Inorganic Sulfur Research Articles

Insight into Structural and Physicochemical Properties of ZrO2-SiO2 Monolithic Catalysts with Hierarchical Pore Structure: Effect of Zirconium Precursor

Zirconia–silica monolithic catalysts with hierarchical micro/macroporous structure were obtained in a sol-gel process combined with phase separation using inorganic salts, i.e., oxychloride, oxynitrate and sulphate, as a zirconium source. It was found that the use of zirconium oxychloride and prehydrolysis of tetraethoxysilane (TEOS) resulted in materials characterized by a well-developed continuous structure of macropores with a diameter of ca. 10 μm. For zirconium oxynitrate and sulfate modified materials, the prehydrolysis hardly affected the macropore size. The micropores with a diameter of 1.5 nm in the skeleton of all materials provided a large surface area of 550–590 m2/g. A high dispersion of zirconia in the silica skeleton in all studied materials was shown. However, the largest surface concentration of Lewis and Brönsted acid sites was found in the monolith synthesized with zirconium oxychloride. The monoliths were used as a core for continuous-flow microreactors and high catalytic activity was confirmed in the deacetalization of benzylaldehyde dimethyl acetal. The process was characterized by a high efficiency at low temperature, i.e., 35 °C.

Airborne desert dust in the Northern Adriatic area (Croatia): Different sources

During the implementation of the INTERREG IT-HR project ECOMOBILITY, whose one of the goals was to estimate the impact of ship emissions on air quality in the port city of Rijeka (Croatia) and Venice (Italy), two particular weekly samples were collected in Rijeka, during the first and the thirteen weeks of sampling, i.e. S01 (16.10.-23.10.2018) and S13 (24.04.-30.04.2019.), respectively. Both samples have similarities regarding species characteristic for desert dust contribution, but HYSPLIT analyses excluded Saharan desert to be the source of the S01 sample. Unlike Saharan dust, this sample had a high contribution of fine and ultrafine particles (>50 % and 9.8 %, respectively), as well as secondary inorganic (sulfates, ammonium) and organic (water soluble organic compounds - WSOC) aerosols. Detailed synoptic situation and HYSPLIT backward trajectories pointed out the Syrian Desert as the source of this collected sample. The same source was proved by MERRA-2 reanalysis of the desert dust emission. Although the Saharan dust episodes, mostly in precipitation, are well known in the Northern Adriatic area, this is the first time to indicate Syrian Desert as a source of airborne particulates. This assumption was confirmed with chemical species characteristic for the Syrian Desert, i.e. higher content of potassium from K- feldspar and phosphates.

Collective production of hydrogen sulfide gas enables budding yeast lacking MET17 to overcome their metabolic defect.

Assimilation of sulfur is vital to all organisms. In S. cerevisiae, inorganic sulfate is first reduced to sulfide, which is then affixed to an organic carbon backbone by the Met17 enzyme. The resulting homocysteine can then be converted to all other essential organosulfurs such as methionine, cysteine, and glutathione. This pathway has been known for nearly half a century, and met17 mutants have long been classified as organosulfur auxotrophs, which are unable to grow on sulfate as their sole sulfur source. Surprisingly, we found that met17Δ could grow on sulfate, albeit only at sufficiently high cell densities. We show that the accumulation of hydrogen sulfide gas underpins this density-dependent growth of met17Δ on sulfate and that the locus YLL058W (HSU1) enables met17Δ cells to assimilate hydrogen sulfide. Hsu1 protein is induced during sulfur starvation and under exposure to high sulfide concentrations in wild-type cells, and the gene has a pleiotropic role in sulfur assimilation. In a mathematical model, the low efficiency of sulfide assimilation in met17Δ can explain the observed density-dependent growth of met17Δ on sulfate. Thus, having uncovered and explained the paradoxical growth of a commonly used "auxotroph," our findings may impact the design of future studies in yeast genetics, metabolism, and volatile-mediated microbial interactions.

