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Paramagnetic radiation-induced defect centres and their correlation with the optical properties of irradiated advanced ceramic breeder pebbles 顺磁辐射诱导缺陷中心及其与辐照高级陶瓷增殖石光学性质的关系
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-12-01 DOI: 10.1016/j.nme.2025.102035
Andris Antuzevics , Guna Krieke , Jekabs Cirulis , Magdalena Rzepna , Maria Gonzalez , Julia M. Leys , Regina Knitter , Arturs Zarins
Advanced ceramic breeder (ACB) pebbles, primarily composed of lithium orthosilicate (Li4SiO4) with lithium metatitanate (Li2TiO3) as a second phase, are currently under development and testing as the European Union’s reference material for tritium breeding in future thermonuclear fusion reactors. In the present work, the formation and accumulation of paramagnetic radiation-induced defect centres is investigated and compared for the first time in the untreated and thermally pre-treated ACB pebbles under exposure to different types of ionising radiation. Electron paramagnetic resonance (EPR) spectroscopy is employed, with particular focus on correlating the detected EPR signals with the optical properties of the irradiated pebbles. The stability of the radiation-induced optical absorption bands and the positions of the main peaks in the thermally stimulated luminescence (TSL) glow curves are correlated to the annealing of the EPR signals at g = 2.04 and g = 2.00. Within the same temperature range, transformations occur among various radiation-induced electron-type centres, originating from structurally related sites formed in the bulk of the material. The annealing of these electron-type centres proceeds in multiple stages up to 350 °C, involving recombination with hole-type centres that exhibit different stabilities. The obtained results highlight the important role of paramagnetic centres in determining the optical properties of the irradiated ACB pebbles.
先进的陶瓷增殖剂(ACB)鹅卵石,主要由正硅酸锂(Li4SiO4)和偏钛酸锂(Li2TiO3)作为第二阶段组成,目前正在开发和测试中,作为欧盟未来热核融合反应堆中氚增殖的参考材料。在本研究中,首次研究了未处理和热预处理的ACB鹅卵石在不同类型电离辐射下顺磁辐射诱导缺陷中心的形成和积累。采用电子顺磁共振(EPR)光谱学,特别侧重于将检测到的EPR信号与辐照鹅卵石的光学性质相关联。在g = 2.04和g = 2.00时,辐射诱导光吸收带的稳定性和TSL发光曲线中主峰的位置与EPR信号的退火有关。在相同的温度范围内,在各种辐射诱导的电子型中心之间发生转变,这些中心起源于材料主体中形成的结构相关的位置。这些电子型中心的退火分多个阶段进行,温度可达350°C,涉及与表现出不同稳定性的空穴型中心的复合。所得结果强调了顺磁中心在确定辐照ACB鹅卵石光学性质中的重要作用。
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引用次数: 0
Tribological and microstructure evaluation of 17Cr ferritic ODS steel fabricated through vacuum hot pressing 真空热压制备17Cr铁素体ODS钢的摩擦学及显微组织评价
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-12-01 DOI: 10.1016/j.nme.2025.102041
G. Dharmalingam , Vishal Naranje , Vikas Sisodia
The wear behavior of high performance 17Cr Ferritic steel is crucial for their successful implementation in various industrial high temperature applications such as nuclear cladding tube, aerospace, engine exhaust chambers etc. This study focuses on the wear behavior analysis of 17Cr Ferritic Oxide Dispersion Strengthened (ODS) steel fabricated through the vacuum hot pressing (VHP) route. The wear resistance of the ODS steel is evaluated under different operating conditions, different sliding distance (500 m,1000 m &1500 m) and constant applied load followed by pin on disc wear testing. Comparisons are made with base material 430L ferritic steel(Sample 1) and Ferritic ODS steel (430L + 0.3Y2O3 + 0.5ZrO2 + 0.1Ti)wt% Sample 2 to compute the potential benefits of the ODS steel in terms of the density, hardness, microstructures and wear characteristics. It was observed that Ferritic ODS steel(Sample 2) shows better wear resistance than the base material (sample 1).
