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Steroids can be used as biomarkers in clinical metabolomics and other fields related to human toxicology. This chemical group is known for its complexity, considering its number of isobaric compounds and the wide variety of phases I and II metabolic pathways that parent compounds can undergo. For a successful analysis of steroids in biological samples, liquid chromatography separation must be finely tuned. It is especially challenging for glucuronidated and sulfated steroids derivatives that bear polar heads and can be affected by non‐specific adsorption. The benefits of a biphenyl stationary phase chemistry for the selectivity of the separation of steroids and their phase II metabolites and the extent to which nonspecific adsorption phenomena could degrade chromatographic performance were investigated. Replacing a conventional hardware by a passivated hardware allowed to considerably reduce peaks width and asymmetry of sulfated species. The addition of weak ion pairing agents in the mobile phase could also help to reduce non‐specific adsorption but are detrimental to mass spectrometry detection. As confirmed by the successful detection of 52 steroids in plasma, the use of a biphenyl stationary phase complemented by a passivated column hardware is of great help for a successful biomedical analysis of steroids and their phase II metabolites. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: It remains an urgent task to develop alternative hole‐transporting layer (HTL) materials beyond commonly used PEDOT:PSS to increase the shelf‐life of organic solar cells (OSCs). Inorganic metal oxide type materials, such as NiOx, CoOx and VOx, with suitable work functions have attracted numerous research attention recently. In this work, more abundant and easily accessible oxygenated salt, vanadyl sulfate (VOSO4) has been demonstrated to be excellent choice as HTL for OSCs. The VOSO4‐based HTL can be readily processed by spin‐coating from the precursor solution with subsequent thermal annealing and UVO treatment. As a consequence, a high power conversion efficiency (PCE) of 18.72% can be achieved for PM8:L8‐BO based OSCs with the VOSO4‐based HTL. High transmittance, smooth film surface, suitable energy level and high conductivity were revealed to contribute to the high OSC performance. More importantly, compared to device with PEDOT:PSS, VOSO4‐based OSCs exhibit improved stability when stored in the N2 filled glove box. After being stored for 600 h, VOSO4‐based device can retain 89% of its initial efficiency. Notably, VOSO4 can be used as general HTL in PM6:BTP‐BO‐4Cl and PM6:IT‐4F based OSCs, yielding high PCEs of 17.87% and 13.85%, respectively. [ABSTRACT FROM AUTHOR]

Nonlinear optical (NLO) crystals that have the capability of achieving tunable lasers through frequency conversion are of great importance in solid‐state lasers. Herein, three new deep‐UV transparent alkali‐scandium sulfates with strong second‐harmonic generation (SHG) response and high thermal stability, A3Sc(SO4)3 (A = K, Rb, Cs), are successfully obtained. It is interesting that the slightly distorted [ScO6] octahedrons are in an ordered/oriented arrangement, which is in favor of the generation of SHG response. Especially, K3Sc(SO4)3 not only exhibits a strong phase‐matching SHG response of 1.6 × KDP, a short deep‐ultraviolet (deep‐UV) cutoff edge of 190 nm, a wide transparent window covering from the deep‐UV region to mid IR, a high laser‐induced damage threshold of 165 MW cm−2 and easy growth of large single crystal, but also behaves thermal stable up to 900 °C under an air atmosphere. Crystal structures and theoretical calculations reveal that their strong SHG responses mainly stem from the slightly distorted [ScO6] octahedron. This study highlights A3Sc(SO4)3 (A = K, Rb, Cs) as promising deep‐UV transparent NLO crystals and offers a new approach for the pursuit of high‐performance NLO crystals. [ABSTRACT FROM AUTHOR]

Bromine chemistry is responsible for the catalytic ozone destruction in the atmosphere. The heterogeneous reactions of sea‐salt aerosols are the main abiotic sources of reactive bromine in the atmosphere. Here, we present a novel mechanism for the activation of bromide ions (Br−) by O2 and H2O in the absence of additional oxidants. The laboratory and theoretical calculation results demonstrated that under dark conditions, Br−, O2 and H3O+ could spontaneously generate Br and HO2 radicals through a proton–electron transfer process at the air–water interface and in the liquid phase. Our results also showed that light and acidity could significantly promote the activation of Br− and the production of Br2. The estimated gaseous Br2 production rate was up to 1.55×1010 molecules cm−2 ⋅ s−1 under light and acidic conditions; these results showed a significant contribution to the atmospheric reactive bromine budget. The reactive oxygen species (ROS) generated during Br− activation could promote the multiphase oxidation of SO2 to produce sulfuric acid, while the increase in acidity had a positive feedback effect on Br− activation. Our findings highlight the crucial role of the proton‐electron transfer process in Br2 production; here, H3O+ facilitates the activation of Br− by O2, serves as a significant source of atmospheric reactive bromine and exerts a profound impact on the atmospheric oxidation capacity. [ABSTRACT FROM AUTHOR]

Fe‐based sulfate materials have attracted much attention in the cathode of sodium‐ion batteries (SIBs) due to their low cost and high operating voltage, as well as possessing application prospects comparable to hard carbon in the anode based on Fe0/Fe2+/Fe3+ redox properties. However, the poor conductivity and the tendency to agglomerate have limited their further application. Herein, the study constructs a dual‐conductive structure that the Na2.31Fe1.72(SO4)3 particles with amorphous carbon in situ‐coated embedded in ketjen black (KB) conducting carbon networks (NFS/KB) via a solid phase ball‐milling strategy, which effectively enhanced inherent conductivity and electron transfer efficiency among particles of the Fe‐based sulphate. The NFS/KB can provide a reversible capacity of 92 mAh g−1 at 0.1 C and stable cycling stability at high current (85% retention after 500 cycles at 20 C) as cathode of SIBs. Surprisingly, as anode of SIBs, the NFS/KB delivers a rate performance (149 mAh g−1 at 10 C) that is superior to that of hard carbon. Notably, further application of the material to symmetric SIBs also achieves favorable results. This work effectively enhances the performance of Fe‐based sulphate materials in SIBs with a low‐cost carbon modification method, providing a new approach for the low‐cost symmetric SIBs. [ABSTRACT FROM AUTHOR]

Mesozoic oceanic anoxic events were characterized by relatively low seawater sulphate concentrations ([SO42−$$ {{\mathrm{SO}}_4}^{2-} $$]), which likely regulated the development and evolution of these major palaeoceanographic phenomena. However, there is little reliable sedimentary evidence for low [SO42−$$ {{\mathrm{SO}}_4}^{2-} $$] in ancient marine waters and understanding of how such a seawater chemistry potentially impacted oceanic anoxic events is limited. This study presents an integrated sedimentological, mineralogical and geochemical investigation of the mineral siderite hosted in dark grey shale and sideritic concretions of Early Aptian (coeval with Oceanic Anoxic Event 1a) from the Tibetan Himalaya. Siderite is present throughout the section and possesses similar morphological characteristics whether in dark grey shale or concretions. Siderite can be present as disseminated and rhombic crystals formed during early diagenesis, or minor spherical crystals formed during late diagenesis. The evidence from redox elements, middle rare‐earth element bulge patterns and extremely low carbon‐isotope values of the sideritic concretions indicates that the iron carbonate was formed in the Fe‐reduction zones by the process of dissimilatory iron reduction. This process would have required conditions of low [SO42−$$ {{\mathrm{SO}}_4}^{2-} $$], reducing environment, abundant iron and high alkalinity. Additionally, the coexistence of siderite and pyrite may indicate that dissimilatory iron reduction occurred close to the microbial sulphate reduction zone, with seawater [SO42−$$ {{\mathrm{SO}}_4}^{2-} $$] hovering around the tipping point at which pyrite could form once seawater sulphate increased. Such an increase during Oceanic Anoxic Event 1a could have resulted from basalt–seawater interaction and associated enhanced continental weathering, and/or hydrothermal activity. This study's observations support the previous hypothesis that low [SO42−$$ {{\mathrm{SO}}_4}^{2-} $$] for Oceanic Anoxic Event 1a was probably caused by massive gypsum burial in the proto‐South Atlantic. Subsequently, enhanced sulphate input could have promoted microbial sulphate reduction and accompanying oxidation of organic matter, which likely further enhanced nutrient recycling, increased primary productivity and organic‐carbon burial, leading to more oxygen consumption and expansion of oxygen minimum zones, as reconstructed for many oceanic anoxic events. [ABSTRACT FROM AUTHOR]