Transformation and migration mechanism of carbon and sulfur in lignite’s chemical looping gasification using carbide slag

In the process of lignite’s chemical looping gasification using carbide slag, carbon, and sulfur are present in both the gas and solid phases. To analyze the migration and transformation of carbon and sulfur in lignite’s chemical looping gasification using carbide slag, theoretical calculations along with experiments were conducted. The results showed that the migration transformation of carbon consisted of three main parts. First part was the transformation of organic carbon to inorganic gaseous carbon, which was followed by the mutual transformation of inorganic gaseous carbon. Finally, the inorganic carbon in gas was transformed into solid phase. The transformation of gaseous inorganic carbon to solid inorganic carbon, and that of inorganic carbon to gaseous carbon occurred at the reaction temperature of more than 1073 K. During the reaction, the migration transformation of sulfur consisted of two main steps. The transformation of organic sulfur to inorganic gaseous sulfur (H2S) through lignite’s gasification, and the transformation of inorganic gaseous sulfur (H2S) to inorganic solid sulfur (CaS). In-situ solidification of sulfur could be achieved through lignite-H2S-CaS reaction. This work provides fundamental knowledge about the mechanism of the transformation of carbon and sulfur during lignite’s chemical looping gasification and provides support for controlling the in-situ solidification of sulfur and carbon-containing gases during lignite’s chemical looping gasification using carbide slag.

Quantification of elemental sulfur in pulping liquors by thin-layer chromatography

The inorganic sulfur compounds that are used as pulping agents in the production of pulp and paper from wood are converted into a variety of sulfur species during processing. How sulfur is allocated to different streams and products in a pulp mill is relevant for efficient mill operation and to avoid harmful emissions. Pulping liquors are a highly challenging and potentially destructive sample matrix. We describe a thin-layer chromatographic method for the direct quantification of elemental sulfur in pulping liquors. The liquors are spotted (not sprayed!) directly onto the plate without prior purification, extraction, or workup. Sulfur is then eluted with cyclo-hexane and detected by densitometry at 285 nm or fluorescence quenching close to the solvent front. The method was validated for a calibrated range from 60 to 2000 ng sulfur on plate. The limit of detection was determined at 20 ng; measurement uncertainty was about 20%. With this method, 27–54 mg/L elemental sulfur were found in Kraft pulping liquors, which corresponds to 0.24–0.48% of the total sulfur in these samples.

Optimization of fucoidan recovery by ultrasound-assisted enzymatic extraction from South African kelp, Ecklonia maxima

Fucoidan, a sulphated polysaccharide, is found exclusively in brown seaweeds and has been reported to possess a wide range of biological functionalities. Fucoidans are found within the cell wall of brown seaweeds, which is composed of recalcitrant cellulose and hemicellulose. This hampers the recovery of fucoidans. In addition, fucoidans are found within a network of viscous hydrocolloids, alginates, further complicating their recovery. Traditionally, the hot water extraction method is used to recover fucoidans from brown seaweed, however, this is characterized by low yields and long extraction time. To combat these issues, several novel extraction technologies have been introduced, these include ultrasound-assisted extraction and enzyme-assisted extraction. Thus, the main aim of this study was to investigate and optimize fucoidan recovery from Ecklonia maxima based on ultrasound-assisted enzymatic extraction. The impact of temperature (40–65 °C), ultrasound intensity (0–118 W·cm−2), enzyme dosage (0–0.05 ml·g−1) and pH (4.5–6) on total dissolved, total carbohydrates and inorganic sulphates yields was studied. The application of ultrasound-assisted enzymatic extraction mainly improved the extraction of total carbohydrates. Ultrasound significantly improves the kinetics and extraction of fucoidan, but there was no merit when it was applied with enzymes. Results reveal that at optimized conditions, the fucoidan extracted 79.13 mg⋅g−1 (7.9 % w/w) of algal dry weight. The present study provides insight into the extraction potentials of enzyme-assisted extraction, ultrasound-assisted extraction, and ultrasound-assisted enzymatic extraction.

