Sulfur Concentration Research Articles

Swelling Behaviors of Natural Rubber/Solvent Systems Based on the Extended Modified Double Lattice Model

AbstractSwelling experiments are conducted on nonfiller natural rubber using four solvents (toluene, cyclohexane, tetrahydrofuran (THF), and methylethylketone (MEK)) over temperatures from 10 to 70 °C. Toluene, cyclohexane, and THF, classified as effective solvents, show swelling ratios between 3 and 7, influenced by the crosslink density of the rubber. MEK, however, has a lower ratio of 1.5 to 2. Temperature has a minor impact on swelling compared to the crosslink density. The study evaluates the Extended Modified Double Lattice (EMDL) model for its mixing contribution in polymer network swelling, aiming to improve the Flory–Hüggins (FH) model. The superiority of EMDL above FH is in the boundary condition at the unvulcanized state, the former aligning its interaction energy with values from solvent activities in primary linear polymer/solvent solutions, unlike the FH model. The EMDL model also accounts for oriented interactions in polar solvents through a secondary lattice, linking specific interaction energy with solvent dipole moments. The study observes a nonlinear correlation between crosslinking density and sulfur amount, proposing a nonrandom mixing at lower sulfur concentrations. This model shows strong alignment with experimental data, suggesting that replacing the FH model's mixing contribution with the EMDL model could improve results with minimal additional complexity.

Eco-friendly catalyst in ultrasonic-assisted oxidative desulfurization of dibenzothiophene compound

10 W t.% WO3@activated carbon was prepared from apple peel and used as a catalyst in ultrasonic-assisted oxidative desulfurization of dibenzothiophene@octane in the presence of H2O2 as an oxidant. The physical characteristics of the prepared catalyst were investigated using X-ray diffraction, N2-adsorption-desorption, and scanning electron microscope. The reaction time, oxidant dose, catalyst dose, and sulfur compound concentration were studied to reach 99 % dibenzothiophene removal at ambient conditions and after four cycles the efficiency of dibenzothiophene removal can reach 97.7 %. The kinetic parameters were studied and indicate the ultrasonic-assisted oxidative desulfurization reaction is pseudo-second order.

Effective Carrier Lifetime in Ultrashort Pulse Laser Hyperdoped Silicon: Sulfur Concentration Dependence and Practical Limitations

Charge carrier lifetime is a crucial material parameter in optoelectronic devices and knowing the dominant recombination channels points the way for improvements. The effective carrier lifetime τeff of surface‐passivated hyperdoped (hSi) and nonhyperdoped “black” (bSi) silicon by quasi‐steady‐state photoconductance decay (QSSPC) measurements and its evolution upon controlled wet‐chemical etching are studied. Sample preparation involves the irradiation of Si by numerous ultrashort laser pulses either in SF6 for hSi or ambient atmosphere for bSi. Findings suggest that the hSi is composed of a double layer: 1) an amorphous resolidified top layer with about 92% of the total incorporated sulfur that accounts for the sub‐bandgap absorptance and 2) a crystalline layer underneath in which sulfur concentration tails off toward the Si substrate. The effective lifetime is deconstructed by a 1D simulation to quantify the impact of the local lifetime of the defect‐rich top layer, τtop. It is found that by the QSSPC method, a maximum τtop for 1) can be estimated. For 2), τtop between 2 and 8 ns is estimated. The bSi sample shows a faster lifetime recovery upon etching which suggests that in hSi samples purely laser‐induced defects are not limiting the carrier lifetime compared to sulfur‐related defects.

