Sulfur Species Research Articles

Multi-defense Pathways against Electrophiles through Adduct Formation by Low Molecular Weight Substances with Sulfur Atoms.

There is a variety of electrophiles in the environment. In addition, there are precursor chemicals that undergo metabolic activation by enzymes and conversion to electrophiles in the body. Although electrophiles covalently bind to protein nucleophiles, they also form adducts associated with adaptive or toxic responses. Low molecular weight compounds containing sulfur are capable of blocking such adduct formation by capturing the electrophiles. In this review, we present out findings on the capture and inactivation of electrophiles by 1) intracellular glutathione, 2) reactive sulfur species and 3) extracellular cysteine (formed during the production of sulfur adducts). These actions not only substantially suppress electrophilic activity but also regulate protein adduct formation.

Supergene formation of sulfur-rich, tochilinite-bearing serpentinites in the Oman ophiolite

Mass transfer processes between fluids and ultramafic rocks produce subsurface environments encompassing a wide range of redox conditions. A notable locality where an extensive range of redox conditions is observed in one location is Hole BA1B, a ∼ 400 m borehole drilled by the Oman Drilling Project. A sulfur-enriched serpentinite zone, containing up to 0.6 wt% S, occurs between shallow oxidized serpentinites (<30 m) and deep partially serpentinized harzburgite (>150 m). All three alteration zones are predominantly composed of serpentine. However, microanalysis of samples from the sulfur-enriched zone shows that mesh textures after olivine are composed of serpentine, brucite, and tochilinite mixtures, yielding optically black thin-section samples that characterize this sulfidic zone. It is proposed that sulfur accumulates in this zone via a process similar to those found in supergene ore deposits. Reaction-path models show that at shallow conditions open to atmospheric input, sulfur is mobilized via oxidative weathering of serpentinized dunite and harzburgite. Sulfate-bearing fluids percolate deeper and react with host rocks in a system closed to atmospheric input. As fluids become more reduced, dissolved sulfate is precipitated as sulfide minerals yielding rocks with ∼0.4 wt% S, like those observed in Hole BA1B. Despite enrichment of S in the sulfidic zone in Hole BA1B, Ni and Co contents are uniform throughout all three layers in the borehole. This is consistent with model results which show that Ni (and, by analogy, Co) is less mobile than S, and can be hosted in serpentine and NiFe alloys in addition to sulfides. The sulfur enrichment process may occur abiotically. However, sulfide enrichment via microbial reduction of sulfate and other sulfur species can also facilitate the formation of the sulfidic zone. Bioenergetic calculations show that abundant energy is available for sulfur reducing microbes, consistent with previous work demonstrating the presence of active, sulfate-reducing microorganisms in Hole BA1B and other nearby boreholes. This suggests that the observed sulfur enrichment is an ongoing process. Overall, this work shows that variable redox conditions are attained as fluids percolate and react with serpentinized ultramafic rocks at variable extents of interaction between aquifer fluids, host ultramafic rocks, and the atmosphere.

Hydrothermal vents supporting persistent plumes and microbial chemoautotrophy at Gakkel Ridge (Arctic Ocean).

Hydrothermal vents emit hot fluids enriched in energy sources for microbial life. Here, we compare the ecological and biogeochemical effects of hydrothermal venting of two recently discovered volcanic seamounts, Polaris and Aurora of the Gakkel Ridge, in the ice-covered Central Arctic Ocean. At both sites, persistent hydrothermal plumes increased up to 800 m into the deep Arctic Ocean. In the two non-buoyant plumes, rates of microbial carbon fixation were strongly elevated compared to background values of 0.5-1 μmol m-3 day-1 in the Arctic deep water, which suggests increased chemoautotrophy on vent-derived energy sources. In the Polaris plume, free sulfide and up to 360 nM hydrogen enabled microorganisms to fix up to 46 μmol inorganic carbon (IC) m-3 day-1. This energy pulse resulted in a strong increase in the relative abundance of SUP05 by 25% and Candidatus Sulfurimonas pluma by 7% of all bacteria. At Aurora, microorganisms fixed up to 35 μmol IC m-3 day-1. Here, metal sulfides limited the bioavailability of reduced sulfur species, and the putative hydrogen oxidizer Ca. S. pluma constituted 35% and SUP05 10% of all bacteria. In accordance with this data, transcriptomic analysis showed a high enrichment of hydrogenase-coding transcripts in Aurora and an enrichment of transcripts coding for sulfur oxidation in Polaris. There was neither evidence for methane consumption nor a substantial increase in the abundance of putative methanotrophs or their transcripts in either plume. Together, our results demonstrate the dominance of hydrogen and sulfide as energy sources in Arctic hydrothermal vent plumes.