Metagenomic insight into the acidophilic functional communities driving elemental geochemical cycles in an acid mine drainage lake

Acidophiles play a key role in the generation, evolution and attenuation of acid mine drainage (AMD), which is characterized by strong acidity (pH<3.5) and high metal concentrations. In this study, the seasonal changes of acidophilic communities and their roles in elemental cycling in an AMD lake (pH∼3.0) in China were analyzed through metagenomics. The results showed eukaryotic algae thrived in the lake, and Coccomyxa was dominant in January (38.1%) and May (33.9%), while Chlorella in July (9.5%). The extensive growth of Chlamydomonas in December (22.7%) resulted in an ultrahigh chlorophyll a concentration (587 μg/L), providing abundant organic carbon for the ecosystem. In addition, the iron-oxidizing and nitrogen-fixing bacterium Ferrovum contributed to carbon fixation. Ammonia oxidation likely occurred in the acidic lake, as was revealed by archaea Ca. Nitrosotalea. To gain a competitive advantage in the nutrient-poor environment, some acidophiles exhibited facultative characteristics, e.g. the most abundant bacterium Acidiphilium utilized both organic and inorganic carbon, and obtained energy from organic matter, inorganic sulfur, and sunlight simultaneously. It was suggested that sunlight, rather than chemical energy of reduced iron-sulfur was the major driver of elemental cycling in the AMD lake. The results are beneficial to the development of bioremediation strategies for AMD.

Impacts of spatial expansion by Phragmites australis on spatiotemporal variation of sulfur fractions in marsh soils of the Min River estuary, Southeast China

To investigate the impacts of spatial expansion by Phragmites australis on spatiotemporal variations of sulfur (S) fractions in marsh soils of the Min River estuary (Southeast China), the contents of total sulfur (TS) and inorganic sulfur (IS) fractions (Water-Soluble-S, W-S-S; Adsorbed-S, A-S; HCl-Soluble-S, H-S-S; and HCl-Volatile-S, H-V-S) were determined in soils of Cyperus malaccensis marsh (before expansion, BE stage), P. australis-C. malaccensis marsh (during expansion, DE stage) and P. australis marsh (after expansion, AE stage) by space-for-time substitution method. Results showed that the expansion of P. australis greatly altered the spatiotemporal variations of TS and IS fractions in marsh soils. The TS contents in soils at AE stage were significantly lower than those at DE and BE stages throughout a year (p < 0.01). Higher levels of W-S-S, A-S, H-S-S and total inorganic sulfur (TIS) generally occurred in soils at DE and AE stages, whereas higher values of H-V-S were observed in soils at BE stage. Although P. australis expansion did not alter the temporal variations of TS stock in soils greatly, the values during autumn and winter were generally higher than those in spring and summer (p < 0.05). The highest TIS stocks in soils of different expansion stages were observed in spring, while the lowest values occurred in summer. The expansion of P. australis significantly increased the IS supply capacity of soils and, compared with the BE stage, stocks of W-S-S, A-S, H-S-S and TIS in soils of all sampling seasons at DE and AE stages increased by 51.40 %, 50.76 %, 63.35 %, 50.52 % and 20.00 %, 31.46 %, 42.93 %, 27.56 %, respectively. It was worth noting that stocks of H-V-S in soils at DE and AE stages showed a decreasing trend compared to the BE stage, implying that the expansion of P. australis might reduce the production of sulfides. This paper found that, compared with C. malaccensis, the increased available IS stocks in soils might be an effective strategy for P. australis to maintain its expansion advantage and the decreased volatile-S in soils might be more favorable for boosting its competitiveness. Our study provided valuable information for understanding the interspecific competition mechanism between P. australis and C. malaccensis. Next step, in order to protect the diversity of marsh vegetations in the Min River estuary, effective measures should be taken to suppress the rapid expansion of P. australis.

Unveiling the Halogenation-Induced Formation of Hg3Se2X2 (X = Cl, Br, and I) Compounds for Multiphase Mercury Cycling.

The interaction between mercury (Hg) and inorganic compounds, including selenium (Se), sulfur (S), and halogens (X = Cl, Br, or I), plays a critical role in the global mercury cycle. However, most previously reported mercury compounds are susceptible to reduction, leading to the release of elemental mercury (Hg0) and causing secondary pollution. In this study, we unveil a groundbreaking discovery that underscores the vital role of halogenation in creating exceptionally stable Hg3Se2X2 compounds. Through the dynamic interplay of Hg, Se, and halogens, an intermediary stage denoted [HgSe]m[HgX2]n emerges, and this transformative process significantly elevates the stabilization of mercury. Remarkably, halogen ions strategically occupy pores at the periphery of HgSe clusters, engendering a more densely packed atomic arrangement of Hg, Se, and halogen components. A marked enhancement in both thermal and acid stability is observed, wherein temperatures ascend from 130 to 300 °C (transitioning from HgSe to Hg3Se2Cl2). This sequence of escalating stability follows the order HgSe < Hg3Se2I2 < Hg3Se2Br2 < Hg3Se2Cl2 for thermal resilience, complemented by virtually absent acid leaching. This innovative compound formation fundamentally alters the transformation pathways of gaseous Hg0 and ionic mercury (Hg2+), resulting in highly efficient in situ removal of both Hg0 and Hg2+ ions. These findings pave the way for groundbreaking advancements in mercury stabilization and environmental remediation strategies, offering a comprehensive solution through the creation of chemically stable precipitates.