Contamination of depressional wetlands in the Mpumalanga Lake District of South Africa near a global emission hotspot

The Mpumalanga Lake District (MLD) of South Africa hosts a regionally unique cluster of water bodies of great importance for wetland biodiversity. It is also located close to a global hotspot for coal-fired power station emissions but the local impacts from these sources of pollution are poorly understood. Sediment cores from three contrasting wetlands were 210Pb dated and analysed for a range of contaminants linked to fossil fuel combustion, including trace elements, Hg, sulphur and spheroidal carbonaceous fly-ash particles (SCPs). At the two sites with pre-industrial (1900) baseline sediments, Pb, Zn and especially Cr concentrations and fluxes showed significant increases in the impact period (post-1975). Mercury showed the greatest proportional increase in flux (>4-fold) of all trace metals. Mercury and sulphur concentrations and fluxes showed highly significant correlations with emissions over the corresponding periods, while SCPs in sediments also closely tracked emissions. In a global context, levels of sediment contamination are relatively minor compared with other heavily industrialised regions, with only Cr exceeding the sediment Probable Effects Concentration for biological impact post-1975. Despite the relatively large increases in Hg, concentrations do not reach the Threshold Effects Concentration. The unexpectedly low levels of contamination may be due to i) low levels of many trace contaminants in South African coals compared to global averages, ii) prevailing recirculation patterns which transport pollution away from the study area during the wet season, minimising wet deposition, and iii) pollutant remobilisation through desiccation of wetlands or volatilization. The effects of hydrology and sediment accumulation rates lead to differential transport and preservation of organic-associated and more volatile contaminants (e.g. Hg, S) relative to non-volatile trace elements in wetlands of the MLD. The greatest fluxes of Hg and S are recorded in the site with the highest catchment: lake area ratio, lowest salinity and greatest sediment organic matter content.

Impact of sulfur addition on the structure and dynamics of Ni–Nb alloy melts

We investigated the change in the structure and dynamics of a Ni–Nb bulk metallic glass upon sulfur addition on both microscopic and macroscopic scales. With the sulfur concentration of 3 at. %, where the composition Ni58Nb39S3 exhibits the best glass forming ability in the investigated sulfur concentration range, both the equilibrium and undercooled melt dynamics remain almost unchanged. Only in the glassy state does sulfur seem to result in mass transport less decoupled to the viscosity of the undercooled liquid, where the measured Ag tracer diffusion coefficient is slower in the ternary alloy. With the structural disorder introduced by the alloying sulfur, the improved glass forming ability is attributed to geometrical frustration, where crystal nucleation requires a depletion of sulfur and hence long range diffusion, as long as no primary sulfur-containing crystalline phase is involved.

Potentially Harmful Elements (As, Sb, Cd, Pb) in Soil Polluted by Historical Smelting Operation in the Upper Silesian Area (Southern Poland)

This study aimed at determining the concentration and possibility of migration of potentially harmful elements (PHEs) in soils and mining and metallurgical waste in the Silesian-Cracow region. Our research was carried out in selected locations of Ruda Śląska, Świętochłowice, Bytom, and in the Olkusz region (Bukowno) in southern Poland. The concentrations of metals (e.g., Ag, Ba, Ca, Cd, Cu, Fe, Mg, Mn, Pb, Sr, Zn), metalloids (As, Sb), and sulphur were determined in 33 soil samples (with a depth range of 0.0–0.3 m) and 12 slag samples. These studies show an increased concentration of metals, metalloids, and sulphur, exceeding the level of regional geochemical background. The research results indicate that the degree of the chemical transformation of soils in the analysed regions of Ruda Śląska, Bytom, and Bukowno is advanced. This highlights the high concentrations of most metals, i.e., arsenic, antimony, and sulphur, in the surface layer of soils (topsoil) due to historic Zn-Pb ore mining and Zn and Fe metallurgy. The presence of both primary and secondary metal sulphides, sulphates, carbonates, oxides/hydroxides, silicates, and aluminosilicates was found in the mineral composition of soils and slags.

