Microscopy X-ray Research Articles

Preparation of a nano aluminum phosphate enhanced hydroxyapatite coating for marble conservation

Open-air marble relics in Beijing are experiencing degradation due to sugaring, dissolution and other illnesses. Therefore, it is necessary to apply a protective and reinforcing coating to the weathered surface. Hydroxyapatite (HAP) has significantly lower solubility and dissolution rate compared to calcite. Additionally, HAP has similar lattice parameters with calcite, suggesting that a cohesive layer of HAP can be formed over calcite. In fact, HAP exhibits a lattice mismatch of 5 % with calcite, which might potentially lead to stress if the layer exceeds a few nanometre in thickness. On the other hand, aluminum phosphates (ideally, B-AlPO4) only exhibit a 1 % mismatch with calcite and have a solubility lower than that of calcite. In this study, in order to improve the property of HAP in marble conservation, sol–gel method was employed to synthesize nano AlPO4, which were then incorporated into the phosphate solution to produce protective coating on the stone surface. The coatingʼs morphology and the structure were characterized by Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), high capacity 3D X-ray microscopy (XRM), optical microscope, and scanning electron microscopy coupled with energy dispersive spectroscopy (SEM-EDS). Moreover, the color, the contact angle, the three-point bending strength measurements, as well as the simulated acid rain test and freeze–thaw treatment were performed to assess the chromatic aberration, hydrophilicity, reliability, and durability of the coating. Results indicated that the nano AlPO4, with its matched lattice parameters and nucleation site provision, facilitated the formation a coherent HAP layer of crystal flakes. Subsequently, the anti‑corrosion property, freeze-thaw resistance and consolidation property of the coating were improved, demonstrating the potential application the hybrid of HAP with nano AlPO4 in the preservation of marble.

Monolithic deformable mirror based on lithium niobate single crystal for high-resolution X-ray adaptive microscopy

X-ray microscopy is very promising not only for nondestructive and high-spatial-resolution observation of the internal structure of a sample but also for elemental distribution and chemical state analysis. However, the spatial resolution of microscopes remains unsatisfactory owing to the fabrication error in the objective lens. To realize an ultra-high-resolution, we propose and develop a monolithic deformable mirror based on a lithium niobite single crystal and a novel adaptive imaging system based on it. An X-ray interferometer confirmed that shape modification is possible with an accuracy of 0.67 nm in peak to valley under high stability (0.17 nm over 7 h) and hysteresis-free deformation control. Introducing this adaptive mirror into an X-ray microscope based on advanced Kirkpatrick-Baez mirror optics and correcting the wavefront aberration demonstrated that the X-ray image quality could be significantly improved.

Controlled Mechanical Property Gradients Within a Digital Light Processing Printed Hydrogel-Composite Osteochondral Scaffold.

Tissue engineered scaffolds are needed to support physiological loads and emulate the micrometer-scale strain gradients within tissues that guide cell mechanobiological responses. We designed and fabricated micro-truss structures to possess spatially varying geometry and controlled stiffness gradients. Using a custom projection microstereolithography (μSLA) system, using digital light projection (DLP), and photopolymerizable poly(ethylene glycol) diacrylate (PEGDA) hydrogel monomers, three designs with feature sizes < 200μm were formed: (1) uniform structure with 1MPa structural modulus ( ) designed to match equilibrium modulus of healthy articular cartilage, (2) = 1MPa gradient structure designed to vary strain with depth, and (3) osteochondral bilayer with distinct cartilage ( = 1MPa) and bone ( = 7MPa) layers. Finite element models (FEM) guided design and predicted the local mechanical environment. Empty trusses and poly(ethylene glycol) norbornene hydrogel-infilled composite trusses were compressed during X-ray microscopy (XRM) imaging to evaluate regional stiffnesses. Our designs achieved target moduli for cartilage and bone while maintaining 68-81% porosity. Combined XRM imaging and compression of empty and hydrogel-infilled micro-truss structures revealed regional stiffnesses that were accurately predicted by FEM. In the infilling hydrogel, FEM demonstrated the stress-shielding effect of reinforcing structures while predicting strain distributions. Composite scaffolds made from stiff μSLA-printed polymers support physiological load levels and enable controlled mechanical property gradients which may improve in vivo outcomes for osteochondral defect tissue regeneration. Advanced 3D imaging and FE analysis provide insights into the local mechanical environment surrounding cells in composite scaffolds.

