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Background: Q fever is a zoonosis caused by the obligate intracellular bacterium Coxiella burnetii. The two long-term complications, after primary infection, are chronic Q fever in ∼1% of patients, and a chronic fatigue syndrome in 10-20%. However, the existence of a protracted decreased health status after Q fever remains controversial., Aim: To determine the health status of the patients of the Q fever outbreak in The Netherlands in 2007, 1 year after primary infection., Design: Cross-sectional case-control study., Methods: Health status of the patients from the 2007 Dutch Q fever outbreak was compared to age-, sex- and geographically matched and Q fever seronegative controls. Health status of both patients and controls was assessed with the Nijmegen Clinical Screening Instrument (NCSI)., Results: Fifty-four Q fever patients provided 34 years of age- and sex-matched controls from the same neighbourhood. Eleven controls had positive Q fever serology and were excluded. Q fever patients had significantly more problems on the subdomains of symptoms and functional impairment. Overall quality of life was decreased in both patients and controls, 59% vs. 39%, respectively, ns). Severe fatigue levels were present in 52% of patients vs. 26% in controls (P < 0.05)., Conclusion: These data support a sustained decrease in many aspects of health status in Q fever patients in The Netherlands, 1 year after primary infection.

This study describes the primary characteristics of the selected kidney stones surgically removed from the patients at the Mersin University Hospital in the southern Turkey and interprets their formation via petrographic, geochemical, XRD, SEM-EDX, and ICP-MS/OES analyses. The analytical results revealed that the kidney stones are composed of the minerals whewellite, struvite, hydroxyapatite, and uric acid alone or in different combinations. The samples occur in staghorn, bean-shaped composite, and individual rounded particle shapes, which are controlled by the shape of the nucleus and the site of stone formation. The cross-section of the samples shows concentric growth layers due to variations in saturation, characterizing the metastable phase. Kidney stone formation includes two main stages: (i) nucleation and (ii) aggregation and/or growth. Nucleation was either Randall plaque of hydroxyapatite in tissue on the surface of the papilla or a coating of whewellite on the plaque, or crystallization as free particles in the urine. Subsequently, aggregation or growth occurs by precipitation of stone-forming materials around the plaque or coating carried into the urine, or around the nucleus formed in situ in the urine. Urinary supersaturation is the main driving force of crystallization processes; and is controlled by many factors including bacterially induced supersaturation., (© 2023. The Author(s), under exclusive licence to Springer Nature B.V.)

Calcium oxide and silicon oxide are combined to form calcium silicate. Since calcium silicate materials offer tuneable physical, chemical, mechanical, and optical characteristics, these materials have found uses in various applications such as luminescence, batteries, bioimaging, supercapacitors, and concrete materials. In the majority of applications, high-purity calcium silicate is produced from chemical precursors such as calcium/silicate oxides or nitrites, even though this method could be expensive, environmentally harmful, and non-biocompatible. As an alternative, natural calcium and silica from biomass are usually economical and abundant, yet they contain impurities but sometimes the trace impurities influence the properties of material in positive ways. Silica can be extracted from wheat husk, rice husk, and sugarcane bagasse, which are frequently dumped in rivers, ponds, and other water bodies, contributing to ecological and health problems, likewise, calcium oxide can be extracted from eggshells, marble waste, snail shell. The trash may recycle or utilized to create marketable, value-added items with significant ecological and financial benefits rather than being dumped. The purpose of this review paper is to discuss the composition, processing, and applications of calcium silicate derivatives. The analysis shows that calcium silicate derivatives have enormous potential for using waste as a replacement of organic precursor materials. [ABSTRACT FROM AUTHOR]

In response to the need for improvement in the utilization of ammonium-rich solutions after the electrochemical reduction of nitrate (NO3−–RR), this study combined phosphorus-containing wastewater and adopted the electrochemical precipitation method for the preparation of struvite (MAP) to simultaneously recover nitrogen and phosphorus resources. At a current density of 5 mA·cm−2 and an initial solution pH of 7.0, the recovery efficiencies for nitrogen and phosphorus can reach 47.15% and 88.66%, respectively. Under various experimental conditions, the generated struvite (MgNH4PO4·6H2O) exhibits a typical long prismatic structure. In solutions containing nitrate and nitrite, the coexisting ions have no significant effect on the final product, struvite. Finally, the characterization of the precipitate product by X-ray diffraction (XRD) revealed that its main component is struvite, with a high purity reaching 93.24%. Overall, this system can effectively recover ammonium nitrogen from the NO3−–RR solution system after nitrate reduction, with certain application prospects for the recovery of ammonium nitrogen and phosphate. [ABSTRACT FROM AUTHOR]

Water seepage flow can dissolve soluble minerals that exist in rock formations. With the development of the excavated area due to dissolution, the water seepage velocity (discharge) into the dissolved rock will also increase. Therefore, water seepage and dissolution propagation are two interrelated processes. Mosul Dam foundation has experienced these processes since its construction, resulting in karstification in the reservoir and foundation of the dam. The present seepage-dissolution measure to minimize this phenomenon relies on traditional cementitious grouts. However, this measure has not been able to address the issue effectively. Currently, there are a few studies on the chemical remediation of soluble rocks under the influence of high-velocity water flow and water pressure. Therefore, the first part of the current study focuses on the impact of high-velocity water flow and water pressure on the dissolution acceleration of gypsum/anhydrite rocks. In the second part, the waterproof capacity of silica colloidal and its impact on the solubility reduction of the rocks is evaluated. Two distinct laboratory models were designed to simulate rock dissolution in the dam abutments and under the dam. Two sets of experiments were conducted on untreated and silica-treated samples. The experiments were executed on the samples extracted from Fatha Formation outcrop and problematic layers of brecciated gypsum situated at varying depths of the Mosul Dam foundation. The obtained findings reveal that the colloidal silica grout markedly prevents the water seepage impact on the soluble rock and that it can be very useful as an alternative to cement-based grouts. [ABSTRACT FROM AUTHOR]

This study combined inorganic α-hemihydrate gypsum (α-HHG) with organic polyacrylamide (PAM) hydrogel to create a novel α-HHG/PAM composite material. Through this facile composite strategy, this fabricated material exhibited a significantly longer initial setting time and higher mechanical strength compared to α-HHG. The effects of the addition amount and the concentration of PAM precursor solution on the flowability of the α-HHG/PAM composite material slurry, initial setting time, and mechanical properties of the hardened specimens were investigated. The structural characteristics of the composite material were examined using XRD, FE-SEM, and TGA. The results showed that the initial setting time of the α-HHG/PAM composite material was 25.7 min, which is an extension of 127.43% compared to that of α-HHG. The flexural strength and compressive strength of the oven-dried specimens were 23.4 MPa and 58.6 MPa, respectively, representing increases of 34.73% and 84.86% over values for α-HHG. The XRD, FE-SEM, and TGA results all indicated that the hydration of α-HHG in the composite material was incomplete. The incompleteness is caused by the competition between the hydration process of inorganic α-HHG and the gelation process of the acrylamide molecules for water, which hinders some α-HHG from entirely reacting with water. The enhanced mechanical strength of the α-HHG/PAM composite material results from the tight interweaving and integrating of organic and inorganic networks. This study provides a concise and efficient approach to the modification research of hemihydrate gypsum. [ABSTRACT FROM AUTHOR]

