Fate of radiocesium in sewage treatment process released by the nuclear accident at Fukushima

The nuclear accident at the Fukushima Daiichi Nuclear Power Plant (FDNPP) which occurred after the Great East Japan Earthquake on March 11, 2011 resulted in releases of radionuclides such as ¹³⁴Cs (half-life:T_1/2 = 2.06 yr), ¹³⁷Cs (T_1/2 = 30.04 yr) and ¹³¹I (T_1/2 = 8.05 d) to the environment. For this paper, we observed the monthly variations of radiocesium (¹³⁴Cs and ¹³⁷Cs) and stable Cs concentrations in influent, effluent, sewage sludge, and sludge ash collected from a sewage treatment plant 280 km north of the FDNPP from July to December, 2011. Using the stable Cs results, we concluded the mass balance of Cs in the sewage treatment plant showed that about 10% of the Cs entering the sewage treatment plant would be transferred to the sewage sludge, and then Cs in the sewage sludge was totally recovered in the sludge ash. The behavior of Cs was similar to that of Rb, but it was not similar to that of K in the sewage treatment process.     

Water at interfaces

Electrolyte cations and anions in aqueous solutions are hydrogen bond breaker. We found that most of anions are strong hydrogen bond breaker whereas cations are not. Further, the electro-reduction of Mg(H₂O)₆²⁺ to Mg(OH)₂ and the growth of the Mg(OH)₂ were observed on Au electrode surface at negative electrode potential. Water molecules in an electric double layer exhibit an ordered and a disordered structure at negative and pzc (point of zero charge) potentials, respectively. Therefore, electrode potential polarization (negative or pzc potential application) from an equilibrium potential operates an electrified interface to cause increased or decreased ordering, orientation and charge transfer of water molecules as well as dissociation of water on the electrode surface.     

论价值意识整合与安全价值取向的形成

探讨了安全价值意识转变中的整合作用机制和价值取向的形成机制。分析了价值意识整合方式及其价值互动、价值认同、价值顺应的作用原理 ,论述了价值取向的形成模式及文化模式与价值取向的交互作用过程     

N2O Emissions at Solid Waste Disposal Sites in Osaka City

Nitrous oxide (N₂O) is a trace gas contributing to stratospheric ozone depletion and global warming. Although a large quantity of information exists about N₂O emissions from various ecosystems, this study was initiated to demonstrate the features of N₂O emissions from sea-based waste disposal sites in Osaka City in relation to CH₄ emissions.

Average N₂O emissions at an active landfill (S-Site) were several times higher than those at a closed landfill (N Site). Average CH₄ emissions were also much greater at the S-Site. Regarding the nature of N₂O emissions, remarkable emissions often were observed with aerobic waste layers at the N-Site, suggesting almost inversely related N₂O emissions with CH₄ production at the N-Site. However, at the S-Site a few exceptionally high N₂O emissions were noted in cases of high CH₄ emissions.     

减灾活动与社会经济协调发展的哲学思考

论述了减灾工作中,应遵循的减灾投入与社会经济状况的统一性原则,发展减灾与发展经济的比例协调性原则;减灾发展的超前性原则;减灾的宏观协调与微观协调辩证统一的原则;减灾活动的协调与不协调辩证统一的原则。     

90Sr, 137Cs and (239,240)Pu concentration surface water time series in the Pacific and Indian Oceans--WOMARS results

Under an IAEA's Co-ordinated Research Project "Worldwide Marine Radioactivity Studies (WOMARS)" 90Sr, 137Cs and (239,240)Pu concentration surface water time series in the Pacific and Indian Oceans have been investigated. The Pacific and Indian Oceans were divided into 17 latitudinal boxes according to ocean circulation, global fallout patterns and the location of nuclear weapons test sites. The present levels and time trends in radionuclide concentrations in surface water for each box were studied and the corresponding effective half-lives were estimated. For the year 2000, the estimated average 90Sr, 137Cs and (239,240)Pu concentrations in surface waters of the Pacific and Indian Oceans varied from 0.1 to 1.5 mBq/L, 0.1 to 2.8 mBq/L, and 0.1 to 5.2 microBq/L, respectively. The mean effective half-lives for 90Sr and 137Cs in surface water were 12+/-1 years for the North, 20+/-1 years for the South and 21+/-2 years for the Equatorial Pacific. For (239,240)Pu the corresponding mean effective half-lives were 7+/-1 years for the North, 12+/-4 years for the South and 10+/-2 years for the Equatorial Pacific. For the Indian Ocean the mean effective half-lives of 137Cs and (239,240)Pu were 21+/-2 years and 9+/-1 years, respectively. There is evidence that fallout removal rates before 1970 were faster than those observed during recent decades. The estimated surface water concentrations of 90Sr, 137Cs and (239,240)Pu in latitudinal belts of the Pacific and Indian Oceans for the year 2000 may be used as the average levels so that any new contribution from nuclear facilities, nuclear weapons test sites, radioactive waste dumping sites and from possible nuclear accidents can be identified.