Sulfur Oxidation Research Articles

Impact of soil bacteria on amylose synthesis in maize kernels under the substitution of manure nitrogen for mineral fertilizer nitrogen

Long-term and large-scale application of mineral fertilizer destroys soil microbial structure and crop quality. To reduce the harm of mineral fertilizer, a 6-year localization experiment was conducted to study the effects of replacing 0 % (CF), 25 % (M25), 50 % (M50), 75 % (M75), and 100 % (M100) of 225 kg ha−1 mineral fertilizer nitrogen with manure nitrogen on soil bacterial community structure and crop quality. The results showed that an increase in soil Longimicrobiaceae elicited a reduction in amylose. The impact of soil bacteria on the soluble sugar showed no significant difference. Compared with CF, substitution treatments significantly reduced Ktedonobacteria and C0119 by 53.42–81.28 %, and significantly decreased cyanobacteria, cellulolysis, aerobic chemoheterotrophy, phototrophy, photoautotrophy and oxygenic photoautotrophy by 3.27–196.58 %, and significantly increased dark sulfur oxidation, dark thiosulfate oxidation, nitrogen fixation and chitinolysis by 15.73–508.50 %. M50, M75, and M100 significantly reduced Holophagae and Subgroup 7 by 24.96–37.91 % relative to CF. M75 significantly increased Chao index, whereas significantly reduced Simpson index compared with M25. The Simpson indices of M75 and M100 were significantly lower than that of CF. Bacillaceae and Env.OPS 17 can be used as the main basis for the classification of soil samples in the equivalent substitution of nitrogen mineral fertilizer with manure.

Partially Amorphous Ru-Doped CoSe Nanoparticles with Optimized Intermediates Adsorption for Highly Efficient Sulfur Oxidation Reaction.

The application of thermodynamically more favorable sulfur oxidation reaction (SOR) to replace oxygen evolution reaction (OER) in electrocatalytic water electrolysis is an appealing strategy to achieve low-energy hydrogen production while removing toxic sulfur ions from wastewater. However, the study of SOR catalysts with both activity and stability still faces great challenges. Herein, this study prepares partially amorphous Ru-doped CoSe (pa-Ru-CoSe) nanoparticles for SOR. The doping of Ru keeps Co in an electron-deficient state, which enhances the adsorption of SOR intermediates and improves the catalytic activity. Meanwhile, the partially amorphous selenide possesses great corrosion resistance to sulfur species, thus ensuring stability in long-term SOR. In addition, the pa-Ru-CoSe requires only 0.566V to reach a current density of 100mA cm-2 in the SOR-HER coupled system and remains stable for 200 h. This work provides a promising partially amorphous strategy for SOR catalysts with both catalytic activity and long-term stability, enabling hydrogen production with low energy consumption and simultaneous sulfur production.

Mechanism of Intracellular Elemental Sulfur Oxidation in Beggiatoa leptomitoformis, Where Persulfide Dioxygenase Plays a Key Role.

Representatives of the colorless sulfur bacteria of the genus Beggiatoa use reduced sulfur compounds in the processes of lithotrophic growth, which is accompanied by the storage of intracellular sulfur. However, it is still unknown how the transformation of intracellular sulfur occurs in Beggiatoa representatives. Annotation of the genome of Beggiatoa leptomitoformis D-402 did not identify any genes for the oxidation or reduction of elemental sulfur. By searching BLASTP, two putative persulfide dioxygenase (PDO) homologs were found in the genome of B. leptomitoformis. In some heterotrophic prokaryotes, PDO is involved in the oxidation of sulfane sulfur. According to HPLC-MS/MS, the revealed protein was reliably detected in a culture sample grown only in the presence of endogenous sulfur and CO2. The recombinant protein from B. leptomitoformis was active in the presence of glutathione persulfide. The crystal structure of recombinant PDO exhibited consistency with known structures of type I PDO. Thus, it was shown that B. leptomitoformis uses PDO to oxidize endogenous sulfur. Additionally, on the basis of HPLC-MS/MS, RT-qPCR, and the study of PDO reaction products, we predicted the interrelation of PDO and Sox-system function in the oxidation of endogenous sulfur in B. leptomitoformis and the connection of this process with energy metabolism.