Insights into the mechanism of enhancing resistance of MnAlOx-Str NH3-SCR catalyst derived from streptomycin waste residue and LDHs

Streptomycin waste residue composited with Layered double hydroxides (LDHs) derived Mn1Al1Ox-Str-2 catalyst was proposed for NH3 selective catalytic reduction (NH3-SCR) denitration technology, which improved the overall catalytic performance. In the wide temperature range of 150-300℃, the preferred Mn1Al1Ox-Str-2 catalyst had Nitrogen oxides (NOx) conversion of exceeded 96%, which was higher than that of the control Mn1Al1Ox and Mn/Al2O3 catalysts. In addition, Mn1Al1Ox-Str-2 catalyst had better resistance to SO2 and/or H2O, as well as good regeneration ability. Various analytical techniques had confirmed that the Mn1Al1Ox-Str-2 catalyst derived from streptomycin residue composite LDHs precursor had better surface properties with more active species, abundant surface oxygen, higher reduction capacity and better adsorption of NOx and NH3. Analytical techniques revealed that the Lewis acid site on the surface of Mn1Al1Ox-Str-2 catalyst was involved in SCR reaction and both the Eley-Rideal mechanism and Langmuir-Hinshelwood mechanism existed simultaneously in the NH3-SCR reaction, and SO2 had a weak effect on the adsorption of reactants with fewer sulfate species formation. This work provided feasible strategies for efficient and stable SCR technology and efficient utilization of streptomycin residue waste resources, which was significant for the design and application of SCR technology in the future.

Chip−like high−entropy oxide catalysts enhance fast sulfur evolution reaction for long−life lithium−sulfur batteries

Many catalysts have shown excellent activity for the sulfur reduction reaction (SRR), but sluggish electrochemistry kinetics have hindered the development of lithium–sulfur batteries. It has been found that the activity of catalysts for the sulfur evolution reaction (SER) plays a crucial role in determining the overall reaction kinetics. To address this issue, the rational design of catalysts is crucial. Here, we proposed a popular rule to accelerate SER by using chip–like high–entropy perovskite oxide La0.7Sr0.3(Fe0.2Co0.2Ni0.2Zn0.2Mn0.2)O3-δ (LMO–HEO) as advanced electrocatalysts. The strong interaction between the adjacent metal atoms in different metals of LMO–HEO electrocatalysts could lead to a "cocktail effect", which not only greatly improved the catalytic capacity toward sulfur species, but also accelerated the oxidation reaction kinetics of Li2S. As a result, the S/La0.7Sr0.3(Fe0.2Co0.2Ni0.2Zn0.2Mn0.2)O3-δ cathodes delivered excellent cyclic stability with a capacity decay of only 0.025% after 1200 cycles at 2 C. This work has provided a rational design idea for new multifunctional electrocatalysts with high catalytic capacity.

