Electroreductive dechlorination of chlorophenols with Pd catalyst supported on solid electrode

Electroreductive dechlorination of chlorophenols with Pd catalyst supported on solidelectrode was studied. As solid electrodes, carbon cloth (CC), carbon felt (CF) and titanium mesh were used, and palladium was plated on solid electrodes by either electrolytic or electroless method. On each electrode with Pd, chlorophenols were qualitatively dechlorinated to phenol, while they were entirely intact on electrodes without Pd. Moreover, neither base electrode nor plating method significantly affected the activity of Pd as far as it was sufficiently loaded on the electrode. Based on the results in the experiments using one electrode repeatedly, Pd catalyst proved to possess a satisfactory duarability under the present condition. It was suggested that the reactive species responsinble for the dechlorination of chlorophenols could be formed during preliminary electrolysis. Thus, (Pd)_x-H resulting from the adsorption of electrogenerated hydrogen on metallic Pd might be assumed most probable.     

Electroreductive dechlorination of chlorophenols with Pd catalyst supported on solid electrode

Electroreductive dechlorination of chlorophenols with Pd catalyst supported on solidelectrode was studied. As solid electrodes, carbon cloth (CC), carbon felt (CF) and titanium mesh were used, and palladium was plated on solid electrodes by either electrolytic or electroless method. On each electrode with Pd, chlorophenols were qualitatively dechlorinated to phenol, while they were entirely intact on electrodes without Pd. Moreover, neither base electrode nor plating method significantly affected the activity of Pd as far as it was sufficiently loaded on the electrode. Based on the results in the experiments using one electrode repeatedly, Pd catalyst proved to possess a satisfactory duarability under the present condition. It was suggested that the reactive species responsinble for the dechlorination of chlorophenols could be formed during preliminary electrolysis. Thus, (Pd)_x-H resulting from the adsorption of electrogenerated hydrogen on metallic Pd might be assumed most probable.     

The cost of stratospheric climate engineering revisited

Stratospheric aerosol injection (SAI) has been receiving increasing attention as a possible option for climate engineering. Its direct cost is perceived to be low, which has implications for international governance of this emerging technology. Here, we critically synthesize previous estimates of the underlying parameters and examine the total costs of SAI. It is evident that there have been inconsistencies in some assumptions and the application of overly optimistic parameter values in previous studies, which have led to an overall underestimation of the cost of aircraft-based SAI with sulfate aerosols. The annual cost of SAI to achieve cooling of 2 W/m² could reach US$10 billion with newly designed aircraft, which contrasts with the oft-quoted estimate of “a few billion dollars.” If existing aircraft were used, the cost would be expected to increase further. An SAI operation would be a large-scale engineering undertaking, possibly requiring a fleet of approximately 1,000 aircraft, because of the required high altitude of the injection. Therefore, because of its significance, a more thorough investigation of the engineering aspects of SAI and the associated uncertainties is warranted.     

Electrostatic hazards of charging of bedclothes and ignition in medical facilities

We investigated the charge generated on bedclothes (cotton and polyester) during bedding exchange with different humidities and the ignitability of an alcohol-based hand sanitizer (72.3 mass% ethanol) due to static spark with different temperatures to identify the hazards of electrostatic shocks and ignitions occurring previously in medical facilities. The results indicated that charging of the polyester bedclothes may induce a human body potential of over about 10?kV, resulting in shocks even at a relative humidity of 50%, and a human body potential of higher than about 8?kV can cause a risk for the ignition of the hand sanitizer. The grounding of human bodies via footwear and flooring, therefore, is essential to avoid such hazards (or to reduce such risks).     

Chlorophyll maxima in Kuroshio and adjacent area

Fluorometric determination of chlorophyll a and pheopigments was carried out in the sea area off southern Japan. Maximum concentration of chlorophyll pigments was determined to be at or below the lower limit of the euphotic zone, namely from 50 to 150 m depth. To estimate the activity of phytoplankton in this maximum chlorophyll layer, changes of chlorophyll concentration and number of cells were measured in samples taken from this layer before and after exposure to different light intensities. It was concluded that the growth of shade-adapted phytoplankton and the deterioration of chlorophyll pigments by light are the main factors causing the chlorophyll maximum to occur in a rather deep oceanic layer.     