Intimate microbe-water-mineral interactions mediate alkalization in the pyroxene-rich iron ore mines in Panxi area, Southwest China

In contrast to acid mine drainage, the microbial assembly and (bio)geochemical processes in alkaline mine conditions remain under-investigated. Here, microbe-water-mineral interactions were systematically investigated in two representative iron mines with alkaline conditions in the Panxi mining area, Southwest China. Compared to reference riverine samples less interfered by mining activities, the iron ore samples, composed of vanadium-titanium magnetite and pyroxene-rich bedrocks, exhibited elevated levels of Fe, HCl-extractable Fe(II), total sulfur, nitrate and sulfate, but lower total carbon (TC). Meanwhile, the mine drainage showed significantly higher sulfate, but lower TC concentrations than the riverine samples. Intriguingly, the Serpentinimonas spp., typically reported in serpentinites, prevailed in the microbial communities from the mine samples exhibiting higher pH. This suggests that the alkaline environments in Panxi mines result from serpentinization-like reactions. Enrichment of Thiobacillus spp. was observed in the mine-dwelling microbial communities, positively correlated with total sulfur, sulfate, nitrate, and Fe(II). Genome-resolved metagenomics suggested a chemoautotrophic lifestyle for the Thiobacillus species (e.g., carbon fixation, sulfur oxidation, and oxygen respiration), which may generate H+ and mitigate alkalization. This study provides valuable insights into progressive development of alkaline mine ecosystems and offers guidance for developing appropriate engineering strategies to restore the abandoned alkaline mines.

Spring Water pH in Forest Catchments Is Modified through Fluctuating Discharge under Climate Change

Over the course of industrialization in the 20th century, vast emissions of air pollutants have occurred. The exhaust gasses contain sulfur and nitrogen oxides, which are converted to sulfuric acid and nitric acid in the atmosphere. This causes acid rain to enter aquatic and terrestrial ecosystems, the most serious consequence of which is large-scale forest dieback across Europe and North America. However, through various political measures, the exhaust gasses have been reduced and, thus, acid rain and forest dieback were stopped. Nevertheless, the lingering effects of this pollution are still present today and are reflected in hydrochemistry. More recently, fluctuating precipitation regimes are causing additional stress to ecosystems in Central Europe. Climatic extremes are becoming more pronounced with climate change. Substantial differences between drought years and years with regular precipitation are directly altering the discharge of springs. Now, two overlapping and interacting syndromes of environmental pressures can be studied in these small catchments at a landscape scale: (1) acidification and (2) climate change. In this long-term study, the waters of 102 forest springs, located in two neighboring forest landscapes in north-eastern Bavaria, Germany (Frankenwald and Fichtelgebirge), were investigated over 24 years (1996 to 2020). By linking changes in pH values with changes in precipitation and spring discharge, we found that pH increases with decreasing discharge and decreasing precipitation. This effect was strongest in the Frankenwald compared to the Fichtelgebirge. We hypothesize that this temporal pattern reflects the longer residence time and, in consequence, the increased buffering of acidic interflow in small catchments during periods of drought. However, this should not be misinterpreted as rapid recovery from acidification because this effect fades in times of enhanced precipitation. We recommend that fluctuations in weather regimes be considered when investigating biogeochemical patterns throughout forest landscapes.

Stark seasonal contrast of fine aerosol levels, composition, formation mechanism, and characteristics in a polluted megacity.