JWST/NIRISS Reveals the Water-rich “Steam World” Atmosphere of GJ 9827 d

With sizable volatile envelopes but smaller radii than the solar system ice giants, sub-Neptunes have been revealed as one of the most common types of planet in the galaxy. While the spectroscopic characterization of larger sub-Neptunes (2.5–4 R ⊕) has revealed hydrogen-dominated atmospheres, smaller sub-Neptunes (1.6–2.5 R ⊕) could either host thin, rapidly evaporating, hydrogen-rich atmospheres or be stable, metal-rich “water worlds” with high mean molecular weight atmospheres and a fundamentally different formation and evolutionary history. Here, we present the 0.6–2.8 μm JWST/NIRISS/SOSS transmission spectrum of GJ 9827 d, the smallest (1.98 R ⊕) warm (T eq,A=0.3 ∼ 620 K) sub-Neptune where atmospheric absorbers have been detected to date. Our two transit observations with NIRISS/SOSS, combined with the existing HST/WFC3 spectrum, enable us to break the clouds–metallicity degeneracy. We detect water in a highly metal-enriched “steam world” atmosphere (O/H of ∼4 by mass and H2O found to be the background gas with a volume mixing ratio of >31%). We further show that these results are robust to stellar contamination through the transit light source effect. We do not detect escaping metastable He, which, combined with previous nondetections of escaping He and H, supports the steam atmosphere scenario. In water-rich atmospheres, hydrogen loss driven by water photolysis happens predominantly in the ionized form, which eludes observational constraints. We also detect several flares in the NIRISS/SOSS light curves with far-UV energies of the order of 1030 erg, highlighting the active nature of the star. Further atmospheric characterization of GJ 9827 d probing carbon or sulfur species could reveal the origin of its high metal enrichment.

Potential for formation of methylated thioarsenates in geothermal environments

Geothermal waters typically have elevated arsenic (As) concentrations. Various As species have been identified, including methylated thioarsenates, which present a high environmental and health risk due to high mobility and toxicity. Upon discharge from hot springs, temperature and geogenic sulfide excess decrease, while redox potential increases. The combined effects of those parameters on activities of sulfate-reducing bacteria and methanogens and thereby on extent of As methylation versus thiolation is currently unknown. Here, we incubated sediments from alkaline hot springs and outflow channels at the Tengchong geothermal region in southwestern China, where inorganic and methylated thioarsenates had been detected, at temperatures between 20 to 90 °C with different initial aqueous As and sulfur species. Results from field samples and incubation experiments showed methylated thioarsenates, but no methylated oxyarsenates, implying quantitative thiolation even at low sulfide concentrations. Enrichment cultures derived from one sediment with quantitative formation of dimethyl-dithioarsenate (DMDTA) at 55 °C, showed a dominance of inorganic trithioarsenate at 35 °C and monomethylated thioarsenates at 55 °C when incubated with two other sediments. The rate-limiting step was microbially mediated As methylation from arsenite, which was not observed at 20 °C or >= 75 °C, in contrast to thiolation of already methylated arsenates. Addition of free sulfide and thiosulfate to incubation experiments promoted formation of inorganic or monomethylated high-thiolated arsenates, while sulfate promoted full methylation and formation of DMDTA, probably due to continuous low supply of microbially produced sulfide. Since DMDTA is more mobile and toxic than inorganic and monomethylated thioarsenates, understanding constraints to its formation is especially important for future risk assessment

Increased hydrogen sulfide turnover serves a cytoprotective role during the development of replicative senescence

The mammalian gasotransmitter hydrogen sulfide (H2S) is produced by enzymes such as cystathionine β-synthase (CBS), cystathionine γ-lyase (CSE), 3-mercaptopyruvate sulfurtransferase (3-MST). Prior studies suggest that H2S may have cytoprotective and anti-aging effects. This project explores the regulation and role of endogenous H2S in a murine model of replicative senescence. H2S and polysulfide levels in RAW 264.7 murine macrophages (control cells: passage 5–10; senescent cells: passage 30–40) were measured using fluorescent probes. The expression of H2S-related enzymes and the activity of senescence marker beta-galactosidase (SA-β-Gal) were also analyzed. CBS, CSE, and 3-MST were inhibited using selective pharmacological inhibitors. Senescence led to a moderate upregulation of CBS and in a significant increase in CSE and 3-MST. H2S degradation enzymes were also elevated in senescence. Inhibition of H2S-producing enzymes reduced H2S levels but increased polysulfides. Inhibition of H2S production during senescence suppressed cell proliferation, and elevated SA-β-Gal and p21 levels. Comparing young and old mice spleens revealed downregulation of CBS and ETHE1 and upregulation of rhodanese and SUOX in older mice. The results demonstrate that increased reactive sulfur turnover occurs in senescent macrophages and that reactive sulfur species supports cell proliferation and regulate cellular senescence