Multiphase interactions between sulfur dioxide and secondary organic aerosol from the photooxidation of toluene: Reactivity and sulfate formation

There is growing evidence that the interactions between sulfur dioxide (SO2) and organic peroxides (POs) in aerosol and clouds play an important role in atmospheric sulfate formation and aerosol aging, yet the reactivity of POs arising from anthropogenic precursors toward SO2 remains unknown. In this study, we investigate the multiphase reactions of SO2 with secondary organic aerosol (SOA) formed from the photooxidation of toluene, a major type of anthropogenic SOA in the atmosphere. The reactive uptake coefficient of SO2 on toluene SOA was determined to be on the order of 10−4, depending strikingly on aerosol water content. POs contribute significantly to the multiphase reactivity of toluene SOA, but they can only explain a portion of the measured SO2 uptake, suggesting the presence of other reactive species in SOA that also contribute to the particle reactivity toward SO2. The second-order reaction rate constant (kII) between S(IV) and toluene-derived POs was estimated to be in the range of the kII values previously reported for commercially available POs (e.g., 2-butanone peroxide and 2-tert-butyl hydroperoxide) and the smallest (C1-C2) and biogenic POs. In addition, unlike commercial POs that can efficiently convert S(IV) into both inorganic sulfate and organosulfates, toluene-derived POs appear to mainly oxidize S(IV) to inorganic sulfate. Our study reveals the multiphase reactivity of typical anthropogenic SOA and POs toward SO2 and will help to develop a better understanding of the formation and evolution of atmospheric secondary aerosol.

Genome sequencing and metabolic network reconstruction of a novel sulfur-oxidizing bacterium Acidithiobacillus Ameehan.

Sulfur-oxidizing bacteria play a crucial role in various processes, including mine bioleaching, biodesulfurization, and treatment of sulfur-containing wastewater. Nevertheless, the pathway involved in sulfur oxidation is highly intricate, making it complete comprehension a formidable and protracted undertaking. The mechanisms of sulfur oxidation within the Acidithiobacillus genus, along with the process of energy production, remain areas that necessitate further research and elucidation. In this study, a novel strain of sulfur-oxidizing bacterium, Acidithiobacillus Ameehan, was isolated. Several physiological characteristics of the strain Ameehan were verified and its complete genome sequence was presented in the study. Besides, the first genome-scale metabolic network model (AMEE_WP1377) was reconstructed for Acidithiobacillus Ameehan to gain a comprehensive understanding of the metabolic capacity of the strain.The characteristics of Acidithiobacillus Ameehan included morphological size and an optimal growth temperature range of 37-45°C, as well as an optimal growth pH range of pH 2.0-8.0. The microbe was found to be capable of growth when sulfur and K2O6S4 were supplied as the energy source and electron donor for CO2 fixation. Conversely, it could not utilize Na2S2O3, FeS2, and FeSO4·7H2O as the energy source or electron donor for CO2 fixation, nor could it grow using glucose or yeast extract as a carbon source. Genome annotation revealed that the strain Ameehan possessed a series of sulfur oxidizing genes that enabled it to oxidize elemental sulfur or various reduced inorganic sulfur compounds (RISCs). In addition, the bacterium also possessed carbon fixing genes involved in the incomplete Calvin-Benson-Bassham (CBB) cycle. However, the bacterium lacked the ability to oxidize iron and fix nitrogen. By implementing a constraint-based flux analysis to predict cellular growth in the presence of 71 carbon sources, 88.7% agreement with experimental Biolog data was observed. Five sulfur oxidation pathways were discovered through model simulations. The optimal sulfur oxidation pathway had the highest ATP production rate of 14.81 mmol/gDW/h, NADH/NADPH production rate of 5.76 mmol/gDW/h, consumed 1.575 mmol/gDW/h of CO2, and 1.5 mmol/gDW/h of sulfur. Our findings provide a comprehensive outlook on the most effective cellular metabolic pathways implicated in sulfur oxidation within Acidithiobacillus Ameehan. It suggests that the OMP (outer-membrane proteins) and SQR enzymes (sulfide: quinone oxidoreductase) have a significant impact on the energy production efficiency of sulfur oxidation, which could have potential biotechnological applications.