In this study, we investigated the temporal variation of organic and inorganic aerosol with its optical properties in Mumbai (India), an urban coastal region. Mean PM2.5concentrations during the sampling period were 175μg/m3 (winter) and 90μg/m3 (summer). During winter, the average concentrations of organic (OC), elemental (EC), and water-soluble organic carbon (WSOC) were three times higher than in summer. Secondary organic carbon (SOC) contribution in OC was higher in summer (78%) than in winter (53%), and strong solar radiation in summer likely caused this outcome. Aerosols were slightly acidic in both seasons, with an average pH of 5.7 (winter) and 6.0 (summer). A correlation was observed between SOC and the acidity of particles in summer (R2 = 0.6), indicating some amount of acid-catalysed SOC formation. In both seasons, the sulphate oxidation ratio (SOR) was higher than the nitrate oxidation ratio (NOR), which may reflect a preference for SO2 oxidation over NO2 or the difference in partitioning ammonium nitrate into ammonium sulphate under high RH. The dominant mechanism of SOC formation (gas vs aqueous phase oxidation) also showed seasonal variation. In winter, a relatively steep reduced major axis (RMA) slope of O3/CO suggests gas phase oxidation was the dominant mechanism of SOC production. Winter has more BrC fraction than summer, indicating higher absorbing aerosols, though the efficiency of absorbing the light was higher in summer. To assess the radiative forcing of PM2.5 on a local scale, an effective carbon ratio (ECR) was computed. The findings pointed to a local radiative heating impact caused by PM2.5. The spectral slope ratio and MAE at 250 to 300nm ratio (E2/E3) revealed a higher abundance of high molecular weight species in WSOC during summer than in winter.

Spatiotemporal Characterization and Driving Factors of Fine Particulate Matter and Its Chemical Components in the Huaihe River Basin

According to the data sets of fine particulate matter （PM2.5） and its components in 35 cities in the Huaihe River Basin from 2015 to 2021, the temporal and spatial distribution patterns of pollutants were analyzed. The influence of meteorological factors on PM2.5 concentrations was examined using a random forest model. The original series of PM2.5, sulfate （SO42-）, nitrate （NO3-）, ammonium salt （NH4+）, organic matter （OM）, and black carbon （BC） were rebuilt using KZ （Kolmogorov-Zurbenko） filtering and multiple linear regression （MLR） to quantify the effects of meteorological conditions. The results demonstrated that from 2015 to 2021, the declining rates of PM2.5, SO42-, NO3-, NH4+, OM, and BC in the Huaihe River Basin were 4.71, 0.99, 1.05, 0.77, 1.01, and 0.19 μg·（m3·a）-1, respectively. The high mass concentrations of PM2.5 and its components were concentrated in the central and western regions of the HRB, whereas those in coastal and southern cities were lower. The variance contributions of the short-term, seasonal, and long-term components of PM2.5 to the original PM2.5 sequences in 35 cities were 51.6%, 35.9%, and 7.0%, respectively. The PM2.5 in coastal cities were more affected by the short-term components. The meteorological conditions were unfavorable for PM2.5 reduction in the HRB from 2015 to 2018, whereas the meteorological conditions supported the PM2.5 decrease from 2019 to 2021. From 2015 to 2021, the contribution rates of meteorological conditions to the long-term component reductions of PM2.5, SO42-, NO3-, NH4+, OM, and BC were 28.3%, 29.1%, 31.0%, 29.3%, 27.8%, and 28.6%, respectively. The contribution rates of meteorological conditions to the long-term PM2.5 reduction were 43.4%, 25.6%, 25.5%, and 20.6% in the HRB cities in Anhui, Shandong, Jiangsu, and Henan Provinces, respectively. With the decrease in PM2.5 concentration in the HRB, the sulfur oxidation rate （SOR） increased significantly, while the nitrogen oxide oxidation rate （NOR） changed little.

Cold seep nitrogen fixation and its potential relationship with sulfur cycling.

