrominated dibenzo-p-dioxin, the vapor pressure predicted in the present study was 1.8 x 10(-8) Pa, obviously lower than those predicted by Rordorf.

Non-electrolytic synthesis of copper oxide/carbon nanocomposite by surface plasma in super-dehydrated ethanol.

Electrolytic processes are widely used to synthesize different nanomaterials and it does not depend on what kind of the method has been applied (wet-chemistry, sonochemistry, plasma chemistry, electrolysis and so on). Generally, the reactions in the electrolyte are considered to be reduction/oxidation (REDOX) reactions between chemical reagents or the deposition of matter on the electrodes, in line with Faraday’s law. Due to the presence of electroconductive additives in any electrolyte, the polarization effect of polar molecules conducting an electrical current disappears, when external high-strength electric field is induced. Because initially of the charge transfer always belongs of electroconductive additive and it does not depend on applied voltage. The polarization of ethanol molecules has been applied to conduct an electric current by surface plasma interaction for the synthesis of a copper oxide/carbon nanocomposite material.