Influences of Sulfur-Containing Components on the Key Phases of FeS Spontaneous Combustion Dynamics

ABSTRACT In petroleum storage tanks, sulfur-containing crude oil continues to corrode equipment, generating sulfur corrosion products such as FeS. These products exhibit rapid exothermic reactions upon contact with air, thereby increasing the risk of fires and explosions. Additionally, sulfur monomers precipitated from sulfur or other compounds present in crude oil can adhere to FeS, consequently altering its spontaneous combustion characteristics. To explore the impact of associated sulfur content on the spontaneous combustion characteristics of FeS during its formation, this research synthesized FeS and its sulfur mixtures with sulfur concentrations of 5%, 10%, 15%, and 20%. These mixtures were prepared using a liquid-phase method, which involved the synthesis of self-made active FeS followed by the addition of different sulfur components. Differences in the spontaneous combustion characteristics of the five groups of samples were investigated in stages by simultaneous thermal analysis. The trends of the characteristic parameters of spontaneous combustion of FeS with different percentages of sulfur-containing components were analyzed. Finally, the apparent activation energy values of FeS with FeS and its associated sulfur were calculated by using thermodynamic analysis in the room-temperature spontaneous combustion stage (RT-75℃) and high temperature combustion stage (160–250℃). The findings indicate that the presence of sulfur components enhances the reactivity of FeS, yet reduces its oxygen absorption saturation threshold, thus advancing the oxygen absorption endpoint and facilitating entry into the high-temperature combustion stage. Moreover, FeS and its associated sulfur exhibit prolonged sustained combustion times when the sulfur component percentage is below 10%, favorably influencing the combustion behavior of FeS. As the percentage of sulfur component increases (from 10% to 20%), the combustion duration temperature rises from 60°C to 95°C. Additionally, an increase in the percentage of sulfur component (from 10% to 20%) leads to a higher combustion temperature. The activation energies of the five samples were determined using the Flynn-Wall-Ozawa (FWO) and Kissinger-Akahira-Sunose (KAS) kinetic methods. During the room temperature spontaneous combustion stage, the activation energy increases from 65.05 kJ/mol to 112.44 kJ/mol as the percentage of sulfur component rises from 0% to 20%. During the high temperature combustion stage, the activation energy increased from 108.32 kJ/mol to 214.49 kJ/mol with the increase in the percentage of sulfur component. FeS and its associated sulfur necessitate energy to propel the process due to heat absorption from the melting of sulfur monomers. As the reaction progresses into the high temperature stage, the required activation energy escalates accordingly.

Factors influencing the hydration kinetics of ye'elimite; effect of free lime

This study investigates factors influencing the hydration of ye'elimite, comparing stoichiometric ye'elimite-rich clinkers with and without free lime (Y-C and Y, respectively). Although the hydration sequences and products were similar, there were notable differences in their kinetics. Y-C exhibited rapid hydration upon contact with water, followed by a significant slowdown within minutes. Contrary, Y demonstrates a slower early hydration, but reached the main hydration period earlier and proceeded more rapidly thereafter. Solution analyses revealed higher initial calcium and aluminium concentrations for Y-C, while the sulfur concentration was reduced. This was attributed to the rapid dissolution of free lime, along with some ye'elimite, resulting in the instantaneous formation of ettringite and aluminium hydroxide. Consequently, the solution composition was altered, causing delayed onset of monosulfate formation and main hydration period. These findings contribute to understanding the hydraulic reactivity of ye'elimite and its potential implications for cement production processes.