The transport of sulfate-bearing brines is closely relevant to mineralization of sulfide deposits as metal-sulfate complexes exist in hydrothermal fluids. Liquid-liquid phase separation evidently occurs in various metal-sulfate systems with transport and precipitating different from homogeneous fluids. Previous studies have revealed a new species with a Raman peak at ~1020 cm-1 in rich concentration phase of liquid-liquid phase separated MgSO4 solution, and it was interpreted as chain structure polymers. Ab initio molecular dynamics simulations (AIMD) and autocorrelation functions for frequency calculation have been performed to disclose the speciation. The results show that more Mg2+ ions surrounding a SO42- anion lead to higher wavenumber of Raman peaks, which indicates the formation of complicate clusters with ion associations similar to kieserite. Besides, the splitting peaks of v-980 Raman bands at ~980, 990, and 1005 cm-1 in homogeneous solution represent more monodentate Mg-Os (Os: O of SO42-) associations instead of certain species, which favors the formation of prenucleation clusters. Furthermore, bidentate Mg-SO4 ligand is less stable than monodentate ligands at 543 K by applying free energy calculations. Our findings give atomic level recognition of concentrated phase in liquid-liquid phase separated MgSO4 fluids and theoretical explanation of the 980 cm-1 Raman peak shifting, which will further inspire understandings on nucleation processes of hydrated sulfate minerals and Raman spectra resolving of other sulfate systems. [ABSTRACT FROM AUTHOR]

Acute Q fever is a generally self-limiting infection caused by the intracellular gram-negative bacterium Coxiella burnetii. For yet unknown reasons, a subset of patients develops chronic infection. Furthermore, chronic fatigue syndrome (CFS) as post-acute Q fever sequelae has been described. We here investigated the rates of chronic Q fever and incidences of CFS 6 years after one of the largest European Q fever outbreaks that occurred in Jena, Germany in 2005 with 331 reported cases, who lived in proximity of a grazing flock of sheep. A total of 80 patients and their 52 non-diseased household members from the former outbreak, were enrolled 6 years after the outbreak. Blood samples were collected and tested for chronic Q fever which was determined by seroprevalence using referenced immunofluorescence assays. Also, the presence of CFS was assessed using the Short Form Symptom Inventory developed by the Centers (United States) for Disease Control and Prevention (SF CDC- SI). In 80 out of 132 (60.6%) study participants, previous Q fever infection was confirmed serologically, while no previous infection was detected in the 52 household members. None of the participants fulfilled the serological criteria of chronic Q fever. The evaluation of the CDC-SI did not show any differences between the two groups. Also, there was no difference between both groups regarding fulfillment of CFS-defining criteria (n = 3 (3.8%; sero-positive) versus n = 2 (3.8%; sero-negative), p = 0.655). Our 6-year follow-up study of a large Q fever outbreak did not find evidence of chronic Q fever or post Q fever CFS. There was no asymptomatic sero-positivity in household members of Q fever patients., (© 2021 The Authors. Transboundary and Emerging Diseases published by Wiley-VCH GmbH.)

Phosphorus recovered from cow urine rich in nutrients serves as an alternative form of fertilizer when recovered as magnesium ammonium phosphate termed as struvite (MgNH4PO4·6H2O). Extraction of struvite was investigated through bench scale experiments, and its yield was measured by surface spread method and plain sedimentation method. Magnesium (Mg): phosphorus (P) ratio of 5: 1 yielded 77.5 mg/L and 10 mg/L of struvite by surface spread method and plain sedimentation method, respectively. A 15-fold increase in phosphorus recovery was obtained through plain sedimentation method. The mean width and length of struvite crystals obtained from plain sedimentation method were 4.4 µm and 18.4 µm, respectively. Struvite crystal size decreased by 77.78% when the rate of mixing was increased from 40 to 120 rpm. SEM analysis depicted the needle-like and lath-shaped morphology of struvite crystals. EDS analysis revealed the presence of Ca2+ and Na+ ions, and the XRD results confirmed the co-precipitation of other magnesium phosphates such as bobierrite and newberyite and sequential precipitation of K-struvite. [ABSTRACT FROM AUTHOR]

This review article delves into the growing recognition of fractal structures in mesoscale phenomena. The article highlights the significance of realistic fractal-like aggregate models and efficient modeling codes for comparing data from diverse experimental findings and computational techniques. Specifically, the article discusses the current state of fractal aggregate modeling, with a focus on particle clusters that possess adjustable fractal dimensions ( D f ). The study emphasizes the suitability of different models for various D f –intervals, taking into account factors such as particle size, fractal prefactor, the polydispersity of structural units, and interaction potential. Through an analysis of existing models, this review aims to identify key similarities and differences and offer insights into future developments in colloidal science and related fields. [ABSTRACT FROM AUTHOR]

Today, the search for disease biomarkers and techniques for their detection is one of the most important focuses in modern healthcare. Extracellular vesicles (EVs) are known to be related to the pathogenesis of various illnesses, such as cancer, neurodegenerative disease, and cardiovascular disease. Specific EV detection and potential control of their amount in biological fluids can provide a promising therapeutic strategy that involves reduction in EV production and circulation to normal levels to prevent disease progression. To provide a foundation for such research and development, we report the application of photonic integrated circuits in the form of a Mach–Zehnder interferometer coupled with microfluidics for monitoring each step of a covalent linkage between receptors and silicon nitride. We show that such a biosensor can be used for biological marker quantification, such as EVs containing a specific membrane protein HER2. The developed platform provides real-time results by using microliter volumes of the test sample. This research can be used as a first step toward creation of a laboratory on a chip for the precise control of coating in terms of chemical applications and monitoring the effectiveness of the chosen treatment for medical applications. [ABSTRACT FROM AUTHOR]

The direct incorporation of Sb(V) ions into a polycondensed silsesquioxane network based on heptaisobutyl POSS units (Sb(V)-POSSs) through a corner-capping reaction is reported for the first time in this work. As a reference sample, a completely condensed monomeric Sb(III)-POSS was prepared using a similar synthetic protocol. The chemical properties of both Sb-containing POSSs were investigated with different analytical and spectroscopic techniques. The analyses confirm the success of the corner-capping reaction for both samples and indicate that an Sb(V)-POSS sample is characterized by a heterogenous multimeric arrangement with an irregular organization of POSS cages linked to Sb(V) centers, and has a more complex structure with respect to the well-defined monomeric Sb(III)-POSS. [ABSTRACT FROM AUTHOR]

We present a comparison of common electron microscopy sample preparation methods for studying crystallisation processes from solution using both scanning and transmission electron microscopy (SEM and TEM). We focus on two widely studied inorganic systems: calcium sulphate, gypsum (CaSO 4 ·2H 2 O) and calcium carbonate (CaCO 3 ). We find significant differences in crystallisation kinetics and polymorph selection between the different sample preparation methods, which indicate that drying and chemical quenching can induce severe artefacts that are capable of masking the true native state of the crystallising solution. Overall, these results highlight the importance of cryogenic (cryo)-quenching crystallising solutions and the use of full cryo-TEM as the most reliable method for studying the early stages of crystallisation., (© 2024 The Authors. Journal of Microscopy published by John Wiley & Sons Ltd on behalf of Royal Microscopical Society.)