Accelerated Reversible Conversion of Li2S2 to Li2S by Spidroin Regulated Li+ Flux for High-performance Li-Sulfur Batteries.

Regulating the transformation of sulfur species is the key to improving the electrochemical performance of lithium-sulfur (Li-S) batteries, in particular, to accelerate the reversible conversion between solid phase Li2S2 and Li2S. Herein, we introduced Spidroin, which is a main protein in spider silk, as a dual functional separator coating in Li-S batteries to effectively adsorb polysulfides via the sequence of amino acids in its primary structure and regulate Li+ flux through the β-sheet of its secondary structure, thus accelerating the reversible transformation between Li2S2 and Li2S. Spidroin-based Li-S cells exhibited an exceptional electrochemical performance with a high specific capacity of 744.1 mAh g-1 at 5 C and a high areal capacity of 7.5 mAh cm-2 at a low electrolyte-to-sulfur (E/S) ratio of 6 μL mgs -1 and a sulfur loading of 8.6 mgs cm-2.

Accelerated Reversible Conversion of Li2S2 to Li2S by Spidroin Regulated Li+ Flux for High‐performance Li‐Sulfur Batteries

Regulating the transformation of sulfur species is the key to improving the electrochemical performance of lithium‐sulfur (Li‐S) batteries, in particular, to accelerate the reversible conversion between solid phase Li2S2 and Li2S. Herein, we introduced Spidroin, which is a main protein in spider silk, as a dual functional separator coating in Li‐S batteries to effectively adsorb polysulfides via the sequence of amino acids in its primary structure and regulate Li+ flux through the β‐sheet of its secondary structure, thus accelerating the reversible transformation between Li2S2 and Li2S. Spidroin‐based Li‐S cells exhibited an exceptional electrochemical performance with a high specific capacity of 744.1 mAh g‐1 at 5C and a high areal capacity of 7.5 mAh cm‐2 at a low electrolyte‐to‐sulfur (E/S) ratio of 6 μL mgs‐1 and a sulfur loading of 8.6 mgs cm‐2.

Seasonal evaluation of sulfur species identified in PM2.5 obtained in Monterrey, Mexico

Seasonal evaluation of sulfur species identified in PM2.5 obtained in Monterrey, Mexico

Conductive Li2S‐NbSe2 Cathode Material Capable of Bidirectional Self‐Activation for High‐Performance All‐Solid‐State Lithium Metal Batteries

AbstractAll‐solid‐state lithium metal batteries (ASSLBs) offer an alternative route to safe and high energy density power sources. Sulfur‐based cathodes with high theoretical specific capacity and low cost are crucial for advancing ASSLBs. However, the electronic insulation and sluggish kinetics of sulfide materials like Li2S severely limit battery performance. Herein, the strategy is proposed that a highly electronic conductive Li2S‐NbSe2 material enhances the electrochemical performance through bidirectional self‐activation. The chemical interaction between Li2S and NbSe2 induces NbSe2‐xSx and Li2Se derivatization, serving as the basis for activation. The carrier transport properties, chemical evolution and self‐activation mechanism of Li2S‐NbSe2 during the oxidation–reduction process are revealed. The chemical activation of NbSe2‐xSx is explored to accelerate the electrochemical processes by modifying the conductivity of sulfur species and the conversion pathways without insulating Li2S and S aggregation. Therefore, ASSLBs using Li2S‐NbSe2 as cathode active material achieve an electrode‐level energy density of 394 Wh kg−1 and a power density of 524 W kg−1 at 1 C (4.35 mA cm−2) and 25 °C. The capacity retention after 100 cycles at 0.5 C is ≈99.3% with almost no degradation. This work provides new options and insights for the rational design and development of chalcogenide cathode active materials for high‐performance ASSLBs.

