Search Results (62)

Recently, the occurrence of phosphine-resistant pests has been increasingly reported in many countries. In this study, the efficacy of carbonyl sulfide (COS) on phosphine-resistant and phosphine-susceptible strains of the rice weevil, Sitophilus oryzae, was evaluated to determine the applicability of COS as a fumigant to control phosphine resistance. S. oryzae at the egg, larval and adult stages was treated with phosphine and COS to determine the 50 and 99% lethal concentration time (LCt₅₀ and LCt₉₉, respectively) values. The LCt₅₀ values of phosphine for phosphine-susceptible S. oryzae at the egg, larval and adult stages were 1.44, 0.63, and 0.66 mg h/L, respectively, and those for phosphine-resistant S. oryzae were 30.65, 17.60, and 8.37 mg h/L, respectively. In contrast, the LCt₅₀ values of COS for phosphine-susceptible S. oryzae at the egg, larval, and adult stages were 284.19, 171.11 and 212.55 mg h/L, respectively, and those for phosphine-resistant S. oryzae were 289.78, 149.87 and 229.06 mg h/L, respectively. The COS-resistance ratios were 1.02, 0.88, and 1.08 for S. oryzae at the egg, larval, and adult stages, respectively. These results indicate that the efficacy of COS is similar for phosphine-susceptible and phosphine-resistant pests, suggesting that COS can be used to control phosphine-resistant grain pests. Full article

It is necessary to find sustainable alternatives to the conventional fossil fuels used by the transportation sector today. For the hard-to-abate aviation and heavy transport, liquid hydrocarbon fuels derived from biomass via pyrolysis are a viable option. Biomass pyrolysis oils need upgrading by hydroprocessing before they can be further processed into fuels at a refinery. Due to reactor plugging and catalyst deactivation in one-step hydroprocessing, it has been proposed to add a stabilization step at a lower temperature to convert the most reactive compounds in pyrolysis oil, such as carbonyls, to less reactive species such as alcohols. Three different catalysts, Ni/Al₂O₃, sulfided NiMo/Al₂O₃, and Pt/Al₂O₃, were studied for stabilizing three different model compounds, furfural, guaiacol, and octanoic acid, alone and as a mixture in a batch reactor at 90 bar initial H₂ pressure and 180 °C. The order of performance was determined to be Ni/Al₂O₃ > Pt/Al₂O₃ > sulfided NiMo/Al₂O₃ in these conditions. The Ni/Al₂O₃ catalyst showed both the highest overall conversion, the most fully hydrogenated compounds, and the highest carbonyl conversion. The effect of adding 1172 wt-ppm sulfur to the feed was also investigated, which showed that Ni/Al₂O₃ was the most sensitive catalyst to sulfur poisoning. Full article

β-Keto sulfides are a class of compounds containing both carbonyl (C=O) and thioether (C–S–C) functionalities, exhibiting significant potential in the field of medicinal chemistry. This study employs the silyl enol ether as the substrate, enabling the formation of C–S bonds under catalyst- and additive-free conditions, thereby facilitating the efficient synthesis of β-keto sulfides. The reaction proceeds rapidly and efficiently, exhibiting a broad substrate scope, and a total of 31 target compounds were synthesized with up to 95% yields. Full article

Hydrogen sulfide (H₂S), nitric oxide (NO), and carbon monoxide (CO) are now recognized as key gasotranmitters that regulate vascular function, contributing to vasodilation, angiogenesis, inflammation control, and oxidative balance. Initially regarded as toxic gases, they are produced on demand by specific enzymes, including cystathionine γ-lyase (CSE), endothelial nitric oxide synthase (eNOS), and heme oxygenase-1 (HO-1). Their activity is tightly controlled by redox-sensitive pathways. Reactive oxygen species (ROS), particularly superoxide and hydrogen peroxide, modulate gasotransmitter biosynthesis at the transcriptional and post-translational levels. Moreover, ROS affect gasotransmitter availability through oxidative modifications, including thiol persulfidation, nitrosative signaling, and carbonylation. This redox regulation ensures a tightly coordinated response to environmental and metabolic cues within the vascular system. This review synthesizes the current understanding of redox–gasotransmitter interactions, highlighting how ROS modulate the vascular roles of H₂S, NO, and CO. Understanding these interactions provides critical insights into the pathogenesis of cardiovascular diseases and offers potential redox-targeted therapies. Full article