Considerable efforts are made worldwide to reduce inorganic scale in reverse osmosis plants, boilers and heat exchangers, evaporators, industrial water systems, geothermal power plants and oilfield applications. These include the development of new environmentally friendly antiscalants and the improvement of conventional ones. The present report is dedicated to the unconventional application of spruce wood shavings in combination with polyacrylate (PAA-F1) in a model case of gypsum scale formation. The electrical conductivity of freshly prepared gypsum solutions with a saturation SI = 2.3 and a concentration of 0.05 mol·dm−3 was analyzed over time at 25°C. It is demonstrated that the small amounts of wood shavings (0.1% by mass) alone, after being in contact with CaCl2 and Na2SO4 stock solutions for 15 min, increase the induction time tind by 25 min relative to the blank experiment (tindblank). In the presence of PAA-F1 (0.1 mg·dm−3), the difference Δtind = tind − tindblank constitutes 110 min, whereas the sequential treatment of the stock solutions with the shavings followed by PAA-F1 injection gives Δtind = 205 min. The observed synergism is associated with the selective removal of colloidal Fe(OH)3solid and Al(OH)3solid nanoimpurities from the stock solutions via their sorption to the well-developed surface of wood. Wood shavings therefore represent a very promising and environmentally friendly material that can significantly improve the effectiveness of conventional antiscalants. [ABSTRACT FROM AUTHOR]

Smectitic clay minerals are unique indicators of paleoenvironmental conditions and exhibit a unique reactivity in the mineral world. Smectites may exhibit tetrahedral substitutions (Al3+, and sometimes Fe3+, can substitute for Si4+ in tetrahedral sites), resulting in a layer-charge increase, thereby impacting their properties (e.g. swelling and sorption capacities, catalytic properties, expandable abilities). The objective of the present study was to determine the influence of pH conditions on the hydrothermal production of smectite end-members exhibiting tetrahedral Al substitutions (saponite, beidellite, and nontronite), using X-ray diffraction (XRD) and Fourier-transform infrared (FTIR) methods. The results of a series of syntheses conducted at various pH values allowed discussion of the crystallization pathways of these smectites from a mechanistic point of view. Altogether, the present study provided easily reproducible protocols for the hydrothermal production of pure saponite, nontronite, or beidellite (i.e. with no other mineral). The successful synthesis of pure saponite was achieved by exposing the starting gels to 230°C for 4 days in solutions at pH ranging from 5.5 to 14. The successful synthesis of pure beidellite was achieved by exposing the starting gels to 230°C for 9 days in a solution at pH 12. The successful synthesis of pure nontronite was achieved by exposing the starting gels to 150°C for 2.5 days in a solution at pH 12.5. Although extrapolating experimental results to natural settings remains difficult, the results of the present study may be of great help to constrain better the geochemical conditions existing or having existed on extraterrestrial planetary bodies. [ABSTRACT FROM AUTHOR]

Accurate evaluation of human epidermal growth factor receptor type 2 (HER2) expression is crucial for determining chemotherapy regimens in gastric cancer. However, formalin fixation status has been identified as an important factor affecting HER2 assessment reliability. This retrospective cohort study aimed to investigate the correlation between sample collection day (weekday vs. weekend) and source (biopsy vs. surgical specimens) in assessing HER2 expression in patients with unresectable advanced/recurrent gastric cancer. Data were collected from gastric cancer patients who received chemotherapy at a single public hospital in Japan from 2008 to 2021. The analysis included 177 patients (109 men, 68 women) with a median age of 68.0 (21–88) years, and the primary outcome was the HER2 positivity rate. The overall HER2 positivity rate was 18.1%, with higher rates on weekdays (20.0%) compared to weekends (12.8%). Biopsies had higher positivity rates on weekdays (23.9%) but lower rates on weekends (11.1%) than surgical specimens. Significant differences were observed in formalin fixation times between weekdays and weekends for both biopsies and surgical samples. The study findings suggest that longer formalin fixation times on weekends may lead to underestimating HER2 expression, particularly in biopsies. Therefore, it is crucial to be cautious of excessive formalin fixation when collecting samples, especially during weekend biopsies. [ABSTRACT FROM AUTHOR]

Label-free optical biosensing holds great promise for a variety of applications in biomedical diagnostics, environmental and food safety, and security. It is already used as a key tool in the investigation of biomolecular binding events and reaction constants in real time and offers further potential additional functionalities and low-cost designs. However, the sensitivity of this technology does not match the routinely used but expensive and slow labelling methods. Therefore, label-free optical biosensing remains predominantly a research tool. Here we discuss how one can go beyond the limits of detection provided by standard optical biosensing platforms and achieve a sensitivity of label-free biosensing that is superior to labelling methods. To this end we review newly emerging optical implementations that overcome current sensitivity barriers by employing novel structural architectures, artificial materials (metamaterials and hetero-metastructures) and using phase of light as a sensing parameter. Furthermore, we elucidate the mechanism of plasmonic phase biosensing and review hyper-sensitive transducers, which can achieve detection limits at the single molecule level (less than 1 fg mm−2) and make it possible to detect analytes at several orders of magnitude lower concentrations than so far reported in literature. We finally discuss newly emerging layouts based on dielectric nanomaterials, bound states in continuum, and exceptional points. [ABSTRACT FROM AUTHOR]

The precipitation of struvite from wastewater is a potential alternative for the recovery of nutrients, especially phosphorus, which is an essential macronutrient for agriculture but can be harmful to the environment when improperly disposed of in water bodies. In addition, struvite has elements of great added value for agricultural activity (P, N, and Mg) and is, therefore, considered a sustainable alternative fertilizer. In its formation process, several intervening physicochemical factors may be responsible for the production yield levels. Optimization processes can help to define and direct the factors that truly matter for precipitation. In this context, a sequential design of experiments (DOE) methodology was applied to select and optimize the main struvite precipitation factors in wastewater. Initially, a screening was performed with eight factors with the aid of Plackett–Burman design, and the factors with a real influence on the process were identified. Then, a Doehlert design was used for optimization by applying the response surface methodology and the desirability function. The results were used to identify the optimal points of the pH (10.2), N/P ratio (≥4), and initial phosphorus concentration (183.5 mg/L); these values had a greater effect on phosphorus recovery and the production of struvite, which was confirmed through thermochemical analysis of the decomposition of its structure by differential scanning calorimeter—glass transition temperature (DSC-TG) and phase identification by X-ray diffraction (XRD). The determination of the best synthesis conditions is an enormous contribution to the control of the process because these conditions lead to better yields and higher levels of phosphorus recovery. [ABSTRACT FROM AUTHOR]