A combination of fixed dose tablet containing 0.5 mg lobeglitazone sulfate (LBZ) and 1 mg glimepiride (GLM) has demonstrated efficacy in enhancing glycemic control in diabetes. The projected work aimed to develop and validate a high‐performance thin‐layer chromatographic (HPTLC) methodology for the precise quantification of both the drugs in tablet formulations. The HPTLC analysis utilized aluminium plates layered with silica gel 60F254, and the solvent system consisted of ethyl acetate, benzene, and hexane (4:3:1 v/v/v) followed by densitometric scanning at 238 nm. The Rf value was found to be 0.68 ± 0.001 for LBZ and 0.48 ± 0.002 for GLM. The methodology exhibited linearity in the range of 100–2000 ng/band for LBZ and 200–4000 ng/band for GLM, with correlation coefficients of 0.9988 and 0.9981, respectively. Exceptional sensitivity was observed, with detection limits of 23.86 ng/band for LBZ and 58.26 ng/band for GLM, along with quantification limits of 72.32 ng/band for LBZ and 176.55 ng/band for GLM. The method demonstrated precision (% relative standard deviation of peak area < 2) and accuracy (recovery between 97% and 102%). The suggested method is suitable for quantifying both the drugs in tablets, making it useful for routine quality control in laboratories. [ABSTRACT FROM AUTHOR]

For the first time, a method for the synthesis of 2,3‐dihydropyrazine 1,4‐dioxide derivatives was devised. The presented approach is based on the reaction of N,N′‐(2,3‐dimethylbutane‐2,3‐diyl)bis(hydroxylamine) with α‐ketoaldehydes. A distinctive feature of the proposed protocol is the application of sulfate of the aforementioned bis‐hydroxylamine in the considered condensation. The advantages of the newly developed route are a one‐step synthetic procedure involving easily available starting materials, atom economy, and simple work‐up of the reaction mixture. The structure of one of the obtained products was confirmed by x‐ray analysis. [ABSTRACT FROM AUTHOR]

Transition metal sulfides (TMS) exhibit significant promise as non‐noble‐metal electrocatalysts for the oxygen evolution reaction (OER) in alkaline environments, notwithstanding their susceptibility to long‐term instability due to the gradual leaching of surface‐reconstructed sulfate ions (SO42−). In this study, a sulfate ion‐assisted strategy is proposed to stabilize the surface‐reconstructed SO42− of FeNiS2. The findings reveal that SO42− experiences considerable loss in KOH due to the infinite concentration gradient of SO42− on the surface. Conversely, in K2SO4/KOH, this strategy mitigates rapid leaching and preserves the predominant surface‐reconstructed SO42−, thereby enhancing stability in both accelerated degradation (5000 cycles) and long‐term (≥120 h) tests, with ≈95% current density retained. Furthermore, the optimal concentration of SO42− proves to be crucial, as supported by both experimental and theoretical results. This approach offers insights into bolstering the long‐term OER stability of TMS and similar compounds, thereby advancing the prospects for widespread application in electrocatalytic water splitting. [ABSTRACT FROM AUTHOR]

The fish‐derived bile salt 5α‐cyprinol sulfate (CPS) has been identified as a kairomone inducing the predator avoidance behavior "diel vertical migration" (DVM) in Daphnia magna in response to fish. However, conclusions about the ecological significance of CPS have been derived from laboratory experiments only. Using a mesocosm approach, we investigate whether the role of CPS as a kairomone can be confirmed in the field. We demonstrate that CPS induces downward migration during daytime in a field‐derived Daphnia community mainly consisting of Daphnia longispina and Daphnia cucullata within the experiment. In the study lake, the actual population of D. longispina shows a similar pattern of DVM, while concomitant quantification of CPS by HPLC‐MS confirms that CPS in situ concentrations are sufficiently high for induction of daytime downward migration of D. longispina in this oligo‐mesotrophic lake. Together, these observations infer that CPS is a significant kairomone‐inducing DVM‐like behavior in Daphnia. [ABSTRACT FROM AUTHOR]

Rhamnan sulphate (RS) is a sulphated polysaccharide found in green algae such as Monostroma nitidum that exhibits various biological functions, including anticoagulant, antitumour, antiviral, and anti‐obesity properties. In our previous clinical trial, we demonstrated that RS intake improves constipation. However, no specific bacteria showed a significant (p <.05) change. Notably, these results were obtained after a short RS inoculation period of only 2 weeks. In the present study, to evaluate the long‐term effects of RS on the gut microbiota, we orally administered RS to BALB/c mice for 11 weeks, analyzed their blood biochemical data, and performed 16s rRNA‐sequencing. Oral administration of RS increased body weight with increased food intake, whereas plasma total cholesterol and fasting plasma glucose levels decreased. RS‐fed mice showed lower fasting insulin levels (p <.1) and decreased homeostatic model assessment for insulin resistance (HOMA‐IR, p <.0001), suggesting that RS improved insulin resistance. In the feces of mice, the amounts of acetic and propionic acids increased. In the gut microbiota, predictive metagenomic profiling using the phylogenetic investigation of communities by reconstruction of unobserved states (PICRUSt2) revealed functional alterations in Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathways in RS‐fed mice. Corresponding to the blood glucose‐lowering effect, the glycolysis and tricarboxylic acid (TCA) cycle pathways were activated. In addition, the Firmicutes/Bacteroides (F/B) ratio, which may be associated with various health outcomes, was also reduced. These results suggest that the blood glucose‐lowering effect, improvement in insulin resistance, and lipid‐lowering effect of RS may be due to changes in the intestinal microbiota. [ABSTRACT FROM AUTHOR]

Sulfates with a large bandgap are always promising optical candidates. However, due to insufficient birefringence, their applications are restricted. Here, in terms of this deficiency, two strategies are proposed to rationally modulate the optical anisotropy of sulfates by cations and anions, respectively. For the cation modulation, the [C(NH2)3]Al(SO4)2·6H2O crystal is investigated, which exhibits an unprecedented birefringence (0.098 @ 546 nm) compared with other deep‐ultraviolet transparent sulfates, resulting from the synergy of π‐conjugated [C(NH2)3]+ and non‐π‐conjugated [SO4]2− groups. For the anion modulation, a novel functional group, [S3O6]2−, with a large polarizability anisotropy, is designed. Thus, a new crystal, NaKS3O6, is obtained, which exhibits a large birefringence of 0.130 @ 546 nm with a short ultraviolet absorption cutoff edge of 215 nm. These results confirm the validity of the strategies. Therefore, the strategies play an important role in improving sulfate's birefringence and then promoting their potential applications in advanced optical systems. [ABSTRACT FROM AUTHOR]