Use of carbon-encapsulated zero-valent iron nanoparticles from waste biomass to hydrogen sulphide wet removal.

This study evaluates the use of carbon-encapsulated zero-valent iron nanoparticles for biogas upgrading in wet systems. The nanoparticles were produced by hydrothermal carbonization, using olive mill waste (OMW) or microalgae as carbon sources. The solids were characterized to investigate the specific surface area, total and zero-valent iron content, pHPZC and chemical and crystalline composition. Their adsorption performance towards hydrogen sulphide (H2S) was tested by treating two types of synthetic biogas with and without CO2. In both cases, the starting H2S concentration was approximately 60 ppm and the experiments lasted until the complete saturation of the nanoparticles. Optimal Fe/C ratios of 0.05 for OMW nanoparticles and 0.2 for microalgae nanoparticles demonstrated H2S-specific adsorption capacities of 9.66 and 9.55 , respectively, in a synthetic biogas without CO2. The addition of CO2 in biogas reduced adsorption, possibly due to system acidification. X-ray photoelectron spectroscopy analysis revealed surface compounds on the surface of the spent nanoparticles, including disulphides, polysulphides and sulphate. The saturated adsorbents were effectively regenerated with air, leading to the oxidation of sulphur species and desorption. The regeneration allowed a total adsorption capacity of 53.25 and 34.14 , after 10 consecutive cycles of adsorption/regeneration with a single batch of olive mill and microalgae nanoparticles, respectively.

Evaluation of environmental geochemical signatures due to RO rejects on arid agricultural farms and tangible solutions

The impact of reverse osmosis (RO) rejects in the groundwater presents a significant challenge in arid regions. This study collected groundwater samples, product water, and reverse osmosis brine (ROB) from evaporation ponds and analyzed them for major ions and trace elements. Test boreholes were drilled near the ROB site along the flow direction, and borehole sediment samples were collected. The samples were predominantly gravelly sand, and the depth to water level fluctuated around 30 m below ground level (bgl), with minerals mainly consisting of calcite, gypsum, and Quartz. Data loggers reflected a rise in water level (<22 m bgl) corresponding to higher electrical conductivity (>16 mS/Cm) during the cropping period in many locations, confirming the impact of ROB in groundwater. The results were further supported by enriched signatures of δ18O (∼ +1.5‰) and δ2H (∼ +15‰). The saturation index of the minerals reflected that carbonate minerals (Calcite > Dolomite) were saturated in the ROB relative to the groundwater. The vertical variation of mineral assemblages in the boreholes indicated gypsum precipitation in the capillary zone along with calcite and dolomite. The assemblage varies as the groundwater moves from the disposal site. The speciation of different compounds along the groundwater path indicated higher carbonate and sulfate species (CaCO3 > CaHCO3> CaSO4 > NaSO4 > MgSO4) near the disposal site, with variations along the flow direction. Considering the significant variation in temperature in the region (5 to 50 ℃), the water sample composition was modeled using PHREEQC, suggesting that the increase in temperature led to supersaturation of Epsomite and Gypsum compositions. The ROB was theoretically mixed with groundwater and product water in different proportions, and an optimum composition (10:90) for safe disposal was derived and tested fit for reuse in agriculture.