The mechanism of the nonclassical crystallization pathway of calcium sulfate dihydrate (gypsum) with calcium sulfate hemihydrate (bassanite) as a precursor has been considered in many studies. However, studies on the crystallization of gypsum in natural environments have rarely been reported, especially with regard to natural estuaries, which are one of the most important precipitation environments for calcium sulfate. Here, surface sediments (0–5 cm) of Lingding Bay of the Pearl River Estuary in China were sampled and analyzed. X-ray powder diffraction (XRD) analysis showed that calcium sulfate in the surface sediments mainly existed in the form of gypsum. In high-resolution transmission electron microscopy (HR-TEM) analysis, calcium sulfate nanoparticles were observed in the surface sediments. These particles mainly included spherical calcium sulfate nanoparticles (diameter ranging from 10–50 nm) and bassanite nanorod clusters (sizes ranging from 30 nm × 150 nm to 100 nm × 650 nm), and their main elements included O, S and Ca, with small amounts of N, Si, Na and Mg. The bassanite nanorods self-assembled into aggregates primarily co-oriented along the c axis (i.e., [001] direction). In epitaxial growth into larger bassanite nanorods (100 nm × 650 nm), the crystal form of gypsum could be observed. Based on the observations and analyses, we proposed that the crystallization of gypsum in surface sediments of the natural estuary environment could occur through the nonclassical crystallization pathway. In this pathway, bassanite nanoparticles and nanorods appear as precursors (nanoscale precursors), grow via self-assembly, and are finally transformed into gypsum. This work provided evidence supporting and enhancing the understanding of the crystallization pathway of calcium sulfate phases in the natural estuary environment. Furthermore, the interactions between calcium sulfate nanoparticles and the natural estuary environment were examined. [ABSTRACT FROM AUTHOR]

Phosphogypsum is widely used as a filler. However, gypsum fillers exhibit poor water resistance, compromising the performance of subsequent products. To address this issue, we modified α‐hemihydrate phosphogypsum (α‐HH) with myristic acid (ΜΑ), a low surface energy material used to prepare super hydrophobic (SHP) surfaces. The MA concentration, temperature, and modification time were optimized using a Box‐Behnken experimental design method. The surface properties, microstructure, and thermal stability of the modified powders were characterized using contact angle measurements, X‐ray diffraction (XRD), Fourier transform infrared (FT‐IR) spectroscopy, Raman spectrum, X‐ray photoelectron spectroscopy (XPS), scanning electron microscopy coupled with energy‐dispersive X‐ray spectroscopy (SEM‐EDS), and thermal gravimetry‐differential scanning calorimetry (TG‐DSC). Additionally, we discussed the hydrophobic modification mechanism of the modified α‐HH. The modified α‐HH/MA prepared with 11.0×10−4 mol L−1 MA at 60 °C for 60 min exhibited high hydrophobicity. During modification, MA bound to the calcium ions on the surface of α‐HH to form calcium myristate, thereby forming a hydrophobic film. The thermal stability of α‐HH was improved by MA modification. The modified powder maintained high hydrophobicity even at 250 °C. [ABSTRACT FROM AUTHOR]

Polycationic polypeptides prompt the polycondensation of inorganic oxides, most notably of silica. Hen egg-white lysozyme is a small polycationic protein that is quite conveniently used to this end. The fate of the protein after the completion of the polycondensation reaction is still a matter of debate. We have recently proven that lysozyme strongly interacts with silica. In this study, we use spin-label-based EPR spectroscopy to investigate whether the protein shows an orientational preference with respect to the silica surface within the composite. We find that a large share of the protein behaves as when it is adsorbed on pre-formed silica, albeit with a more marked preference for orientations that point the patches with higher surface charge density toward the material. In addition, a part of the protein shows a less-defined behavior. With this study, we provide additional information on the nature of the protein-material interactions in this class of bioinspired solids. [ABSTRACT FROM AUTHOR]

Deposits of calcium sulfate scale on the surfaces of industrial equipment in distillation facilities, reverse osmosis desalination plants, in oil and gas industries lead to significant clogging of pipes and membranes and to a serious increase in production costs. For the mitigation of scale formation, the wide spectrum of antiscalants is applied. The present work is dedicated to the study of calcium sulfate deposition from supersaturated aqueous solutions in the presence of polyacrylic antiscalant with fluorescent marker (naphthalimide fragment) PAA-F1, which provides traceability of the scale inhibitor and a better understanding of its efficacy. A paradoxical phenomenon is being described here. Antiscalant causes a change in the crystal phase from bassanite to gypsum, significantly reduces the amount of deposit, but does not reveal the presence of its molecules either at the kink, step, or at selected edge sites of deposited crystals. Contrary to the predictions of the theory, it either stays in the aqueous phase, or forms its own separate phase Ca-PAA-F1. It is demonstrated that the antiscalant does not block the surfaces of calcium sulfate nuclei or crystal surfaces, but rather the foreign particles of nanodust with particle sizes around 1 nm, naturally occurring in any aqueous solution. As a result, the number of calcium nucleation sites is reduced, and the rate of scale formation decreases without any apparent antiscalant–scale interaction. On the grounds of the current experiment, the substoichiometric effect of scale inhibition obtained an alternative, quite stoichiometric explanation. [ABSTRACT FROM AUTHOR]

Per- and polyfluoroalkyl substances (PFAS) are widespread in the environment. Properly developed QSAR/QSPR models can be used to assess the impact of these chemicals on humans and the environment. This work assesses 38 in silico models developed for this group of compounds, which mainly show physicochemical (22), and also toxic (8) and ecotoxic (8) properties. The evaluation of the models was carried out based on the (Q)SAR Model Reporting Format (QMRF), which was found in the QSAR Database (5) or was prepared manually, according to the information contained in scientific publications based on the QMRFEditor-v3.0.0 format (33). We based our evaluations on an individual assessment of each of the OECD principles described in the document and then summing up everything together. During the analysis, we identified 22 models as scientifically valid and could be used in the prediction of new compounds. Twelve of them contained all the information necessary to reproduce the model, and another 10, despite the lack of some information, are still reproducible. The other 16 models do not contain enough information to reproduce them and therefore they are scientifically invalid. The present work allows identifying the remaining gaps, needs, and recommendations that should be considered in further development of predictive models in the PFAS area. [ABSTRACT FROM AUTHOR]

Equipment scaling leads to reduced production efficiency in a wide range of industrial applications worldwide. Various antiscaling agents are currently commonly used to mitigate this problem. However, irrespective of their long and successful application in water treatment technologies, little is known about the mechanisms of scale inhibition, particularly the localization of scale inhibitors on scale deposits. The lack of such knowledge is a limiting factor in the development of applications for antiscalants. Meanwhile, fluorescent fragments integrated into scale inhibitor molecules have provided a successful solution to the problem. The focus of this study is, therefore, on the synthesis and investigation of a novel fluorescent antiscalant: (2-(6-morpholino-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)yl)ethylazanediyl)bis(methylenephosphonic acid) (ADMP-F) which is an analog of the commercial antiscalant: aminotris(methylenephosphonic acid) (ATMP). ADMP-F has been found to effectively control the precipitation of CaCO3 and CaSO4 in solution and is a promising tracer for organophosphonate scale inhibitors. ADMP-F was compared with two other fluorescent antiscalants—polyacrylate (PAA-F1) and bisphosphonate (HEDP-F)—and was found to be highly effective: PAA-F1 > ADMP-F >> HEDP-F (CaCO3) and PAA-F1 > ADMP-F > HEDP-F (CaSO4·2H2O). The visualization of the antiscalants on the deposits provides unique information on their location and reveals differences in the "antiscalant-deposit" interactions for scale inhibitors of different natures. For these reasons, a number of important refinements to the mechanisms of scale inhibition are proposed. [ABSTRACT FROM AUTHOR]