Engineered cementitious composites (ECC) are a class of high‐performing fibre‐reinforced cementitious materials recognised for their increased ductility and durability compared to conventional cement‐based materials, owing to their autogenously controlled tight crack widths, even when subjected to high strains. To reduce ECC's environmental impact, this research examines the use of a low‐clinker binder − limestone‐calcined clay cement (LC3) − as an alternative to portland cement (PC), along with fly ash to further reduce the clinker proportion and the embodied CO2 of the formulations. In conventional concrete, LC3 hydrates to a denser microstructure resulting from the synergistic reaction between limestone and calcined clay. At the lower water contents typical of ECC and with the presence of fly ash, the influence of the binder composition on the microstructure is difficult to anticipate. To examine the influence of these compositional variables on microstructure, permeability and durability, the sulphate resistance of LC3‐based ECC is explored. Specifically, the ECC‐LC3 blends are designed with high clinker replacement rate of 75% by mass of binder and contain either conventional fly ash or reclaimed fly ash at 50% by mass of binder. Expansion of ECC‐LC3 samples subjected to standard sodium sulphate test conditions was measured up to 12 months and the depth of penetration of sulphates into the ECC‐LC3 of varying compositions was quantified using micro‐X‐Ray Fluorescence (microXRF) imaging and modelling. The expansion results show that the ECC‐LC3 formulations performed better than the PC samples and can provide adequate resistance to external sulphate attack, even when reclaimed fly ashes are used in place of the conventional ash. In addition, the shallow penetration of sulphate into these cementitious composites demonstrates the low diffusion coefficients values that were determined using the quantitative data from MicroXRF imaging. [ABSTRACT FROM AUTHOR]

Soil fertility diagnosis often omits subsoil measurements, impacting precision. Our objective was to compare the vertical distribution of nitrate and sulfate in agricultural Mollisols. Both anions were measured in 34 Mollisols of the Pampean region (Argentina) sampled to 160‐cm depth at 20 cm intervals. Nitrate exhibited a continuous downward trajectory, with maximum values at 0–20 cm (12.7 mg N kg−1) and minimum values at 140–160 cm (3.3 mg N kg−1). Sulfate displayed a sinuous pattern, with a minimum at 60–80 cm (3 mg S kg−1). The 60–160/0–160 cm concentration ratio was 42% for nitrate and 60% for sulfate, indicating greater topsoil stratification for nitrate. Predicting deep‐layer nitrate concentrations from topsoil data was more accurate than for sulfate. This poses a challenge for assessing soil S bioavailability, as subsoil sulfates go undetected in conventional sampling. Core Ideas: Nitrate content consistently decreased from the shallowest to the deepest soil layer.In contrast, sulfate exhibited a sinuous trajectory, with minimum values at 60–80 cm.Compared to sulfates, the stratification toward the topsoil was 35% higher for nitrates.Sulfates in the upper layers failed to predict sulfate concentrations in deep layers.Nitrate at 20–60 cm was an acceptable predictor of subsoil nitrate (60–160 cm). [ABSTRACT FROM AUTHOR]

Sulfate surfactants in cosmetic products raise concerns due to their skin irritating impact and sustainability. Rhamnolipid, a green and safe biosurfactant, was studied from the perspective of rheology to help develop a formulation with natural and effective ingredients for cosmetics. The viscosity of rhamnolipids was investigated by changing pH, concentration and adding additives like inorganic salts (NaCl, MgCl2) and polymers (Carbopol® Ultrez 20, Carbopol® Aqua SF‐1, Carbopol® 940 and cationic guar gum), showing that the viscosity of rhamnolipid had a positive correlation with the increase of concentration, a negative correlation with the increase of pH, and that polymers instead of inorganic salts were suitable for thickening rhamnolipid. Further rheology tests indicated that Carbopol® Aqua SF‐1 imparted gel properties of rhamnolipid while cationic guar gum determined the liquid properties. In addition, the rhamnolipid‐containing moisturizing cream consisting of stearic acid/squalane ratios all showed shear‐thinning and gel behavior the same as the commercial ones. Visual appearance and particle size analysis indicated that all formulations exhibited high storage stabilities. The knowledge gained from this study may be useful for designing "sulfonate‐free" shampoo and cream with rheological properties that can be tailed for specific commercial cosmetic applications. [ABSTRACT FROM AUTHOR]

Sonopiezoelectric therapy (SPT) has gained ever‐increasing prominence in tumor therapy as a combination of ultrasound (US) and piezoelectric nanomaterials to generate cytotoxic reactive oxygen species (ROS) for tumor suppression. In this study, the facile hydrothermal method is used to construct the distinct 2D piezocatalyst Bi2Fe4O9 nanosheets (BFO NSs). The engineered BFO NSs can create a piezoelectric field when exposed to US irradiation, facilitating the separation of electron–hole (e−–h+) pairs to play a crucial role in Fe3+/Fe2+ circulation, which catalyzes the activation of peroxymonosulfate (PMS), resulting in an amplified production of cytotoxic sulfate radical (SO4•−). The produced SO4•− combines with ROS generated by SPT including hydroxyl radicals (•OH), and singlet oxygen (1O2), leading to the augmented oxidative tumor suppression. The BFO NSs and PMS are further integrated into a thermal hydrogel (BFO/PMS‐Gel) for in vitro and in vivo investigations on their catalytic antitumor effects. In both in vitro and in vivo studies, it is validated that BFO/PMS‐Gel, under US irradiation, significantly enhances radicals generation efficiency, which achieves superior antitumor performance while maintaining high therapeutic biocompatibility and biosafety, providing a representative paradigm of US‐activated multiple radicals production as enabled by piezoelectric nanomedicine for antitumor treatment. [ABSTRACT FROM AUTHOR]

Balantioides coli (=Balantidium coli), a large ciliated protozoan, is reported in multiple free‐ranging and captive primate species, often in association with a clinical presentation that requires medical intervention. This report describes the clinical effectiveness of paromomycin sulfate against B.coli in zoo‐kept mandrill monkeys (Mandrillus sphinx, at orally doses of 8–31 mg/kg, once daily (SID) for 7 days) and gorillas (Gorilla gorilla gorilla, at orally doses of 1.4–3.1 mg/kg, SID for 5 days). [ABSTRACT FROM AUTHOR]

Objective: The purpose of this in vitro study was to evaluate the effect of potassium aluminum sulfate (alum) application on the stainability and translucency of computer‐aided design and computer‐aided manufacturing (CAD‐CAM) materials after coffee thermocycling (CTC). Materials and Methods: Disk‐shaped specimens (Ø10 × 1 mm; N = 200) were fabricated by using additively (Crowntec [CT] and Varseo Smile Crown Plus [VS]) and subtractively manufactured (Brilliant Crios [RCR], CEREC Block [FC], and Vita Enamic [VE]) CAD‐CAM materials and polished. All specimens were randomly divided into two groups as alum applied and control (n = 10). All specimens were then subjected to CTC (10,000 cycles at 5–55°C) and color coordinates were measured at each time interval. Color differences (ΔE00) and relative translucency parameters (RTPs) were calculated and the data were statistically analyzed (a = 0.05). Results: Among tested time intervals, alum applied specimens had their lowest ΔE00 after alum application (p ≤ 0.006), except for FC (p = 0.177). In addition, alum applied RCR had lower ΔE00 values than its control specimens (p = 0.029). Alum applied specimens had their lowest RTP after CTC (p < 0.001) and alum application decreased the RTP of CT (p = 0.010). CTC reduced the RTP of all materials in control groups (p < 0.001). Alum applied CT had higher RTP than its control specimens (p = 0.049). Conclusions: Alum application's effect on color change varied depending on the material and alum mostly resulted in clinically acceptable changes in translucency. CTC led to unacceptable color and translucency changes based on previously reported threshold values. Clinical Significance: Optical properties of CAD‐CAM materials and the sustainability of these properties over time is critical for longevity. Alum may improve the color stability of reinforced composite resin when subjected to long‐term coffee consumption. [ABSTRACT FROM AUTHOR]