369 Effects of Supplementing Sources of Zinc on Digestibility Parameters of Beef Steers

Abstract Zinc (Zn) has numerous functions and many life-sustaining processes depend on the presence of Zn within the body. The objective of this study was to determine if apparent digestibility differed by Zn source. In this study, Angus steers (n = 12, 226 kg ± 16.17) underwent three isozinc treatments: Organic Zn glycinate, Inorganic Zn sulfate (ZnSO4), and Zn hydroxychloride (Phibro Animal Health, Teaneck, NJ). On day 1, steers were weighed, rumen fluid collected, liver biopsy performed, and blood collected. Steers were then placed in metabolism crates for a 4-day adaptation period. Each steer was assigned a source of Zn in a completely randomized design (4 steers/treatment). Steers had ad libitum access to hay and treatments were fed once daily. Treatments contained the assigned source of Zn 0.063 g/d, soybean pellets 0.063 g/d, ground corn 0.063 g/d, and molasses 0.2 g/d. Orts were quantified daily, and total fecal samples were collected and sampled daily at time of feeding (0600h) for 5 consecutive days (d 5 to d 10). On d 10, steers were removed from metabolism crates, weighed, rumen fluid collected, liver biopsy performed, and blood collected. Feed and fecal samples were composited for the entirety of the collection period. Each sample was dried, ground, and analyzed to determine DM, NDF, ADF, fat, protein, and mineral content. Data were analyzed using the proc mixed procedure of SAS. Digestibility results for Organic Zn, Inorganic ZnSO4, and Zn hydroxychloride were DM (70.74, 70.64, 72.46, respectively), NDF (75.98,76.03, 77.79, respectively), ADF (83.00, 82.47, 84.00, respectively), Fat (67.28, 66.00, 70.04, respectively), and protein (69.14, 68.56, 70.12, respectively). Hemicellulose and organic matter (OM) were calculated and determined, with digestibility of Organic Zn, Inorganic ZnSO4, and Zn hydroxychloride to be OM (74.13,73.50, 75.67, respectively), and hemicellulose (57.66, 59.27, 61.65, respectively). The results of proximate analysis reported digestibility of DM, NDF, ADF, fat, protein, OM, and hemicellulose, were not affected (P &amp;lt; 0.05) by treatment. Mineral analysis was performed by Inductively coupled plasma spectroscopy. Treatment did not affect Zinc liver concentrations. However, numerical differences indicate additional research is needed on rumen dynamics to fully understand the impact of mineral source within the animal, and ultimately its final environmental impact.

The effect of anaerobic remineralization of the seagrass Halophila stipulacea on porewater biogeochemistry in the Gulf of Aqaba

IntroductionSeagrasses form oxidizing microenvironments around their roots, creating complex and strong redox gradients, thus affecting the rates of microbial carbon mineralization in their surrounding sediments. Since seagrasses are continuously being lost worldwide, a deeper understanding of the changes that occur within different seagrass sediments following the disappearance of the plants is of ecological and global importance.MethodsWe conducted a slurry experiment with sediments that have different characteristics from the northern tip of Gulf of Aqaba; the different sediments included different compartments of the tropical seagrass Halophila stipulacea (old and young leaves, rhizomes, or roots). We measured the changes over time in dissolved inorganic carbon (DIC), alkalinity, ferrous iron (Fe2+), hydrogen sulfide (H2S), sulfate (SO42-), and sulphur isotope ratios in sulfate within water. These measurements were used to calculate the rate of remineralization of each seagrass compartment, allowing us to predict the potential effects of the disappearance of different H. stipulacea compartments on key microbial processes in the surrounding environment.ResultsWe show that H. stipulacea’s rhizomes had the fastest decomposition rates, followed by the young leaves, roots, and old leaves (which also indicates the preservation potential of old leaves).DiscussionHigh concentrations of hydrogen sulfide were detected only in the slurries containing rhizomes and young leaves. High sulfide concentrations can lead to seagrass mortality and cause a positive feedback loop where the loss of seagrass due to sulfide generates further sulfide accumulation. This positive feedback loop can also be further reinforced by the loss of burrowing fauna in the sediment. This emphasizes the importance of understanding the extent of different pathways of seagrass disappearance on the surrounding environment and other geochemical feedbacks.