高性能17Cr铁素体钢的磨损性能对于其在核包层管、航空航天、发动机排气室等各种工业高温应用中的成功实施至关重要。对真空热压(VHP)工艺制备的17Cr氧化铁素体弥散强化(ODS)钢的磨损行为进行了研究。ODS钢在不同工况、不同滑动距离(500米、1000米和1500米)和恒定载荷下的耐磨性进行了评估,然后进行了销盘磨损试验。将基体材料430L铁素体钢(试样1)和铁素体ODS钢(430L + 0.3Y2O3 + 0.5ZrO2 + 0.1Ti)wt%试样2进行比较,计算ODS钢在密度、硬度、显微组织和磨损特性方面的潜在优势。结果表明,铁素体ODS钢(样品2)的耐磨性优于母材(样品1)。
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引用次数: 0
Investigations on boronisation in the full-tungsten ASDEX UPGRADE 全钨ASDEX UPGRADE中硼化的研究
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-12-01 DOI: 10.1016/j.nme.2025.102036
Volker Rohde, Karl Krieger, Tim-Oliver Hohmann, Andreas Redl, Jörg Hobirk, Sehoon An, Sangeetha Sasidharan, ASDEX UPGRADE Team , EUROfusion Tokamak Exploitation Team
Conditioning of the Plasma-Facing Surfaces (PFSs) in fusion devices is essential for reliable plasma operation. In ASDEX Upgrade (AUG), boronisation by a glow discharge in helium (He) with 10% of deuterated diborane is used as a standard wall conditioning technique. The recent transition of the PFSs in ITER to full tungsten has triggered considerable interest in the wall-conditioning methods employed in present-day full-metal fusion devices. In this paper first results on new investigation at AUG are reported. Although plasma start-up without boronisation in ITER-like divertor configuration was not successful, applying boronisation, even with only half of the anodes active, enabled easy operation. Spectroscopic investigations of limiters indicate that the reduction in tungsten erosion is not due to boron layer coverage, but due to the reduction of oxygen content, which is the dominant ion responsible for sputtering tungsten. Quartz microbalance instruments installed at AUG at different positions allow insitu realtime measurement of the deposition for each boronisation. Switching off one anode reduces the deposition by less than a factor of two, in contrast to simulations that predicted strongly localized boron (B) deposition near anodes, with reduction of 2 to 3 orders of magnitude in regions between them. This discrepancy may arise from the sticking coefficient of the precursor species, a key factor in layer homogeneity, as indicated bya cavity probe.
Witness samples of different substrates exposed during coating using a manipulator allow to analyse the layers by ion beam techniques. The amount of boron deposited depends on the kind of substrate. For relevant materials, deuterium (D) to boron (B) ratio, D/B < 0.3 is found, indicating chemically active layers. Silicon and carbon substrates show higher D content specially after exposure to tokamak plasmas. The D content in the layers is strongly reduced after exposure to air.
在聚变装置中,等离子体面(pfs)的调节是等离子体可靠运行的必要条件。在ASDEX Upgrade (AUG)中,在氦气(He)中加入10%的氘化二硼烷,通过辉光放电进行硼化,作为标准的壁调节技术。最近,ITER中pfs向全钨的转变引发了人们对目前全金属聚变装置中采用的壁面调节方法的极大兴趣。本文报道了在AUG上新研究的初步结果。虽然在类似iter的分流器配置中,没有硼化的等离子体启动并不成功,但即使只有一半的阳极是活跃的,应用硼化也可以使操作变得容易。限制剂的光谱研究表明,钨腐蚀的减少不是由于硼层的覆盖,而是由于氧含量的减少,氧含量是导致钨溅射的主要离子。安装在AUG不同位置的石英微天平仪器允许对每个硼化的沉积进行现场实时测量。与预测阳极附近强烈局部硼(B)沉积的模拟结果相反,关闭一个阳极减少的沉积量不到两倍,在阳极之间的区域减少了2到3个数量级。这种差异可能是由前驱体的粘附系数引起的,这是层均匀性的关键因素,如腔探针所示。在涂层过程中,使用操纵器对暴露的不同衬底样品进行观察,从而可以通过离子束技术对层进行分析。硼的沉积量取决于衬底的种类。相关材料中氘(D)与硼(B)之比D/B <; 0.3,表明存在化学活性层。硅基片和碳基片经托卡马克等离子体照射后,其D含量更高。在暴露于空气后,层内的D含量明显降低。
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引用次数: 0
In-situ water signal calibration method for thermal desorption spectroscopy 热解吸光谱原位水信号定标方法
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-12-01 DOI: 10.1016/j.nme.2025.102029
Thomas Schwarz-Selinger, Thomas Dürbeck, Armin Manhard
