Liquid Lithium Research Articles

Poly(ionic) Liquid-Enhanced Ion Dynamics in Cellulose-Derived Gel Polymer Electrolytes.

Gel polymer electrolytes (GPEs) are regarded as a promising alternative to conventional electrolytes, combining the advantages of solid and liquid electrolytes. Leveraging the abundance and eco-friendliness of cellulose-based materials, GPEs were produced using methyl cellulose and incorporating various doping agents, either an ionic liquid (1-Butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide [Pyr14][TFSI]), its polymeric ionic liquid analogue (Poly(diallyldimethylammonium bis(trifluoromethylsulfonyl)imide) [PDADMA][TFSI]), or an anionically charged backbone polymeric ionic liquid (lithium poly[(4-styrenesulfonyl)(trifluoromethyl(S-trifluoromethylsulfonylimino) sulfonyl) imide] LiP[STFSI]). The ion dynamics and molecular interactions within the GPEs were thoroughly analyzed using Attenuated Total Reflectance Fourier-Transform Infrared Spectroscopy (ATR-FTIR), Heteronuclear Overhauser Enhancement Spectroscopy (HOESY), and Pulsed-Field Gradient Nuclear Magnetic Resonance Diffusion (PFG-NMR). Li+ transference numbers (tLi+) were successfully calculated. Our study found that by combining slow-diffusing polymeric ionic liquids (PILs) with fast-diffusing lithium salt, we were able to achieve transference numbers comparable to those of liquid electrolytes, especially with the anionic PIL, LiP[STFSI]. This research highlights the influence of the polymer's nature on lithium-ion transport within GPEs. Additionally, micro supercapacitor (MSC) devices assembled with these GPEs exhibited capacitive behavior. These findings suggest that further optimization of GPE composition could significantly improve their performance, thereby positioning them for application in sustainable and efficient energy storage systems.

Preparation and ferroelectric properties of metal-organic frame lithium ion liquid crystal composites

ABSTRACT Two series of lithium ion liquid-crystalline composites (LCCs) containing metal-organic frame (MOF) materials were fabricated via a self-assembly process by use of poly(4-styrenesulfonic acid) lithium polymers, a cholesteryl-based liquid-crystalline monomer with terminal sulphonic acid group, and Fe-MIL-53_NH2. The chemical structure, chiral smectic C mesophase and ferroelectric property of the LCCs were characterised by various instruments, and the effect of liquid crystal monomer and lithium polymers on the ferroelectric property were investigated. The cholesteryl-based liquid crystal monomer presents a dominant role in the ferroelectric property of the LCCs, in which the asymmetric carbon atoms are responsible for the spontaneous polarisation. For the LCCs, the mechanical properties and porous loading characteristics of liquid crystal polymer are improved by the MOF materials, and the lithium-ion polymer connects the liquid crystal monomer with the MOF by ionic bond and improves the polarity of the material. When the electric field changed from −10 V and 10 V, the maximum residual polarisation strength (Pr) of the LCCs reached 74.82 nC/cm2. Because the LCCs showed excellent ferroelectric and mechanical properties, it has some potentials of application in the field of ferroelectric materials.

Eliminating the effect of pH: Dual-matrix modulation adsorbent enables efficient lithium extraction from concentrated seawater

Lithium ion sieve adsorbents frequently extract liquid lithium resources due to their adsorption effect and cost advantages. However, the adsorption effect is significantly influenced by the ambient pH. The pH effects on the adsorption process can be categorized into two main areas: the competition adsorption of impurity ions and the difference in surface zeta potential. A dual-matrix modulation adsorbent was prepared, comprising a carrier matrix modified with zwitterionic quaternary ammonium bases and an adsorption matrix modified with carboxylation. The zwitterionic quaternary ammonium base groups were employed to mitigate the competitive adsorption of impurity ions by acid-base neutralization. Furthermore, the negative charge of carboxyl groups was employed to diminish the discrepancy in surface zeta potential. The adsorption effect of the ion sieve adsorbent under natural conditions appeared to be significantly enhanced by the dual-matrix modulation, with the saturated adsorption capacity (28 mg/g) and adsorption selectivity (α(Li+/Mg2+)=24.23) being 6.3 and 7.8 times higher than that of the manganese-based adsorbent (HMO) under the same conditions, respectively. Moreover, the adsorption effect was found to be consistent with HMO under alkaline conditions. The results demonstrate that by optimizing the adsorption conditions of the adsorbent, the detrimental impact of pH on the adsorption process of lithium ion sieves can be eliminated.