Structural Evolution of GaOx-Shell and Intermetallic Phases in Ga-Pt Supported Catalytically Active Liquid Metal Solutions.

We present a comprehensive scale-bridging characterization approach for supported catalytically active liquid metal solutions (SCALMS) which combines lab-based X-ray microscopy, nano X-ray computed tomography (nano-CT), and correlative analytical transmission electron microscopy. SCALMS catalysts consist of low-melting alloy particles and have demonstrated high catalytic activity, selectivity, and long-term stability in propane dehydrogenation (PDH). We established an identical-location nano-CT workflow which allows us to reveal site-specific changes of Ga-Pt SCALMS before and after PDH. These observations are complemented by analytical transmission electron microscopy investigations providing information on the structure, chemical composition, and phase distribution of individual SCALMS particles. Key findings of this combined microscopic approach include (i) structural evolution of the SCALMS particles' GaOx shell, (ii) Pt segregation toward the oxide shell leading to the formation of Ga-Pt intermetallic phases, and (iii) cracking of the oxide shell accompanied by the release of liquid Ga-Pt toward the porous support.

Effect of starch granule size on the properties of dough and the oil absorption of fried potato crisps

Starch is a key element in fried potato crisps, however, the effect of starch granule size on oil absorption of the product have yet to be fully investigated. The study explored the impact of starch granule size on both the dough characteristics and oil absorption in potato crisps. The dough composed of small-sized potato granules showed more compact and uniform network system. Additionally, X-ray Microscope analysis showed that potato crisps prepared with small-sized potato granules had limited matrix expansion and fewer pores, cracks, and voids. The small-sized potato and small-sized wheat starches granule addition crisps displayed a significantly greater average cell thickness (52.05 and 53.44 μm) than other samples, while exhibiting notably lower average porosity (61.37 % and 60.28 %) compared to other samples. Results revealed that potato crisps with medium and small potato granules had 12.91 % and 21.92 % lower oil content than those containing large potato starch. Potato crisps with B-type wheat starch showed 16.36 % less oil absorption than those with A-type wheat starch. Small-sized starches significantly influence the dough structure and contribute to the reduction of oil absorption in fried products. The generated insights may provide monitoring indexes for cultivating potato varieties with low oil absorption.

Investigating the influence of natural dye extracts from Ocimum gratissimum, Solanum melongena, Piper guineese, and their blend in the fabrication of perovskite solar cells

Perovskite solar cells (PSCs) represent a promising alternative to conventional silicon solar cells but face challenges like instability stemming from structural defects, environmental toxicity due to the selection of precursors and additives, and concerns regarding long-term reliability. To address these issues, we investigated the viability of cost-effective and eco-friendly PSCs by strategically incorporating natural dyes derived from indigenous plants, including Ocimum gratisimum, Solanum melongena, and Piper guineese, into the MAPbI3 perovskite crystal, using a two-step sequential drop-casting technique. The resulting perovskite films underwent comprehensive analysis for their structural, morphological, optical and elemental composition using an X-ray diffractometer (XRD), scanning electron microscopy (SEM), UV–visible spectrophotometer (UV–Vis) and energy dispersive X-ray microscopy (EDX). Performance evaluation was conducted through J-V curve analysis using a solar simulator. The XRD analysis revealed polycrystalline films with enhanced diffraction intensities corresponding to a hexagonal structure, and the UV–Vis analysis demonstrated substantial improvements in light absorption with improved optical properties. SEM studies provided crucial correlations between morphology and performance, with each sample exhibiting unique attributes, and EDX analysis confirmed essential elements within the films. The current density-voltage analysis demonstrated a 1.83 % power conversion efficiency (PCE) for the natural dye-doped device under air, surpassing the pristine device. This study advances the understanding of the synergies between natural dyes and perovskite materials, emphasizing their potential to enhance PSC efficiency. The findings underscore the considerations for designing and optimizing PSCs, paving the way for further exploration of natural dye-based approaches in sustainable photovoltaic technologies.