N2 fixation is an important source of biologically available in carbon-dominated cold seep systems as little nitrogen is released by hydrocarbon seepage, thereby promoting biological productivity and the degradation of non-nitrogenous organic matter. Cold seeps are rich in diverse sources of dissolved organic matter (DOM) derived from the sinking of photosynthetic products in euphotic layer and the release of chemosynthesis products on the seafloor. However, it remains unclear whether N2 fixation is coupled to the metabolic processes of DOM, as determined by e.g., carbon, nitrogen, phosphorus, and sulfur content, for energy acquisition in sulfur-rich cold seeps. In this study, diazotroph community structure and its response to DOM compositions were revealed. Moreover, the metagenomics analysis suggested that Dechloromonas genus plays a dominant role in potential coupling N2 fixation and sulfur oxidation. Our study highlighted that sulfur oxidation in deep-sea cold seeps may serve as an energy source to drive N2 fixation.

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.

Spatial-temporal characteristics of port infrastructures on sulfur-oxide concentrations of coastal port in China

Port infrastructure is an important guarantee to support the development of shipping trade and a main link to connect shipping routes, where its construction and expansion promote economic progress whereas exacerbating regional pollution. Based on the panel data of 18 above-scale coastal ports in China from 2005 to 2020, the spatial characteristics and correlation of sulfur-oxide (SOX) concentrations are first analyzed, then the spatial Durbin model (SDM) is established to evaluate the extent of port infrastructure's impact on the concentrations, further the intermediation effects of three dimensions on the concentrations are explored. From the outcome, the influences of port infrastructures on the SOX concentrations are from decreasing the SOX concentrations through improving the operational efficiencies and increasing the SOX concentrations by adding the operational equipment, which also shows significant spatial spillover effects. In addition, the mechanical dimension as a mediation makes the trade dimension have an indirect effect on the SOX concentrations. This paper employs a spatial econometric model to analyze panel data from 18 coastal ports and ports of higher tiers in China, spanning from 2005 to 2020. It uncovers the intricate mechanism by which port infrastructure influences SOX concentration, thus providing a scientific foundation and decision support for environmental protection and sustainable port development.

To Study the Effects of Microemulsion Based Hybrid Biofuel on Emission Characteristics of CI Engine: A Short Review

AbstractMicroemulsion based fuels (MBF) have gained significant attention in recent years due to their potential to enhance combustion efficiency, reduce emissions, and improve overall engine performance. This research paper enlightens the effects of physiochemical properties on the emission characteristics of CI engine. The microemulsions are formulated using surfactants, co‐surfactants, water or alcohols, and fuel components. The effects of density, viscosity, calorific value, cold flow properties, and cetane number along with the stability and the multi‐component characteristics of (MBF) has been taken into consideration to examine its effects on Emission characteristics such as nitrogen oxides (NOx), sulfur oxides (SOx), carbon monoxide (CO), particulate matter (PM), and unburned hydrocarbons (UHC). Microemulsion‐based fuels lower emissions of NOx and PM, recognized to the more complete combustion. The review highlights various studies that have investigated the benefits of microemulsion fuels, including reduced emissions of different pollutants and thus reduce the adverse effect on environment.In conclusion, microemulsion‐based fuels show likely physiochemical properties, as well as favorable emission characteristics, with reduced NOx, SOx, CO, PM, and UHC emissions. This study highlights the potential of microemulsion‐based fuels as environment friendly alternatives, flagging the way for further research.

Hydrochemical gradients driving extremophile distribution in saline and brine groundwater of southern Poland.

Extreme environments, such as highly saline ecosystems, are characterised by a limited presence of microbial communities capable of tolerating and thriving under these conditions. To better understand the limits of life and its chemical and microbiological drivers, highly saline and brine groundwaters of Na-Cl and Na-Ca-Cl types with notably diverse SO4 contents were sampled in water intakes and springs from sedimentary aquifers located in the Outer Carpathians and the Carpathian Foredeep basin and its basement in Poland. Chemical and microbiological methods were used to identify the composition of groundwaters, determine microbial diversity, and indicate processes controlling their distribution using multivariate statistical analyses. DNA sequencing targeting V3-V4 and V4-V5 gene regions revealed a predominance of Proteobacteriota, Methanobacteria, Methanomicrobia, and Nanoarchaea in most of the water samples, irrespective of their geological context. Despite the sample-size constraint, redundancy analysis employing a compositional approach to hydrochemical predictors identified Cl/SO4 and Cl/HCO3 ratios, and specific electrical conductivity, as key gradients shaping microbial communities, depending on the analysed gene regions. Analysis of functional groups revealed that methanogenesis, sulphate oxidation and reduction, and the nitrogen cycle define and distinguish the halotolerant communities in the samples. These communities are characterised by an inverse relationship between methanogens and sulphur-cycling microorganisms.