Subwavelength grating (SWG) metamaterial waveguides and ring resonators on a silicon nitride platform are proposed and demonstrated. The SWG waveguide is engineered such that a large overlap of 53% of the Bloch mode with the top cladding material is achieved, demonstrating excellent potential for applications in evanescent field sensing and light amplification. The devices, which have critical dimensions greater than 100 nm, are fabricated using a commercial rapid turn‐around silicon nitride prototyping foundry process using electron beam lithography. Experimental characterization of the fabricated device reveals excellent ring resonator internal quality factor (2.11 × 105) and low propagation loss (≈1.5 dB cm−1) in the C‐band, a significant improvement of both parameters compared to silicon‐based SWG ring resonators. These results demonstrate the promising prospects of SWG metamaterial structures for silicon nitride based photonic integrated circuits. [ABSTRACT FROM AUTHOR]

Niclosamide is an FDA-approved anthelmintic that is being studied in clinical trials as a chemotherapeutic and broad-spectrum antiviral. Additionally, several other applications are currently in the preclinical stage. Unfortunately, niclosamide is a poorly water soluble molecule, with reduced oral bioavailability, which hinders its use for new indications. Moreover, niclosamide is a poor glass former; in other words, the molecule has a high tendency to recrystallize, and it is virtually impossible to generate a stable amorphous solid employing the neat molecule. Previously, our group reported the development of an amorphous solid dispersion (ASD) of niclosamide (niclosamide ASD) that generates nanoparticles during its dissolution, not only increasing niclosamide's apparent solubility from 6.6 ± 0.4 to 481.7 ± 22.2 µg/mL in fasted state simulated intestinal fluid (FaSSIF) but also its oral bioavailability 2.6-fold in Sprague–Dawley rats after being administered as a suspension. Nevertheless, niclosamide ASD undergoes recrystallization in acidic media, and an enteric oral dosage form is needed for its translation into the clinic. In this work, we further characterized the nanoparticles that generated during the dissolution of the niclosamide ASD. Cryogenic transmission electron microscopy (Cryo-TEM) and wide-angle X-ray scattering (WAXS) revealed that the nanoparticles were amorphous and had a particle size of ~150 nm. The oral dosage forms of niclosamide ASD were formulated using commercial enteric capsules (Capsuline® and EudracapTM) and as enteric-coated tablets. The enteric dosage forms were tested using pH-shift dissolution and acid-uptake tests, using the USP type II dissolution apparatus and the disintegration apparatus, respectively. The capsules exhibited a higher percentage of weight gain, and visual rupture of the Capsuline capsules was observed. Eudracap capsules protected the formulation from the acidic media, but polymer gelling and the formation of a nondispersible plug were noted during dissolution testing. In contrast, enteric-coated tablets protected the formulation from acid ingress and maintained the performance of niclosamide ASD granules during dissolution in FaSSIF media. These enteric-coated tablets were administered to beagle dogs at a niclosamide dose of 75 mg/kg, resulting in plasma concentrations of niclosamide higher than those reported in the literature using solubilized niclosamide at a higher dose (i.e., 100 mg/kg). In summary, an enteric oral dosage form of niclosamide ASD was formulated without hindering the generation of nanoparticles while maintaining the increase in the niclosamide's apparent solubility. The enteric-coated tablets successfully increased the niclosamide plasma levels in dogs when compared to a niclosamide solution prepared using organic solvents. [ABSTRACT FROM AUTHOR]

Insight into the nucleation, growth and phase transformations of calcium sulphate could improve the performance of construction materials, reduce scaling in industrial processes and aid understanding of its formation in the natural environment. Recent studies have suggested that the calcium sulphate pseudo polymorph, gypsum (CaSO4·2H2O) can form in aqueous solution via a bassanite (CaSO4·0.5H2O) intermediate. Some in situ experimental work has also suggested that the transformation of bassanite to gypsum can occur through an oriented assembly mechanism. In this work, we have exploited liquid cell transmission electron microscopy (LCTEM) to study the transformation of bassanite to gypsum in an undersaturated aqueous solution of calcium sulphate. This was benchmarked against cryogenic TEM (cryo‐TEM) studies to validate internally the data obtained from the two microscopy techniques. When coupled with Raman spectroscopy, the real‐time data generated by LCTEM, and structural data obtained from cryo‐TEM show that bassanite can transform to gypsum via more than one pathway, the predominant one being dissolution/reprecipitation. Comparisons between LCTEM and cryo‐TEM also show that the transformation is slower within the confined region of the liquid cell as compared to a bulk solution. This work highlights the important role of a correlated microscopy approach for the study of dynamic processes such as crystallisation from solution if we are to extract true mechanistic understanding. [ABSTRACT FROM AUTHOR]

The synthesis and characterization of novel luminescent amorphous POSS-based polysilsesquioxanes (PSQs) with Tb3+ and Eu3+ ions directly integrated in the polysilsesquioxane matrix is presented. Two different Tb3+/Eu3+ molar ratios were applied, with the aim of disclosing the relationships between the nature and loading of the ions and the luminescence properties. Particular attention was given to the investigation of site geometry and hydration state of the metal centers in the inorganic framework, and of the effect of the Tb3+ → Eu3+ energy transfer on the overall optical properties of the co-doped materials. The obtained materials were characterized by high photostability and colors of the emitted light ranging from orange to deep red, as a function of both the Tb3+/Eu3+ molar ratio and the chosen excitation wavelength. A good energy transfer was observed, with higher efficiency displayed when donor/sensitizer concentration was lower than the acceptor/activator concentration. The easiness of preparation and the possibility to finely tune the photoluminescence properties make these materials valid candidates for several applications, including bioimaging, sensors, ratiometric luminescence-based thermometers, and optical components in inorganic or hybrid light-emitting devices. [ABSTRACT FROM AUTHOR]

Asteroids and comets are thought to form in the inner and outer solar systems, respectively. Chondritic porous and smooth interplanetary dust particles (CP IDPs and CS IDPs, respectively) in the stratosphere are regarded as dust grains from comets and hydrated asteroids, respectively. Here, we describe an Antarctic micrometeorite (AMM) composed of lithologies of both CP and CS IDPs. In addition to the CS IDP‐like compact lithology that experienced severe aqueous alteration, the CP IDP‐like porous lithology shows evidence of very weak aqueous alteration. The structure of the organic matter in the porous lithology varies from that in the CP IDPs to aromatic‐rich organic matter. In contrast, the structure of the organic matter in the compact lithology is homogenous, which is consistent with higher degrees of aqueous alteration. Its structure is more similar to that of CP IDPs and Wild 2 samples than that of meteoritic insoluble organic matter, suggesting that the compact lithology formed from the porous lithology. Some CP IDPs are related to cometary dust streams, such as those originating from 26P/Grigg‐Skjellerup. In addition, the presence of this AMM indicates an additional origin of the CP IDPs and their equivalent AMMs. The mineralogy and organic chemistry of this AMM suggest that its parent body was composed of the same building blocks as those of the comets, and later experienced incomplete aqueous alteration. The AMM probably formed as microbreccia in the regolith layer composed of materials from a CP IDP‐like crust and a hydrated interior. [ABSTRACT FROM AUTHOR]