Unveiling nano-scale chemical inhomogeneity in surface oxide films formed on V- and N-containing martensite stainless steel by synchrotron X-ray photoelectron emission spectroscopy/microscopy and microscopic X-ray absorption spectroscopy

Nano-scale chemical inhomogeneity in surface oxide films formed on a V- and N-containing martensite stainless steel and tempering heating induced changes are investigated by a combination of synchrotron- based hard X-ray Photoelectron emission spectroscopy (HAXPES) and microscopy (HAXPEEM) as well as microscopic X-ray absorption spectroscopy (µ-XAS) techniques. The results reveal the inhomogeneity in the oxide films on the micron-sized Cr2N- and VN-type particles, while the inhomogeneity on the martensite matrix phase exists due to localised formation of nano-sized tempering nitride particles at 600 °C. The oxide film formed on Cr2N-type particles is rich in Cr2O3 compared with that on the martensite matrix and VN-type particles. With the increase of tempering temperature, Cr2O3 formation is faster for the oxidation of Cr in the martensite matrix than the oxidation of Cr nitride-rich particles.

A high resolution miniature electron energy spectrometer

In this work we describe how a novel mass spectrometer design we recently reported on can be utilized as an electron spectrometer having excellent resolution and passband width. This new electron spectrometer is referred to as a segmented electrode electron spectrometer (SEES). We discuss the determination of the operating parameters for the instrument and provide a detailed assessment of the energy resolution and passband width. We compare the new instrument to hemispherical deflection analyzers (HDAs), a popular electron spectrometer topology. The instrument presented has a resolution ∼9.1x greater than an idealized HDA and an energy passband ∼2.1x wider. In addition, the instrument has a volume far below an HDA of identical outer radius, enabling simpler integration with other existing instrumentation like x-ray, electron, and/or ion sources and microscopes. The evolution of this instrument demonstrates a new framework for the development of electron spectrometers with improved performance characteristics.

Effective Removal of Nile Blue Dye from Wastewater using Silver-Decorated Reduced Graphene Oxide.

Nile blue (NB) dye is a highly toxic substance that when discharged into sewage presents a significant risk to the environment and human health. Carbon-based nanomaterials, such as graphene oxide (GO), reduced graphene oxide (rGO), and their nanocomposites, offer considerable potential for eliminating hazardous pollutants from aqueous systems. In this study, we have successfully fabricated bare GO and rGO, and then, the rGO was decorated with silver (Ag) nanoparticles to develop the Ag-rGO composite. The as-prepared materials were characterized by various techniques, such as UV-visible (UV-vis) and Fourier transform infrared (FTIR) spectroscopies, X-ray diffraction (XRD), energy-dispersive X-ray (EDX), and scanning electron microscopy (SEM) to elucidate their structure, morphology, and chemical composition. The pollutant removal performance of the as-prepared materials was evaluated through a batch approach under the effect of various experimental variables for removal of NB dye from wastewater. As obvious, the Ag-rGO composite revealed exceptional performance for NB dye removal from wastewater, with a maximum removal percentage of 94% within 60 min, which is remarkably higher than those of the rGO (i.e., 59%) and GO (i.e., 22%), under the same experimental conditions. The adsorption data was analyzed with thermodynamics, isotherms, and kinetics models to better understand the physicochemical mechanisms driving the effective removal of the NB dye. The results reveal that Ag-rGO nanocomposite exhibit excellent adsorption ability as well as favorable thermodynamic and kinetic parameters for NB dye removal. It was also found that the presence of light enhanced the adsorptive removal of NB while using Ag-rGO as an adsorbent. The present study noted significant reusability of the Ag-rGO nanocomposite, likely due to minimal Ag leaching and/or the robust stability of the Ag-rGO. It is suggested that Ag-rGO-based hybrid materials could serve as promising candidates for efficiently adsorbing and catalytically removing various toxic pollutants from wastewater.

