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The actinide-containing mineral monazite–(Ce) is a common accessory rock component that bears petrogenetic information, is widely used in geochronology and thermochronology, and is considered as potential host material for immobilisation of radioactive waste. Natural samples of this mineral show merely moderate degrees of radiation damage, despite having sustained high self-irradiation induced by the decay of Th and U (for the sample studied herein 8.9 ± 0.3 × 10 19  α/g). This is assigned to low damage-annealing temperature of monazite–(Ce) and “alpha-particle-assisted reconstitution”. Here we show that the response of monazite–(Ce) to alpha radiation changes dramatically, depending on the damage state. Only in radiation-damaged monazite–(Ce), 4 He ions cause gradual structural restoration. In contrast, its high-temperature annealed (i.e. well crystalline) analogue and synthetic CePO 4 experience He-irradiation damage. Alpha-assisted annealing contributes to preventing irradiation-induced amorphisation (“metamictisation”) of monazite–(Ce); however, this process is only significant above a certain damage level.

Higher enrichment of nuclear fuel along the manufacturing limit of boron content in steel and aluminum alloys represents a significant challenge in designing spent fuel transport and storage facilities. One possible solution for spent fuel pools and casks is the burnup credit method that allows for decreasing very high safety margins associated with fresh fuel assumption in spent fuel facilities. An alternative solution based on placing neutron absorber material directly into the fuel assembly is proposed here. A neutron absorber permanently fixed in guide tubes decreases system reactivity more efficiently than absorber sheets between the assemblies. The efficiency of the newly proposed concept is demonstrated on the criticality safety analysis of the GBC-32 spent fuel cask. Absorber rods from 8 different elements are placed within Westinghouse OFA 17x17 guide tubes. Currently used boron is a good option because of high absorption cross section, low atomic mass and chemical compatibility with various alloys. Alternative options (e.g., Sm, Eu, Gd, Dy, Hf, Re, Ir) are based on very good absorbers that do not require alloy compatibility since the absorbers can be placed inside zirconium or steel cladding. Because of high efficiency of the newly proposed absorber concept, boron content in BORAL sheets can be decreased to more competitive economics. Moreover, fuel assembly pitch is investigated in order to change cask wall inner diameter that will result in lower material consumption for the cask wall with the same shielding thickness.

In this work, we demonstrate and describe an effective method of protecting zirconium fuel cladding against oxygen and hydrogen uptake at both accident and working temperatures in water-cooled nuclear reactor environments. Zr alloy samples were coated with nanocrystalline diamond (NCD) layers of different thicknesses, grown in a microwave plasma chemical vapor deposition apparatus. In addition to showing that such an NCD layer prevents the Zr alloy from directly interacting with water, we show that carbon released from the NCD film enters the underlying Zr material and changes its properties, such that uptake of oxygen and hydrogen is significantly decreased. After 100–170 days of exposure to hot water at 360 °C, the oxidation of the NCD-coated Zr plates was typically decreased by 40%. Protective NCD layers may prolong the lifetime of nuclear cladding and consequently enhance nuclear fuel burnup. NCD may also serve as a passive element for nuclear safety. NCD-coated ZIRLO claddings have been selected as a candidate for Accident Tolerant Fuel in commercially operated reactors in 2020.

Myeloproliferative neoplasms are caused by mutations in the haematopoietic stem cell (HSC) compartment, and here the authors show that the HSC niche contributes to the pathogenesis; sympathetic innervation of mesenchymal stem cells (MSCs) is reduced in the bone marrow of patients, which leads to reduced MSC numbers and increased mutant HSC expansion, and restoring sympathetic regulation of MSCs with neuroprotective/sympathomimetic drugs prevents mutant HSC expansion. Pathogenesis of myeloproliferative neoplasms The stem cell niche has recently been recognized as an oncogenic unit and an important element in regulating cancer stem cells. Here, Simón Méndez-Ferrer and colleagues demonstrate that sympathetic innervation of nestin-positive mesenchymal stem cells (MSCs) in the bone marrow microenvironment is reduced in patients with myeloproliferative neoplasms. This denervation leads to reduced MSC numbers and increased mutant haematopoietic stem cell (HSC) expansion. When sympathetic regulation of nestin-positive MSCs is restored by neuroprotective drugs, mutant HSC expansion is prevented. Myeloproliferative neoplasms (MPNs) are diseases caused by mutations in the haematopoietic stem cell (HSC) compartment. Most MPN patients have a common acquired mutation of Janus kinase 2 ( JAK2 ) gene in HSCs 1 , 2 , 3 , 4 that renders this kinase constitutively active, leading to uncontrolled cell expansion. The bone marrow microenvironment might contribute to the clinical outcomes of this common event. We previously showed that bone marrow nestin + mesenchymal stem cells (MSCs) innervated by sympathetic nerve fibres regulate normal HSCs 5 , 6 . Here we demonstrate that abrogation of this regulatory circuit is essential for MPN pathogenesis. Sympathetic nerve fibres, supporting Schwann cells and nestin + MSCs are consistently reduced in the bone marrow of MPN patients and mice expressing the human JAK2(V617F) mutation in HSCs. Unexpectedly, MSC reduction is not due to differentiation but is caused by bone marrow neural damage and Schwann cell death triggered by interleukin-1β produced by mutant HSCs. In turn, in vivo depletion of nestin + cells or their production of CXCL12 expanded mutant HSC number and accelerated MPN progression. In contrast, administration of neuroprotective or sympathomimetic drugs prevented mutant HSC expansion. Treatment with β 3 -adrenergic agonists that restored the sympathetic regulation of nestin + MSCs 5 , 6 prevented the loss of these cells and blocked MPN progression by indirectly reducing the number of leukaemic stem cells. Our results demonstrate that mutant-HSC-driven niche damage critically contributes to disease manifestation in MPN and identify niche-forming MSCs and their neural regulation as promising therapeutic targets.