Soil heavy metal contamination poses critical challenges to ecological sustainability in mining regions, particularly in acidic soils from copper sulfide mines. This study developed a sustainable remediation strategy using a carbonyl iron powder–biochar composite (CIP@BC) derived from agricultural waste (rice husk) and industrial byproducts. The composite was synthesized through an energy-efficient mechanical grinding method at a 10:1 mass ratio of biochar to carbonyl iron powder, aligning with circular economy principles. Material characterization revealed CIP particles uniformly embedded within biochar’s porous structure, synergistically enhancing surface functionality and redox activity. CIP@BC demonstrated exceptional Cu²⁺ immobilization capacity (910.5 mg·g⁻¹), achieved through chemisorption and monolayer adsorption mechanisms. Notably, the remediation process concurrently improved key soil health parameters. Soil incubation trials demonstrated that 6% CIP@BC application elevated soil pH from 4.27 to 6.19, reduced total Cu content by 29.43%, and decreased DTPA-extractable Cu by 67.26%. This treatment effectively transformed Cu speciation from bioavailable to residual fractions. Concurrent improvements in electrical conductivity (EC), cation exchange capacity (CEC), soil organic matter (OM), and soil water content (SWC) collectively highlighted the composite’s multifunctional remediation potential. This study bridges environmental remediation with sustainable land management through an innovative waste-to-resource approach that remediates acidic mine soils. The dual functionality of CIP@BC in contaminant immobilization and soil quality restoration provides a scalable solution. Full article

As a renewable and degradable biomass material, cellulose diacetate (CDA) has significant development potential and has gained widespread interest from researchers. However, its poor thermal stability at high temperatures limits its practical use in the extrusion process and restricts its applications in other fields, such as high-heat airflow filters, battery separators and special textile materials. To enhance the thermal stability of CDA, three heat-resistance additives, i.e., polyphenylene sulfide (PPS), polycarbonate (PC) and polyimide (PI), were introduced to synthesize PPS/CDA, PC/CDA and PI/CDA composite materials through melt extrusion. The incorporation of three heat-resistant additives increased the glass transition temperature (T_g), initial melting temperature (T_mⁱ) and final melting temperature (T_m^f) of the composites, and it reduced the heat loss at 195 °C. After conducting the isothermal thermogravimetry test for 3 h at 215 °C in an air atmosphere, the weight loss of PPS/CDA, PC/CDA and PI/CDA composites was 4.6%, 4.1% and 3.7%, respectively, which was 5.1% lower than that of pure CDA. Morphology characterization tests using a 3D digital microscope and a field emission scanning electron microscope (FESEM) revealed the compatibility order with CDA as the following: PC > PPS > PI. Additionally, Fourier transform infrared spectroscopy (FT–IR) disclosed that hydrogen bonds were formed between heat-resistant additives and CDA molecules, and the carbonyl groups in CDA showed conjugation and hyperconjugation effects with the benzene rings in the additives. Therefore, the enhanced thermal stability of CDA composites can be attributed to the molecular entanglement and crosslinking between additives and CDA molecules. Full article

SO₂ emissions are a major source of air pollution, and the catalytic reduction of SO₂ to elemental sulfur by CO represents a promising solution. This study investigates the effects of Fe doping and pre-sulfurization on the catalytic performance of LaCoO₃ perovskite catalysts. A series of Fe-doped LaCoO₃ perovskites were synthesized via the sol–gel method and evaluated for the catalytic reduction of SO₂ by CO. The results showed that LaCo_0.8Fe_0.2O₃ exhibited the highest catalytic performance, achieving 84.0% SO₂ conversion at 500 °C. The oxygen-free sulfurization (OFS) treatment compared with oxygen-assisted sulfurization (OAS) treatment significantly enhanced the activity, reaching a SO₂ conversion of 95.9% from 80.0% at 450 °C with the lower byproduct generation. Characterization analyses demonstrated that the OFS treatment facilitated the formation of active sulfur species and oxygen vacancies on the catalyst surface while also enhancing the adsorption capacity of the catalyst for the reactant gases. These factors were identified as key contributors to the improved catalytic performance, driven by the combination of redox and carbonyl sulfide (COS) intermediate mechanism. The findings suggest that the OFS treatment is an effective strategy to improve the catalytic reduction of SO₂ by CO, offering a more environmentally friendly solution for SO₂ emission control through resource utilization. Full article