Degradation of organic coatings is essential for recycling valuable substrates. Despite the development of strategies for this purpose, the resulting degradations are typically constrained by the composition of the coating. This paper presents a simple strategy utilizing radicals induced by UV for the degradation of diverse organic coatings. The sulfate radicals, generated from UV‐exposed ammonium persulfates, induce the degradation of various organic coatings, including layer‐by‐layer assembled coating composed of alginate and chitosan polymers as well as polydopamine coating. This strategy also facilitates the separation of two adhered substrates by degrading the adhesive polymer layer positioned between them. This novel approach enables the complete degradation of various organic coatings in aqueous conditions without imposing restrictions on their composition, leading to the recovery of the original surface properties of the substrate. [ABSTRACT FROM AUTHOR]

The sulfur (S) mass fraction of carbonate minerals can be used to reconstruct the environmental conditions and S sources at the time of precipitation. As S is present in a wide range of host materials, there is an urgent need to develop a method to extract S from a single mineral phase. We have developed a method to extract structurally substituted sulfate, termed carbonate‐associated sulfate (CAS), from geological and biogenic carbonate minerals using weakly acidic cation exchange resins. Two types of weakly acidic cation exchange resin (methacrylic acid and acrylic acid types) were tested to minimise the blank S contents and decompose carbonate. After repeated cleaning of the resins with high‐purity water or HCl, the blank S contents were reduced to < 0.1 μg, which is < 0.1% of the CAS in the samples. The cleaned resin was used to dissolve 10 and 25 mg of the JCp‐1 carbonate certified reference material (CRM; Japanese National Institute of Advanced Industrial Science and Technology, AIST). Samples and resin were added to 8 ml of high‐purity water at resin/sample ratios of 2, 5, 10 and 20, set on a shaking table, and reacted. The supernatant solutions were sampled sequentially from 0.5 h to 87 h after the start of experiments. The results show that the optimal conditions for decomposing 10 mg of carbonate is a resin/sample ratio of ≥ 10 with a reaction time of ≥ 40 h. Carbonate‐associated S mass fractions were measured for six geological and biogenic carbonate CRMs. The coefficient of variation in carbonate‐associated S mass fractions was ≤ 7%, regardless of the type of resins used. The mass fractions determined with this method recover 74–94% of the total S mass fractions reported in previous studies, suggesting that this method dissolved carbonate, and did not leach other S‐bearing fractions that are not resistant to weak acids. Another benefit of this method is that the decomposed solution can be introduced directly into the ion chromatograph, allowing for more sensitive analyses. We emphasise that this method can also be used for S isotopic measurements, as S contamination from other S‐bearing mineral phases is low. [ABSTRACT FROM AUTHOR]

Secondary ion mass spectrometry was used to test the δ18O and δ34S nanogram‐scale homogeneity of a suite of candidate sulfate minerals, ultimately selecting three barite, two anhydrite, and two gypsum samples from the Royal Ontario Museum that have repeatabilities for their SIMS measurements of better than ±0.39‰ and ±0.37‰ (1s) for oxygen and sulfur isotope ratios, respectively. Metrological splits of each of the seven materials were sent to multiple gas source isotope ratio mass spectrometry laboratories in order to establish their absolute 18O/16O and 34S/32S ratios. The inter‐laboratory results of GS‐IRMS analyses yielded reasonably narrow ranges in δ18OVSMOW, whereas larger variations in δ34SVCDT values were found between the results from the gas source laboratories. All samples have good reproducibility within laboratories of GS‐IRMS 103δ18O values of between ±0.24‰ and ±0.44‰ (1s). The reproducibility within laboratories of GS‐IRMS 103δ34S values range from ±0.07‰ to ±0.99‰ (1s). Here we also discuss some of the current analytical limitations affecting these isotope‐mineral systems. A total of 256 metrological splits have been prepared from each of these seven materials; these aliquots will be made available to the global geochemical community. [ABSTRACT FROM AUTHOR]

The widely discussed single‐atom catalysts (SACs) are regarded as a kind of attractive material for sulfate radical‐based advanced oxidation processes (SR‐AOPs) owing to their maximum atomic utilization efficiency and outstanding stability. Currently, metal–organic frameworks (MOFs) have appeared as prospective precursors for building SACs due to extensive chelating sites, functional adjustability, and structural tunability. However, there are few critical and systematic reviews about the application of MOF‐derived SACs in SR‐AOPs, especially in‐depth analysis of the mechanisms. Therefore, this review seeks to offer a thorough summary of the development of MOF‐derived SACs in SR‐AOPs. First, the unique advantages of MOFs as derivative precursors for SACs are discussed thoroughly. Afterward, the current synthesis strategies are elaborated categorically to unveil the formation process of single atoms and their coordination environments. Notably, the roles of different reaction sites including the generation of reactive species and mediating electron transfer are further analyzed to explain mechanisms comprehensively. Thereafter, the characterization techniques and theoretical calculations for mechanisms studies are also highlighted. Eventually, critical insights into present challenges and future developments are proposed, which are expected to enhance the catalytic efficiency of MOF‐derived SACs in SR‐AOPs. [ABSTRACT FROM AUTHOR]

Sulfate crystals typically exhibit minimal optical anisotropy due to the near‐zero polarizability anisotropy (δ) of [SO4]2− tetrahedra, arising from highly symmetrical electron clouds. Recent research sought to enhance δ via chemical modifications, such as fluorination. However, the resultant crystals often maintain subpar optical anisotropy, frequently with birefringence values below 0.1. In this study, we have uncovered that δ can be significantly strengthened by chemically tailoring the tetrahedral [SO4]2− with anisotropic π‐conjugated modules. This has been demonstrated by several newly proposed S−O‐Org (Org: π‐conjugated organic species) moieties, which show a sharp increase in δ based on theoretical computations. To further validate this experimentally, we synthesized and characterized six new 3‐pyridinesulfonate crystals with the formula A(3‐C5H4NSO3) ⋅ xH2O (A=Li, Ag, K, Rb, Cs, and NH4; x=0 and 1). Notably, these materials exhibit strong optical anisotropy, with birefringence values ranging from 0.240 to 0.312 at 546 nm. These values are approximately 23 to 145.5 times greater than those of corresponding sulfates, and they outperform a vast number of sulfate‐related optical materials, thus verifying the effectiveness of the proposed strategy. Furthermore, the title compounds exhibit diverse microstructure peculiarities influenced by the size and binding natures of the counter cations. [ABSTRACT FROM AUTHOR]

Sulfate crystals typically exhibit minimal optical anisotropy due to the near‐zero polarizability anisotropy (δ) of [SO4]2− tetrahedra, arising from highly symmetrical electron clouds. Recent research sought to enhance δ via chemical modifications, such as fluorination. However, the resultant crystals often maintain subpar optical anisotropy, frequently with birefringence values below 0.1. In this study, we have uncovered that δ can be significantly strengthened by chemically tailoring the tetrahedral [SO4]2− with anisotropic π‐conjugated modules. This has been demonstrated by several newly proposed S−O‐Org (Org: π‐conjugated organic species) moieties, which show a sharp increase in δ based on theoretical computations. To further validate this experimentally, we synthesized and characterized six new 3‐pyridinesulfonate crystals with the formula A(3‐C5H4NSO3) ⋅ xH2O (A=Li, Ag, K, Rb, Cs, and NH4; x=0 and 1). Notably, these materials exhibit strong optical anisotropy, with birefringence values ranging from 0.240 to 0.312 at 546 nm. These values are approximately 23 to 145.5 times greater than those of corresponding sulfates, and they outperform a vast number of sulfate‐related optical materials, thus verifying the effectiveness of the proposed strategy. Furthermore, the title compounds exhibit diverse microstructure peculiarities influenced by the size and binding natures of the counter cations. [ABSTRACT FROM AUTHOR]

