Spectrometry Measurements Research Articles

Juvenile downstream migration patterns of an anadromous fish, allis shad (Alosa alosa), before and after the population collapse in the Gironde system, France.

Diadromous fish have exhibited a dramatic decline since the end of the 20th century. The allis shad (Alosa alosa) population in the Gironde-Garonne-Dordogne (GGD) system, once considered as a reference in Europe, remains low despite a fishing ban in 2008. One hypothesis to explain this decline is that the downstream migration and growth dynamics of young stages have changed due to environmental modifications in the rivers and estuary. We retrospectively analysed juvenile growth and migration patterns using otoliths from adults caught in the GGD system 30 years apart during their spawning migration, in 1987 and 2016. We coupled otolith daily growth increments and laser ablation inductively-coupled plasma mass spectrometry measurements of Sr:Ca, Ba:Ca, and Mn:Ca ratios along the longest growth axis from hatching to an age of 100 days (i.e., during the juvenile stage). A back-calculation allowed us to estimate the size of juveniles at the entrance into the brackish estuary. Based on the geochemistry data, we distinguished four different zones that juveniles encountered during their downstream migration: freshwater, fluvial estuary, brackish estuary, and lower estuary. We identified three migration patterns during the first 100 days of their life: (a) Individuals that reached the lower estuary zone, (b) individuals that reached the brackish estuary zone, and (c) individuals that reached the fluvial estuary zone. On average, juveniles from the 1987 subsample stayed slightly longer in freshwaterthan juveniles from the 2016 subsample. In addition, juveniles from the 2016 subsample entered the brackish estuary at a smaller size. This result suggests that juveniles from the 2016 subsample might have encountered more difficult conditions during their downstream migration, which we attribute to a longer exposure to the turbid maximum zone. This assumption is supported by the microchemical analyses of the otoliths, which suggests based on wider Mn:Ca peaks that juveniles in 2010s experienced a longer period of physiological stress during their downstream migration than juveniles in 1980s. Finally, juveniles from the 2016 subsample took longer than 100 days to exit the lower estuary than we would have expected from previous studies. Adding a new marker (i.e., Ba:Ca) helped us refine the interpretation of the downstream migration for each individual.

Remediate and sense: alginate beads empowered by portable electrochemical strips for copper ion removal and detection at environmental sites.

The contamination of environmental sites due to the presence of persistent species represents an important issue to be tackled. In particular, the presence of high levels of metals in soil and surface water is more frequent. One of the metals that sometimes exceeds the permissible limit set by regulatory authorities is copper. For instance, copper-based fungicides are widely used in viticulture. However, copper ions remain in soil and can enter the food chain, posing threats to human health and environmental safety. Although the rapid detection of copper ions using portable sensors is effective in enhancing early warning, it sometimes solves only half of the problem as remediation is not considered. In this paper, we present a novel integrated/portable approach that merges the remediation and sensing of metals by proposing a remediate-and-sense concept. In order to realize this concept, alginate beads were coupled with printed electrochemical strips for on-site copper detection. Within the same architecture, alginate beads were used to remove copper ions from the soil, and printed electrochemical strips were used to evaluate the efficacy of remediation at the point of need. The concept was applied towards soil containing copper ions at the parts per billion level; with few alginate beads and in the absence of additional species, copper ions were quantitatively removed from the matrix; and 3D printing allowed us to combine the printed strips and spheres within a unique tool. The architecture was optimized and the results were compared to inductively coupled plasma-mass spectrometry (ICP-MS) measurements with a recovery percentage of 90%-110%. It should be noted that this novel portable approach may be applied to other pollutants, opening new possibilities for integrated remediation and sensing.

Quantitative Proteomics of the Intracellular Bacterial Pathogen Salmonella enterica Serovar Typhimurium.