Green synthesis of ZnO nanoparticles using the mangosteen (Garcinia mangostana L.) leaf extract: Comparative preliminary in vitro antibacterial study

Abstract In the realm of public health, the rising threat caused by bacteria resistant to many drugs is a critical concern. In this work, we used the aqueous extract of mangosteen leaves to create zinc oxide (ZnO) nanoparticles (NPs) in an environmentally friendly manner. Through various analytical methods, we thoroughly characterized these biogenic ZnO NPs, including UV−visible, Fourier transform infrared, X-ray photoelectron spectroscopy, Raman spectroscopy, X-ray powder diffraction, field emission-scanning electron microscopy with energy dispersive X-ray and high resolution-transmission electron microscopy. ZnO NPs showed distinctive properties among different characterization techniques, including a small energy bandgap of 2.80 eV, a porous, a minimum crystalline size of 16.99 nm, an average particle size of 14.21 nm, and a spherical nanostructure. Additionally, we performed preliminary antibacterial experiments to assess ZnO NPs, copper oxide (CuO) NPs, and ZnO–CuO nanocomposites for antibacterial activity. Interestingly, ZnO NPs showed significant potential in suppressing the growth of Staphylococcus aureus ATCC BAA-1026, Bacillus subtilis ATCC 6633, Escherichia coli ATCC 25922, and Klebsiella pneumoniae ATCC 13883, with decreasing order of minimum inhibitory concentrations: S. aureus = B. subtilis (15.63 μg·mL−1) &gt; E. coli (62.50 μg·mL−1) &gt; K. pneumoniae (125.00 μg·mL−1). These results highlight the potential of biogenic NPs, particularly ZnO NPs, as effective agents against multi-drug-resistant bacteria.

Experimental analysis and numerical simulation of biomass pyrolysis

AbstractFinding alternatives to fossil fuels is extremely important for economic and environmental considerations. Biomass pyrolysis stands out as an efficient method for generating fuels and chemical intermediates. This study explored the influence of wood particle size (ranging from 1 to 3 cm) and pyrolysis temperature (ranging from about 300 to 480 °C) on the process. Characterization of wood residues utilized energy-dispersive X-ray (EDX) and field emission scanning electron microscopy (FE-SEM) to comprehend surface morphology and resultant biochar structure. Results revealed a significant temperature-dependent impact on pyrolysis product concentrations. Biomass composition analysis indicates lignin, hemicellulose, extractive contents, and cellulose percentages at 11.23%, 39%, 2.15%, and 47.62% mass/mass, respectively. Reduction in particle size to less than 2 mm enhances heat transfer, elevating overall bio-oil production. Major bio-oil components comprise phenolics, acids, alcohols, aldehydes, and ketones. Optimal conditions are identified at a wood particle size of 1 cm and a heating temperature of 480 °C. For every 1.0 kg of wood biomass residues, bio-oil, syngas, and biochar yields are 0.38 kg, 0.22 kg, and 0.4 kg, respectively. Notably, the agreement between Aspen Plus simulation and experimental findings underscored the robustness of the study.

Osteoinductive effect of the nanoparticulate form of Cissus quadrangularis ethanolic extract on implant surface in experimental animals

BackgroundThe purpose of this study was to evaluate the effect of nanoparticles (NPs) of a plant extract on implant osseointegration in vivo. NPs of the Cissus quadrangularis (CQ) extract were synthesized. Twenty Wistar rats were included in the study. The test group (n = 5) had NPs-incorporated, the control group (n = 5) had no incorporation of NPs, and the sham group (n = 5) did not have implants placed. The toxicity profile of NPs was carried out by biochemical analysis before and after the implant placement. The rate of integration was assessed using Cone Beam Computed Tomography (CBCT), Digital X-ray, histology, and scanning electron microscopy (SEM) at intervals of 2, 4, and 6 weeks. Statistical significance between the groups was determined by Analysis of Variance (ANOVA) (p < 0.05) and the differences were uncovered with post hoc Tukey’s test.ResultsRadiographs showed that the bone density around implants with NPs was considerably higher than those without NPs. The osteoid seam along the implant surface was found to be considerably higher in the test group. A noteworthy increase was observed in the bone formation around the implants in bone samples belonging to the test group. Comparing the values at different time intervals, the highest serum Alkaline phosphatase (ALP) activity was noted in the test group after six weeks and the lowest serum Acid phosphatase (ACP) activity was documented in the test group after 6 weeks.ConclusionThe test group samples exhibited an osseointegration rate of less than 2 weeks thus demonstrating CQ NPs to be a potent osteoinductive agent.Graphical abstract