Objective: The aim of this study is to use machine learning models to predict drinking water quality from a public health nursing approach. Design: Machine learning study. Sample: "Water Quality Dataset" was used in the study. The dataset contains physical and chemical measurements of water quality for 2400 different water bodies. The process consists of four stages: Data processing with Synthetic Minority Oversampling Technique, hyperparameter tuning with 10‐fold cross‐validation, modeling and comparative analysis. 80% of the dataset is allocated as training data and 20% as test data. ML models logistic regression, K‐nearest neighbor, support vector machine, random forest, XGBoost, AdaBoost Classifier, Decision Tree algorithms were used for water quality prediction. Accuracy, precision, recall, F1 score and AUC performance metrics of ML models were compared. To evaluate the performance of the models, 10‐fold cross‐validation was used and a comparative analysis was performed. The p‐values of the models were also compared. Results: N this study, where drinking water quality was predicted with seven different ML algorithms, it can be said that XGBoost and Random Forest are the best classification models in all performance metrics. There is a significant difference in all ML algorithms according to the p‐value. The H0 hypothesis is accepted for these algorithms. According to the H0 hypothesis, there is no difference between actual values and predicted values. Conclusion: In conclusion, the use of ML models in the prediction of drinking water quality can help nurses greatly improve access to clean water, a human right, be more knowledgeable about water quality, and protect the health of individuals. [ABSTRACT FROM AUTHOR]

Rationale: Preparation of BaSO4 from samples of atmospheric rain, snow, and aerosols has been used for δ18O and δ34S analyses. In the present study, we investigated the effect of various sample pretreatments on δ18O and δ34S values determined from a Na2SO4 reagent solution and samples of atmospheric precipitation to improve assay time and cost efficiency. Methods: BaSO4 was prepared from a Na2SO4 solution by (a) evaporative concentration, (b) evaporation to dryness, (c) evaporation to dryness after adding HCl, and (d) evaporation to concentration after adding HCl, followed by cooling and then precipitation using a BaCl2 solution. To analyze the atmospheric precipitation samples for δ18O, BaSO4 prepared from the samples was treated with diethylenetriaminepentaacetic acid (DTPA) and SO42− and separated chromatographically. The values of δ18O and δ34S were measured using a continuous‐flow elemental analyzer coupled to an isotope‐ratio mass spectrometer. Results: The δ34S values in BaSO4 precipitated from Na2SO4 solution determined by methods (a)–(c) were consistent within precisions of ±0.5‰. The δ18O values of methods (a) and (b) were consistent within ±0.2‰, whereas the δ18O values of methods (c) and (d) increased with increasing HCl concentrations. Similar results were obtained from samples of atmospheric precipitations. The δ18O values from DTPA‐treated BaSO4 were consistent with those obtained by chromatographic separation within ±0.5‰. Conclusions: We found no significant differences in the effects of various pretreatments (acidification, heating, concentration, and drying) on δ18O and δ34S values in sulfate from samples of atmospheric precipitation and aerosols extracted as BaSO4 if HCl was not added to the sample before heating and BaSO4 was treated with DTPA for the δ18O analysis. [ABSTRACT FROM AUTHOR]

Two neodymium sulfate based purely inorganic networks, [NH4][Nd(SO4)2(H2O)3] ⋅ H2O (1) and [Nd2(SO4)3(H2O)4] ⋅ H2O (2) have been synthesized at different reaction temperatures and pH values. The structure of 1 features a two‐dimensional (2D) anionic corrugated sheet with an sql topological net built up by linking NdO8 units and μ2‐SO42− anions, in which the NH4+ charge‐compensating/templating cations occupy the intersheet layers. While 2 possesses a 3D neutral framework with an unprecedented (3,42,7‐c) net constructed by NdO9 units and μ4‐ and μ6‐SO42− linkers. They exhibit thermally induced irreversible structural transformation associated with the dehydration and the changes in coordination geometry and dimensionality. Both compound 1 and 2 display typical antiferromagnetic interactions between the Nd3+ centres. In addition, the CO2 adsorption isotherms of the desolvated samples 1 and 2 were also investigated. [ABSTRACT FROM AUTHOR]

Aims: Indoxyl sulfate and parathyroid hormone (PTH), which accumulate in chronic kidney disease (CKD), have been reported to reduce cytochrome P450(CYP)3A activity. Homozygotes of the CYP3A5*3 allele have reduced CYP3A5 activity compared to carriers of at least one CYP3A5*1 allele. 4β‐Hydroxycholesterol (4β‐OHC) has been established as an endogenous substrate reflecting CYP3A activity. 4β‐OHC is produced through hydroxylation by CYP3A4 and CYP3A5 and by autoxidation of cholesterol, whereas 4α‐hydroxycholesterol (4α‐OHC) is produced solely by autoxidation of cholesterol. This study focused on CKD patients and evaluated the effects of plasma indoxyl sulfate and intact‐PTH concentrations on plasma 4β‐OHC concentration, 4β‐OHC/total cholesterol ratio and 4β‐OHC–4α‐OHC, with consideration of the influence of CYP3A5 polymorphism. Methods: Sixty‐three CKD patients were analysed and divided into CYP3A5 carrier group (n = 26) and non‐carrier group (n = 37). Results: Plasma indoxyl sulfate significantly correlated inversely with 4β‐OHC concentration and with 4β‐OHC–4α‐OHC in both the CYP3A5*1 carrier group (r = −0.42, P =.034; r = −0.39, P =.050, respectively) and the non‐carrier group (r = −0.45, P =.0054; r = −0.39, P =.019, respectively). However, multiple regression analysis did not identify plasma indoxyl sulfate concentration as a significant independent factor associated with any of the CYP3A activity indices. There was no significant correlation between plasma intact‐PTH concentration and any of the CYP3A activity indices. Conclusions: The present results suggest that plasma indoxyl sulfate and intact‐PTH concentrations do not have clinically significant effects on CYP3A activity in patients with CKD. [ABSTRACT FROM AUTHOR]

Wide bandgap and large birefringence, as well as strong second harmonic effect, are important but often mutually restraint prerequisites for deep‐ultraviolet (DUV) nonlinear optical (NLO) crystals, a type of photoelectronic materials that play an indispensable role in the DUV laser generation. For the long term, the search for new DUV NLO crystals has focused on the alkali‐metal inorganic acid salts where the variations of anionic groups are considered. Herein, another design strategy is reported, in which the alkali‐metal cations are substituted by the asymmetrical non‐π‐conjugated cations to harmonize the above mutual restrictions. Accordingly, LiN2H5SO4 (LNHSO) crystal is obtained by the substitution of [N2H5]+ for alkali‐metal ions in LiMSO4 (M = Na, K, and Rb). Compared with LiMSO4 (M = Na, K, and Rb), LNHSO exhibits a moderate phase‐matching second‐harmonic generation response (0.6 × KH2PO4), increased birefringence (two to three times that of other sulfates), and the widest bandgap (7.69 eV) among all the reported NLO sulfates. The structural analysis and theoretical calculation reveal that the structural anisotropy, arrangement, and packing configuration of the novel NLO‐active [N2H5]+ cation in LNHSO effectively promotes the optical properties and enlarges the bandgap. This work provides an innovative perspective for the rational design and synthesis of DUV NLO materials with excellent performance. [ABSTRACT FROM AUTHOR]