Mass spectrometry-based proteomics provides a wealth of information about changes in protein production and abundance under diverse conditions, as well as mechanisms of regulation, signaling cascades, interaction partners, and communication patterns across biological systems. For profiling of intracellular pathogens, proteomic profiling can be performed in the absence of a host to singularly define the pathogenic proteome or during an infection-like setting to identify dual perspectives of infection. In this chapter, we present techniques to extract proteins from the human bacterial intracellular pathogen, Salmonella enterica serovar Typhimurium, in the presence of macrophages, an important innate immune cell in host defense. We outline sample preparation, including protein extraction, digestion, and purification, as well as mass spectrometry measurements and bioinformatics analysis. The data generated from our dual perspective profiling approach provides new insight into pathogen and host protein modulation under infection-like conditions.

Paper spray mass spectrometry combined with machine learning as a rapid diagnostic for chronic kidney disease.

A new analytical method for chronic kidney disease (CKD) detection utilizing paper spray mass spectrometry (PS-MS) combined with machine learning is presented. The analytical protocol is rapid and simple, based on metabolic profile alterations in urine. Anonymized raw urine samples were deposited (10 μL each) onto pointed PS-MS sample strips. Without waiting for the sample to dry, 75 μL of acetonitrile and high voltage were applied to the strips, using high resolution mass spectrometry measurement (15 s per sample) with polarity switching to detect a wide range of metabolites. Random forest machine learning was used to classify the resulting data. The diagnostic performance for the potential diagnosis of CKD was evaluated for accuracy, sensitivity, and specificity, achieving results >96% for the training data and >91% for validation and test data sets. Metabolites selected by the classification model as up- or down-regulated in healthy or CKD samples were tentatively identified and in agreement with previously reported literature. The potential utilization of this approach to discriminate albuminuria categories (normo, micro, and macroalbuminuria) was also demonstrated. This study indicates that PS-MS combined with machine learning has the potential to be used as a rapid and simple diagnostic tool for CKD.

Polycarbonate-Based Solid-Polymer Electrolytes for Solid-State Sodium Batteries.

Solid-polymer electrolytes comprised of polypropylene carbonate (PPC) and varied sodium bis(fluorosulfonyl)imide (NaFSI) salt concentrations are investigated for implementation as a conductive solid polymer electrolyte into solid-state cathode composites utilizing a sodium-layered oxide active material. The ionic conductivity generally increases with NaFSI salt content, reaching ≈1mScm-1 at 80°C at the highest salt concentration (PPC:NaFSI = 0.5:1). Through an all-in-one slurry casting method, Na2/3Ni1/3Mn2/3O2 cathode composites are fabricated in which the dispersed PPC electrolyte acts as the primary binder. Enabled by a bilayer polymer electrolyte system, cycling performance with the PPC cathode electrolyte is optimized with respect to salt concentration and anode material. The best cyclability is achieved with a moderate salt concentration electrolyte (PPC:NaFSI = 5:1), showcasing an initial capacity of 83mAhg-1 with a remarkable 80% capacity retention after 150 cycles at C/5 rate and 60°C. The superior performance of the lower salt concentration electrolyte is attributed to better electrochemical stability, as confirmed by linear sweep voltammetry and online electrochemical mass spectrometry measurements. These results underscore the potential of carbonate-based polymer electrolytes and the importance of balancing electrolyte conductivity and stability in cell design.

Sensitive Determination of Arsenic by Photochemical Vapor Generation with Inductively Coupled Plasma Mass Spectrometry: Synergistic Effect from Antimony and Cadmium.