Growth, structural, thermal, and optical characteristics of L-asparagine monohydrate doped magnesium sulphate heptahydrate semiorganic crystals

A novel semi-organic crystal has been grown using slow evaporation technique by doping organic compound L-asparagine monohydrate (C4H8N2O3·H2O) with inorganic material Magnesium sulphate heptahydrate (MgSO4·7H2O). The crystallographic parameters like strain, dislocation density and crystallite size were calculated by powder X-ray diffraction method. Functional groups were identified and bond length, force constants were calculated from FT-IR spectroscopy. Energy dispersive X-ray (EDX) analysis was used to identify the constituent elements of the crystal. Kinetic and thermodynamic parameters, such as, activation energy Ea, change in Gibb's free energy (ΔG) and change in enthalpy (ΔH) have been determined by thermogravimetric analysis (TGA) analysis. Ea, ΔH and ΔG show positive values and change in entropy (ΔS) shows negative ones. The thermal degradation behavior of the crystals has been analyzed by differential scanning calorimetry (DSC) analysis. Various optical constants such as optical band gap, lattice dielectric constant, absorbance, extinction coefficient, the ratio of free charge carrier concentration to the effective mass, Urbach energy, optical and electrical conductivities were estimated from UV–vis transmittance data. High optical conductivity (1010 s−1) justifies the good photo response nature of the semi-organic crystal.

Robust Scale Dissolver Mitigates Mixed-Scale Issue in South China Sea

_ This article, written by JPT Technology Editor Chris Carpenter, contains highlights of paper SPE 211187, “Tackling Mixed-Scales Issue in an Oil Field Using a Novel Robust Scale Dissolver,” by Nora Aida Ramly, Luky Hendraningrat, SPE, and Latief Riyanto, SPE, Petronas, et al. The paper has not been peer reviewed. _ The evaluation of a recently developed robust solid dissolver (RSD), from the laboratory phase through pilot deployment, is presented in the complete paper. Based on laboratory tests, the RSD can dissolve mixed scales completely in 24 hours at well temperatures while experiencing no incompatibility issues with production chemicals and all pumping and wireline components. The RSD was developed based on the total organic system that can prevent corrosion and is compatible with hydrocarbon. The RSD was piloted at oil Well 1 in Field PN and successfully removed mixed scales, allowing the well’s revival. Introduction Solid scale deposition is one of the most frequent flow-assurance issues both in subsurface and at the surface. The scale can be classified as organic (wax or asphaltenes), inorganic (calcites, sulphates, sulfides, halites, carbonates, and oxides), soap-related (naphthenates and carboxylates), gas-related (hydrates), or mixed scales. Scale occurrence, quantity, and severity mainly are determined by mineralogy, water chemistry, reservoir pressure and temperature, and the flow characteristics of the producing fluid in the well. Furthermore, scale formation is exacerbated by higher pH conditions and a higher water-cut environment, as would be expected in oil fields where water is to be injected for pressure maintenance. The most common type of scales found in Malaysian oil fields are organic and inorganic scales. The operator’s previously deployed scale-dissolving chemical in its fields only could cater to a single type of scale treatment at a time, which was ineffective for dissolving mixed scales simultaneously. Another method is the use of a mechanical solution using a coiled tubing unit (CTU). Removal mechanically by CTU in tubulars is a successful method in removing hard barite scales, but the cost is high and the method requires several days of production deferment. An improved and cheaper mixed-scale removal approach was needed to clean out mixed-scale issues in more-challenging brownfields. The RSD technology was developed for wellbore cleanout caused by mixed scale based on a stable microemulsion solution consisting of acid and solvent components. The solution was proposed to dissolve both organic and inorganic scales simultaneously in the near-wellbore area and tubing string of an oil well. The very small droplet size formed by the surfactant system and solvent is a significant advantage of using microemulsion and can allow penetration even in tight formations with small pore throats and promotes more-uniform surface coverage because of the increased interfacial area of the droplets. Previous studies have reported that the microemulsion can be pumped without causing a significant increase in pumping pressure.