Optimized sulfur curing of pulse-damping rubber tubes

In pumping systems present in the industrial field, positive displacement pumps are used due to the high manometric loads and the characteristics of the extracted fluid. However, this type of pump provides a pulsating flow in the system that causes large pressure fluctuations, reducing the useful life of the installations. Because of this problem, pulsation dampers (attenuators) are used in the system in order to promote a more continuous flow and the good functioning of the process. In-line type attenuators feature a flexible tube composed of elastomer, whose viscoelastic behavior causes flow attenuation. The objective of this work is to evaluate whether there is a relationship between the sulfur content present in blends of natural rubber (NR) and synthetic rubber of the Butadiene Styrene (SBR) and the performance of tubular attenuators in a pumping system with pulsating flow. Four NR/SBR rubber blends with different sulfur concentrations in the formulation (0.5; 1.5, 3.0 and 4.5 phr) were tested. The rubbers were characterized using Fourier Transform Infrared Spectroscopy (FTIR) and their mechanical properties were analyzed using mechanical tensile tests. The efficiency of the attenuators was evaluated through bench tests that simulate pumping systems in the field. The results of the mechanical tests showed significant relationships with the performance of the attenuators in experimental tests. In attenuation tests, blends with 1.5; 3.0 and 4.5 phr sulfur had attenuation results of 27.06 %, 9.70 % and 1.61 %, respectively. The 0.5 phr attenuator could not withstand the applied loads due to lack of elastic properties. Thus, it was found that materials with a lower modulus of elasticity had greater efficiency in attenuating the pulsating flow and greater compliance, in which the attenuator that was formulated with 1.5 phr of sulfur showed 25.45 % greater pulsation damping than the stiffer material.

Thiourea modulated supercapacitive behavior of reduced graphene oxide

In this report, we investigated the role of the concentration of nitrogen and sulfur containing thiourea in modulating the electrochemical properties of reduced Graphene Oxide (rGO) by controlling the percentage of heteroatoms on the rGO surface. The synthesis route involved the preparation of Graphene Oxide (GO) using an improved method of synthesis in an economical way by reducing the volume of concentrated acids used. Furthermore, GO is reduced by using different mass proportions of thiourea via a simple reflux method. Characterization of the rGO samples by Fourier Transform Infrared (FTIR) spectroscopy, Raman spectroscopy, X-ray Diffraction (XRD), Scanning Electron Microscopy with Energy Dispersive X-ray Spectroscopy (SEM-EDAX) and elemental analysis through CHNS analyzer exhibited successful doping and impact of nitrogen and sulfur atoms on the graphene framework. The comparative electrochemical performance from Cyclic Voltammograms (CV), Galvanostatic Charge Discharge (GCD) profiles and Electrochemical Impedance Spectroscopy (EIS) measurements on the various rGO samples revealed the superiority of 1:8rGO having 15.190 wt% of nitrogen and 26.849 wt% of sulfur and S/N ratio of 1.768, in delivering highest specific capacitance of 465.21 F·g−1 at 1 mV·s−1 scan rate with a remarkable cyclic stability exhibiting a capacitive retention of 119 % and offering lowest charge transfer resistance and diffusion resistance. The study also demonstrated detrimental effect of excess thiourea on electrochemical properties of rGO. This work suggests an effective and simple approach for optimizing the nitrogen and sulfur content in rGO to enhance its electronic properties using thiourea.

A study on structural and electronic properties of WS2/SnS2 composite thin films by CBD method

The composite WS2/SnS2 thin films deposited by CBD have been studied for variations in deposition time and sulfur concentration. XRD results show a polycrystalline hexagonal phase with crystallite size varying from ∼ 3.56 nm to ∼ 16.35 nm in composite thin films. The optical absorption spectra of S-2 show maximum absorption peaks in 380 nm to 800 nm. The band gap was calculated to be ∼ 1.52 eV to ∼ 2.5 eV. We measured the current–voltage characteristics across the junction to determine the transport properties. A photodetector application involving the WS2/SnS2 composite structure shows a maximum specific detectivity of 6.2 x 1013 Jones. The reason for varying the electrical parameters discussed in this work.