Selective ion channel adsorbents facilitate efficient and low environmental impact extraction of liquid lithium resources

As lithium is the cornerstone of green energy development, it is crucial to realize a low environmental impact and efficient lithium extraction process. Ion-sieve adsorption is the most widely used method to extract liquid lithium resources, but this method is only efficient under alkaline conditions for H+ and Mg2+ competing adsorption. Conventional methods are often accompanied by the consumption of quantities of alkali, the generation of solid waste, and the acidification of liquid lithium resources. To address these issues, a selective ion-channel adsorbent was constructed. The composition comprises an ion sieve adsorbent and an organic carrier with a zwitterionic quaternary ammonium base group. This group storages OH-in situ, hinders H+ diffusion, slows down Mg2+ diffusion, and accelerates Li+ diffusion by relying on the difference in binding energies, which reduces the competing adsorption and avoids acidification and solid waste generation. The saturated adsorption capacity (21.38mg/g) and selectivity of the adsorbent are 4.7 and 24 times higher than that of conventional ion-sieve adsorbent under neutral conditions respectively. The dosage of alkali is 1/256 of the traditional method, the effluent remains neutral and no solid waste is generated. This study presents an environmental and effective adsorbent for lithium extraction.

Boosting electrochemical performance by regulating rigid-flexible microphase separation of multiblock copolymers

The growth of lithium dendrites and associated safety issues hinder the further development of liquid lithium metal batteries. A novel rigid-flexible multiblock copolymer PBC-mb-PBS was successfully synthesized based on molecular design. Incorporating crystalline rigid phase polybutylene succinate (PBS) into PBC-mb-PBS significantly enhances its tensile strength and low-temperature toughness through physical crosslinking. The flexible polydibutyl 2-(2-cyanoethyl)malonate (PBC) phase with side-chain cyano groups facilitate ionic conduction, forming a LiN-rich stabilized interfacial layer, thereby improving oxidative stability and high-voltage cathode compatibility. A series of multiblock copolymers with varying segment lengths were synthesized to balance mechanical properties and ionic conductivity by adjusting microphase separation. The quasi-solid-state polymer electrolyte (QSPE), derived from PBC-mb-PBS with the molar block ratio of 0.42, exhibits optimal electrochemical performance with ionic conductivity of 6.20 × 10−5 S cm−1 at 30 °C and 4.22 × 10−4 S cm−1 at 60 °C. Due to its bicontinuous microphase structure, it also shows excellent mechanical strength and promotes uniform lithium deposition at high current densities. Li//LiFePO4 and Li//LiNi0.83Co0.05Mn0.12O2 cells demonstrate high capacity retention, confirming the potential of this polymer electrolyte in high-voltage applications. This design strategy offers insights for developing quasi-solid-state lithium metal batteries with superior overall performance.

Chemical and structural durability of α-Al2O3 and γ-LiAlO2 layers formed on ODS FeCrAl alloys in liquid lithium lead stirred flow

The protection performance of an α-Al2O3 layer formed on oxide dispersion-strengthened (ODS) FeCrAl alloys in liquid LiPb flow was investigated by means of the corrosion tests under stirred-flow condition at 873 K for 1000 h. The result of STEM/EELS analysis indicated the Li adsorption and diffusion into α-Al2O3 layer. The ODS FeCrAl alloys in-situ formed a durable γ-LiAlO2 layer on their bare surface in liquid LiPb. The results of micro scratch tests on the protective layers indicated that they revealed strong resistance against the exfoliation in a shearing direction after the immersion to liquid LiPb.

Coupled model for liquid lithium plasma facing components

Numerical analysis provides the design choice and operating window of liquid metal Plasma Facing Components (PFC) concepts. Coupled analysis of boundary plasma together with the surrounding boundary structures is required. To achieve this goal, PPPL is developing a comprehensive multi-physics model for modeling of PFCs in fusion devices. The model includes the fluid-kinetic code SOLPS-ITER and the flow and heat transfer code CFX from ANSYS. SOLPS-ITER was augmented with a liquid metal boundary condition algorithm, allowing direct two-way coupling of the plasma analysis with the two-dimensional analytical slab flow model which includes heat convection in the liquid metal PFC. The target heat flux resulting from this coupled analysis is used as a boundary condition for detailed 3D Computational Fluid Dynamics (CFD) Magneto Hydro Dynamics (MHD) and heat transfer analysis. A new formulation of MHD equations is introduced in the numerical procedure ensuring current conservation of the discretized equations. Results of the 3D analysis are used for final validation of the coupled model. A PFC design where a porous wall is used to stabilize the liquid metal surface, while MHD drive is used to push the liquid metal flow inside the PFC, will be investigated in the regimes where vapor shielding is created for enhanced volumetric plasma heat dissipation.