In contemporary times, wastewater treatment plants (WWTPs) were recognized as substantial sources of odorous emissions, potentially impacting nearby communities’ sensory experience. This study investigates the half-lives (T½) of odorous compounds emitted from WWTPs and their degradation due to atmospheric hydroxyl radicals (•OH) in different environmental settings. The calculated half-lives of specific odorants in rural areas ranged from 31.36 min to 517.33 days, in urban areas from 42.50 min to 1550 days, and in the marine boundary layer from 42.50 min to 129,861 days. These results show that compounds with high reactivity and short T½, such as methanethiol and ethanethiol, degrade rapidly and are less likely to contribute to long-term odor nuisances. In contrast, compounds with longer half-lives, such as carbonyl sulfide and ammonia, persist longer in the atmosphere, with higher potential for sustained odor issues. The findings suggest that •OH plays a significant role in degrading odorous compounds. These insights into odorant–oxidant kinetics may aid in predicting atmospheric half-lives and their contribution to secondary aerosol formation, thus informing regulatory and mitigation strategies to improve air quality. Full article

The complex of hypofluorous acid with acetonitrile—HOF•CH₃CN—is the only substance possessing a truly electrophilic oxygen. This fact makes it the only tool suitable for transferring oxygen atoms to sites that are not accessible to this vital element. We will review here most of the known organic reactions with this complex, which is easily made by bubbling dilute fluorine through aqueous acetonitrile. The reactions of HOF•CH₃CN with double bonds produce epoxides in a matter of minutes at room temperature, even when the olefin is electron-depleted and cannot be epoxidized by any other means. The electrophilic oxygen can also substitute deactivated tertiary C-H bonds via electrophilic substitution, proceeding with full retention of configuration. Using this complex enables transferring oxygen atoms to a carbonyl and oxidizing alcohols and ethers to ketones. The latter could be oxidized to esters via the Baeyer–Villiger reaction, proving once again the validity of the original Baeyer mechanism. Azines are usually avoided as protecting groups for carbonyl since their removal is problematic. HOF•CH₃CN solves this problem, as it is very effective in recreating carbonyls from the respective azines. A bonus of the last reaction is the ability to replace the common ¹⁶O isotope of the carbonyl with the heavier ¹⁷O or ¹⁸O in the simplest and cheapest possible way. The reagent can transfer oxygen to most nitrogen-containing molecules. Thus, it turns practically any azide or amine into nitro compounds, including amino acids. This helps to produce novel α-alkylamino acids. It also attaches oxygen atoms to most tertiary nitrogen atoms, including certain aromatic ones, which could not be obtained before. HOF•CH₃CN was also used to make five-member cyclic poly-NO derivatives, many of them intended to be highly energetic materials. The nucleophilic sulfur atom also reacts very smoothly with the reagent in a wide range of compounds to form sulfone derivatives. While common sulfides are easily converted to sulfones by many orthodox reagents, electron-depleted ones, such as R_f-S-Ar, can be oxidized to R_f-SO₂-Ar only with this reagent. The mild reaction conditions also make it possible to synthesize a whole range of novel episulfones and offer, as a bonus, a very easy way to make S^xO₂, x being any isotope variation of oxygen. These mild conditions also helped to oxidize thiophene to thiophen-S,S-dioxide without the Diels–Alder dimerizations, which usually follow such dioxide formation. The latter reaction was a prelude to a series of preparations of [all]-S,S-dioxo-oligothiophenes, which are important for the efficient preparation of active layers in field-effect transistors (FETs), as such oligomers are considered to be important for organic semiconductors for light-emitting diodes (LEDs). Several types of these oligothiophenes were prepared, including partly or fully oxygenated ones, star-oligothiophenes, and fused ones. Several [all]-S,S-dioxo-oligo-thienylenevinylenes were also successfully prepared despite the fact that they also possess carbon–carbon p centers in their molecules. All oxygenated derivatives have been prepared for the first time and have lower HOMO-LUMO gaps compared to their parent compounds. HOF•CH₃CN was also used to oxidize the surface of the nanoparticles of oligothiophenes, leaving the core of the nanoparticle unchanged. Several highly interesting features have been detected, including their ability to photostimulate the retinal neurons, especially the inner retinal ones. HOF•CH₃CN was also used on elements other than carbon, such as selenium and phosphor. Various selenides were oxidized to the respective selenodioxide derivatives (not a trivial task), while various phosphines were converted efficiently to the corresponding phosphine oxides. Full article