The nanosheet-seeding growth (NSG) technique is an interesting synthesis method for preparing two-dimensional (2D) materials by employing ultrathin nanosheets as templates. In this work, the synthesis of 2D TiO2 nanoplates using Ti0.87O2 nanosheets via the NSG process is thoroughly studied to achieve a better understanding of this process. The influence of various synthesis conditions on the morphology and phase composition has been carefully examined. The study of synthesis time reveals that the TiO2 grows in the Stranski–Krastanov mode on the templates and the growth follows second-order kinetics. It is also found that the concentration of precursors and the synthesis time are the effective parameters in controlling the thickness of TiO2 nanoplates. The phase of the sample changes from anatase TiO2 to NH4TiOF3 and the morphology changes from flake to disk with the increase in the precursor concentration. The synthesis temperature has a large influence on the morphology and thickness of the sample but has little effect on the phase composition. However, the synthesis temperature changes the color of the sample, and a high temperature enlarges the light absorption range of the sample. [ABSTRACT FROM AUTHOR]

EFSA's aim by 2030, is that the Agency and its partners will be equipped for the routine implementation of human health risk assessment to multiple chemicals, across EFSA's domains of activity. To facilitate this effort, a roadmap for action has been developed by mapping the methods, data and tools that are currently available for mixture risk assessment and identifying current scientific gaps including challenges and blockers. The results shows that extensive methods, data and tools are available for dietary mixture risk assessment for pesticides, but that several scientific gaps still exist for the non‐dietary mixture exposure to pesticides. For food additives and for certain contaminants, the regulatory readiness for mixture risk assessment was also found to be fairly high compared to food contact materials and cross‐silo mixture risk assessment. The scientific gaps identified were prioritised according to their impact on the implementation of mixture risk assessment and, as a result, ten multi‐annual project proposals were defined to address these scientific gaps on the short‐term, mid‐term and long‐term. The roadmap also proposes and prioritises a number of working areas in the regulatory domains of pesticides, food contact materials, contaminants, food additives, as well as in the overarching domain of chemicals. Besides the scientific proposals, recommendations to improve stakeholder engagement and communication on mixture risk assessment was investigated. These included, among others, creating an online catalogue of tools, methods and data for mixture risk assessment, as well as the organisation of regular webinars/workshop to promote exchange of information between stakeholders and making more efficient use of national communication hubs for food safety in communicating with the general public. [ABSTRACT FROM AUTHOR]

Acute febrile illness (AFI) is a morbid condition with a sudden onset of fever with at least seven days of evolution, where no signs or symptoms related to an apparent infection have been identified. In Latin America, a high proportion of disease is typically due to malaria and arboviruses. However, among the infectious etiologies, tick-borne diseases (TBDs) should also be considered, especially in areas where people come into direct contact with these arthropods. This study aims to describe the etiology and epidemiology related to tick-borne agents in patients with AFI and the tick's natural infection by agents of TBD in the rural tropical Magdalena Medio region in Colombia, and explore the factors associated with the presence of Coxiella burnetii infection. We conduct a cohort study enrolling 271 patients with AFI to detect the bacteria of the genera Anaplasma, Ehrlichia, Coxiella, Rickettsia, Borrelia, and Francisella through molecular techniques, and additionally evaluate the presence of IgG antibodies with commercially available kits. We also conduct tick collection in the patient's households or workplaces for the molecular screening of the same bacterial genera. Seropositivity to IgG antibodies was obtained for all the bacteria analyzed, with Francisella being the most common at 39.5% (107/271), followed by R. rickettsii at 31.4% (85/271), Ehrlichia at 26.9% (73/271), R. typhi at 15.5% (42/271), Anaplasma at 14.4% (39/271), and Borrelia at 6.6% (18/271). However, these bacteria were not detected by the molecular techniques used. Coxiella burnetii infection was detected in 39.5% of the patients: 49.5% only by phase I and II IgG antibodies, 33.6% only by real-time PCR, and 16.8% had a concordant positive result for both techniques. A total of 191 adult ticks, 111 females and 80 males, were collected and identified as Rhipicephalus sanguineus s.l. and Rhipicephalus microplus. In the 169 adult ticks in which natural infection was evaluated, Ehrlichia spp. was detected in 21.3% (36/169), Coxiella spp. in 11.8% (20/169), and Anaplasma spp. in 4.7% (8/169). In conclusion, we identified the prior exposition to Francisella, Anaplasma, Ehrlichia, Rickettsia, Borrelia, and Coxiella in patients through serological tests. We also detected the infection of C. burnetii using molecular techniques. In the ticks, we identified bacteria of the genera Coxiella, Anaplasma, and Ehrlichia. These results suggest the importance of these zoonotic agents as possible causes of AFI in this region. [ABSTRACT FROM AUTHOR]

Organic–inorganic composite materials with tailored properties can be designed in the lab through bio-inspired approaches. In this context, we exploited the particle-based crystallisation process of calcium sulfate, a technologically important mineral, to hybridise inorganic and organic matter. We identified and synthesised an organic polymer showing strong affinity to bind to the surfaces of mineral precursors as well as intrinsic tendency to self-organise. Subsequently, polymer-coated building units were allowed to self-assemble via oriented attachment, aggregation and phase transformation, which produced ordered superstructures where the organic polymer is intercalated between the subunits and surrounds the hybrid core as a shell. This specific architecture across multiple length scales leads to unique mechanical properties, comparable to those of natural biominerals. Thus, our results devise a straightforward pathway to prepare organic–inorganic hybrid structures via bottom-up self-assembly processes innate to the crystallisation of the inorganic phase. This approach can likely be transferred to other inorganic minerals, affording next-generation materials for applications in the construction sector, biomedicine and beyond. [ABSTRACT FROM AUTHOR]

Magnesium phosphate-based cements (MPCs) have recently attracted great attention as materials for bone repair. However, the lack of macroporosity, fundamental for cells permeation and bone ingrowth, is one of the main limitations hampering MPCs full exploitation. In this work gelatin microparticles are exploited as templating agents for the creation of macroporosities in MPCs. In addition, gelatin particles were loaded with a well-recognized drug for the treatment of osteoporosis, alendronate, to locally release the therapeutic agent. Gelatin microparticles of different size were prepared with a simple water-in-oil emulsion method and included in MPCs at various concentrations. The properties of both the MPCs and the final material were characterized by assessing the composite in terms of injectability, setting time, infrared spectroscopy, scanning electron microscopy and confocal Raman microscopy. The MPC-gelatin composites were then incubated in water at physiological temperature, to promote the dissolution of the gelatin, obtain a macroporous cement, and release gelatin and alendronate. The obtained results show that gelatin microparticles have a twofold action as they allow for the formation of MPC with an interconnected and hundreds of µm-sized porosity and the local release of alendronate, resulting in a material with ideal features for bone repair. [ABSTRACT FROM AUTHOR]

Crystal nucleation determining the formation and assembly pathway of first organic materials is the central science of various scientific disciplines such as chemical, geochemical, biological, and synthetic materials. However, our current understanding of the molecular mechanisms of nucleation remains limited. Over the past decades, the advancements of new experimental and computational techniques have renewed numerous interests in detailed molecular mechanisms of crystal nucleation, especially structure evolution and solution chemistry. These efforts bifurcate into two categories: (modified) classical nucleation theory (CNT) and non-classical nucleation mechanisms. In this review, we briefly introduce the two nucleation mechanisms and summarize current molecular understandings of crystal nucleation that are specifically applied in polymorphic crystallization systems of small organic molecules. Many important aspects of crystal nucleation including molecular association, solvation, aromatic interactions, and hierarchy in intermolecular interactions were examined and discussed for a series of organic molecular systems. The new understandings relating to molecular self-assembly in nucleating systems have suggested more complex multiple nucleation pathways that are associated with the formation and evolution of molecular aggregates in solution. [ABSTRACT FROM AUTHOR]