Fusing together an outline design for sustained fuelling and tritium self-sufficiency.

Ensuring tritium fuel self-sufficiency while maintaining continuous and high-specification fuel flow to the tokamak via a low tritium inventory and controllable fuel cycle is a significant challenge to the STEP plant design. Effective and high-quality fuelling and exhaust design is required to sustain and control a stable plasma, whereas fuel sufficiency is required to prevent depletion of available tritium supply. Concerns regarding the lack of tritium availability preventing continuous tritium import are countered by breeding, where highly energetic neutrons from the core fusion reactions interact with lithium atoms suspended in the surrounding breeder blanket to produce tritium. The compact nature of STEP prohibits the integration of inboard breeder blankets posing a significant challenge for the design team looking to ensure more tritium is bred and made available than consumed within the core plasma. This paper outlines how purposeful technology selection and system architecting has converged on the outline of a conceivable and tritium-capable fuel cycle and breeder blanket design. Before introducing the STEP fuel cycle design outline and summarizing the approach undertaken to address the challenges facing plasma fuelling, key aspects of fuel self-sufficiency are discussed. This includes discussing a proposed helium-cooled liquid lithium breeder blanket and possible technology options for tritium extraction from lithium. Lastly, there is a brief process modelling overview, which emphasizes the central contribution of various employed modelling methods. Reflections on the presented fuel cycle design outline conclude that substantial development work is still required to realize a continuous tritium fuel cycle design and overcome the major challenges posed by tritium and lithium handling. Reflections on the presented breeder blanket design proposal conclude that while many substantial risks and blockers remain to achieve fuel self-sufficiency, high breeding ratios are expected to be achievable with a compact spherical tokamak configuration. Nonetheless, it is recognized that further consideration is required to ensure that the selection of liquid lithium as a breeder medium provides the overall simplest route to a self-sufficient and realizable design.This article is part of the theme issue 'Delivering Fusion Energy - The Spherical Tokamak for Energy Production (STEP)'.

Mxene-based lithium-ion sieve polymer membrane for sustainable lithium adsorption

Lithium, an emerging mineral of critical global significance, is recognized as a strategic resource by major economies worldwide, leading to an increased demand for this essential element. The extraction of lithium from rich sources, such as seawater and brine, has become commonplace. Among various liquid lithium extraction techniques, the lithium-ion sieve (LIS) adsorption method has attracted substantial attention owing to its simplicity, high recovery rate, and relatively low energy consumption. Despite significant advancements in LIS technology, the powdery nature of these materials poses challenges to handling and recycling, leading to inevitable adsorbent loss and limited practical applications. LISs are typically recycled through powder shaping, but the commonly employed shaping methods may result in a reduction in the adsorbent’s adsorption capacity. Therefore, it is urgent to develop a technology that can not only realize the recycling of LISs but also avoid the loss of the adsorbent’s adsorption capacity. We synthesized a titanium-based LIS (HTO) hybrid membrane by incorporating 2D MXene, known for its excellent properties across various applications. The incorporation of MXene into the membrane significantly increased the pore structure, enhancing adsorption site exposure and facilitating Li+ migration. The HTO/MXene@PVC hybrid film demonstrated favorable adsorption properties, with an Li+ adsorption capacity of 25.4 mg·g−1 within 24 h. Additionally, the film exhibited notable selectivity capacity and maintained its adsorption capacity above 90 % even after eight adsorption–desorption cycles, indicating excellent cycling performance. This study introduces a novel design concept for adsorbents, specifically for extracting Li+ from liquid lithium sources, offering new insights for the development of Li+ adsorbents aimed at enhancing lithium recovery.