Influence of Biofloc Technology and Continuous Flow Systems on Aquatic Microbiota and Water Quality in Japanese Eel Aquaculture

Biofloc technology (BFT) systems heavily rely on microbiota to mitigate ammonia toxicity and manage essential nutrient cycling. Understanding the diversity and functional role of microbiota within BFT-applied aquaculture systems is crucial for ensuring sustainable operations. Though some studies exist on BFT microbiota, research on microbial differences in Japanese eel aquaculture is still limited, hindering the wider application of BFT systems. In this study, we analyzed the characteristics of water quality factors and microbiota in Japanese eel (Anguilla japonica) breeding water, applying the BFT system. Using a metabarcoding approach, the diversity and community structure of aquatic microbiota were compared between BFT and continuous flow (CF) systems. The pH was significantly higher in CF water, while total ammonia nitrogen (TAN) and nitrite (NO2−-N) was higher in BFT water. Alpha diversity was significantly higher in BFT compared to CF systems, and it was correlated significantly with pH and TAN. In both BFT and CF water, the phyla Proteobacteria and Bacteroidota were found to be the most abundant. In the BFT water, a diverse array of bacterial taxa, including BFT-specific clades, were consistently present, while the microbiota in CF water was more variable and contained fewer specific taxa. In addition, bacterial functions related to nitrate reduction, sulfur compound oxidation, and chitinolysis were significantly more abundant in BFT than in CF systems. These findings highlight differences in water quality and microbiota between aquaculture systems, which can inform future research on the use of BFT for sustainable fish farming.

Investigation of blood pressure regulatory effect of bioactive peptides in complex enzyme-assisted hydrolysate from Paralichthys olivaceus

This study aimed to identify the bioactive peptides of protamex-pepsin hydrolysate obtained from Paralichthys olivaceus (POppH) and to investigate their potential vasorelaxation and blood pressure regulatory properties, both in vitro and in vivo. The effects of the peptides on endothelium-derived relaxing factors (EDRFs), such as nitric oxide and hydrogen sulfate levels, were analyzed in EA.hy926 cells, and the vasorelaxation-related PI3K/AKT/eNOS pathway activity was analyzed in EA. hy926 cells. An in vitro study revealed that POppH and leucine-glutamic acid-arginine (IER) peptide did not show any cytotoxic effects and significantly increased EDRF production via the regulation of vasorelaxation-associated PI3K/AKT/eNOS protein expression in EA.hy926 cells. An in vivo study suggested that oral administration of IER reduced systolic, diastolic, and mean arterial blood pressure in a spontaneously hypertensive rat model. The bioactive peptide IER derived from Paralichthys olivaceus could be used in the development of functional food products with blood pressure regulatory properties.

Sulfur oxidation of ferrate synthesized from sludge in the aspect of desulfurization: A parametric study