The potential of the electrospray deposition technique as new method to make nanosheet-based multilayer films is evaluated. Densely packed nanosheet-based films with thicknesses of 1–20 nm with rms roughnesses of 2.1–2.4 nm were fabricated on samples of 1 cm2 size with a growth rate of 0.5 nm/min. Electrosprayed Ti0.87O2 nanosheet films were successfully used as oriented growth templates for 40 nm perovskite SrRuO3 thin films grown by pulsed laser deposition. The electrospray method provides a fast and easy alternative to the more commonly used Langmuir–Blodgett (LB) deposition method for nanosheet films. [ABSTRACT FROM AUTHOR]

Calcium sulfate is an important construction material. More than 1600 million square meters of interior surfaces are covered with plasterboards in Europe each year. Plasterboard is manufactured by transforming mined or recycled gypsum (CaSO4 × 2 H2O) to bassanite (CaSO4 × ½H2O) in a time‐ and energy‐consuming heating process. A fast and sustainable way to produce bassanite by solvent‐assisted milling, thereby eliminating the need for energy‐intensive dehydration, is described. The milling reaction is complete after ≈200 min. Kinetic studies revealed that gypsum crystals transform to bassanite by shear forces during milling. 1H nuclear magnetic resonance (NMR) spectroscopic techniques and Fourier‐transform infrared spectroscopy (FT‐IR) show that the resulting bassanite nanocrystals are stabilized by surface functionalization with the auxiliary solvent methanol. Bassanite particles produced over extended milling times of 990 min form long‐term stable dispersions without stabilizers and no signs of precipitation. Addition of water to bassanite leads to instant agglomeration, followed by a phase change to gypsum. The dispersibility in volatile methanol and the elucidation of the crystallization mechanism allow also for applications of the bassanite nanocrystals in hybrid materials. [ABSTRACT FROM AUTHOR]

Nucleation and crystal growth of CaSO4 ∙ 0.5H2O (calcium sulphate hemihydrate) was studied under conditions simulating scale formation in phosphoric acid production evaporators. Phosphoric acid, calcium hydrogen phosphate, and sulphuric acid were mixed at 88°C. The induction time was determined using a turbidimeter across a range of supersaturation from 1.3–3.5. Crystallization equations, taking as input the induction time and supersaturation, were used to calculate surface energy, nucleation rate, free energy, and the critical nucleus radius of CaSO4 ∙ 0.5H2O with and without the addition of 75 mg/L of various scale inhibitors: polyacrylic acid (PAA) 8000 g/mol, poly(diallyldimethylammonium chloride) (PDADMAC) <100 000 g/mol, or polyethyleneimine (PEI) 60 000 g/mol. The results suggest that PEI is capable of inhibiting crystal growth through the impediment of crystal nucleation. [ABSTRACT FROM AUTHOR]

In this study, novel lanthanide-containing double-decker polyhedral oligomeric silsesquioxanes (POSS) were prepared by combining the partially condensed TetraSilanolPhenyl POSS with terbium (Tb3+) and europium (Eu3+) ions. This open-cage POSS possesses four diametrically opposite silanol groups that are able to coordinate, under mild conditions, different luminescent ions through a simple corner-capping method. The two metal-containing POSS functionalized with Tb3+ and with an equimolar combination of Tb3+ and Eu3+ show a completely condensed structure with different luminescent properties. Their emission features depend on the chemical nature of the metal ions incorporated in the framework. An improved stokes shift was detected in the bimetallic compound containing both the Tb3+ and Eu3+ ions, promoted by the occurrence of a Tb3+→Eu3+ energy transfer mechanism. These characteristics identify this metal-functionalized silica platform as a potential candidate for the development of novel luminescent devices. [ABSTRACT FROM AUTHOR]

Ordinary γ‐CaSO4 is a metastable calcium sulfate, while γ‐CaSO4 from the hyperarid region on Earth and from Mars has been found with abnormally high stability. In this study, we used multiple microanalyses to characterize the chemical and structural properties of two such γ‐CaSO4: one from Atacama soil (#10‐d30) and the other from Martian meteorite MIL03346,168. Silicon was determined to be quasi‐homogeneously distributed in Atacama γ‐CaSO4, while both silicon and phosphorus were detected in Martian γ‐CaSO4. We found the abnormally high stability of those γ‐CaSO4 from hyperarid environments was due to the chemical impurities which filled their structural tunnels and blocked the entrance of atmospheric H2O, with non‐detectable structural distortion. We propose that the γ‐CaSO4 with Si or Si and P impurities could have igneous origin or evaporative origin. Due to the extreme similarity in the structures of bassanite and γ‐CaSO4, their XRD patterns are almost non‐distinguishable; thus some martian "bassanite" minerals identified by Curiosity's CheMin instrument at Gale crater can actually be γ‐CaSO4. The structural tunnels in γ‐CaSO4 would allow ions and ionic groups to fill, thus providing meaningful insights about the geological and geochemical processes experienced by it during the formation and transformation. The Raman spectrometer carried by the Perseverance and by ExoMars rovers will help the selection of samples enriched in γ‐CaSO4 at Jezero Crater and Oxia Planum, which should be sampled for in‐depth analysis on Mars and back to Earth. Plain Language Summary: In the laboratory, ordinary γ‐CaSO4 would adsorb atmospheric H2O in minutes and transform to bassanite. However, the γ‐CaSO4 from the hyperarid region on Earth and from Mars has been found maintaining abnormally high stability for years. We used multiple microanalyses to characterize the chemical and structural properties of γ‐CaSO4 from Atacama soil and Martian meteorite MIL03346,168. We found that silicon is quasi‐homogeneously distributed in Atacama γ‐CaSO4, while both silicon and phosphorus were determined in Martian γ‐CaSO4. Our study demonstrated that abnormally high stability of γ‐CaSO4 was due to chemical impurities, which filled the structural tunnels that blocked the entrance of atmospheric H2O. Due to extreme similarity in the structures of bassanite and γ‐CaSO4, their XRD patterns are almost non‐distinguishable. We anticipate that some "bassanite" identified by Curiosity's CheMin instrument at Gale crater could actually be γ‐CaSO4. Our study shows that the structural tunnels in γ‐CaSO4 could be readily filled by ions and ionic groups, and even organic molecules as demonstrated by other studies. The Raman spectrometer carried by the Perseverance and ExoMars rovers would help the selection of samples enriched in γ‐CaSO4, for in‐depth analyses on Mars and return to Earth. Key Points: High stability of γ‐CaSO4 from hyperarid areas was found due to chemical impurities that filled tunnels and blocked entrance of H2OThe impure γ‐CaSO4 could have igneous and evaporative origins, significant for understanding geochemical processSome "bassanite" minerals identified by the CheMin instrument on Mars can actually be γ‐CaSO4 [ABSTRACT FROM AUTHOR]