A method is presented that allows to quantify water desorption in a thermal desorption spectroscopy (TDS) setup in-situ. It is based on deuterium (D) desorption from D-containing tungsten covered with a thin, electro-chemically grown tungsten oxide layer. The method is based on the fact that diffusing deuterium is known to react with amorphous tungsten oxide, forming HDO and D2O. A stable deuterium reservoir underneath the oxide is accomplished by MeV tungsten ion irradiation to create a so-called self-damaged tungsten layer that is loaded with deuterium with a low-temperature plasma prior to oxidation. The total deuterium amount in the sample is determined with 3He Nuclear Reaction Analysis (3He-NRA) before the TDS measurement. Detecting all deuterium-containing molecules desorbing during TDS and closing the particle balance with the known total deuterium amount from 3He-NRA, the calibration factor for water can be determined. The calibration factor is found to be close to the one of e.g. deuterium or hydrogen. It agrees with tabulated values but contradicts the usual assumption that water cannot be treated in a quantitative manner in TDS because it is highly likely to stick to surfaces and thus would be lost on the way to the mass spectrometer. The result suggests that this general assumption is not always applicable. At least for the case where the gas flow does not consist solely of water but is a mixture of water and hydrogen molecules, quantification is still possible. Because the method simply relies on the desorption of gases from a sample of typical size it can be applied to any existing TDS setup without modifying the latter. However, care must be taken for TDS systems were the sample environment is undefined and water signals stem not from the sample under investigation alone but from undefined outgassing of the surrounding materials.
提出了一种在原位热解吸光谱(TDS)装置中定量测定水解吸的方法。它是基于氘(D)解吸从含D的钨覆盖薄,电化学生长的氧化钨层。该方法是基于这样一个事实,即扩散的氘已知与无定形氧化钨反应,形成HDO和D2O。通过MeV钨离子辐照形成所谓的自毁钨层,在氧化前用低温等离子体装载氘,从而在氧化物下方形成稳定的氘储层。在TDS测量之前,用3He核反应分析法(3He- nra)测定样品中的总氘量。检测TDS过程中所有含氘分子的解吸,并与已知的3He-NRA总氘量关闭粒子平衡,可以确定水的校准因子。校正因子与氘或氢等元素的校正因子相近。它与表中的值一致,但与通常的假设相矛盾,即水不能在TDS中以定量的方式处理,因为水很可能粘在表面上,因此会在通往质谱仪的途中丢失。结果表明,这种一般假设并不总是适用的。至少对于气体流不完全由水组成,而是水和氢分子的混合物的情况,量化仍然是可能的。由于该方法仅依赖于典型尺寸样品的气体解吸,因此可以应用于任何现有的TDS装置,而无需修改后者。然而,对于TDS系统,如果样品环境是不确定的,水信号不是单独来自被调查的样品,而是来自周围材料的不确定的脱气,则必须小心。
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引用次数: 0
Thermal cycling experiment of biphasic Li4SiO4-Li2TiO3 EU reference tritium breeder ceramics 双相Li4SiO4-Li2TiO3铕参考氚增殖陶瓷的热循环实验
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-12-01 DOI: 10.1016/j.nme.2025.102038
Julia Leys, Oliver Leys, Regina Knitter
The thermal cycling behaviour of Advanced Ceramic Breeder (ACB) pebbles was investigated in a temperature range from 300 to 800 °C in a He + 0.1 vol% H2 gas atmosphere for up to 30 cycles. For the experiment, two batches of ACB pebbles, each with a nominal composition of 70  mol% Li4SiO4 and 30  mol% Li2TiO3 and comparable material properties, were selected. One cycle comprised 12  h at 300 °C and 12  h at 800 °C (heating rate: 10  K/min, cooling rate: ∼0.5  K/min). Different material properties were measured before the experiment and after 2, 14, and 30 cycles. Comparable to previous long-term thermal treatments, the ACB pebbles also show a good performance during thermal cycling. They remain stable with regard to their chemical and phase composition. No significant changes occur with regard to their microstructure and porosity. The mechanical stability is decreased after 2 cycles and remains stable afterwards.