Design of a 3D-printed liquid lithium divertor target plate and its interaction with high-density plasma

A liquid Li divertor is a promising alternative for future fusion devices. In this work a new divertor model is proposed, which is processed by 3D-printing technology to accurately control the size of the internal capillary structure. At a steady-state heat load of 10 MW m−2, the thermal stress of the tungsten target is within the bearing range of tungsten by finite-element simulation. In order to evaluate the wicking ability of the capillary structure, the wicking process at 600 °C was simulated by FLUENT. The result was identical to that of the corresponding experiments. Within 1 s, liquid lithium was wicked to the target surface by the capillary structure of the target and quickly spread on the target surface. During the wicking process, the average wicking mass rate of lithium should reach 0.062 g s−1, which could even supplement the evaporation requirement of liquid lithium under an environment > 950 °C. Irradiation experiments under different plasma discharge currents were carried out in a linear plasma device (SCU-PSI), and the evolution of the vapor cloud during plasma irradiation was analyzed. It was found that the target temperature tends to plateau despite the gradually increased input current, indicating that the vapor shielding effect is gradually enhanced. The irradiation experiment also confirmed that the 3D-printed tungsten structure has better heat consumption performance than a tungsten mesh structure or multichannel structure. These results reveal the application potential and feasibility of a 3D-printed porous capillary structure in plasma-facing components and provide a reference for further liquid−solid combined target designs.

Optimization of lithium vapor box divertor evaporator location on NSTX-U using SOLPS-ITER

Commercial fusion reactors will be faced with extremely high divertor target heat fluxes that will require mitigation. Simulations of detachment in an NSTX-U scenario projected to have 92 MW m−2 unmitigated peak target heat flux are presented, which reaches sub-10 MW m−2 target heat flux using a highly dissipating lithium vapor box divertor design. The lithium vapor box is a detached divertor design which employs lithium vapor evaporation and condensation to contain lithium below the X-point. Previous SOLPS modeling has indicated a lithium vapor box can reduce the heat flux down to 10 MW m−2 via simultaneous evaporation from the Private Flux Region (PFR) and the Common Flux Region (CFR) sides of the vapor box. It is found here that PFR evaporation has improved access to the separatrix leading to significantly more efficient power dissipation than CFR evaporation. Simulations of target evaporation with an evaporation distribution that is self-consistent with the temperature of a Capillary Porous System with Fast flowing liquid lithium could reach nLi / ne∼ 0.025–0.030 at the Last Closed Flux Surface (LCFS) depending on the liquid metal flow speeds and lithium sputtering yield, while PFR-side evaporation can reach acceptable heat fluxes with nLi / ne∼ 0.038 at the LCFS. However, PFR evaporator performance can be improved if the target is allowed to be hot enough such that it reflects lithium, reaching nLi / ne∼ 0.028 and reducing required lithium evaporation. Ultimately PFR evaporation and target evaporation are found to have similar ability to produce acceptable heat flux solutions with minimal upstream concentration.

New developments of hydrogen impurity online-monitoring in liquid lithium of IFMIF-DONES

On the way to future nuclear fusion power plants, the International Fusion Materials Irradiation Facility (IFMIF) – DEMO Oriented Neutron Source (DONES), is an important key element between ITER and DEMO to study before the influence of DEMO-neutron irradiation on foreseen fusion materials. The core of DONES, currently under construction near Granada, Spain, is based on a circuit containing liquid lithium at elevated temperatures acting as a functional material for the (d,n)-Li reaction in a materials test cell. In addition to this actual function of DONES, there are important aspects of maintenance in which hydrogen isotopes are generated under operating conditions and dissolved in this aggressive and very reactive alkali metal. This implies strong unfavourable effects on the applied structural materials, e.g. hydrogen embrittlement and others.To counteract these unfavourable effects, endangering the safe operation, an Impurity Control System (ICS) is an integral part of the DONES instrumentation. As part of the tasks of the European Neutron Source (ENS) to develop redundant systems for monitoring impurities, a special sub-task was defined for the development of an electrochemical H-sensor for concentrations in liquid lithium, ECHSLL. It is determined by detecting the electrical potentials of the lithium melts compared to a standard Li-based chemical reference system. This allows an inherent material property to be directly correlated (i.e. through appropriate electrochemical instrumentation) with chemical concentration values. This article presents important advancements in the applied ECHSLL technique, such as improving laboratory measurements from stagnant conditions to dynamic and realistic flow conditions of the liquid lithium material, as well as appropriate approaches to overcome the challenges in distinguishing the hydrogen isotopes by ECHSLL system (protium and deuterium among given laboratory conditions).