A novel method for the determination of trace arsenic (As) by photochemical vapor generation (PVG) with inductively coupled plasma mass spectrometry measurement was developed in this study. The synergistic effect from antimony (Sb) and cadmium (Cd) was found for the photochemical reduction of As for the first time. Effective photochemical reduction of As was obtained in the system containing 10% (v/v) acetic acid, 5.0 mg L-1 Sb(III), and 20.0 mg L-1 Cd(II) with 100 s UV irradiation. Analytical sensitivity of As(III) was comparable with that of As(V) under the tested conditions, making direct determination of total As feasible. Compared to the pneumatic nebulization method, analytical sensitivity of the developed method was enhanced about 50 folds. The PVG efficiency was estimated up to be 99 ± 3%. The limit of detection (LOD) (3σ) was found to be 2.1 ng L-1 for As, which was improved about 30-fold compared to that using direct sample introduction solution nebulization. Considering the sample dilution prior to analysis (usually one-fold), the LOD was actually enhanced about 15 folds. The relative standard deviations of seven replicate measurements of 1.0 μg L-1 As(III) and As (V) standard solutions were 2.3 and 2.9% for As(III) and As(V), respectively. The proposed method was successfully applied for the detection of As in certified reference materials of sediments (GBW07303a and GBW07305a), as well as three water samples. The mechanism of the PVG system was investigated by using gas chromatography mass spectrometry, electron paramagnetic resonance, and X-ray photoelectron spectroscopy. (CH3)3As along with (CH3)3Sb were synthesized under UV irradiation. Besides, volatile species of Cd were also found. The result obtained in this study is useful for developing efficient "sensitizers" in PVG and understanding the transformation of As in the presence of hydride/cold vapor forming elements in the photochemical process.

Sparse linear dictionary reconstruction for removing microphonic noise from nuclear spectrometry measurements

The deployment of precise and sensitive nuclear spectroscopy instrumentation, using high purity germanium (HPGe), requires sustained cryogenic temperatures that can be achieved with cryocooler heat pumps. However, these pumps introduce microphonic noise that broaden the peaks of the spectra. This work demonstrates the efficacy of L1-norm regularization for the purpose of removing microphonic noise generated by the cryocooler, while still recovering the correct detector pulse amplitudes. Data are first collected from an He3 neutron detector with an attached cryocooler which enables the controlled addition of microphonic noise. A dictionary is then created by combining two relatively incoherent matrices, the first is the Fourier basis and the second is a matrix created from normalized and shifted pulses. By applying this dictionary to background noise, the regularization parameter λ is obtained. Using an L1-regularization least squares solver, microphonic noise can be effectively separated, therefore reducing the variance of the detector pulses while preserving the correct amplitude.

Mass Spectrometry Study about In Vitro and In Vivo Reaction between Metformin and Glucose: A Preliminary Investigation on Alternative Biological Behavior.

Metformin is the most prescribed glucose-lowering drug worldwide; globally, over 100 million patients are prescribed this drug annually. Some different action mechanisms have been proposed for this drug, but, surprisingly, no metabolite of metformin has ever been described. It was considered interesting to investigate the possible reaction of metformin with glucose following the Maillard reaction pattern. The reaction was first performed in in vitro conditions, showing the formation of two adducts that originated by the condensation of the two molecular species with the losses of one or two water molecules. Their structures were investigated by liquid chromatography coupled with mass spectrometry (HPLC-MS), tandem mass spectrometry (MS/MS) and accurate mass measurements (HRMS). The species originated via the reaction of glucose and metformin and were called metformose and dehydrometformose, and some structural hypotheses were conducted. It is worth to emphasize that they were detected in urine samples from a diabetic patient treated with metformin and consequently they must be considered metabolites of the drug, which has never been identified before now. The glucose-related substructure of these compounds could reflect an improved transfer across cell membranes and, consequently, new hypotheses could be made about the biological targets of metformin.