Adequate distribution of mineral sulphur (S) nutrition to nodules mediated by sulphate transporters is crucial for nitrogen fixation in symbiosis establishment process. However, the molecular mechanisms underlying this process remain largely unknown. In this study, we characterized the function of Early Senescent Nodule 2 (MtESN2), a gene crucial to nitrogen fixation in Medicago truncatula. Mutations in MtESN2 resulted in severe developmental and functional defects including dwarf shoots, early senescent nodules, and lower nitrogenase activity under symbiotic conditions compared to wild‐type plants. MtESN2 encodes an M. truncatula sulphate transporter that is expressed only in roots and nodules, with the highest expression levels in the transition zone and nitrogen‐fixing zone of nodules. MtESN2 exhibited sulphate transport activity when expressed in yeast. Immunolocalization analysis showed that MtESN2‐yellow fluorescent protein fusion protein was localized to the plasma membranes of both uninfected and infected cells of nodules, where it might transport sulphate into both rhizobia‐infected and uninfected cells within the nodules. Our results reveal an unreported sulphate transporter that contributes to effective symbiosis and prevents nodule early senescence in M. truncatula. Summary statement: In the present study, we performed detailed phenotypic studies of loss‐of‐function mutants and functional characterization of MtESN2 and found that MtESN2 is a sulphate transporter localized on the plasma membrane of infected and uninfected nodule cells with an important role in nitrogen fixation. Our findings have expanded knowledge of an indispensable role of the subgroup II sulphate transporter MtESN2 in legume‐rhizobial symbiosis and nodule senescence. [ABSTRACT FROM AUTHOR]

Metal halide perovskite light‐emitting diodes (PeLEDs) are promising high‐definition display candidates due to their narrow emission bandwidth and wide color gamut. However, efficient and stable pure‐red PeLEDs have rarely been achieved. Herein, a robust and strongly‐coordinated sulfate anion passivation strategy is reported to achieve a spectrally stable and efficient pure‐red PeLED with an electroluminescent peak at 630 nm and full width at half maximum of 27 nm. Octylammonium sulfate is employed to construct a PbSO4 layer on the surface of CsPbI3−xBrx nanocrystals, which can effectively inhibit phase separation under UV light, humidity, or heat treatment. Using sulfate passivated CsPbI3−xBrx NC film, pure red PeLEDs with high external quantum efficiency of 12.6%, excellent spectral stability, and an operational half‐life time of over 300 min (T50@100 cd cm−2) are fabricated. This work provides a new avenue to improve performance of pure red PeLEDs via strong‐coordinated sulfate passivation. [ABSTRACT FROM AUTHOR]

The accumulation of authigenic carbonate in marine sediments has been regarded as a significant contributor to the carbon cycle over Earth's history. However, accurate quantification of the extent of authigenic carbonate formation in both modern and ancient oceans has been challenging due to limited approaches. Here, we analyzed calcium, magnesium, dissolved inorganic carbon, and alkalinity pore‐water profiles of 153 sites influenced by methane diffusion from the northern South China Sea. By combining these data with published data of diffusive sulfate flux, we found a significant positive correlation between carbonate precipitation rate and sulfate flux in the subseafloor. This correlation can be used to quantify the regional extent of authigenic carbonate formation, representing an advantage over a spatial interpolation approach. We therefore propose that the observed correlation can serve as a new approach for quantifying authigenic carbonate formation in shallow sediments along continental margins for both modern and ancient oceans. Plain Language Summary: Carbonate mineral precipitation through removing seawater dissolved inorganic carbon—the marine carbonate factory—plays a critical role in shaping marine carbon cycling and global climate. The formation of authigenic carbonate from pore‐water of marine sediments represents a variable share of the marine carbonate factory throughout geological history. However, it is challenging to quantify the extent of such authigenic carbonate formation. By analyzing pore‐water parameters from 153 sites influenced by methane diffusion of the northern South China Sea, we found a significant positive correlation between the rate of carbonate precipitation and the diffusive flux of sulfate into shallow sediments. Given the existence of estimates on the sizes of the seawater sulfate pool and diffusive fluxes of sulfate into sediments over Earth's history, we propose that the observed correlation can be used for quantifying authigenic carbonate formation in shallow sediments along continental margins through time, which will greatly advance our understanding for past carbon cycling and its relation to climate. Key Points: Porewater parameters from 153 sites of the northern South China Sea were evaluated to quantify the extent of authigenic carbonate formationRate of carbonate formation strongly correlates with diffusive flux of sulfate into sediments affected by methane diffusionA correlation of carbonate formation rate with sulfate flux is used to quantify most of authigenic carbonate formation in shallow sediments [ABSTRACT FROM AUTHOR]

A regioselective fluoromethylation by ring‐opening of cyclic sulfamidates and sulfates with α‐fluorocarbanions and subsequent reductive desulfonylation is developed. Fluorobis(phenylsulfonyl)methane (FBSM) was explored as fluoromethide equivalent and the reaction was extended to the α‐fluorocarbanion of ethyl 2‐fluoroacetoacetate. This approach allows access to γ‐ and δ‐fluoroamines as well as γ‐ and δ‐fluoroalcohols in high yields. [ABSTRACT FROM AUTHOR]

Four salts, namely, 2,4,6‐triaminopyrimidinium 6‐chloronicotinate dihydrate, C4H8N5+·C6H3ClNO2−·2H2O, (I), 2,4,6‐triaminopyrimidinediium pyridine‐2,6‐dicarboxylate dihydrate, C4H9N52+·C7H3NO42−·2H2O, (II), 2,4,6‐triaminopyrimidinediium sulfate monohydrate, C4H9N52+·SO42−·H2O, (III), and 2,4,6‐triaminopyrimidinium 3,5‐dinitrobenzoate dihydrate, C4H8N5+·C7H3N2O6−·2H2O, (IV), were synthesized and characterized by X‐ray diffraction techniques. Proton transfer from the corresponding acid to the pyrimidine base has occurred in all four crystal structures. Of the four salts, two [(I) and (IV)] exist as monoprotonated bases and two [(II) and (III)] exist as diprotonated bases. In all four crystal structures, the acid interacts with the pyrimidine base through N—H...O hydrogen bonds, generating an R22(8) ring motif. The sulfate group mimics the role of the carboxylate anions. The water molecules present in compounds (I)–(IV) form water‐mediated large ring motifs. The formation of water‐mediated interactions in these crystal structures can be used as a model in the study of the hydration of nucleobases. Water molecules play an important role in building supramolecular structures. In addition to these strong hydrogen‐bonding interactions, some of the crystal structures are further enriched by aromatic π–π stacking interactions [(I) and (II)]. [ABSTRACT FROM AUTHOR]

The possibility of using heterogeneous construction waste such as masonry rubble as a raw material for the production of lightweight aggregates similar to expanded clays or even pumice has already been reported earlier. This approach has been consistently pursued. As a current aspect, the extent to which gypsum‐containing masonry rubble is also suitable as a raw material was investigated. This not only avoids (expensive) landfilling of this material, but at the same time makes a contribution to at least partially filling the "gypsum gap" created by the elimination of flue gas desulfurization gypsum. The first part of this publication reports on laboratory‐scale tests. The second part focuses on testing the process in the pilot plant. [ABSTRACT FROM AUTHOR]

Heterogeneous construction waste such as masonry rubble has potential as a raw material for the production of lightweight aggregates similar to expanded clays or even pumice. In the present paper, the suitability of feedstocks with considerable gypsum contents was investigated in a pilot plant. Based on the results, initial technological statements could be made. According to these, energetic advantages can be expected in comparison with lightweight aggregates made from expanded clays. [ABSTRACT FROM AUTHOR]

Water quality parameters from 2000 to 2020 were used to identify the spatial and temporal sulfate variations in estuaries of the northwestern Gulf of Mexico. Sulfate enrichment relative to conservative mixing was found to be associated with a low river discharge period from 2012 to 2014 in all estuaries. Based on reaction stoichiometry, sedimentary sulfide oxidation holds significant potential for reducing the alkalinity in estuarine waters. However, during this extreme drought, alkalinity enrichment was also occasionally observed in some of the southern estuaries along with sulfate enrichment, and when alkalinity depletion occurred, the magnitude of depletion was usually much less than what would be expected based on sulfide oxidation alone. This discrepancy can be partially explained by carbonate dissolution and other proton removal pathways (e.g., Fe‐oxide dissolution), and by the uncertainties in the model used to estimate alkalinity enrichment/depletion. Under a changing climate, the close coupling between river discharge variation and estuarine sulfate dynamics will significantly impact estuarine carbonate chemistry. [ABSTRACT FROM AUTHOR]