Update of the 5 MW Beam-on-Target Requirements for improvement of the materials irradiation performance at IFMIF-DONES

IFMIF-DONES is a facility under construction in Granada, whose main goal is the validation and characterization of materials under a fusion prototypic irradiation field. This field is created by the interaction of a high energy intense continuous deuteron beam and a flowing liquid lithium target. The requirements imposed on the beam at the interaction point are a complex trade-off among the scientific experimental needs for the materials irradiation defined at the top-level requirements (20 dpa in a volume of 0.3 dm3 and 50 dpa in 0.1 dm3), and the technical constraints of several systems such as the Accelerator Systems, the Lithium Systems, and the Test Systems. Recent simulations with the initial definition of beam-on-target requirements showed the necessity of redefining them in order to fulfill the irradiation needs. This contribution will address the main challenges to gather the inputs for the definition and reassessment of the beam-on-target requirements. A comparison detailing the main changes compared to the previous ones will be given, together with a short overview of the studies ongoing by different systems to analyze the impact of each beam-on-target requirements on the performance of the whole facility.

Thermal hydraulic and structural analysis of the IFMIF-DONES liquid-lithium target system

In the IFMIF-DONES neutron source a single accelerator line delivers 125 mA of deuterons at 40 MeV to a flowing liquid lithium target with a free surface facing the deuteron beam.Neutrons with fusion-relevant spectrum are generated by a stripping reaction and used for material samples irradiation.This report presents a numerical thermal–hydraulic and structural analysis using updated design of the target system and neutronics analysis results. Simulation scope includes the target assembly, vacuum chamber with beam ducts, outlet channel, quench tank vessel and connecting elements.Simulations have been conducted with the commercial CFD code Simcenter Star-CCM + . The computational domains consist total of 47.4x106 fluid and 14x106 structure cells.The following aspects have been analyzed:•Temperature distribution in lithium and target system structure during beam-on operation;•Transient mixing of lithium in the quench tank with temperature change during the beam switch-on phase.•Thermal displacements and stresses in the TA and QT structures.Simulations using the new distribution of nuclear heating show no significant changes in the temperature field in liquid lithium. Calculated unwanted temperature hotspots in the target structure demonstrate the need for optimization of the target design.

Selective biosorption of Li+ in aqueous solution by lithium ion-imprinted material on the surface of chitosan/attapulgite

The extraction of Li+ from liquid lithium resources is a pivotal focus of current research endeavors. Attapulgite (ATP), characterized by its distinctive layered structure and inherent ion exchange properties, emerges as an exceptional material for fabricating lithium-ion sieve. Ion-imprinted chitosan/ATP composite materials are successfully synthesized, demonstrating efficacy in selectively absorbing Li+. The results emphasize the rich functional groups present in H-CTP-2, enhancing its absorbability and selectivity, with an adsorption capacity of 37.56 mg•g−1. The adsorption conforms to the Langmuir and pseudo-second-order kinetic model. Li+ coordination involves amino and hydroxyl group, indicating a chemisorption process. Furthermore, the substantial pore structure and significant specific surface area of ATP significantly promote Li+ adsorption, suggesting its participation not only in chemisorption but also in physical adsorption. The fabricated ion-imprinted materials boast substantial adsorption capacity, exceptional selectivity, and rapid kinetics, highlighting their potential for effectively separating Li+ from aqueous solution.

Validation activities at ENEA Brasimone in support of the IFMIF-DONES design

IFMIF-DONES is a powerful neutron source which is being designed with the main purpose of qualifying structural materials (EUROFER being the first candidate) to be used in DEMO and fusion power plants envisaged after it. This source relies on one high current (125 mA) deuterons beam accelerated to 40 MeV which impacts on a liquid lithium target to produce an intense neutron flux through Li(d,n) stripping reactions able to simulate the nuclear responses expected on the first wall of the reactor. The engineering design of IFMIF-DONES is presently being carried out mainly in the framework of the EUROfusion Work Package Early Neutron Source (WPENS). Since 2021, a new phase has started with the launch of the FP9 WPENS workplan whose objective is to continue advancing the engineering design of the facility, putting special effort on the experimental validation of those aspects which still need to be qualified to demonstrate the fulfillment of functional and safety requirements. The ENEA Brasimone Research Centre has been and still is strongly committed in several validation tasks concerned in particular with the lithium systems design and the Remote Handling (RH) maintenance.In this paper, an overview of the most relevant validation activities carried out in recent years or still in progress or planned at the ENEA Brasimone Research Centre in both of the aforementioned areas is presented, including the erosion/corrosion tests in the Lifus 6 loop; the nitrogen-gettering materials qualification in the ANGEL facility; and the RH and prototypes testing in the DRP laboratory for the validation of the High Flux Test Module electric connectors and the pre-heating of the Target Assembly.