Abstract The emission of sulfur in the atmosphere poses a significant threat to human health and the environment. To address this issue, stringent regulations have been implemented to limit the sulfur content in diesel, and novel desulfurization technologies are being developed. One notable technology is oxidative desulfurization (ODS), which employs oxidants to transform sulfur compounds into their corresponding sulfones, which are relatively easier to recover. The application of high-shear mixing in ODS has been studied to increase sulfur-to-sulfone conversion by creating smaller droplets and reducing mass transfer resistance. This research investigates the application of potassium ferrate derived from drinking water treatment sludge (DWTS), in the mixing-assisted oxidative desulfurization (MAOD) of a dibenzothiophene (DBT) model fuel. Potassium ferrate was synthesized using the wet oxidation method. The study evaluated the effects of ferrate concentration (400 to 600 ppm), agitation speed (4,400 to 10,800 rpm), and temperature (40 to 60 °C) on the efficiency of DBT conversion. The results revealed that 493.2 ppm DBT conversion was achieved at 550 ppm Fe(VI) concentration, 7,600 rpm agitation speed, and 50 °C temperature. Notably, increasing Fe(VI) concentration, agitation speed, and temperature had significant effects on sulfur reduction. This study demonstrates the potential of using potassium ferrate derived from DWTS in MAOD for effective desulfurization and discusses insights into the effects of operating conditions to enhance desulfurization efficiency. Ultimately, the study contributes to the development of environmentally friendly and cost-effective desulfurization technologies.

Genomic analysis and biodesulfurization potential of a new carbon-sulfur bond cleaving Tsukamurella sp. 3OW.

Direct combustion of sulfur-enriched liquid fuel oil causes sulfur oxide emission, which is one of the main contributors to air pollution. Biodesulfurization is a promising and eco-friendly method to desulfurize a wide range of thiophenic compounds present in fuel oil. Previously, numerous bacterial strains from genera such as Rhodococcus, Corynebacterium, Gordonia, Nocardia, Mycobacterium, Mycolicibacterium, Paenibacillus, Shewanella, Sphingomonas, Halothiobacillus, and Bacillus have been reported to be capable of desulfurizing model thiophenic compounds or fossil fuels. In the present study, we report a new desulfurizing bacterium, Tsukamurella sp. 3OW, capable of desulfurization of dibenzothiophene through the carbon-sulfur bond cleavage 4S pathway. The bacterium showed a high affinity for the hydrocarbon phase and broad substrate specificity towards various thiophenic compounds. The overall genome-related index analysis revealed that the bacterium is closely related to Tsukamurella paurometabola species. The genomic pool of strain 3OW contains 57 genes related to sulfur metabolism, including the key dszABC genes responsible for dibenzothiophene desulfurization. The DBT-adapted cells of the strain 3OW displayed significant resilience and viability in elevated concentrations of crude oil. The bacterium showed a 19 and 37% reduction in the total sulfur present in crude and diesel oil, respectively. Furthermore, FTIR analysis indicates that the oil's overall chemistry remained unaltered following biodesulfurization. This study implies that Tsukamurella paurometabola species, previously undocumented in the context of biodesulfurization, has good potential for application in the biodesulfurization of petroleum oils.

Research on smoke cleaning based on Mg(OH)2/NaClO2 seawater solution

Abstract Ship exhaust emissions contain a large amount of sulfur oxides and nitrogen oxides, which have attracted widespread attention from the international community for their pollution of the atmospheric environment. In order to reduce the emissions of these pollutants, the International Maritime Organization (IMO) and other national institutions have established strict emission standards and promoted the research and application of ship exhaust desulfurization and denitrification technology. Experimental and simulation analyses were conducted on the denitrification effect of Mg(OH)2/NaClO2 solution using a cyclic spray method. Simulation analysis was carried out using cyclic spraying. The experiment compared the reaction degree and reaction time of NO in NaClO2 seawater, NaClO2 water, and Mg(OH)2/NaClO2 marine solution. The experimental result is that in the process of cyclic spray, the removal rate of NO by these three solutions can reach 100%. The reaction time of NO is 71, 86, and 90 minutes, respectively. Under the same conditions, the simulation results showed that the reaction rate of NaClO2 water solution with NO was faster, followed by NaClO2 seawater solution. The reaction rate of Mg(OH)2/NaClO2 seawater solution with NO was the slowest of the three. When the pH value exceeds 7, it effectively inhibits the production of ClO2 gas by NaClO2. The removal rate of Mg(OH)2/NaClO2 seawater solution is directly proportional to the initial concentration of NaClO2. In addition, it could be seen from the simulation cloud diagram that the removal speed of NO in the spray reactor slows down as the concentration of NO increases.

