New Technology for Conducting Radiation Hazard Assessments: The Application of the Underwater Radiation Spectral Identification System (URSIS) at the Massachusetts Bay Industrial Waste (U.S.A.)

The Underwater Radiation Spectral Identification System (URSIS) is a portable spectrometer used for the in situ detection of radioactivity in the marine environment. This paper reports on the first time application of this technology to assess, in a preliminary manner, the potential radiation threat to the public and environment at an aquatic disposal site – the Massachusetts Bay Industrial Waste Site (IWS). Utilizing the meneuvering capabilities of ROV and manned submersible vehicles, the URSIS was successfully positioned close (5–10 cm) to waste containers for a period sufficient to detect, in real time, the presence of radioactive materials. Spectral data from 45 individual targets indicated that the radionuclides present in sediments which draped or partially buried waste containers were consistent with natural background concentrations. No man-made radionuclides were detected at any of the target or background measurement locations. These data support the conclusion that low-level radiation does not pose an imminent and widespread human health or ecological threat in Massachusetts Bay.     

Distribution of radionuclides among the main components of Lake Chervyanoe in the Eastern Ural Radioactive Trace

Radioecological conditions have been estimated in Lake Chervyanoe located on the central axis of the Eastern Ural Radioactive Trace (EURT) about 100–110 km northeast of the Mayak Production Association. Data on the ⁹⁰Sr and ¹³⁷Cs contents in the main components of the lake, the distribution of these radionuclides over the profile of bottom sediments, and their amounts in the lake are presented. The experimental data have been used to construct mathematical models for estimating changes in the radionuclide concentrations and amounts in the water and bottom sediments of the lake over a long period after the nuclear accident, as well as the tritium content of the lake water in different periods of time.     

14C and 125I Labelling of Humic Material for Use in Environmental Studies

Humic and fulvic acids are present in nearly all natural waters. These acids are known to affect the transport of environmental contaminants such as metals and hydrophobic organics through the terrestrial environment. an understanding of their role in the transport of contaminants is therefore essential and is facilitated if the acid is labelled with a suitable radioactive label. This paper reports the use of ¹⁴C-methylamine and ¹²⁵I to label humic acid with either ¹⁴C or ¹²⁵I and investigates factors which affect the yield of these reactions. the stability and mobility of the labelled humic material through sand is also reported.     

纳米Fe掺杂MIL-101(Cr)及其吸附放射性碘研究

目的改进并提高MIL-101(Cr)吸附气态碘单质的性能,以期用于核事故放射性碘富集吸收。方法通过水热法制备MIL-101(Cr)材料,并利用纳米Fe掺杂改性,运用SEM、XRD等对掺杂前后的材料进行表征。将材料在75℃条件下对气态碘单质进行吸附,并比较不同Fe掺杂量下材料对气态碘吸附性能的差异。结果纳米Fe成功掺杂于基体材料MIL-101中,并对基体材料晶体结构无破坏作用。吸附性能研究表明,掺杂纳米Fe质量分数为1%的Fe@MIL-101吸附性能最优,对气态碘的饱和吸附量可达3.42 g(I2)/g(MIL-101)。结论纳米Fe掺杂改性的MIL-101材料在高温条件下对气态碘单质具有良好的吸附效果,有望应用于核反应堆事故中对放射性碘的富集或捕集。     

放射性污染的危害及防护措施

环境巾的各种放射性污染都能影响人类健康。介绍了放射性污染性质、来源和特点,重点介绍了各种影响人类生活的放射性污染。和环境中的其他污染小同,它不易察觉,但容易在人体中积累,人们要关注放射性污染,对它有一个科学的认识,才能保护自身的健康。     

施灰田土壤及所产蔬菜铀、钍和钾、钼、镁、锌含量变化及影响评价

U和Th是放射性元素,K、Fe、Mo、Mg和Zn是植物生长需要的必要营养元素。粉煤灰中U、Th、Fe和Mo的含量略高于空白土壤中Fe和Mo的含量,K、Mg和Zn的含量低于空白土壤中K、Mg和Zn的含量。掺施粉煤灰并没有引起施灰土壤及所产蔬菜中各元素含量的明显变化。与国家土壤环境质量标准及食品、卫生标准的限值相比,施灰土壤及所产蔬菜的U、Th、K、Fe、Mo、Mg和Zn的含量均在正常范围内波动。     

辐射污染防治地方立法评析

由于国家立法的缺失,近年来中国的辐射污染防治地方立法十分活跃。将放射性污染防治和电磁辐射污染防治合并,制定综合性的辐射污染防治法已成为地方立法的趋势。两种辐射污染同中有异,在污染特性、危害原理和危害程度上有明显的区别,综合性立法既有必要又具可行性。但现有立法未能反映两种辐射污染防治的根本不同,特别是回避和混淆两种辐射污染的防治原则,确立电磁辐射污染防治适用风险预防原则是当务之亟。     

Fate and transport of the β-adrenergic agonist ractopamine hydrochloride in soil–water systems

The feed additive ractopamine hydrochloride was fortified at four concentrations into batch vials containing soils that differed in both biological activity and organic matter(OM).Sampling of the liquid layer for 14 days demonstrated that ractopamine rapidly dissipated from the liquid layer. Less than 20% of the fortified dose remained in the liquid layer after 4 hr,and recoveries of dosed ractopamine ranged from 8 to 18% in the liquid layer at 336 hr. Sorption to soil was the major fate for ractopamine in soil:water systems, i.e., 42%–51% of the dose at14 days. The major portion of the sorbed fraction was comprised of non-extractables; a smaller fraction of the sorbed dose was extracted into water and acetone, portions which would be potentially mobile in the environment. Partitioning coefficients for all soils suggested strong sorption of ractopamine to soil which is governed by hydrophobic interactions and cation exchange complexes within the soil OM. Ractopamine degradation was observed, but to mostly non-polar compounds which had a higher potential than ractopamine to sorb to soil. The formation of volatiles was also suggested. Therefore, despite rapid and extensive soil sorption,these studies indicated a portion of ractopamine, present in manures used to fertilize soils,may be mobile in the environment via water-borne events.     

柠檬酸对核电站低放废液中110mAg吸附去除性能的影响

具有γ放射性的~(110m)Ag是核电站放射性废液中的主要核素之一,半衰期长,并且可以通过食物链在海洋生物中富集,研究其高效去除技术具有重要的意义.核电站化学去污过程加入的络合剂(如柠檬酸)对~(110m)Ag的化学形态和吸附性能有重要的影响.因此,本文首先模拟核电站水化学环境,研究了柠檬酸对~(110m)Ag化学形态的影响规律,其次研究了不同形态的~(110m)Ag物种在几种优选材料上的吸附性能.结果表明,由于核电站放射性废液的来源不同,柠檬酸与~(110m)Ag同时形成离子态络合物和~(110m)Ag0/柠檬酸纳米金属复合物;采用过氧化氢与紫外线联合高级氧化的方法能够破坏柠檬酸络合离子及~(110m)Ag0/柠檬酸复合物结构,形成单独的离子态~(110m)Ag+,从而有效地提高了~(110m)Ag物种的吸附去除性能.     

文丘里洗涤过滤型FCVS性能评价述评及建议

通过调研对国内外文丘里洗涤过滤型FCVS性能评价进展进行了阐述与比较,指出国内开展文丘里洗涤过滤型FCVS出厂性能评价不全面,需进一步开展相关性能评价技术研究;FCVS在现场的安装质量如何,随着时间的推移性能变化如何,并未开展试验验证,结合法规要求等,建议开展FCVS现场试验评价技术的研究。