研究了高级陶瓷增殖剂(ACB)鹅卵石在300 ~ 800℃的温度范围内,在He + 0.1 vol% H2气氛中进行30次循环的热循环行为。在实验中,选择了两批ACB鹅卵石,每批鹅卵石的标称成分为70 mol% Li4SiO4和30 mol% Li2TiO3,材料性能相当。一个循环包括在300°C下12小时和在800°C下12小时(加热速率:10 K/min,冷却速率:~ 0.5 K/min)。分别在实验前、循环2次、循环14次和循环30次后测量不同材料的性能。与之前的长期热处理相比,ACB鹅卵石在热循环过程中也表现出良好的性能。它们的化学和相组成保持稳定。在微观结构和孔隙度方面没有明显的变化。机械稳定性在2次循环后下降,之后保持稳定。
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引用次数: 0
Biasing effects on hydrogen isotope transport and permeation in the gaps of monoblock plasma-facing components 偏置效应对单块等离子体组件间隙中氢同位素输运和渗透的影响
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-12-01 DOI: 10.1016/j.nme.2025.102040
Qian Xu , Haishan Zhou , Gakushi Kawamura , Xuechun Li , Haodong Liu , Guang-Nan Luo
Hydrogen isotope (HI) permeation through millimeter-scale gaps in tungsten monoblocks poses a critical challenge to tritium safety in fusion reactors. Although substrate biasing is widely employed to simulate the fusion boundary environment, its specific impact on hydrogen transport and permeation within these gaps remains inadequately understood. By integrating experimental measurements from the PREFACE facility with 2D3V particle-in-cell (PIC) simulations, this study clarifies how a negative bias of –100 V affects HI permeation behavior. Contrary to initial expectations, biasing enhances ion flux but does not lead to a net increase in permeation flux at the gap bottom. Simulations reveal that this results from a key decoupling between ion deposition and net retention: the applied bias directs ions toward the gap bottom with elevated impact energies (∼100 eV), which promotes sputtering and reflection, thereby reducing effective retention. In contrast, under floating conditions, funnel-like sheath fields guide ions through multiple sidewall reflections, gradually channeling low-energy particles to the bottom region, where permeation is more efficient. This work clarifies the biasing effect on permeation by establishing electric-field-controlled ion energy and trajectory as the governing mechanism, offering valuable insights for the design of plasma-facing components to mitigate tritium leakage.
氢同位素(HI)通过钨块中毫米级间隙的渗透对聚变反应堆中氚的安全性提出了关键挑战。尽管衬底偏置被广泛用于模拟聚变边界环境,但其对这些间隙内氢传输和渗透的具体影响仍未充分了解。通过将前言设备的实验测量与2D3V的电池内粒子(PIC)模拟相结合,本研究阐明了-100 V的负偏置如何影响HI渗透行为。与最初的预期相反,偏置增强了离子通量,但并不导致间隙底部渗透通量的净增加。模拟表明,这是离子沉积和净保留之间的关键解耦的结果:施加的偏压使离子以更高的冲击能量(~ 100 eV)朝向间隙底部,这促进了溅射和反射,从而降低了有效保留。相比之下,在漂浮条件下,漏斗状鞘场引导离子通过多次侧壁反射,逐渐将低能粒子引导到底部区域,在那里渗透效率更高。本研究通过建立电场控制离子能量和轨迹作为控制机制,阐明了偏态对渗透的影响,为设计面向等离子体的元件来减轻氚泄漏提供了有价值的见解。
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引用次数: 0
Recollections for the 50th anniversary of the plasma surface interactions (PSI) in controlled fusion devices conference 受控聚变装置等离子体表面相互作用(PSI)会议50周年回顾
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-12-01 DOI: 10.1016/j.nme.2025.102037
A. Grosman , J. Roth , J. Winter , J. Li , N. Ohno , R. Maingi
The Plasma Surface Interactions in Controlled Fusion Devices (PSI) conference reached an important milestone in 2024 with its 50th anniversary. It was celebrated at its venue in Marseille by a special round table discussion gathering 6 former chairmen of its Programme Committees, who gave some highlights presented at the conference during the five decades. The article provides a summary of this overview.