Carbonyl sulfide (COS) is the most abundant and longest-lasting organic reduced sulfur compound in the atmosphere. Removing it is a critical and challenging aspect in desulfurization technology in order to comply with global restrictions on harmful emissions. Catalytic hydrolysis refers to the process whereby COS reacts with water under the influence of a catalyst to generate carbon dioxide and hydrogen sulfide. Due to its high conversion rate, minimal side reactions, no hydrogen consumption, and mature technology, it has emerged as the most crucial COS removal method at present. Since its inception in the 1940s, research on the catalytic hydrolysis of COS has witnessed encouraging progress over the past several decades. This review summarizes recent advancements in this field. In this review, the evaluation metrics, influencing factors, and reaction mechanism for the COS hydrolysis reaction are briefly introduced. The recent advancements in COS hydrolysis catalysts in recent years are emphasized. Additionally, the existing challenges and potential solutions in this field are also proposed. Finally, the future development directions for this research area are envisioned. The purpose of this review is to offer a reference for the subsequent design and research of high-activity and high-stability hydrolysis catalysts. Full article

We report in this contribution the synthesis and in vitro biological evaluation of a novel class of chiral thiazoloisoindolinone scaffolds as potent inhibitors against human farnesyltransferase (FTase-h). The targeted products, sulfides (4), sulfoxides (5,6), and sulfones (7), containing up to three points of diversification, were obtained in a short-step sequence starting from the available and cost-effective L-cysteine hydrochloride (1), which is the source of N and S atoms and the chiral pool, and α-carbonyl benzoic acids (2), which are isoindolinone precursors. Concisely, the key ester intermediates (1) provide (a) sulfide-amides (4) by solvent-free amidation, (b) sulfoxides (5,6) by selective S-oxidation using NaIO₄, and (c) sulfones (7) by oxidation using MMPP. Finally, the obtained N,S-acetal systems have shown promising inhibitory activities on FTase-h in the nanomolar range with excellent half maximal inhibitory concentration (IC₅₀) values up to 4.0 nanomolar (for example, 25.1 nM for sulfide 4bI, 67.3 nM for sulfone 7bG, and more interesting of 4.03 nM for sulfoxide 5bG). Full article

In this work, a highly sensitive, selective, and industrially compatible gas sensor prototype is presented. The sensor utilizes three distributed-feedback quantum cascade lasers (DFB-QCLs), employing wavelength modulation spectroscopy (WMS) for the detection of hydrogen sulfide (H₂S), methane (CH₄), methyl mercaptan (CH₃SH), and carbonyl sulfide (COS) in the spectral regions of 8.0 µm, 7.5 µm, and 4.9 µm, respectively. In addition, field-programmable gate array (FPGA) hardware is used for real-time signal generation, laser driving, signal processing, and handling industrial communication protocols. To comply with on-site safety standards, the QCL sensor prototype is housed in an industrial-grade enclosure and equipped with the necessary safety features to ensure certified operation under ATEX/IECEx regulations for hazardous and explosive environments. The system integrates an automated gas sampling and conditioning module, alongside a purge and pressurization system, with intrinsic safety electronic components, thereby enabling reliable explosion prevention and malfunction protection. Detection limits of approximately 0.3 ppmv for H₂S, 60 ppbv for CH₃SH, and 5 ppbv for COS are demonstrated. Noise-equivalent absorption sensitivity (NEAS) levels for H₂S, CH₃SH, and COS were determined to be 5.93 × 10⁻⁹, 4.65 × 10⁻⁹, and 5.24 × 10⁻¹⁰ cm⁻¹ Hz^−1/2. The suitability of the sensor prototype for simultaneous sulfur species monitoring is demonstrated in process streams of a hydrodesulphurization (HDS) and fluid catalytic cracking (FCC) unit at the project’s industrial partner, OMV AG. Full article