Synthesis &amp; Characterization of Carbon Nanostructures.

Synthesis In this research a study was conducted on the Synthesis and dimensional structural characterization of nanostructures consisting of Graphene, Nanotubes and Fullerenes C60 and C70 carbon research project consists of a synthesis and characterization in its theoretical and experimental framework to test yields in the synthesis of each nanostructure. Synthesis for Multiple Synthesis Rector MSR will be held in the exploder and electric fields in the toroidal coil Tesla coil. As for the structural dimensional characterization of nanostructured materials carbon is carried out by Raman spectroscopy, diffraction X-ray (XRD) and Transmission Electron Microscopy (TEM) Scanning Electron Microscopy (SEM) Atomic Force Microscopy (AFM) and EELS (Energy Electron loss Spectrum). Justification Synthesis System The main justification synthesis system is to generate nanostructures (Nanotubes, Nanofibers, Fullerenes, graphene) easily and economically; all using little equipment and a simple process which is reflected in lower costs simple synthesis as current processes are very expensive and too complex. Justification Synthesis System The main objective of this system is the generation synthesis of nanostructures by using a Tesla coil (Plasma Generator) as the main component of the system being accessible, simple and inexpensive technology. Another goal is to optimize the generation of nanostructures to its widespread use in industry, nanotechnology and materials science. Through a system very inexpensive and simple synthesis.

Methods for research on structures and functions of traditional Chinese medicine proteins

Traditional Chinese medicine proteins(TCMPs) not only have nutritional values and biological activities but also serve as key enzymes in the synthesis of pharmacodynamic components in traditional Chinese medicines. They play a role in the synthesis of pharmacodynamic components by regulating biosynthesis and selective synthesis pathways and controlling drug quality and stability. The recent years have witnessed great progress in the research on the structures and functions of proteins using various methods and technologies. However, the research on the structures and functions of TCMPs lags behind. Therefore, it is urgent to study the structures and functions of TCMPs using modern means to promote the discovery of innovative drugs based on TCMPs and clarify the synthesis pathways of pharmacodynamic components. This study introduces the latest techniques for studying protein structures and functions, including spectroscopy, mass spectrometry, nuclear magnetic resonance, X-ray crystal diffraction, microscopy, and structure prediction. Furthermore, this paper introduces the methods for protein functional studies, including liquid chromatography-mass spectrometry, co-immunoprecipitation, yeast two-hybrid, and pull-down assay. By systematically reviewing these techniques and methods, this paper provides technical references for the structural identification and functional studies of TCMPs, with the aim of promoting the in-depth exploration of the structures and functions of TCMPs.

Enhancing interfacial synergies for the preparation of high mechanical strength and interconnected porosity of alumina extrudates through pre-wetting method

The forming of catalyst supports is a crucial step in the application of industrial catalysts. Alumina, a widely employed catalyst support, is often shaped using nitric acid as a peptizer to enhance mechanical strength. However, the use of large amounts of nitric acid typically results in a decrease in specific surface area and damage to the pore structure due to chemical corrosion. In this work, we present a more practical approach that is pre-filling the open pores of pseudo-boehmite powder with water instead of directly filling them with nitric acid solution. The binder with a small quantity of nitric acid plays a synergistic role in functioning as a glue on the particle surfaces. And through this method, high-strength (231 N cm−1) alumina support can be prepared more efficiently through extrusion. Besides, the pore structure of the extrudates was characterized by multi-scale methods, including nitrogen physical sorption and XRM (X-ray microscopy), which revealed abundant interconnected hierarchical pores deriving from the pre-wetting shaping process. This proposed approach enables the attainment of high mechanical strength and interconnected porosity for alumina extrudates with less use of acid, which holds a significant practical application value.