受控聚变装置中的等离子体表面相互作用(PSI)会议在2024年迎来了50周年纪念,这是一个重要的里程碑。会议在马赛举行,由6位规划委员会前任主席参加的特别圆桌讨论会庆祝,他们介绍了50年来在会议上提出的一些亮点。本文提供了这一概述的摘要。
{"title":"Recollections for the 50th anniversary of the plasma surface interactions (PSI) in controlled fusion devices conference","authors":"A. Grosman ,&nbsp;J. Roth ,&nbsp;J. Winter ,&nbsp;J. Li ,&nbsp;N. Ohno ,&nbsp;R. Maingi","doi":"10.1016/j.nme.2025.102037","DOIUrl":"10.1016/j.nme.2025.102037","url":null,"abstract":"<div><div>The Plasma Surface Interactions in Controlled Fusion Devices (PSI) conference reached an important milestone in 2024 with its 50th anniversary. It was celebrated at its venue in Marseille by a special round table discussion gathering 6 former chairmen of its Programme Committees, who gave some highlights presented at the conference during the five decades. The article provides a summary of this overview.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 102037"},"PeriodicalIF":2.7,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145694164","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tensile properties of EUROFER97-3 after neutron irradiation at 330 °C and 540 °C to damage doses of 19–23 dpa 在330°C和540°C中子辐照19 - 23dpa损伤剂量下,EUROFER97-3的拉伸性能
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-12-01 DOI: 10.1016/j.nme.2025.102034
Vladimir Chakin, Carsten Bonnekoh, Ramil Gaisin, Rainer Ziegler, Michael Duerrschnabel, Michael Klimenkov, Bronislava Gorr, Michael Rieth
The reduced activation ferritic-martensitic (RAFM) EUROFER97-3 steel of two heat treatments (EUROFER97-3_1100/700 and EUROFER97-3_980/780) after irradiation in the BOR-60 fast reactor at temperatures of 330 °C and 540 °C, with damage doses ranging from 19.2 to 23.3 dpa exhibited fundamentally different changes in tensile properties depending on the irradiation temperature, regardless of the heat treatment used. Significant radiation hardening and embrittlement were observed after irradiation at 330 °C. In contrast, irradiation at 540 °C resulted in only minor alterations to the tensile properties compared to the unirradiated reference state. These changes can be attributed to the formation of radiation-induced defects and fine precipitates, as well as an evolution in the original phase structure.
两种热处理(EUROFER97-3_1100/700和EUROFER97-3_980/780)的还原活化铁素体-马氏体(RAFM) EUROFER97-3钢在330℃和540℃的BOR-60快堆中辐照后,损伤剂量范围为19.2 ~ 23.3 dpa,无论采用何种热处理方式,其拉伸性能随辐照温度的变化都有根本的不同。在330°C辐照后,观察到明显的辐射硬化和脆化。相比之下,与未辐照的参考状态相比,540°C辐照只导致拉伸性能的微小变化。这些变化可以归因于辐射诱导缺陷和细小沉淀的形成,以及原始相结构的演变。
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引用次数: 0
Application of an improved WallDYN surface model to estimate ITER boronization layer lifetime 应用改进的WallDYN表面模型估算ITER硼化层寿命
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-12-01 DOI: 10.1016/j.nme.2025.102033
K. Schmid
The WallDYN code was developed to model the coupled evolution of the impurity influx onto the first wall, the surface composition and the flux of impurities back into the plasma in fusion devices. It was recently shown that its default surface erosion/deposition model is poorly suited to describe cases where impurity sources deplete over time, causing net deposition zones to become net erosion zones, because it has a limited memory of previously deposited materials amounts. Therefore, the model was augmented by a dedicated deposition layer that records the deposited material allowing to re-erode it later and thus maintain a global material balance. The augmented surface model is compared to dynamic SDTrimSP calculations to verify its ability to model layer growth/recession and mixed material formation. Finally, recently published calculations on the B migration in ITER are repeated with the improved model and predictions on the B layer lifetime in the main chamber and layer deposition in divertor are refined.