Background and Purpose: GABAA receptors are regulated by numerous classes of allosteric modulators. However, regulation of receptor macroscopic desensitisation remains largely unexplored and may offer new therapeutic opportunities. Here, we report the emerging potential for modulating desensitisation with analogues of the endogenous inhibitory neurosteroid, pregnenolone sulfate. Experimental Approach: New pregnenolone sulfate analogues were synthesised incorporating various heterocyclic substitutions located at the C‐21 position on ring D. The pharmacological profiles of these compounds were assessed using electrophysiology and recombinant GABAA receptors together with mutagenesis, molecular dynamics simulations, structural modelling and kinetic simulations. Key Results: All seven analogues retained a negative allosteric modulatory capability whilst exhibiting diverse potencies. Interestingly, we observed differential effects on GABA current decay by compounds incorporating either a six‐ (compound 5) or five‐membered heterocyclic ring (compound 6) on C‐21, which was independent of their potencies as inhibitors. We propose that differences in molecular charges, and the targeted binding of analogues to specific states of the GABAA receptor, are the most likely cause of the distinctive functional profiles. Conclusions and Implications: Our findings reveal that heterocyclic addition to inhibitory neurosteroids not only affected their potency and macroscopic efficacy but also affected innate receptor mechanisms that underlie desensitisation. Acute modulation of macroscopic desensitisation will determine the degree and duration of GABA inhibition, which are vital for the integration of neural circuit activity. Discovery of this form of modulation could present an opportunity for next‐generation GABAA receptor drug design and development. [ABSTRACT FROM AUTHOR]

The impacts of cloud mixing and uptake on wet scavenging are not adequately resolved in global models which can lead to an overestimation of the removal of water‐soluble gases and aerosols from the atmosphere. To address this issue, we develop and implement novel parameterizations to consider the impacts of these processes. Our analysis of vertical profiles of nitric acid, inorganic nitrate, ammonium, and sulfate concentrations during the Atmospheric Tomography Mission periods indicates that air refreshing limitation has a significant impact above 800 hPa, while cloud ice uptake limitation plays an important role above 500 hPa. Incorporating these two processes resulted in a reduction of wet depositions of these species across source regions and a slight increase in their downwind regions. Wet depositions of nitrate, ammonium, and sulfate were reduced in source regions by 22.7%, 8.4%, and 8.3%, respectively and increased in downwind regions by 10.1%, 7.0%, and 4.3%, respectively. Plain Language Summary: Atmospheric species in cloud‐free or rain‐free air need time to be transported and mixed with those in cloudy or rainy air before being influenced by wet scavenging. Additionally, the efficiency of rainout of water‐soluble aerosols for cold clouds is expected to be limited by cloud ice uptake. The removal of water‐soluble aerosols from cold clouds only occurs when they are taken up by ice crystals. However, current models do not adequately address these two processes. In this study, we derived new approaches that consider the effects of air refreshing and cloud ice uptake limitations on wet scavenging. We found that these new approaches have significant impacts on the vertical profiles and wet deposition fluxes of nitrate, ammonium, and sulfate. Key Points: Air refreshing and cloud ice uptake limitations are not well resolved in global modelsAir refreshing limitation impacts vertical concentration profiles <800 hPa, while cloud ice uptake limitation is important above 500 hPaIn combination, the two processes reduced wet depositions across source regions and slightly increased wet depositions in downwind regions [ABSTRACT FROM AUTHOR]

The synthesis of polysaccharide sulfates without harmful solvents used is a serious environmental problem. A method for the synthesis of xylan sulfate using the sulfamic acid–urea melt as a sulfating agent without solvents is proposed. The melt is prepared by heating the sulfamic acid–urea mixture with a molar ratio of 1 : 1 at a temperature of 110 °C. This ratio allows significant reduction of side reactions, in particular, carbamation of xylan. Sulfation is carried out at temperatures of 110,115, 120, 125, and 130 °C. The maximum yield and degree of substitution (DSsulfate 1.40) are attained at atemperature of 115 °C. The proposed method makes it possible to synthesize xylan sulfate rapidly (for 0.5 h) and without contamination of the obtained product with toxic solvents, e. g., dimethyl sulfoxide, pyridine, etc. The composition and structure of initial and sulfated xylan are confirmed by FTIR, NMR, GC, and elemental analysis. [ABSTRACT FROM AUTHOR]

This study aimed to compare the effect of sodium hypochlorite (NaOCl) and calcium hypochlorite [Ca(OCl)2] on the bond strength to pulp chamber dentin when followed or not by the use of sodium thiosulfate (Na2S2O3). The pulp chamber of fifty human molars were divided into five groups (n = 10) according to the immersion protocol: 2.5% NaOCl; 2.5% NaOCl + 5% Na2S2O3; 2.5% Ca(OCl)2; 2.5% Ca(OCl)2 + 5% Na2S2O3; and 0.9% sodium chloride (NaCl; control). Subsequently, the samples were restored with resin composite. Three sticks each were obtained and subjected to microtensile testing. SEM/EDS analyses of the pulp chamber roof (n = 8) were carried out for mineral quantification. Elemental analysis data were investigated via one‐way ANOVA and Tukey's post hoc, and bond strength data by post hoc pairwise comparisons using the Kruskal–Wallis test. Use of 2.5% NaOCl was associated with the lowest value of bond strength, while 2.5% Ca(OCl)2 had similar bond strength to that of the 0.9% NaCl control. Using 5% Na2S2O3 was able to increase the bond strength after 2.5% NaOCl, but not after 2.5% Ca(OCl)2. The group treated only with 2.5% Ca(OCl)2 had a higher Ca/P ratio on the dentin surface. Dentin treated with Ca(OCl)2 was not affected by Na2S2O3 and showed bond strength similar to the 0.9% NaCl. [ABSTRACT FROM AUTHOR]

Background and Objective: Acute exacerbations of chronic obstructive pulmonary disease (AECOPD) are associated with worsening health outcomes and effective treatment of each episode is essential. In this study, we aimed to investigate if plasma levels of heparan sulphate (HS) are associated with the aetiology of AECOPD. Methods: COPD patients (N = 1189), GOLD grade II–IV, from a discovery cohort (N = 638) and from a validation cohort (N = 551), were included in the study. HS and heparanase (HSPE‐1) were measured longitudinally in plasma at stable state, at AECOPD and at 4 weeks follow‐up. Results: Plasma HS was higher in patients with COPD as compared with non‐COPD controls and was significantly increased at AECOPD as compared to stable state (p < 0.001) in the discovery and in the validation cohorts. Four distinct exacerbation groups were classified based on aetiology (no‐infection/bacterial‐infection/viral‐infection/bacterial and viral coinfection) in the validation cohort. The fold‐increase of HS from stable state to AECOPD was associated with the aetiology of exacerbation and was higher in cases with bacterial and viral coinfections. HSPE‐1 was also significantly increased at AECOPD, however, there was no association of HSPE‐1 levels with the aetiology of these events. The probability of having an infection at AECOPD was raised as HS levels increased from stable state to AECOPD. This probability was higher for bacterial infections than viral infections. Conclusion: The results of our study indicate that circulating levels of HS are increased at AECOPD and this increase may be associated with the aetiology of these events. [ABSTRACT FROM AUTHOR]