Carbonyl sulfide (COS), an organosulfur compound commonly present in industrial gases, poses significant challenges for environmental protection and industrial processes due to its toxicity. This paper reviews recent advancements in the development of catalysts for COS hydrolysis, emphasizing the effects of various supports and active components on catalyst performance, as well as the mechanisms underlying the hydrolysis reaction. Traditional supports like γ-Al₂O₃ demonstrate high activity for COS hydrolysis but are susceptible to deactivation. In contrast, novel supports such as activated carbon, TiO₂, and ZrO₂ have garnered attention for their unique structures and properties. The incorporation of active components, including alkali metals, alkaline earth metals, transition metals, and rare earth metals, significantly enhances the hydrolysis efficiency and resistance to deactivation of the catalysts. Additionally, this paper outlines three primary mechanisms for COS hydrolysis: the alkali-catalyzed mechanism, the Langmuir–Hinshelwood model, and the Eley–Rideal model mechanism, as well as the thiocarbonate intermediate mechanism, which collectively elucidate the conversion of COS into the H₂S and CO₂ catalyzed by these systems. Future research efforts will concentrate on developing high-activity, high-stability, and cost-effective COS hydrolysis catalysts, along with a more in-depth exploration of the reaction mechanisms to facilitate the efficient removal of COS from industrial emissions. Full article

The gas phase reaction of fluorine atoms with carbonyl sulfide, F + OCS → SF + CO (1), has been investigated over a wide temperature range, T = 220–960 K, in a discharge-flow system combined with mass spectrometry for the analysis of the reactive mixture. The reaction rate coefficient was determined as a function of temperature using both absolute (under pseudo-first-order conditions using an excess of F atoms) and relative rate methods: k₁ = (8.95 ± 0.52) × 10⁻¹¹ exp((102 ± 20)/T) cm³ molecule⁻¹ s⁻¹ (with an estimated total uncertainty of 15% independent of temperature). The SF radical was observed as the main primary reaction product. The experimental results are supported by theoretical calculations, which evidence that the reaction is exothermic with a weak negative temperature dependence. Full article

During the process of liquefied petroleum gas (LPG) exploitation, various sulfide-containing gases are produced, which significantly bring about corrosion attacks to copper equipment and facilities. Investigations on the effects of sulfides, hydrogen sulfide (H₂S), carbonyl sulfide (COS), and ethanethiol (C₂H₆S) on copper corrosion and synergistic mechanisms are of great significance for LPG production. This paper studied the synergistic corrosion effects of mixed sulfide-containing gases in LPG on copper plates, including the influence of H₂S + COS, H₂S + C₂H₆S, as well as H₂S + COS + C₂H₆S. The results showed that there exists an apparent synergistic effect between different sulfide-containing gases, which decreased the critical point of corrosion and enhanced the severity of copper corrosion. SEM observation on corrosion products with the addition of different sulfide-containing gases demonstrated that the microstructures of corrosion products are significantly different, which reveals different corrosion mechanisms. By characterizing the corrosion products on copper surfaces, corresponding corrosion mechanisms were proposed. Individual H₂S reacts with copper directly as chemical corrosion. The presence of water leads to the dissolution of H₂S into water film at the copper surface and results in electrochemical corrosion in nature. COS tends to decompose into acidic gas H₂S and CO₂, which accelerates the electrochemical corrosion at the copper surface. C₂H₆S can react with copper directly as chemical corrosion. A mixture of different sulfur-containing gases enhanced the corrosion attack by synergistic effect. Full article