Combination Effects of Sulfur Fertilizer and Rhizobium Inoculant on Photosynthesis Dynamics and Yield Components of Soybean

Sulfur (S) fertilization and rhizobium inoculation are important agronomic practices for improving soybean growth and yield. However, their combined effects on yield components and the resultant impacts on yield need further investigation. Our study aimed to verify the combined effects of S fertilizer and rhizobium inoculant on the yield components and seed yield of soybeans, as well as photosynthesis dynamics during the V5–R6 growth stages. A randomized block design incorporating two factors was employed for field experiments on soybean, involving the application of five rates of sulfur (0, 5.0, 9.8, 14.8, and 19.6 kg S ha−1) with rhizobium inoculation or without. A reduction of 50% in mineral fertilizer according to farmer practice (FP) was applied alongside different rates of sulfur for field experiments on soybeans. The findings indicated that the application of sulfur fertilization significantly enhanced soybean yield by increasing the number of grains per plant (NG) and the number of pods per plant (NP). Maximum grain yield was reached under treatment with an S rate of 19.6 kg S ha−1, which increased NG by 39% more than an S rate of 0 kg S ha−1. Correlation analysis indicated that higher photosynthesis was closely associated with increased yield components. This study demonstrated that applying S fertilizers could improve soybean production by combining the appropriate sulfur concentration and rhizobia inoculation.

Activated carbon modification for real diesel adsorptive deep desulfurization: experiments and modeling

This study examined the desulfurization capacity of a high specific surface area activated carbon (AC) and its modifications for real diesel fuel of different sulfur concentrations. Adsorbent’s evaluation strategy included desulfurization experiments under batch and continuous conditions. Batch experiments were conducted by a homogeneous stirring of adsorbent and diesel fuel, while for the continuous tests, a fixed bed reactor was used to generate breakthrough desulfurization curves. In the fixed bed reactor’s tests, the sulfur removal – considering an initial concentration of about 6 parts per million weight (ppmw) – was substantial for the first 30 ml fuel per gram of adsorbent. For this specific quantity, the total sulfur content of the cumulatively processed fuel was less than 2 ppmw. The batch experimental results are elaborated using a mechanistic kinetic model for batch adsorption considering the total sulfur mass balance. Mass transfer coefficients are derived this way for all the conditions and adsorbents tested. The adsorption equilibrium data from batch experiments are utilized to model the fixed bed experimental results. In this way, mass transfer coefficients for the fixed bed are derived. In any case, the modeling results indicate that sulfur is not the only adsorbate of the process, but other adsorbates act competitively to sulfur, thereby complicating the process.

Characterization of low molecular weight sulfur species in seaweed from the Antarctic continent.

Antarctic seaweeds are vital components of polar marine ecosystems, playing a crucial role in nutrient cycling and supporting diverse life forms. The sulfur content in these organisms is particularly interesting due to its implication in biogeochemical processes and potential impacts on local and global environmental systems. In this study, we present a comprehensive characterization of seaweed collected in the Antarctic in terms of their total sulfur content and its distribution among different classes of species, including thiols, using various methods and high-sensitivity techniques. The data presented in this paper are unprecedented in the scientific literature. These methods allowed for the determination of total sulfur content and the distribution of sulfur compounds in different fractions, such as water-soluble and proteins, as well as the speciation of sulfur compounds in these fractions, providing valuable insights into the chemical composition of these unique marine organisms. Our results revealed that the total sulfur concentration in Antarctic seaweeds varied widely across different species, ranging from 5.5 to 56gkg-1 dry weight. Furthermore, our investigation into the sulfur speciation revealed the presence of various sulfur compounds, including sulfate, and some thiols, which were quantified in all ten seaweed species evaluated. The concentration of these individual sulfur species also displayed considerable variability among the studied seaweeds. This study provides the first in-depth examination of total sulfur content and sulfur speciation in brown and red Antarctic seaweeds.

Effect of Co-Inoculation with Growth-Promoting Bacteria and Arbuscular Mycorrhizae on Growth of Persea americana Seedlings Infected with Phytophthora cinnamomi.