Ultra-Trace Electrochemical Determination of Glyphosate Using Bimetallic Metal–Organic Frameworks (MOFs) with Differential Pulse Voltammetry

Hierarchically bimetallic Zr-Cu metal–organic framework combined with 1,3,5-benzenetricarboxylic acid (Zr-CuBTC MOFs) was synthesized using hydrothermal reaction and used as modifier for investigation of non-electroactive glyphosate. These MOFs were dropcasted on a glassy carbon electrode (GCE) and non-electroactive glyphosate were tested by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and differential pulse voltammetry (DPV). Glyphosate in water was recognized by the difference of currents in spiked and non-spiked glyphosate samples. At the same time, CuBTC and Fe-CuBTC were investigated for the best material for sensor development. The results showed the bimetallic Zr-CuBTC MOF is the most promising for the determination of glyphosate. Morphological and structural studies showed the coordination of Cu2+ with the presence of Zr4+ ions with BTC ligands provided a highly porous framework with active surface area up to 1337 m2 g−1. The pore diameter and pore volume increased to 1.75 nm and 0.687 cm3 g−1, respectively. Under optimal conditions, Zr-CuBTC modified on GCE (Zr-CuBTC/GCE) sensor is able to indirectly detect glyphosate in a water environment at a detection limit as low as 9 × 10−13 M. The developed sensor was employed to determine glyphosate in the surface water samples collected from the Red River, North Vietnam. The results showed good recoveries (94.6–107.1%) which were in agreement with liquid chromatography coupled tandem mass spectrometry (LC-MS/MS) measurements. These results demonstrate the possibility of using this MOF material in sensor applications to determine trace pesticides in the contaminated water.

Electrophilic MiniFrags Revealed Unprecedented Binding Sites for Covalent HDAC8 Inhibitors.

Screening of ultra-low-molecular weight ligands (MiniFrags) successfully identified viable chemical starting points for a variety of drug targets. Here we report the electrophilic analogues of MiniFrags that allow the mapping of potential binding sites for covalent inhibitors by biochemical screening and mass spectrometry. Small electrophilic heterocycles and their N-quaternized analogues were first characterized in the glutathione assay to analyze their electrophilic reactivity. Next, the library was used for systematic mapping of potential covalent binding sites available in human histone deacetylase 8 (HDAC8). The covalent labeling of HDAC8 cysteines has been proven by tandem mass spectrometry measurements, and the observations were explained by mutating HDAC8 cysteines. As a result, screening of electrophilic MiniFrags identified three potential binding sites suitable for the development of allosteric covalent HDAC8 inhibitors. One of the hit fragments was merged with a known HDAC8 inhibitor fragment using different linkers, and the linker length was optimized to result in a lead-like covalent inhibitor.

Efficiency Enhancement of Perovskite Solar Cells Based on Graphene Nanocomposites as Electrons and Holes Transport Layers

This study investigates the use of TiO2/G and ZrO2/G transport layers in perovskite solar cells. The hydrothermal technique was used to synthesize the transport layers. According to the results, using TiO2/G as an electron transport layer enhances the transfer of negative charges from perovskites, which increases the efficiency of the solar cell. This is thanks to improved electrical conductivity and less loss of negative charges in the transport layer. The positive gap transition from the perovskite layer to the gap transport layer was enhanced using ZrO2/G. The chemical and physical properties of ZrO2/G help to build a strong interface with perovskite, which promotes gap crossing and reduces the loss of positive charges. Regarding the photonic layer, the efficiency of the solar cell increased significantly when CsPbBr3 quantum dots were used as the active element due to their strong abilities to absorb light from the visible light spectrum according to absorption spectrometry measurements. The efficiency of converting light into electrical charges increases because they can absorb more sunlight, including low-level solar energy. Quantum dots have efficient charge transfer paths, which reduces charge loss and improves conversion efficiency. CsPbBr3 quantum dots are chemically and crystallineally stable. These factors work together to increase the efficiency of the perovskite solar cell when using CsPbBr3 quantum dots from 10.004% to 10.425%.