Associations of Long-Term Exposure to PM2.5 and Its Constituents with Erythrocytosis and Thrombocytosis in Rural Populations.

Evidence on the effect of long-term exposure to fine particulate matter (PM2.5) on erythrocytosis and thrombocytosis prevalence was limited. We aimed to investigate the association of PM2.5 and its constituents with the risks of erythrocytosis and thrombocytosis. The present study included a total of 33,585 participants from the Henan Rural Cohort at baseline between 2015 and 2017. A hybrid satellite-based model was employed to estimate the concentrations of PM2.5 mass and its constituents (including black carbon [BC], nitrate [NO3-], ammonium [NH4+], inorganic sulfate [SO42-], organic matter [OM], and soil particles [SOIL]). The logistic regression model was used to assess the associations of single exposure to PM2.5 and its constituents with the risks of erythrocytosis and thrombocytosis, and the quantile G-computation method was applied to evaluate their joint exposure risk. For the independent association, the odds ratios for erythrocytosis/thrombocytosis with 1 μg/m3 increase was 1.049/1.043 for PM2.5 mass, 1.596/1.610 for BC, 1.410/1.231 for NH4+, 1.205/1.139 for NO3-, 1.221/1.359 for OM, 1.300/1.143 for SO42-, and 1.197/1.313 for SOIL. Joint exposure to PM2.5 and its components was also positively associated with erythrocytosis and thrombocytosis. The estimated weight of NH4+ was found to be the largest for erythrocytosis, while OM had the largest weight for thrombocytosis. PM2.5 mass and its constituents were positively linked to prevalent erythrocytosis and thrombocytosis, both in single-exposure and joint-exposure models. Additionally, NH4+/OM was identified as a potentially responsible component for the association between PM2.5 and erythrocytosis/thrombocytosis.

Cysteine facilitates the lignocellulolytic response of Trichodermaguizhouense NJAU4742 by indirectly up-regulating membrane sugar transporters

BackgroundFilamentous fungi possess a rich CAZymes system, which is widely studied and applied in the bio-conversion of plant biomass to alcohol chemicals. Carbon source acquisition is the fundamental driver for CAZymes-producing sustainability and secondary metabolism, therefore, a deeper insight into the regulatory network of sugar transport in filamentous fungi has become urgent.ResultsThis study reports an important linkage of sulfur assimilation to lignocellulose response of filamentous fungus. Inorganic sulfur addition facilitated biodegradation of rice straw by Trichodermaguizhouense NJAU4742. Cysteine and glutathione were revealed as major intracellular metabolites responsive to sulfur addition by metabolomics, cysteine content was increased in this process and glutathione increased correspondingly. Two membrane sugar transporter genes, Tgmst1 and Tgmst2, were identified as the critical response genes significantly up-regulated when intracellular cysteine increased. Tgmst1 and Tgmst2 were both positively regulated by the glucose regulation-related protein (GRP), up-regulation of both Tgmst1 and Tggrp can cause a significant increase in intracellular glucose. The transcriptional regulatory function of GRP mainly relied on GSH-induced glutathionylation, and the transcription activating efficiency was positively related to the glutathionylation level, furthermore, DTT-induced deglutathionylation resulted in the down-regulation of downstream genes.ConclusionsInorganic sulfur addition induces a rise in intracellular Cys content, and the conversion of cysteine to glutathione caused the increase of glutathionylation level of GRP, which in turn up-regulated Tgmst1 and Tgmst2. Subsequently, the sugar transport efficiency of single cells was improved, which facilitated the maintenance of vigorous CAZymes metabolism and the straw-to-biomass conversion.