Interleukin-1β (IL-1β) is a master regulator of inflammation. Increased activity of IL-1β has been implicated in various pathological conditions including myeloproliferative neoplasms (MPNs). Here we show that IL-1β serum levels and expression of IL-1 receptors on hematopoietic progenitors and stem cells correlate with JAK2 -V617F mutant allele fraction in peripheral blood of patients with MPN. We show that the source of IL-1β overproduction in a mouse model of MPN are JAK2 -V617F expressing hematopoietic cells. Knockout of IL-1β in hematopoietic cells of JAK2 -V617F mice reduces inflammatory cytokines, prevents damage to nestin-positive niche cells and reduces megakaryopoiesis, resulting in decrease of myelofibrosis and osteosclerosis. Inhibition of IL-1β in JAK2 -V617F mutant mice by anti-IL-1β antibody also reduces myelofibrosis and osteosclerosis and shows additive effects with ruxolitinib. These results suggest that inhibition of IL-1β with anti-IL-1β antibody alone or in combination with ruxolitinib could have beneficial effects on the clinical course in patients with myelofibrosis. Inflammatory cytokines are elevated in patients with myeloproliferative neoplasms (MPN). Here the authors show that the JAK2-V617F mutation is associated with increased expression of IL-1 in MPN patients and that loss of IL-1β in JAK2-V617F mutant hematopoietic cells reduces MPN symptoms and myelofibrosis in a mouse model.

The long-known presence of a sharp OH absorption band in the tetragonal fluoride mineral sellaite, MgF2, inspired us to conduct a detailed study of the OH incorporation modes into this IR-transparent (where IR stands for Infrared) material as well as to search for hydrogen traces in two other IR-translucent halides—villiaumite (NaF) and fluorite (CaF2). Among these three phases, sellaite is the only one to incorporate ‘intrinsic’ OH groups, most commonly as O–H∙∙∙F defects oriented nearly perpendicular to the c-axis along the shortest edge of the constituent MgF6 polyhedra, in analogy with the isostructural mineral rutile, TiO2. Another defect type, seen only scarcely in untreated natural material, develops when subjecting sellaite to temperatures above 900 °C. It involves an O–H∙∙∙O cluster along the 2.802 Å edge of the original MgF6 dipyramid, as fluorine atoms are progressively expelled from the structure, being replaced by O2- anions. This is corroborated by the appearance of spectral absorption features typical for brucite (Mg(OH)2) and ultimately periclase (MgO), the presence of which could be proven via powder diffraction of the heat-treated material. Except for a ‘dubious’ peak most probably caused by included phases, neither villiaumite (NaF) nor fluorite (CaF2) showed any presence of ‘intrinsic’ OH defects. They do however decompose along a similar route into the respective oxide and hydroxide phases at high temperature. This thermal decomposition of the studied halide phases is accompanied by the emission of gaseous (HF)n species at temperatures well below their established melting point - a subject which seems to be quite overlooked.

Carbon-free thermally driven district cooling systems (DCS) can effectively mitigate the excessive electricity consumption and carbon emissions associated with the cooling sector. This study proposes a DCS that employs nuclear heat as the primary energy source. The system comprises three main subsystems: heat station, heat transmission, and cooling station. A heat-only small modular reactor called Teplator, gas boilers, and heat storage are considered to supply the heat required to drive absorption chillers; cold storage and compression chillers are the supplementary units. The technoeconomic aspects of the system are formulated, and an algorithm is developed to determine the optimal design and operation. The method is examined for supplying a typical cooling demand profile with a peak of 2050 MWc. The resulting optimized design includes 11 nuclear plants (150 MWt each), 20 000 MWth heat storage, and 1.9 m diameter heat supply/return pipes. Absorption chillers with a total capacity of 1424 MWc are determined, covering 92% of the total cooling demand, and 244 MWc of compression chillers and 20 000 MWch of cold storage are found to cover the peak and enhance the load following. This system saved 69% of the electricity consumption and carbon emissions and 34% of the costs compared with an electric-based scenario.