Highly efficient CO2 and propylene oxide co-polymerization using Zn glutarate/Zn-Cr double metal cyanide composite catalyst

A highly active zinc glutarate-double metal cyanide (DMC) composite catalyst (ZnGA/Zn-CrDMC) was designed for the carbon dioxide (CO2) and propylene oxide (PO) copolymerization reaction. The composite catalyst was synthesized in a rheological phase reaction and characterized using Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), and scanning electron microscopy (SEM). The synthesized composite catalysed the solvent free reactions of PO and CO2 to afford biodegradable polypropylene carbonate (PPC) copolymer. 1H NMR,13C NMR, FT-IR and ESI-TOF mass spectrometry measurements were employed to confirm the characteristics of the PPC produced. Under optimal reaction conditions (50 bar CO2, 70 °C, 24 h), the ZnGA-Zn3[Cr(CN)6]2 composite displayed higher catalytic activities in the copolymerization reactions than the individual catalysts. The ZnGA:Zn3[Cr(CN)6]2 ratio of 15:1 gave PPC yield of 47.9 g polymer/g cat compared to ZnGA that produced 42.6 g polymer/ g cat in 24 h. In addition, the PPC produced from the composite catalyst displayed higher carbonate linkage content (Fc = 85.4 %) compared to the value of Fc = 33.9 %. obtained using the Zn3[Cr(CN)6]2 catalyst. Similaly, the composite catalsyt produced PPC with molecular weight of 4200 g/mol and narrow polydispersity index of 2.2. The resultant PPC copolymer displayed good thermal stability, exhibiting a high degradation temperatures (TGA-10%) of 229 °C and complete decomposition at 350 °C.

Ensuring quality in 17OHP mass spectrometry measurement: an international study assessing isomeric steroid interference.

Interference from isomeric steroids is a potential cause of disparity between mass spectrometry-based 17-hydroxyprogesterone (17OHP) results. We aimed to assess the proficiency of mass spectrometry laboratories to report 17OHP in the presence of known isomeric steroids. A series of five samples were prepared using a previously demonstrated commutable approach. These samples included a control (spiked to 15.0 nmol/L 17OHP) and four challenge samples further enriched with equimolar concentrations of 17OHP isomers (11α-hydroxyprogesterone, 11β-hydroxyprogesterone, 16α-hydroxyprogesterone or 21-hydroxyprogesterone). These samples were distributed to 38 participating laboratories that reported serum 17OHP results using mass spectrometry in two external quality assurance programs. The result for each challenge sample was compared to the control sample submitted by each participant. Twenty-six laboratories (68 % of distribution) across three continents returned results. Twenty-five laboratories used liquid chromatography-tandem mass spectrometry (LC-MS/MS), and one used gas chromatography-tandem mass spectrometry to measure 17OHP. The all-method median of the control sample was 14.3 nmol/L, ranging from 12.4 to 17.6 nmol/L. One laboratory had results that approached the lower limit of tolerance (minus 17.7 % of the control sample), suggesting the isomeric steroid caused an irregular result. Most participating laboratories demonstrated their ability to reliably measure 17OHP in the presence of the four clinically relevant isomeric steroids. The performance of the 12 (32 %) laboratories that did not engage in this activity remains unclear. We recommend that all laboratories offering LC-MS/MS analysis of 17OHP in serum, plasma, or dried bloodspots determine that the isomeric steroids are appropriately separated.

Dandelion-like Cu-Ni LDH-decorated biochar/aminated chitosan composite for boosting Fenton-like degradation of doxycycline: Insights into performance and mechanism

