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美国能源部拨款2600万美元资助基于同意的乏核燃料选址 快报文章
地球科学快报,2023年第12期
作者:  刘文浩
Microsoft Word(16Kb)  |  收藏  |  浏览/下载:535/0  |  提交时间:2023/06/25
DOE  Spent Nuclear Fuel  Consent-Based Siting  
WNA发布《核燃料报告:2021—2040年全球全球需求和供应情况》 快报文章
地球科学快报,2021年第18期
作者:  刘学
Microsoft Word(14Kb)  |  收藏  |  浏览/下载:722/0  |  提交时间:2021/09/24
Nuclear Fuel  uranium mining  World Nuclear Association  
英国发布先进核燃料循环路线图 快报文章
气候变化快报,2021年第14期
作者:  廖琴
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Net Zero  Advacned Nuclear Fuel  Clean Energy  
Preindustrial (CH4)-C-14 indicates greater anthropogenic fossil CH4 emissions 期刊论文
NATURE, 2020, 578 (7795) : 409-+
作者:  Keener, Megan;  Hunt, Camden;  Carroll, Timothy G.;  Kampel, Vladimir;  Dobrovetsky, Roman;  Hayton, Trevor W.;  Menard, Gabriel
收藏  |  浏览/下载:25/0  |  提交时间:2020/05/13

Atmospheric methane (CH4) is a potent greenhouse gas, and its mole fraction has more than doubled since the preindustrial era(1). Fossil fuel extraction and use are among the largest anthropogenic sources of CH4 emissions, but the precise magnitude of these contributions is a subject of debate(2,3). Carbon-14 in CH4 ((CH4)-C-14) can be used to distinguish between fossil (C-14-free) CH4 emissions and contemporaneous biogenic sources  however, poorly constrained direct (CH4)-C-14 emissions from nuclear reactors have complicated this approach since the middle of the 20th century(4,5). Moreover, the partitioning of total fossil CH4 emissions (presently 172 to 195 teragrams CH4 per year)(2,3) between anthropogenic and natural geological sources (such as seeps and mud volcanoes) is under debate  emission inventories suggest that the latter account for about 40 to 60 teragrams CH4 per year(6,7). Geological emissions were less than 15.4 teragrams CH4 per year at the end of the Pleistocene, about 11,600 years ago(8), but that period is an imperfect analogue for present-day emissions owing to the large terrestrial ice sheet cover, lower sea level and extensive permafrost. Here we use preindustrial-era ice core (CH4)-C-14 measurements to show that natural geological CH4 emissions to the atmosphere were about 1.6 teragrams CH4 per year, with a maximum of 5.4 teragrams CH4 per year (95 per cent confidence limit)-an order of magnitude lower than the currently used estimates. This result indicates that anthropogenic fossil CH4 emissions are underestimated by about 38 to 58 teragrams CH4 per year, or about 25 to 40 per cent of recent estimates. Our record highlights the human impact on the atmosphere and climate, provides a firm target for inventories of the global CH4 budget, and will help to inform strategies for targeted emission reductions(9,10).


Isotopic evidence from ice cores indicates that preindustrial-era geological methane emissions were lower than previously thought, suggesting that present-day emissions of methane from fossil fuels are underestimated.


  
Redox-switchable carboranes for uranium capture and release 期刊论文
NATURE, 2020, 577 (7792) : 652-+
作者:  Marques, Joao C.;  Li, Meng;  Schaak, Diane;  Robson, Drew N.;  Li, Jennifer M.
收藏  |  浏览/下载:31/0  |  提交时间:2020/07/03

The uranyl ion (UO22+  U(vi) oxidation state) is the most common form of uranium found in terrestrial and aquatic environments and is a central component in nuclear fuel processing and waste remediation efforts. Uranyl capture from either seawater or nuclear waste has been well studied and typically relies on extremely strong chelating/binding affinities to UO22+ using chelating polymers(1,2), porous inorganic(3-5) or carbon-based(6,7) materials, as well as homogeneous(8) compounds. By contrast, the controlled release of uranyl after capture is less established and can be difficult, expensive or destructive to the initial material(2,9). Here we show how harnessing the redox-switchable chelating and donating properties of an ortho-substituted closo-carborane (1,2-(Ph2PO)(2)-1,2-C2B10H10) cluster molecule can lead to the controlled chemical or electrochemical capture and release of UO22+ in monophasic (organic) or biphasic (organic/aqueous) model solvent systems. This is achieved by taking advantage of the increase in the ligand bite angle when the closo-carborane is reduced to the nido-carborane, resulting in C-C bond rupture and cage opening. The use of electrochemical methods for uranyl capture and release may complement existing sorbent and processing systems.