Effect of electromagnetic induction drying on the drying–incineration process of dyeing sludge: focus on migration and conversion of sulfur

Secondary sulfur pollution in dyeing sludge (DS) during drying and incineration is a major environmental problem necessitating in-situ control. To robustly immobilise sulfur during drying–incineration, the authors introduce an electromagnetic induction (EMI) drying method and reveal the corresponding migration and conversion of sulfur in DS. The EMI-drying efficiency reached 10.69%/min, five times that of thermal drying. EMI drying increases the relative sulfoxide ratio from that of thermal drying. In a sludge–sulfur model, the proposed treatment promoted the oxidation and decomposition of organic sulfur without noticeably affecting the inorganic sulfur. The selective oxidation process during EMI drying promotes sulfur stabilisation in dried DS, decreasing the performance and stability of DS combustion. The sulfur-containing pollutants released during the incineration of DS mainly contain H2S, followed by CH3SH and SO2. EMI drying increases the outputs of SO2 and CH3SH but decreases the outputs H2S and total sulfur compared with the outputs of thermal drying. Under the sulfur-model conditions, EMI promoted the conversion of inorganic sulfur to sulfur-containing gases (especially H2S) during incineration. In contrast, the sulfur stabilised by partial oxidation of organic sulfur in the EMI-dried DS was not easily converted to gaseous sulfur during subsequent combustion. Overall, EMI inhibits the release of sulfur during the combined drying–incineration process of DS.

Association of Fine Particulate Matter Constituents with the Predicted 10-Year Atherosclerotic Cardiovascular Disease Risk: Evidence from a Large-Scale Cross-Sectional Study.

Little is known concerning the associations of fine particulate matter (PM2.5) and its constituents with atherosclerotic cardiovascular disease (ASCVD). A total of 31,162 participants enrolled from the Henan Rural Cohort were used to specify associations of PM2.5 and its constituents with ASCVD. Hybrid machine learning was utilized to estimate the 3-year average concentration of PM2.5 and its constituents (black carbon [BC], nitrate [NO3-], ammonium [NH4+], inorganic sulfate [SO42-], organic matter [OM], and soil particles [SOIL]). Constituent concentration, proportion, and residual models were utilized to examine the associations of PM2.5 constituents with 10-year ASCVD risk and to identify the most hazardous constituent. The isochronous substitution model (ISM) was employed to analyze the substitution effect between PM2.5 constituents. We found that each 1 μg/m3 increase in PM2.5, BC, NH4+, NO3-, OM, SO42-, and SOIL was associated with a 3.5%, 49.3%, 19.4%, 10.5%, 21.4%, 14%, and 28.5% higher 10-year ASCVD risk, respectively (all p < 0.05). Comparable results were observed in proportion and residual models. The ISM found that replacing BC with other constituents will generate the greatest health benefits. The results indicated that long-term exposure to PM2.5 and its constituents were associated with increased risks of ASCVD, with BC being the most attributable constituent.

Abscisic acid promotes selenium absorption, metabolism and toxicity via stress-related phytohormones regulation in Cyphomandra betacea Sendt. (Solanum betaceum Cav.)

High levels of selenium (Se) uptakes negatively affect plant growth. In this study, the possible molecular mechanism for the effects of abscisic acid (ABA) on Se absorption, metabolism and toxicity in Cyphomandra betacea Sendt. (Solanum betaceum Cav.) young plants were investigated. Se+ABA treatment promoted significant Se absorption in C. betacea while impeding plant growth as compared to Se treatment. The expression levels of sulfate/phosphate transporter protein genes indicated that Se+ABA triggered more S/Se absorption and transportation into chloroplast. Furthermore, Se+ABA promoted higher metabolisms of inorganic sulfur (S)/Se and organic S/Se. The organic Se might be in several forms (SeCysth, SeCys and SeMet) in Se+ABA treatment, whereas SeCysth was the major organic form in Se treatment. More reactive oxygen species production was suggested in Se+ABA treatment from a series of genes involved in antioxidant enzymes and molecules, including superoxide dismutase, peroxiredoxin, glutathione sulfur-transferase and glutathione. Se+ABA further improved the expression levels of genes involved in biosynthesis and signaling transduction genes involved in stress-related phytohormones (jasmonic acid and salicylic acid). Combining with the data in ABA treatment, we hypothesized a model that ABA might first affect the biosynthesis and signaling transduction pathways of stress-related phytohormones, and subsequently altered the metabolic processes responding to Se stress.