Microbial acidification by N, S, Fe and Mn oxidation as a key mechanism for deterioration of subsea tunnel sprayed concrete

The deterioration of fibre-reinforced sprayed concrete was studied in the Oslofjord subsea tunnel (Norway). At sites with intrusion of saline groundwater resulting in biofilm growth, the concrete exhibited significant concrete deterioration and steel fibre corrosion. Using amplicon sequencing and shotgun metagenomics, the microbial taxa and surveyed potential microbial mechanisms of concrete degradation at two sites over five years were identified. The concrete beneath the biofilm was investigated with polarised light microscopy, scanning electron microscopy and X-ray diffraction. The oxic environment in the tunnel favoured aerobic oxidation processes in nitrogen, sulfur and metal biogeochemical cycling as evidenced by large abundances of metagenome-assembled genomes (MAGs) with potential for oxidation of nitrogen, sulfur, manganese and iron, observed mild acidification of the concrete, and the presence of manganese- and iron oxides. These results suggest that autotrophic microbial populations involved in the cycling of several elements contributed to the corrosion of steel fibres and acidification causing concrete deterioration.

Sequential Chemical and Biological Desulphurization of High Sulfur Containing Pakistani Coal

Coal is a rich and affordable source of energy that is extensively used for different industrial purposes. However, its extensive utilization have caused a number of environmental problems. Especially, the release of different oxides of sulfur during combustion have resulted in the ongoing acid rain and global warming issues. To tackle the issue, sequential chemical and biological technologies were applied for the desulfurization of a coal sample, collected from Shahrag coal mines, in Baluchistan, Pakistan. The coal was initially de-pyritized with a 15% nitric acid (HNO3) solution. The chemically treated coal was subsequently biodesulfurized with iron oxide (Fe3O4) coated bacterial consortium IQMJ-5. The de-pyritized and biodesulfurized coal was analyzed with proximate, ultimate, FTIR, XRD, and EDX analysis. The calorific value was determined through an oxygen bomb analyzer. Following desulfurization, about 61% organic sulfur and 86.57% total sulfur were removed from the coal sample. Similarly, an increase of about 93 kcal/kg in the calorific value was detected after the treatment. These results clearly depicts the potentiality of the technology for the desulfurization of fossil fuels at the industrial scale.

Spectroscopic Study of Strain, Oxidation, and Formation of Few-Layer Graphene at Steel Surfaces Tribologically Tested against MoS2 Films.

MoS2 not only has unique optoelectronic properties realizing photonic and semiconductor applications but also serves as a promising solid lubricant in tribological three-body contacts due to its advantageous friction and wear behavior. Its functionality is defined by elementary processes including strain, oxidation processes, and material mixing. However, these mechanisms were not elucidated for MoS2 having transferred from the MoS2 film synthesized at the main body to a steel counter body during tribological ball-on-disk tests. Using spatially and spectrally high-resolved Raman spectroscopy, we study the compressive and tensile strain within the MoS2 transfer material and analyze the oxidation of molybdenum, sulfur, and iron. In addition, we elaborate on the impact of transition metals modifying the MoS2 films on the strain distribution and oxidation processes. Decreasing intensities of the MoS2 Raman lines are accompanied with enhanced intensities of sulphur and molybdenum oxide Raman signatures which are particularly agglomerated at the edges of the tribological track. The formation of tribochemical oxides, including Mo4O11 in the Magnéli-phase, depends weakly on the type of modifying element, and an oxidation of a modification element itself is not detected. We also identified a tribologically induced formation of disordered few-layer graphene at counter-body surface areas which experienced weak thermo-mechanical tribological load. Our results characterize structural and chemical features of the MoS2 transfer material, thus predicting material failure at the microscopic level.