Redox-switchable chelation is demonstrated for a carborane cluster molecule, leading to controlled chemical or electrochemical capture and release of uranyl in monophasic or biphasic model solvent systems.


  
Property values and tax rates near spent nuclear fuel storage 期刊论文
ENERGY POLICY, 2018, 123: 433-442
作者:  Munro, Kirstin;  Tolley, George
收藏  |  浏览/下载:1/0  |  提交时间:2019/04/09
Nuclear power  Spent nuclear fuel storage  Property taxes  Real estate values  
Integrated system evaluation of nuclear fuel cycle options in China combined with an analytical MCDM framework 期刊论文
ENERGY POLICY, 2018, 114: 221-233
作者:  Gao, Ruxing;  Nam, Hyo On;  Ko, Won Il;  Jang, Hong
收藏  |  浏览/下载:1/0  |  提交时间:2019/04/09
MCDM framework  Nuclear sustainability  Nuclear fuel cycle  Dynamic model  
Economic potential of fuel recycling options: A lifecycle cost analysis of future nuclear system transition in China 期刊论文
ENERGY POLICY, 2017, 101
作者:  Gao, Ruxing;  Choi, Sungyeol;  Ko, Won Il;  Kim, Sungki
收藏  |  浏览/下载:0/0  |  提交时间:2019/04/09
Levelized cost  Fuel cycle transition  Probabilistic approach  Spent nuclear fuel management  
A Historical Evaluation of the U15 Complex, Nevada National Security Site, Nye County, Nevada 科技报告
来源:US Department of Energy (DOE). 出版年: 2014
作者:  Drollinger, Harold;  Holz, Barbara A;  Bullard, Thomas F;  Goldenberg, Nancy G;  Ashbaugh, Laurence J;  Griffin, Wayne R
收藏  |  浏览/下载:8/0  |  提交时间:2019/04/05
This report presents a historical evaluation of the U15 Complex on the Nevada National Security Site (NNSS) in southern Nevada. The work was conducted by the Desert Research Institute at the request of the U.S. Department of Energy  National Nuclear Security Administration Nevada Field Office and the U.S. Department of Defense  Defense Threat Reduction Agency. Three underground nuclear tests and two underground nuclear fuel storage experiments were conducted at the complex. The nuclear tests were Hard Hat in 1962  Tiny Tot in 1965  and Pile Driver in 1966. The Hard Hat and Pile Driver nuclear tests involved different types of experiment sections in test drifts at various distances from the explosion in order to determine which sections could best survive in order to design underground command centers. The Tiny Tot nuclear test involved an underground cavity in which the nuclear test was executed. It also provided data in designing underground structures and facilities to withstand a nuclear attack. The underground nuclear fuel storage experiments were Heater Test 1 from 1977 to 1978 and Spent Fuel Test - Climax from 1978 to 1985. Heater Test 1 was used to design the later Spent Fuel Test - Climax experiment. The latter experiment was a model of a larger underground storage facility and primarily involved recording the conditions of the spent fuel and the surrounding granite medium. Fieldwork was performed intermittently in the summers of 2011 and 2013  totaling 17 days. Access to the underground tunnel complex is sealed and unavailable. Restricted to the surface  four buildings  four structures  and 92 features associated with nuclear testing and fuel storage experiment activities at the U15 Complex have been recorded. Most of these are along the west side of the complex and next to the primary access road and are characteristic of an industrial mining site  albeit one with scientific interests. The geomorphological fieldwork was conducted over three days in the summer of 2011. It was discovered that major modifications to the terrain have resulted from four principal activities. These are road construction and maintenance  mining activities related to development of the tunnel complex  site preparation for activities related to the tests and experiments  and construction of drill pads and retention ponds. Six large trenches for exploring across the Boundary geologic fault are also present. The U15 Complex  designated historic district 143 and site 26NY15177  is eligible to the National Register of Historic Places under Criteria A  C  and D of 36 CFR Part 60.4. As a historic district and archaeological site eligible to the National Register of Historic Places  the Desert Research Institute recommends that the area defined for the U15 Complex  historic district 143 and site 26NY15117  be left in place in its current condition. The U15 Complex should also be included in the NNSS cultural resources monitoring program and monitored for disturbances or alterations.