A bifunctional thiobenzamide additive for improvement of cathode kinetics and anode stability in lithium-sulfur batteries

Lithium-sulfur batteries (LSBs) are considered as the key candidates for the next generation of energy storage devices. However, the practical applications of LSBs are hindered by the slow conversion of sulfur species and the inhomogeneous Li+ precipitation /stripping of lithium anode. Here, we report a bifunctional thiobenzamide electrolyte additive, 4-(trifluoromethyl) thiobenzamide (TFBCA), which synergistically improves cathode redox kinetics and anode stability. Polysulfides (LiPSn) are in-situ transferred to more reactive polysulfide intermediates (T-Sn-T), which significantly improve the liquid–solid reduction process by promoting the deposition dimension of Li2S. A LiF/Li3N-rich solid electrolyte interphase is formed with TFBCA, the uniform lithium deposition is achieved and the growth of lithium dendrites is suppressed. Correspondingly, LSBs with TFBCA show a high capacity (888 mAh·g−1 at 5C) and cycling stability (0.055 % per cycle after 600 cycles at 2C). Even under high sulfur loading (7.1 mg·cm−2) and low E/S ratio of 7, the LSBs also exhibit an areal capacity of 7 mAh·cm−2 after 50 cycles, and an energy density of 314 Wh·kg−1 is achieved for the pouch cell. This work demonstrates an efficient additive strategy through molecular structure design to construct high-performance LSBs.

Enhancing the activity and sulfur resistance of CuFeAlOx catalyst via the structure effect for the simultaneous removal of Hg0 and NO at wide temperature

The efficient strategy for improving SO2 resistance and catalytic activity is structural modification. Herein, the CuFeAlOx catalysts with different structures, including one-dimensionally disordered mesoporous nanoparticles structure (CuFeAl-N), one-dimensionally ordered mesoporous nanoparticles structure (CuFeAl-C), three-dimensionally ordered porous honeycomb-like structure (CuFeAl-P) and three-dimensionally ordered porous flower-like structures (CuFeAl-CP), were synthesized via a template method to investigate structure effect on activity and sulfur resistance of the catalyst for simultaneously removing NO and Hg0 at wide temperature. The results showed that the various surface characteristics resulted in distinct behaviours with regards to SO2 tolerance. CuFeAl-CP and CuFeAl-C exhibits excellent SO2 resistance, but CuFeAl-N catalyst presents poor SO2 resistance. The CuFeAl-CP with the flower-like structure possesses large specific surface area, which can expose more active sites and exhibited highly dispersed active component. More importantly, it reacts with SO2 to generate reactive sulfate providing additional acid sites, which significantly promotes high-temperature catalytic performance. One-dimensionally ordered mesoporous and three-dimensionally ordered porous effectively facilitates mass transfer of reactants and ammonium sulphate decomposition, thereby inhibiting surface sulfation and ammonium sulfate species deposition. This work lays the foundation for developing highly efficient SCR catalysts that are tolerant to SO2.

Post-Translational Modifications to Cysteine Residues in Plant Proteins and Their Impact on the Regulation of Metabolism and Signal Transduction.

Cys is one of the least abundant amino acids in proteins. However, it is often highly conserved and is usually found in important structural and functional regions of proteins. Its unique chemical properties allow it to undergo several post-translational modifications, many of which are mediated by reactive oxygen, nitrogen, sulfur, or carbonyl species. Thus, in addition to their role in catalysis, protein stability, and metal binding, Cys residues are crucial for the redox regulation of metabolism and signal transduction. In this review, we discuss Cys post-translational modifications (PTMs) and their role in plant metabolism and signal transduction. These modifications include the oxidation of the thiol group (S-sulfenylation, S-sulfinylation and S-sulfonylation), the formation of disulfide bridges, S-glutathionylation, persulfidation, S-cyanylation S-nitrosation, S-carbonylation, S-acylation, prenylation, CoAlation, and the formation of thiohemiacetal. For each of these PTMs, we discuss the origin of the modifier, the mechanisms involved in PTM, and their reversibility. Examples of the involvement of Cys PTMs in the modulation of protein structure, function, stability, and localization are presented to highlight their importance in the regulation of plant metabolic and signaling pathways.