Aqueous inks for ecofriendly processing of organic solar cells: Investigation of morphological changes

Aqueous dispersions of organic semiconducting nanoparticles (NPs) are particularly attractive as inks for the environmentally friendly preparation of organic solar cells. The internal morphology of the NPs, which depends on their elaboration process, is a key parameter, which has a significant influence on the final morphology of the active layer and therefore its effectiveness. In the present study, core-shell (PF2:PC71BM) NPs were prepared by miniemulsion. Their internal morphology including the composition of the two phases was characterized by scanning transmission X-ray microscopy (STXM) showing a core composed of 77% PC71BM and a shell composed of 75% PF2. It was found that thermal annealing promotes PC71BM diffusion from the core to the shell, increasing its proportion in the shell from 25% to 42%. This annealing, when applied after NPs deposition by spincoating, allows partial coalescence of the NPs, reducing the roughness of the active layer, and increases electron mobility, thus demonstrating the formation of PC71BM percolation paths for electron transport. A PCE of 1.6% could thus be obtained after 10 min of thermal annealing at 100°C. At higher temperature, Grazing-Incidence Wide-Angle X-Ray Scattering (GIWAXS) analyses demonstrate the modification of the PF2 structuration from randomly oriented lamella after deposition to edge-on orientation after annealing, leading to an unfavorable decrease of the hole mobility in the direction perpendicular to the substrate, while increasing the hole mobility in the substrate plane. This study demonstrates the need to systematically characterize the internal morphology of NPs in order to rationalize the morphology of the active layer and optimize its properties.

Process-Structure-Property Relationship Development in Large-Format Additive Manufacturing: Fiber Alignment and Ultimate Tensile Strength.

Parts made through additive manufacturing (AM) often exhibit mechanical anisotropy due to the time-based deposition of material and processing parameters. In polymer material extrusion (MEX), printed parts have weak points at layer interfaces, perpendicular to the direction of deposition. Poly(lactic acid) with chopped carbon fiber was printed on a large-format pellet printer at various extrusion rates with the same tool pathing to measure the fiber alignment with deposition via two methods and relate it to the ultimate tensile strength (UTS). Within a singular printed bead, an X-ray microscopy (XRM) scan was conducted to produce a reconstruction of the internal microstructure and 3D object data on the length and orientation of fibers. From the scan, discrete images were used in an image analysis technique to determine the fiber alignment to deposition without 3D object data on each fiber's size. Both the object method and the discrete image method showed a negative relationship between the extrusion rate and fiber alignment, with -34.64% and -53.43% alignment per extrusion multiplier, respectively, as the slopes of the linear regression. Tensile testing was conducted to determine the correlation between the fiber alignment and UTS. For all extrusion rates tested, as the extrusion multiplier increased, the percent difference in the UTS decreased, to a minimum of 8.12 ± 14.40%. The use of image analysis for the determination of the fiber alignment provides a possible method for relating the microstructure to the meso-property of AM parts, and the relationship between the microstructure and the properties establishes process-structure-property relationships for large-format AM.

Lithium-Ion Batteries under the X-ray Lens: Resolving Challenges and Propelling Advancements