Numerical Study on the Local Aggregation of Helium Bubbles in Liquid Lithium and Its Thermal Analysis

Abstract Liquid lithium is widely regarded as an optimal cooling medium for space nuclear reactors due to its exceptional heat transfer properties and low density. However, the helium bubbles generated by liquid lithium under space irradiation pose significant hazards to the safe and stable operation of nuclear reactions. This study employs the COMSOL finite element software to construct the level-set two-phase flow models and bubble stream model separately to investigate the local accumulation of helium bubbles and the overall flow of low-concentration gas–liquid mixtures. The main focus is on examining the different distributions of multiple helium bubbles randomly generated in local liquid lithium and the influence of boundary conditions on their accumulation morphology, as well as the impact of low-concentration bubble stream on their overall heat transfer performance. Agglomerated bubbles with radii between 5 μm and 150 μm are classified into three categories based on local concentrations: circular (≤20.37%), irregular elongated (up to 30.44%), and banded (up to 36.31%).The interconnected banded bubbles can be up to 8 times larger than irregularly elongated ones, and they have a positive effect on the distribution of physical quantities and wall temperature perturbations in the pipeline. The increase in inlet velocity triggers bubble impacts and fragmentation, further reducing thermal resistance and enhancing heat transfer performance. When the bubble diameter is less than 15 μm and the bubble concentration is within 1%, the influence of the mixed flow on overall heat transfer is not significant. This study provides insights for manipulating bubble structure and guiding localized and comprehensive thermal analyses.

An evaluation of a Stenotrophomonas maltophilia outbreak due to commercial arterial blood gas collection kit

BackgroundStenotrophomonas maltophilia is a gram-negative bacterium that can cause hospital infections and outbreaks within hospitals. This study aimed to evaluate an outbreak of Stenotrophomonas maltophilia, caused by ready-to-use commercial syringes containing liquid lithium and heparin for arterial blood gas collection in a university hospital.MethodsUpon detecting an increase in Stenotrophomonas maltophilia growth in blood cultures between 15.09.2021 and 19.11.2021, an outbreak analysis and a case-control study (52 patients for the case group, 56 patients for the control group) were performed considering risk factors for bacteremia. Samples from possible foci for bacteremia were also cultured. Growing bacteria were identified by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. The genetic linkage and clonal relationship isolates were investigated with pulsed-field gel electrophoresis (PFGE) in the reference laboratory.ResultsIn the case-control study, the odds ratio for the central venous catheter [3.38 (95% confidence interval [CI]: 1.444, 8.705 ; p = 0.006)], for surgery [3.387 (95% confidence interval [CI]: 1.370, 8.373 ; p = 0.008)] and for arterial blood gas collection history [18.584 (95% confidence interval [CI]:4.086, 84.197; p < 0.001)] were identified as significant risk factors. Stenotrophomonas maltophilia growth was found in ready-to-use commercial syringes used for arterial blood gas collection. Molecular analysis showed that the growths in the samples taken from commercial syringes and the growths from blood cultures were the same. It was decided that the epidemic occurred because the method for sterilization of heparinized liquid preparations were not suitable. After discontinuing the use of the kits with this lot number, the outbreak was brought under control.ConclusionsAccording to our results, disposable or sterile medical equipment should be included as a risk factor in outbreak analyses. The method by which injectors containing liquids, such as heparin, are sterilized should be reviewed. Our study also revealed the importance of the cooperation of the infection control team with the microbiology laboratory.

Pressure-induced insulator-to-metal transition in the quantum spin liquid candidate lithium ytterbium diselenide

Pressure-induced insulator-to-metal transition in the quantum spin liquid candidate lithium ytterbium diselenide

Liquid-lithium-cooled beryllium target as the p-to-n converter

Thermal analysis and neutron moderation simulations were carried out to assess the feasibility and performance of a proton-beam-driven neutron source where the (p,n) conversion target is a cuvette made of beryllium and cooled by flowing liquid lithium. Using a prototype model with 5 MeV proton beam energy, the simulations show that this type of target can be highly beneficial in upgrading existing facilities operating with a beryllium target, or in designing new compact neutron sources.