This study fabricated a novel biochar/amine chitosan composite (BC/AmCS) decorated with dandelion-like Copper-Nickel layered double hydroxide (Cu-Ni LDH) for Fenton-like degradation of doxycycline (DOX). The Fenton-like degradation of DOX proceeded at varied experimental conditions, implying the superior degradation efficacy of Cu-Ni LDH/BC/AmCS composite at pH = 8, H2O2 = 400 mg/L, and composite dosage = 0.03 g/L. Interestingly, results showed that the Fenton-like degradation % of DOX reached 86.9 % after 1 h at a high concentration of DOX (500 mg/L). Furthermore, it was recorded a synergistic effect between adsorption, and Fenton-like processes during the degradation of DOX, where the adsorption % attained 46.9 %. Moreover, kinetic modeling clarified the fitting of a pseudo-first-order kinetic model to model the degradation of DOX by Cu-Ni LDH/BC/AmCS/H2O2 system. Based on the X-ray photoelectron spectroscopy (XPS), and quenching test, the Fenton-like degradation mechanism of DOX followed a radical pathway forming a continuous redox cycle in Cu-Ni LDH/BC/AmCS. In addition, the degradation pathway was presumed via gas chromatography–mass spectrometry (GC–MS) measurements. The developmental toxicity of the produced intermediates was assessed using quantitative structure–activity relationship (QSAR) prediction. The durability of Cu-Ni LDH/BC/AmCS catalyst was scrutinized by performing a cycling test for 5 runs, and measuring the metal leaching. The H2O2 decomposition was determined via the potassium titanium (IV) oxalate spectrophotometric technique. Eventually, Cu-Ni LDH/BC/AmCS composite could be recommended as a promising catalyst for the efficient degradation of organic pollutants from wastewater.

Expert consensus on pre-treatment of clinical samples by liquid chromatography-tandem mass spectrometry

Liquid chromatography-tandem mass spectrometry (LC-MS/MS) combines the advantages of high separation ability of chromatography and high selectivity, specificity and sensitivity of mass spectrometry, making it one of the most vibrant new technologies in the field of clinical testing. However, the analytical performance is often limited by the characteristics of the sample to be measured. Due to the limited anti-contamination capability of the mass spectrometer, biological samples need to be properly pre-processed to effectively improve the detection performance and achieve accurate detection. The main function of pre-treatment is to selectively separate the target analyte from the biological matrix to reduce interference from other matrix components. At the same time, the target analytes can be concentrated and enriched to improve the analytical sensitivity. At present, there are many kinds of clinical sample pre-treatment methods, and several methods are time-consuming and cumbersome, which brings difficulties to laboratory personnel in method selection, development and standardized operation. Therefore, the purpose of this consensus is to provide guidance for the establishment of laboratory methods and facilitate the standardized development of clinical mass spectrometry measurement.

Bluer Phototruncation: Retro-Diels-Alder of Heptamethine Cyanine to Trimethine Cyanine through an Allene Hydroperoxide Intermediate.

The photoconversion of heptamethine to pentamethine cyanines and of pentamethine to trimethine cyanines was recently reported. Here, we report mechanistic studies and initial experimental evidence for a previously unexplored 4-carbon truncation reaction that converts the simplest heptamethine cyanine to the corresponding trimethine cyanine. We propose a DFT-supported model describing a singlet oxygen (1O2)-mediated formation of an allene hydroperoxide intermediate and subsequent 4-carbon loss through a retro-Diels-Alder process. Fluorescence and mass spectrometry measurements provide evidence of this direct conversion process. This 4-carbon truncation reaction adds to a growing body of cyanine reactivity and may provide an optical tool leading to a substantial blue-shift (Δλem) of ∼200 nm.

Degradation Mechanism Study for Secondary Degradants in Rosuvastatin Calcium and Determination of Degradant Acetaldehyde Using Static Headspace Gas Chromatography Coupled with Matrix Precipitation