Net ecosystem CO2 exchange over a larch forest in Hokkaido, Japan

Larch forests are distributed extensively in the east Eurasian continent and are expected to play a significant role in the terrestrial ecosystem carbon cycling process. In view of the fact that studies on carbon exchange for this important biome have been very limited, we have initiated a long-term flux observation in a larch forest ecosystem in Hokkaido in northern Japan since 2000. The net ecosystem CO₂ exchange (NEE) showed large seasonal and diurnal variation. Generally, the larch forest ecosystem released CO₂ in nighttime and assimilated CO₂ in daytime during the growing season from May to October. The ecosystem started to become a net carbon sink in May, reaching a maximum carbon uptake as high as 186 g C m⁻² month⁻¹ in June. With the yellowing, senescing and leaf fall, the ecosystem turned into a carbon source in November. During the non-growing season, the larch forest ecosystem became a net source of CO₂, releasing an average of 16.7 g C m⁻² month⁻¹. Overall, the ecosystem sequestered 141–240 g C m⁻² yr⁻¹ in 2001. The NEE was significantly influenced by environmental factors. Respiration of the ecosystem, for example, was exponentially dependent on air temperature, while photosynthesis was related to the incident PAR in a manner consistent with the Michaelis–Menten model. Although the vapor pressure deficit (VPD) was scarcely higher than 15 hPa, the CO₂ uptake rate was also depressed when VPD surpassed 10 hPa.     

Dechlorination of PCBs by electrochemical reduction with aromatic radical anion as mediator

Mediated electrochemical reduction was applied to the dechlorination of polychlorinated biphenyls (PCBs) in tetra-n-butylammonium perchlorate/dimethylformamide solution. Rapid and complete dechlorination was possible with biphenyl or naphthalene as the mediator, whereas the reaction was much slower with anthracene or 9,10-diphenylanthracene. The reaction rate was so high with naphthalene or biphenyl radical anion that differences in reactivity could not be observed between congeners. Side reactions, other than biphenyl formation, could occur depending upon the mediators and the substrates, but contributed less than 10% of the total products in the case of naphthalene-mediated dechlorination. Almost all chloride ion formed in the dechlorination remained in the cathode solution. The order of the reaction was determined to be 0.5 for the substrate and 1 for the mediator (naphthalene) in the dechlorination of 2-chlorobiphenyl; identical to results for the mediated dechlorination of 1-chloronaphthalene. The reaction rate in practical PCB dechlorination could be estimated with the use of the initial concentration of the mediator and chlorine content of the solution provided that the problem of the deactivation of the electrode surface could be solved.     

Coral skeletal tin and copper concentrations at Pohnpei, Micronesia: possible index for marine pollution by toxic anti-biofouling paints

We present 40 year-long skeletal chronologies of tin (Sn) and copper (Cu) from an annually-banded coral (Porites sp.) collected from Pohnpei Island, Micronesia (western equatorial Pacific). Both the elements are present in antifouling marine paints and are released inadvertently into ambient seawater. Especially, Sn has often been used in the form of tributyltin (TBT). Based on a stepwise pretreatment examination, Sn and Cu both inside and outside the aragonite lattice of the coral skeleton show a potential for providing marine pollution indicators. High values of extra-skeletal Cu/Ca and Sn/Ca atomic ratios were found between late 1960s and late 1980s during a period of active use of TBT-based antifouling paints worldwide. However, a significant decrease in both the ratios in the beginning of 1990s can be attributed to regulation of the use of TBT on cargo ships by countries such as the USA, Japan and Australia.     

Characteristics of cesium accumulation in the filamentous soil bacterium Streptomyces sp. K202

A filamentous soil bacterium, strain K202, was isolated from soil where an edible mushroom (Boletopsis leucomelas) was growing and identified as belonging to the genus Streptomyces on the basis of its morphological characteristics and the presence of LL-2, 6-diaminopimelic acid. We studied the existence states of Cs and its migration from extracellular to intracellular fluid in the mycelia of Streptomyces sp. K202. The results indicated that Cs accumulated in the cells through at least 2 steps: in the first step, Cs⁺ was immediately and non-specifically adsorbed on the negatively charged cell surface, and in the second step, this adsorbed Cs⁺ was taken up into the cytoplasm, and a part of the Cs entering the cytoplasm was taken up by an energy-dependent transport system(s). Further, we confirmed that a part of the Cs⁺ was taken up into the mycelia competitively with K⁺, because K⁺ uptake into the intact mycelia of the strain was significantly inhibited by the presence of Cs⁺ in the culture media. This suggested that part of the Cs is transported by the potassium transport system. Moreover, ¹³³Cs-NMR spectra and SEM-EDX spectra of the mycelia that accumulated Cs showed the presence of at least 2 intracellular Cs states: Cs⁺ trapped by intercellular materials such as polyphosphate and Cs⁺ present in a cytoplasmic pool.