The quest for high-performance lithium-ion batteries (LIBs) is at the forefront of energy storage research, necessitating a profound understanding of intricate processes like phase transformations and thermal runaway events. This review paper explores the pivotal role of X-ray spectroscopies in unraveling the mysteries embedded within LIBs, focusing on the utilization of advanced techniques for comprehensive insights. This explores recent advancements in in situ characterization tools, prominently featuring X-ray diffraction (XRD), X-ray tomography (XRT), and transmission X-ray microscopy (TXM). Each technique contributes to a comprehensive understanding of structure, morphology, chemistry, and kinetics in LIBs, offering a selective analysis that optimizes battery electrodes and enhances overall performance. The investigation commences by highlighting the indispensability of tracking phase transformations. Existing challenges in traditional methods, like X-ray absorption spectroscopy (XAS), become evident when faced with nanoscale inhomogeneities during the delithiation process. Recognizing this limitation, the review emphasizes the significance of advanced techniques featuring nanoscale resolution. These tools offer unprecedented insights into material structures and surface chemistry during LIB operation, empowering researchers to address the challenges posed by thermal runaway. Such insights prove critical in unraveling interfacial transport mechanisms and phase transformations, providing a roadmap for the development of safe and high-performance energy storage systems. The integration of X-ray spectroscopies not only enhances our understanding of fundamental processes within LIBs but also propels the development of safer, more efficient, and reliable energy storage solutions. In spite of those benefits, X-ray spectroscopies have some limitations in regard to studying LIBs, as referred to in this review.

Impact of external female urinary catheter use on urine chemistry test results

We aimed to evaluate how urine chemistry tests are impacted by collection using a female external urinary catheter employing wicking and suction, to assess this catheter's potential as an alternative to transurethral catheters for collecting urine samples from incontinent patients. We obtained 50 random 40mL refrigerated urine specimens from excess volume submitted to the Michigan Medicine Biochemical Laboratory. Specimens were split into a 10mL "control" sample simulating voided urine, and a 30mL paired "wicked" sample applied dropwise to and collected from a fresh PureWick system simulating collection from an incontinent patient. Each sample pair was tested for glucose, sodium, potassium, creatinine, urea, total protein, and derived ratios of sodium/creatinine, urea/creatinine, and protein/creatinine, then compared using Pearson correlation coefficients. Wicking materials were imaged via absorption contrast tomography on a laboratory X-ray microscope, to study the structure through which urine passes. Control and wicked urine samples had very similar results for all chemical tests evaluated: strong Pearson correlation coefficients ranging from 0.955 (potassium) to 0.997 (glucose). Microscopic assessment of the amorphous wicking materials demonstrated an average pore spacing of 95.38µm. Common urine chemistry tests were unaltered by collection using the PureWick female external catheter system. This external device can be used to collect urine for chemistry tests as an alternative to transurethral catheters.

Are the Fe-rich-clay veins in the igneous rock of the Kansas (USA) Precambrian crust of magmatic origin?

The North American Mid-Continent rift (MCR) is a 1.1 Ga aborted rift, which has recently become an area of intense focus for energy resource exploration following the report of H2 emissions. To document the nature of the producing rocks, we conducted a multi-scale study on preserved drill-core samples from the DR1-A well located in the same area as the H2-producing wells in Kansas. We showed that this well reaches an unmapped part of the MRS composed of fayalite-bearing monzo-diorites in which we identified atypical veins of iddingsite, a complex mixing of Fe-rich phyllosilicates. Combining scanning and transmission electron microscopy (SEM and TEM) with scanning transmission X-ray microscopy (STXM) allowed us to differentiate at least two types of sub-micro-meter Fe-rich veins. A central reduced vein cutting the fayalite, other mafic minerals, the plagioclase, and to a lesser extent the alkali feldspar, contains a complex mix of serpentine, chlorite, and mica. Furthermore, a border vein, with a higher degree of Fe-oxidation, is found to be contained only within the fayalite. This external vein mainly contains iron and silicon, together with a few percent of potassium and calcium, and can be divided into two sub-veins composed of Fe3+-rich interstratified chlorite-smectite and Fe3+-rich serpentine in direct contact with the fayalite. Textures and microstructures of these phyllosilicates suggest that they have crystallized from a late magmatic and differentiated fluid, which precipitation produced the central vein together with the exsolution of an H2O-enriched fluid phase. This exsolved fluid, chemically far from equilibrium with the fayalite, appears to have induced a deuteric alteration of the fayalite, leading to the crystallization of the external veins enriched in ferric iron. These observations bring new perspectives on the history of formation of iron-rich clay minerals, which may, somehow, be related to H2 production.