During the development of headspace gas chromatography (HSGC) method for assessing residual solvents in rosuvastatin calcium (RSV) drug substance, acetaldehyde (AA) was detected in obtained chromatograms, with a calculated concentration of up to 226 ppm. After a series of experiments, it was established that acetaldehyde originates from matrix interference due to direct degradation of Imp-C, which is accompanied by the formation of impurity at relative retention time (RRT) 2.18, without the involvement of impurity at RRT 2.31. The thermal instability of Imp-C also results in the formation of impurity at RRT 2.31 through dehydration and decarboxylation. In addition, cyclization reaction of degradant at RRT 2.18 further resulted in the generation of impurity at RRT 2.22. The structure of these three degradants, were confirmed by liquid chromatography-mass spectrometry (LC-MS), 1D and 2D nuclear magnetic resonance (NMR) measurement. In order to minimize the said matrix interference, a simple precipitation procedure was proposed as a pretreatment to mitigate the impact of Imp-C. Subsequently, an HSGC method was developed for the simultaneous determination of the degradant AA and the other five residual solvents used in RSV synthetic process. The final method was validated concerning precision, limit of detection (LOD) and limit of quantitation (LOQ), linearity, and accuracy.

Availability and reactivity of N2(v) for NH3 synthesis by plasma catalysis

Production of vibrationally excited N2 (N2(v)) in atmospheric pressure nonthermal plasma and loss of N2(v) by gas-phase reactions and reactions on catalytic surfaces are analyzed to examine the role of N2(v) in NH3 formation by plasma catalysis. Vibrational state-to-state kinetic models complemented with molecular beam mass spectrometry (MBMS) measurements demonstrate that N2(v> 0) is produced with densities 100× greater than the density of N radicals by a radiofrequency atmospheric pressure plasma jet. The experimentally measured loss of N2(v) corresponds with a state-to-state kinetic model that describes loss of N2(v) by surface-mediated vibrational relaxation without consideration of reactions that convert N2(v) to NH3 over the catalyst surface. Rate constants for vibrational relaxation of N2(v) on catalyst surfaces exceed upper bounds on proposed rate constants for NH3 formation reactions from N2(v) over Fe when v < 9, Ni when v < 18, and Ag when v < 39, which indicates that only higher vibrational levels can possibly contribute to catalytic NH3 formation faster than they undergo vibrational relaxation on the surface. Densities of N2(v> 8), vibrational levels that can possibly react over Fe to form NH3 faster than they undergo vibrational relaxation, are less than or similar to N densities at the inlet of the catalyst bed and measured NH3 formation for the investigated conditions in this work, while densities of N2(v> 17) and N2(v> 38) are orders of magnitude below the N density at the inlet of the catalyst bed and the measured NH3 formation. The loss of N2(v) by vibrational relaxation on the surface limits the ability of N2(v) to contribute to catalytic NH3 formation and explains why N2(v) does not produce NH3 in quantities that are comparable to NH3 formation from N even though N2(v > 0) is more abundantly produced by the plasma.

Diagenetic history of calcite fractures in Vaca Muerta shales (Argentina) inferred from paired Δ47 and fluid inclusion geothermometry