Background: This study aimed to determine short- and long-term physical and psychosocial impact of Coxiella burnetii infection in three distinct entities: Q-fever fatigue syndrome (QFS), chronic Q-fever, and patients with past acute Q-fever without QFS or chronic Q-fever. Methods: Integrative data analysis was performed, combining original data from eight studies measuring quality of life (QoL), fatigue, physical and social functioning with identical validated questionnaires, from three months to eight years after onset infection. Linear trends in each outcome were compared between Q-fever groups using multilevel linear regression analyses to account for repeated measures within patients. Results: Data included 3947 observations of 2313 individual patients (228 QFS, 135 chronic Q-fever and 1950 patients with past acute Q-fever). In the first years following infection, physical and psychosocial impact was highest among QFS patients, and remained high without significant improvements over time. In chronic Q-fever patients, QoL and physical functioning worsened significantly over time. Levels of fatigue and social participation in patients with past acute Q-fever improved significantly over time. Conclusion: The impact differs greatly between the three Q-fever groups. It is important that physicians are aware of these differences, in order to provide relevant care for each patient group. [ABSTRACT FROM AUTHOR]

In this paper, we explore the impact of yttrium content and thermal annealing on the structural properties and sensing characteristics of YbYxOy sensing membranes deposited on Si substrates through reactive cosputtering for electrolyte-insulator-semiconductor (EIS) pH sensors. X-ray photoelectron spectroscopy and atomic force microscopy were used to study the compositional and morphological features of these membranes as functions of the growth conditions (Y plasma powers of 50, 100, and 150 W; temperatures ranging from 700 to 900 °C). The YbYxOy EIS device prepared under an Y plasma power of 100W with subsequent annealing at 800 °C exhibited the best sensing characteristics (pH sensitivity, hysteresis voltage, and drift rate). We attribute this behavior to the optimal yttrium content in this sensing membrane improving the stoichiometry of YbYxOy membrane and its surface roughness. [ABSTRACT FROM AUTHOR]

Characterizing the pathways by which crystals form remains a significant challenge, particularly when multiple pathways operate simultaneously. Here, an imaging‐based strategy is introduced that exploits confinement effects to track the evolution of a population of crystals in 3D and to characterize crystallization pathways. Focusing on calcium sulfate formation in aqueous solution at room temperature, precipitation is carried out within nanoporous media, which ensures that the crystals are fixed in position and develop slowly. The evolution of their size, shape, and polymorph can then be tracked in situ using synchrotron X‐ray computed tomography and diffraction computed tomography without isolating and potentially altering the crystals. The study shows that bassanite (CaSO4 0.5H2O) forms via an amorphous precursor phase and that it exhibits long‐term stability in these nanoscale pores. Further, the thermodynamically stable phase gypsum (CaSO4 2H2O) can precipitate by different pathways according to the local physical environment. Insight into crystallization in nanoconfinement is also gained, and the crystals are seen to grow throughout the nanoporous network without causing structural damage. This work therefore offers a novel strategy for studying crystallization pathways and demonstrates the significant impact of confinement on calcium sulfate precipitation, which is relevant to its formation in many real‐world environments. [ABSTRACT FROM AUTHOR]

The goal of this study was to describe the variation in hospital-based diagnostic care activities for patients with symptomatology suspect for breast cancer in The Netherlands. Two cohorts were included: the 'benign' cohort (30,334 women suspected of, but without breast cancer) and the 'malignant' cohort (2236 breast cancer patients). Hospital-based financial data was combined with tumor data (malignant cohort) from The Netherlands Cancer Registry. Patterns within diagnostic pathways were analyzed. Factors influencing the number of visits and number of diagnostic care activities until diagnosis were identified in the malignant cohort with multivariable Cox and Poisson regression models. Compared to patients with benign diagnosis, patients with malignant disease received their diagnosis less frequently in one day, after an equal average number of hospital visits and higher average number of diagnostic activities. Factors increasing the number of diagnostic care activities were the following: lower age and higher cM-and cN-stages. Factors increasing the number of days until (malignant) diagnosis were as follows: higher BIRADS-score, screen-detected and higher cN-and cT-stages. Hospital of diagnosis influenced both number of activities and days to diagnosis. The diagnostic care pathway of patients with malignant disease required more time and diagnostic activities than benign disease and depends on hospital, tumor and patient characteristics. [ABSTRACT FROM AUTHOR]

The reaction of 3.65 Å phase <=> clinoenstatite + water was investigated in five experiments at 10GPa, 470-600 °C, using a rotating multi-anvil press. Under these P/T conditions, clinoenstatite exists in its high-pressure modification, which, however, is not quenchable to ambient conditions but transforms back to low-pressure clinoenstatite. The quenched run products were characterized by electron microprobe analyses (EMPA), powder X-ray diffraction (XRD), Raman spectroscopy and by high-resolution transmission electron microscopy (HRTEM) on focused ion beam (FIB)-cut foils. We bracketed the reaction in the T range 470 to 510 °C (at 10 GPa). The hydration of clinoenstatite to the 3.65 Å phase at 470 °C was very sluggish and incomplete even after 96 h. Clinoenstatites range in size from less than 1 to up to 50 µm. Usually clinoenstatite has a very small grain size and shows many cracks. In sub-micron-sized broken clinoenstatite, an amorphous phase (0.91Mg : 1.04Si, with about 20 wt % H2O) was observed, which further transformed with increasing reaction time into the 3.65 Å phase (1Mg : 1Si, with 34 wt % H2O). Thus, the sub-micron-sized fractured clinoenstatite transformed via an amorphous water-bearing precursor phase to the 3.65 Å phase. The dehydration to clinoenstatite was faster but still incomplete after 72 h at 600 °C. From the backscattered electron images of the recovered sample of the dehydration experiment, it is obvious that there is a high porosity due to dehydration of the 3.65 À phase. Again, the grain size of clinoenstatite ranges from less than 1 up to 50 µm. There are still some clinoenstatite crystals from the starting material present, which can clearly be distinguished from newly formed sub-micron-sized clinoenstatite. Additionally, we observe a water-rich crystalline phase, which does not represent the 3.65 Å phase. Its Raman spectra show the double peaks around 700 and 1000 cm-1 characteristic for enstatite and strong water bands at 3700 and 3680 cm-1. The Mg : Si ratio of 0.90 : 1.04 was determined by EMPA, totalling to 81 wt %, in accordance with its high water content. Diffraction patterns from high-resolution images (fast Fourier transform - FFT) are in agreement with an orthoenstatite crystal structure (Pbca). The surprising observation of this study is that, in both directions of the investigated simple reaction, additional metastable phases occur which are amorphous in the hydration and crystalline in the dehydration reaction. Both additional phases are water rich and slightly deviate in composition from the stable products 3.65 À phase and clinoenstatite, respectively. Thus, as a general remark, conventional investigations on reaction progress should be complemented by nanoscale investigations of the experimental products because these might reveal unpredicted findings relevant for the understanding of mantle processes. The extreme reduction in grain size observed in the dehydration experiments due to the formation of nanocrystalline clinoenstatite rather than the slowly released fluids might cause mechanical instabilities in the Earth's mantle and, finally, induce earthquakes. [ABSTRACT FROM AUTHOR]