Key Clinical Message: We report a case of imported taeniasis, under the modality of "visiting friends and relatives", in the context of colon hydrotherapy. This technique allows the detection of proglottids, diagnosed in this case as Taenia saginata based on the gravid proglottid that presented more than 13 uterine branches and showed active motility. Moreover, the patient did not consume pork for religious reasons. The treatment with paromomicin sulfate was effective. In this case, a trip to Ethiopia, together with the ingestion of raw beef, was the cause of parasitization. It is highly advisable to obtain detailed information from the patient on their background, especially their travel and dietary histories. [ABSTRACT FROM AUTHOR]

Detection of anions in complex aqueous media is a fundamental challenge with practical utility that can be addressed by supramolecular chemistry. Biomolecular hosts such as proteins can be used and adapted as an alternative to synthetic hosts. Here, we report how the mutagenesis of the β‐bulge residues (D137 and W138) in mNeonGreen, a bright, monomeric fluorescent protein, unlocks and tunes the anion preference at physiological pH for sulfate, resulting in the turn‐off sensor SulfOFF‐1. This unprecedented sensing arises from an enhancement in the kinetics of binding, largely driven by position 138. In line with these data, molecular dynamics (MD) simulations capture how the coordinated entry and gating of sulfate into the β‐barrel is eliminated upon mutagenesis to facilitate binding and fluorescence quenching. [ABSTRACT FROM AUTHOR]

Detection of anions in complex aqueous media is a fundamental challenge with practical utility that can be addressed by supramolecular chemistry. Biomolecular hosts such as proteins can be used and adapted as an alternative to synthetic hosts. Here, we report how the mutagenesis of the β‐bulge residues (D137 and W138) in mNeonGreen, a bright, monomeric fluorescent protein, unlocks and tunes the anion preference at physiological pH for sulfate, resulting in the turn‐off sensor SulfOFF‐1. This unprecedented sensing arises from an enhancement in the kinetics of binding, largely driven by position 138. In line with these data, molecular dynamics (MD) simulations capture how the coordinated entry and gating of sulfate into the β‐barrel is eliminated upon mutagenesis to facilitate binding and fluorescence quenching. [ABSTRACT FROM AUTHOR]

This study presents an attempt has been carried out to fabricate ion‐selective electrodes (ISEs) for the determination of Atropine sulfate (AT) in pharmaceutical formulas. Three plasticizers; namely, di‐n‐butyl phthalate (DBP), bis (2‐ethyl hexyl) phthalate (BEP), nitrobenzene (NB), and tetrahydrofuran (THF) were used in the fabrication of the three ion selective electrodes after incorporating into polyvinyl chloride (PVC) and symbolized as E1, E2, and E3, respectively. Beyond evaluation of the three ISEs, it has been confirmed that one with DBP experienced the most Nernstian behaviour. For the electrode of interest, the slope and detection limit are 55.02 mV/decade and 1.1×10−6 M, respectively. The linear range was 1.0×10−2–1.0×10−5 M (R2=0.9999) with recording 5 s and 45 days; sequentially, for the response time and shelf life of E1 electrode. The sensor has experienced high selectivity for atropine sulfate, verifying from the selectivity coefficient data for a number of potential interferences. The statistical analysis using t‐test and F‐test indicates the eligibility of constructed electrode for utilization in field of pharmaceutical analysis. A satisfactory accordance has been obtained between the proposed electrode for atropine sulfate and the standard method. This methodology is supposed to be applicable in quality control and even clinical diagnosis. [ABSTRACT FROM AUTHOR]

Anhydrite (CaSO4) and calcite (CaCO3) are two of the main mineral structures on which there is no longer any discussion today. The problem is different when it comes to analyzing the crystal chemical relationships between them and, in particular, the crystallography arising at the epitaxial interfaces between Ca sulfates (deposits) and the peculiar {10.4} form of cleaved calcite (substrate). Recently, Ca sulfates replacing calcite have acquired great importance in addressing the epitaxy challenge. The crystallographic epi‐interactions between CaSO4·2H2O gypsum and CaSO4·0.5H2O bassanite and the {10.4} form of calcite have already been analyzed in detail by this research group [Aquilano et al. (2022). CrystEngComm, 24, 5120–5127; Aquilano et al. (2022). J. Appl. Cryst.55, 1289–1296] (parts I and II, respectively). This work is intended to complete the research, presenting the re‐evaluation (part III) of anhydrite (CaSO4) epitaxially matching on the {10.4} rhombohedron of calcite. [ABSTRACT FROM AUTHOR]

Peatlands are among the largest natural sources of atmospheric methane (CH4) worldwide. Microbial processes play a key role in regulating CH4 emissions from peatland ecosystems, yet the complex interplay between soil substrates and microbial communities in controlling CH4 emissions as a function of global change remains unclear. Herein, we performed an integrated analysis of multi‐omics data sets to provide a comprehensive understanding of the molecular processes driving changes in greenhouse gas (GHG) emissions in peatland ecosystems with increasing temperature and sulfate deposition in a laboratory incubation study. We sought to first investigate how increasing temperatures (4, 21, and 35°C) impact soil microbiome–metabolome interactions; then explore the competition between methanogens and sulfate‐reducing bacteria (SRBs) with increasing sulfate concentrations at the optimum temperature for methanogenesis. Our results revealed that peat soil organic matter degradation, mediated by biotic and potentially abiotic processes, is the main driver of the increase in CO2 production with temperature. In contrast, the decrease in CH4 production at 35°C was linked to the absence of syntrophic communities and the potential inhibitory effect of phenols on methanogens. Elevated temperatures further induced the microbial communities to develop high growth yield and stress tolerator trait‐based strategies leading to a shift in their composition and function. On the other hand, SRBs were able to outcompete methanogens in the presence of non‐limiting sulfate concentrations at 21°C, thereby reducing CH4 emissions. At higher sulfate concentrations, however, the prevalence of communities capable of producing sufficient low‐molecular‐weight carbon substrates for the coexistence of SRBs and methanogens was translated into elevated CH4 emissions. The use of omics in this study enhanced our understanding of the structure and interactions among microbes with the abiotic components of the system that can be useful for mitigating GHG emissions from peatland ecosystems in the face of global change. [ABSTRACT FROM AUTHOR]

The hydrogensulfate‐sulfates Ln(HSO4)(SO4) (Ln: Sm, Eu, Gd, Tb, Dy) have been crystallized from sulfuric acid and their thermal decomposition behavior has been studied. The crystal structures for all members of the series were refined from X‐ray single‐crystal diffraction data (for all: Tb(HSO4)(SO4) structure type, P21, Z=2, a≈6.66 Å, b≈6.63 Å, c≈6.82 Å, β≈104.6°). Optical spectra (Sm–Dy) and magnetic susceptibilities (Eu–Dy) have been measured. For comparison the octahydrates Ln2(SO4)3 ⋅ 8 H2O (Sm, Eu) and the anhydrous sulfates Ln2(SO4)3 (Sm, Eu) have also been characterized by optical spectroscopy and magnetic measurements. Ligand field analyses (angular overlap model) based on these data suggest for the square‐antiprismatic [LnIIIO8] chromophores in the hydrogensulfate‐sulfates a rather weak ligand field, which is comparable only to that in ultraphosphates LnP5O14 and in contrast to the much stronger field observed for most other lanthanoid(III) oxo‐compounds studied so far. [ABSTRACT FROM AUTHOR]

A simple, readily prepared biphenyl bis‐amidinium compound (1⋅Cl2) is able to selectively precipitate sulfate from water. The precipitant is effective at concentrations as low as 1 mM and shows complete selectivity against monovalent anions, and high selectivity even against CO32− and HPO42−. It is highly effective (>90 % sulfate removed) in both seawater and highly acidic conditions relevant to mining waste‐streams. X‐ray crystallography reveals that 1⋅SO4 forms a tightly packed, anhydrous, structure where each sulfate anion receives eight hydrogen bonds from amidinium N−H hydrogen bond donors. [ABSTRACT FROM AUTHOR]