Many low-permeability, hydrocarbon-bearing rocks are productive for petroleum because natural fractures enhance hydrocarbon delivery to wellbores. Exploration and development decisions often must be made in the face of uncertainty about the presence and properties of natural fractures at scales of beds, field and plays, and how they contribute to production. Fractures patterns in subsurface rocks are challenging to predict or characterize owing to the difficulty in obtaining representative samples of fractures and the sparse set of tools for reconstructing how and when fractures grow during sedimentary basin evolution. In this study, we investigate bed-parallel fracture diagenesis in the Vaca Muerta shales (Argentina) based on a set of calcite vein collected from core across a thermal maturity sequence that ranges from the oil to dry gas window. We characterize these samples using secondary ions mass spectrometry (SIMS) measurements of stable isotope ratios, carbonate clumped isotope geothermometry and fluid inclusion analysis. These measurements precisely reconstruct the evolution of fluid geochemistry, temperature and pore fluid pressure during fracture opening. Here we show that within each studied site, all bedding parallel fibrous veins calcite formed at similar ranges of temperature. The fracture mineralization temperature increases substantially at the basin scale, from 90 °C to 120 °C, correlated with host-rock thermal maturity. We compare our constraints on carbonate and fluid temperature with apatite fission track thermal models and find that most of the fractures of the Vaca Muerta shales have formed in a relatively early stage of subsidence of the basin (c.a. 90 to 70 Ma). These ages estimations are consistent with recently published U–Pb ages on calcite veins from the outcropping area (117–61 Ma). The presence of petroleum inclusions (oil, condensate, and gas) in most of the vein's calcite fibers from cores also provides clear evidence that fracture formation was contemporaneous or posterior with petroleum generation, constraining the timing of catagenesis in the Vaca Muerta. Reconstructed paleo pressures conditions of veins formation from fluid inclusion analysis highlight significant fluid overpressure in the shale interval, which likely contributed to fracture initiation and growth. Preserved apparent Δ47 temperatures in fibrous veins carbonates mineralization evolves gradually from 130 °C to 175 °C with increasing host rock thermal maturity. These clumped-isotope-based temperatures are systematically higher than trapping temperatures of associated fluid inclusions; one interpretation of this observation is that carbonate clumped isotope compositions re-equilibrated to near maximum burial conditions by solid-state isotopic re-ordering, yielding a record of the maximum burial temperature the shale unit experienced. The combination of paleothermometry techniques used in this study illustrates the importance of simultaneously exploring several independent geothermometers, particularly the informative combination of fluid inclusion and clumped isotope constraints, which provides a means of understanding the complex diagenesis of old sedimentary rocks that have experienced burial temperatures in the oil and gas thermal windows.

One and two-step electrodeposition of composite films of calcium-deficient hydroxyapatite matrix with nanoscale Ag- and Zn-based particles

A fundamental study regarding the electrochemical synthesis of composite coatings with application in the orthopaedic field has been conducted. In particular, the electrodeposition of calcium phosphate coatings with Ag nanoparticles (AgNPs) from either a single electrolyte (one-step, 1S) or two electrolytes (two-step, 2S) on a β-Ti alloy (Ti-18Mo-6Nb-4Ta in wt%) was investigated. Pulse current deposition was implemented to produce the composite coatings by the 1S approach from a simple solution containing 42 mM Ca(NO3)2·4H2O, 25 mM NH4H2PO4, and 0.5 mM AgNO3 at 65°C. Meanwhile, the calcium phosphate matrix was also deposited by pulse current, and Ag was afterwards grown by direct current from 0.1 M KNO3 + x mM AgNO3 (x = 5, 10) at 25 °C (2S approach). The Ca/P ratio of the matrix was compatible with the formation of calcium-deficient hydroxyapatite (CDHA). The resulting Ag content in the composites could be varied between 4 and 13 wt% as a function of the working conditions. The 2S-derived coatings produced by electroplating Ag at j = –20.8 mA/cm2 from 0.1 M KNO3 + 10 mM AgNO3 furnished an optimal dispersion of the AgNPs on top of the CDHA matrix, while aggregation and/or dendritic growth was observed in other cases. Glow discharge optical emission spectrometry (GDOES) measurements indicated that a given amount of AgNPs becomes engulfed in the CDHA matrix during the 1S electrodeposition, whereas most of them decorate its outer surface in the 2S-derived coatings. The applicability of the two approaches was extended to the case of zinc oxide. ZnO-containing CDHA coatings in which the Zn element was homogeneously distributed across the film surface were obtained from 42 mM Ca(NO3)2·4H2O, 25 mM NH4H2PO4 and 1 mM Zn(NO3)2·6H2O at 65 °C (1S approach). On the contrary, ZnO-NPs could be clearly observed when deposition from 5 mM KNO3 + 5 mM Zn(NO3)2 was performed at 70 °C on top of previously grown CDHA (2S approach). The results indicated that the percentage and location of the antibacterial element (Ag, Zn) in the calcium phosphate matrix can be tuned on demand to a great extent by electrochemical means.