This work presents the results of an investigation of an assemblage of secondary Sc-minerals from the intraplutonic metaluminous pegmatite Kožichovice II, Třebíč Pluton, Czech Republic. The assemblage was formed by hydrothermally-induced dissolution of primary Sc-enriched (≈1.6 wt.% Sc 2 O 3 ) columbite-(Mn) followed by in situ reprecipitation of volumetrically dominant fersmite (≈0.16 wt.% Sc 2 O 3 ) and minor nioboheftetjernite (ScNbO 4 ). Subsequent hydrothermal processes resulted in the formation of fluorcalciomicrolite + Sc-minerals (thortveitite + kristiansenite) + titanite. The mass balance calculations (based on EPMA-derived mineral compositions, mineral proportions obtained from TIMA automated mineralogy and textural observations) revealed that the amount of Sc released from the replaced mass of columbite-(Mn) is significantly higher than the amount of Sc incorporated in the mass of the secondary minerals. This indicates that part of the Sc was mobilised and released to the host rocks (pegmatite and granite). The secondary mineral assemblages indicate elevated Ca activity in the alteration fluids. Other occurrences of Sc-minerals in pegmatites (Baveno Pluton and Heftetjern pegmatite) show remarkable similarities in the paragenetic position of Sc-minerals (late hydrothermal/replacement minerals), including the high activity of Ca in fluids during their formation. The high activity of Ca in fluids during the metasomatic replacement of Sc-enriched precursors causes the formation of the volumetrically dominant Sc incompatible phases, followed by a local supersaturation of Sc resulting in the crystallisation of secondary Sc-minerals.

A multi-methodological study was conducted in order to provide further insight into the structural and compositional complexity of rare earth element (REE) fluorcarbonates, with particular attention to their correct assignment to a mineral species. Polycrystals from La Pita Mine, Municipality de Maripí, Boyacá Department, Colombia, show syntaxic intergrowth of parisite–(Ce) with röntgenite–(Ce) and a phase which is assigned to B3S4 (i.e., bastnäsite-3–synchisite-4; still unnamed) fluorcarbonate. Transmission electron microscope (TEM) images reveal well-ordered stacking patterns of two monoclinic polytypes of parisite–(Ce) as well as heavily disordered layer sequences with varying lattice fringe spacings. The crystal structure refinement from single crystal X-ray diffraction data – impeded by twinning, complex stacking patterns, sequential and compositional faults – indicates that the dominant parisite–(Ce) polytype M1 has space group Cc. Parisite–(Ce), the B3S4 phase and röntgenite–(Ce) show different BSE intensities from high to low. Raman spectroscopic analyses of parisite–(Ce), the B3S4 phase and röntgenite–(Ce) reveal different intensity ratios of the three symmetric CO3 stretching bands at around 1100 cm−1. We propose to non-destructively differentiate parisite–(Ce) and röntgenite–(Ce) by their 1092 cm−1 / 1081 cm−1 ν1(CO3) band height ratio.

Tennantite-(Cd), Cu10Cd2As4S13, was approved as a new mineral species from the Berenguela mining district, Pacajes Province, La Paz, Bolivia. It occurs as black metallic anhedral grains, up to 1 mm across, associated with baryte, montmorillonite and secondary Cd-sulfates (aldridgeite, niedermayrite and voudourisite). In reflected light, tennantite-(Cd) is isotropic and grey with brownish tints. Reflectance data for the four COM wavelengths in air are [λ (nm): R (%)]: 470: 30.0; 546: 30.1; 589: 28.2; and 650: 25.8. Electron microprobe analysis gave (in wt.% - average of 11 spot analyses): Cu 40.56(32), Ag 0.05(5), Fe 0.04(1), Zn 1.91(63), Cd 11.32(1.09), Hg 0.04(7), As 19.04(43), S 26.78(30), total 99.74(53). On the basis of ΣMe = 16 atoms per formula unit (apfu), the empirical formula of tennantite-(Cd) is Cu9.98Ag0.01Cd1.57Zn0.46Fe0.01As3.97S13.05. Tennantite-(Cd) is cubic, I43m, with unit-cell parameters a = 10.3088(2) Å, V = 1095.53(6) Å3 and Z = 2. Its crystal structure was refined by single-crystal X-ray diffraction data to a final R1 = 0.0152 on the basis of 359 unique reflections with Fo > 4σ(Fo) and 22 refined parameters. Tennantite-(Cd) is isotypic with other tetrahedrite-group minerals. Its crystal-chemistry is discussed and previous findings of Cd-rich tetrahedrite-group minerals are briefly reviewed.