Transformation and control of organic sulfur during pyrolysis of sludge under conditions relevant to smoldering combustion: Role of oxygen and CaO

This study focused on the effect of oxygen (0–15 %) and 5 % CaO addition on the organic-S control and transformation behavior during pyrolysis (400–600 °C) of sludge under the conditions relevant to smoldering combustion. The results show that oxygen inhibits the total emission of gaseous sulfur (decreased by 25.6–36.9 %). At low temperatures (<500 °C), oxygen enhances the oxidation of aliphatic-S, aromatic-S/thiophene-S, and sulfide-S, leading more sulfur retains in the form of sulfone-S and sulfate-S in char products, also migrates to water-soluble products (especially sulfone-S). At high temperatures (>500 °C), the formed sulfur species in char products mainly further decompose into water-soluble sulfone-S, and partially generate SO2. After the addition of CaO during oxidative pyrolysis, the synergistic promotion effect on the sulfur fixation in char products is found, mainly due to the generation of more amount of stable sulfone-S and sulfate-S in char products. This leads to a decrease in gaseous sulfur by 12.4–14.6 % and an increase in sulfur content of char products by 31.3–202.9 %.

Sulfur doping induced 3D hierarchical porous BiOI–Bi2S3 S-scheme heterojunction with regulated oxygen vacancies for a four-pronged enhanced photocatalytic degradation towards four representative pollutants

It is challenging and still difficult to adjust and boost the catalytic performance of photocatalysts via the synergistic achievement of heteroatom doping, vacancies engineering, morphology regulation, and appropriate structural design. Herein, we developed an efficient method to synthesize 3D hierarchical porous BiOI–Bi2S3 S-scheme heterojunction with oxygen vacancies (Ov-BBS) induced by sulfur doping and systematically investigated regulation of oxygen vacancies by sulfur doping and their effects on photocatalytic performance. Results showed that sulfur species promoted the formation of S-scheme heterojunction but depleted oxygen vacancies in Ov-BiOI. The optimal sulfur doped catalyst (Ov-BBS-0.1) exhibited excellent UV–vis light photocatalytic activity towards four representative pollutants, affording removal rate of 97.1 % for MB, 97.6 % for RhB, 99.4 % for Cr(VI), and 92.0 % for TC, respectively, which were higher than those of pristine Bi2S3, BiOI, Ov-BiOI, Ov-BiOI/Bi2S3 mixture, Ov-BBS-0.05, and Ov-BBS-0.2. Deep characterizations and theoretical studies certified that the four-pronged enhancement strategy of 3D hierarchical porous structure, oxygen vacancies, sulfur doping and the constructed S-scheme heterojunction, not only enriched accessible active sites, but also promoted electronic polarization and modulated electronic structure, resulting in rapid separation and migration of photogenerated carriers. Moreover, considering the excellent stability and cyclic photocatalytic performance, the film prepared by pumping Ov-BBS dispersion was also satisfactory in the practical application of circulating sewage treatment. Overall, the present work provides a novel approach for the design of more photocatalysts with high efficiency.

Application of X-ray Spectroscopic Techniques to Determine the Inorganic Composition and Sulfur Chemical Speciation of the Amazonian Plant Bixa orellana

Bixa orellana is a plant that has a variety of uses, such as applications in the food and cosmetic industries, as well as culinary uses, and body painting for Indigenous people. Despite its versatility, few studies have explored its inorganic composition, and its sulfur chemical speciation has only been assessed from the point of view of sulfurous amino acids. Here, we report on the inorganic composition of Bixa orellana fruits, pericarps, and seeds obtained using Wavelength Dispersive X-ray Fluorescence (WD-XRF) and sulfur chemical speciation using X-ray Absorption Near-Edge Structure (XANES). Our results show that the seed is a source of potassium, calcium, magnesium, and phosphorous. But also, the pericarp, which is considered waste, contains a high amount of nutrients. From the XANES measurements, the distribution of the oxidation state of the sulfur atom was obtained, and it was shown that although several oxidation states of sulfur are present, oxidized sulfur (sulfate) is the dominant form of sulfur in all samples.