开发了WallDYN代码来模拟聚变装置中杂质流入第一壁、表面组成和杂质流回等离子体的耦合演化。最近的研究表明,其默认的表面侵蚀/沉积模型不太适合描述杂质源随着时间的推移而耗尽的情况,导致净沉积区变成净侵蚀区,因为它对先前沉积的材料量的记忆有限。因此,该模型通过一个专门的沉积层来增强,该沉积层记录了沉积的物质,允许以后重新侵蚀它,从而保持全球物质平衡。将增强表面模型与动态SDTrimSP计算进行比较,以验证其模拟层生长/衰退和混合材料形成的能力。最后,用改进后的模型重复了最近发表的ITER中B层迁移的计算,并对主室中B层寿命和导流器中B层沉积的预测进行了改进。
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引用次数: 0
Modelling of tungsten prompt redeposition at the inner wall of ITER during ramp-up 加速过程中ITER内壁钨离子快速再沉积的模拟
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-11-19 DOI: 10.1016/j.nme.2025.102031
A. Kirschner , C. Baumann , S. Brezinsek , Ch. Linsmeier , R.A. Pitts , A.A. Pshenov , J. Romazanov
The prompt redeposition of sputtered tungsten at the inner wall of ITER during current ramp-up has been simulated with the ERO code. Plasma parameters from SOLPS-ITER for a medium-density (with a peak electron density of 4E12 cm−3 at the inner wall) and a high-density (1E13 cm−3) case have been used as input for ERO. Simulations without anomalous cross-field diffusion for sputtered tungsten ions reveal peaked prompt redeposition profiles in poloidal direction. At the tangency point with largest electron temperature and density, maximum prompt redeposition fractions of about 60 % for the medium density and 80 % for the high density case occur. At a distance of 50 cm away from the tangency point, prompt redeposition decreases to 10 % (medium-density) and 20 % (high-density case). The simulations without anomalous cross-field diffusion show that the overall redeposition is the same as the prompt redeposition thus the overall redeposition is only due to prompt redeposition. An anomalous cross-field diffusion of 1 m2/s leads to slightly increased prompt redeposition, however, for both medium and high-density case there is now also a significant amount of non-prompt redeposition. The modelled profiles of prompt redeposition can be used as input for plasma simulation codes like SOLPS-ITER to improve the assumptions of net tungsten wall sources.
用ERO程序模拟了在电流加速过程中溅射钨在ITER内壁的快速再沉积。从中密度(内壁峰值电子密度为4E12 cm−3)和高密度(1E13 cm−3)的情况下,SOLPS-ITER的等离子体参数被用作ERO的输入。在没有异常交叉场扩散的情况下,对溅射钨离子的模拟显示了在极向方向上的峰值提示再沉积曲线。在电子温度和密度最大的切点处,中等密度和高密度情况下的最大快速再沉积分数分别约为60%和80%。在距离切点50cm处,迅速再沉积下降到10%(中密度)和20%(高密度)。不存在异常交叉扩散的模拟结果表明,总体再沉积与瞬时再沉积相同,因此总体再沉积只是由瞬时再沉积引起的。1 m2/s的异常跨场扩散会导致提示性再沉积略有增加,然而,对于中等和高密度的情况,现在也有大量的非提示性再沉积。模拟的快速再沉积剖面可以作为SOLPS-ITER等等离子体模拟代码的输入,以改进净钨壁源的假设。
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引用次数: 0
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Nuclear Materials and Energy
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