Avocado is one of the most in-demand fruits worldwide and the trend towards its sustainable production, regulated by international standards, is increasing. One of the most economically important diseases is root rot, caused by Phythopthora cinnamomi. Regarding this problem, antagonistic microorganism use is an interesting alternative due to their phytopathogen control efficiency. Therefore, the interaction of arbuscular mycorrhizal fungi of the phylum Glomeromycota, native to the Peruvian coast (GWI) and jungle (GFI), and avocado rhizospheric bacteria, Bacillus subtilis and Pseudomonas putida, was evaluated in terms of their biocontrol capacity against P. cinnamomi in the "Zutano" variety of avocado plants. The results showed that the GWI and Bacillus subtilis combination increased the root exploration surface by 466.36%. P. putida increased aerial biomass by 360.44% and B. subtilis increased root biomass by 433.85%. Likewise, P. putida rhizobacteria showed the highest nitrogen (24.60 mg ∙ g-1 DM) and sulfur (2.60 mg ∙ g-1 DM) concentrations at a foliar level. The combination of GWI and Bacillus subtilis was the treatment that presented the highest calcium (16.00 mg ∙ g-1 DM) and magnesium (8.80 mg ∙ g-1 DM) concentrations. The microorganisms' multifunctionality reduced disease severity by 85 to 90% due to the interaction between mycorrhizae and rhizobacteria. In conclusion, the use of growth promoting microorganisms that are antagonistic to P. cinnamomi represents a potential strategy for sustainable management of avocado cultivation.

Marine fuel restrictions and air pollution: A study on Chinese ports considering transboundary spillovers

Docked vessels in ports can be one of the dirtiest emitters in terms of local air pollutants. This paper evaluates whether the regulation of Emission Control Areas in China reduces air pollutants emissions in port cities. The transboundary spillovers of air pollution, induced by meteorological conditions, results in air pollution concentrations at specific locations encompassing both locally generated pollutants and those originating from elsewhere. Therefore, it is challenging to discern the emission reduction effects of environmental regulatory policies through air pollutant monitoring concentrations. This paper develops an approach to isolate transboundary spillovers induced by the wind, estimate locally produced pollution, and utilize the concentrations of locally produced pollution to identify the treatment effects of the Chinese Emission Control Areas policy. The results find that the policy has significantly reduced the locally produced sulfur dioxide concentrations by 3.41% in port cities. However, the omission of transboundary spillovers could yield contrasting results, suggesting that ignoring the pollution transport could lead to erroneous conclusions. The research findings of this study hold significant policy implications, highlighting the importance of accounting for transboundary transport of air pollution in evaluating the local government’s environmental efforts and implementing supra-city environmental policies to prevent air pollution.

Impact of Seawater Inorganic Carbon Chemistry on Element Incorporation in Foraminiferal Shell Carbonate

AbstractReconstruction of the marine inorganic carbon system relies on proxy signal carriers, such as element/calcium (El/Ca) ratios in foraminiferal shells. Concentrations of boron, lithium, strontium, and sulfur have been shown to vary with carbonate system parameters, but when comparing individual proxy reconstructions based on these elements, they are rarely in complete agreement. This is likely caused by the simultaneous effects of multiple environmental factors on element incorporation. Culture experiments with benthic foraminifera have revealed that the shell's S/Ca reflects the carbon chemistry and can potentially be used as a proxy for seawater []. Aiming to investigate the application potential of sulfur incorporation for carbonate speciation reconstruction, we present S/Ca ratios in five planktonic foraminiferal species, namely Globigerina bulloides, Globigerinoides ruber albus, Globigerinoides ruber ruber, Trilobatus sacculifer, and Neogloboquadrina incompta from core‐top sediments in regions with contrasting [], [], temperature, and salinity. Analyses of B/Ca and Mg/Ca ratios are included here since these elements have been shown to depend to a certain degree on carbon system parameters (e.g., calcite saturation state and pH, respectively) as well. Moreover, foraminiferal Mg/Ca values covary with S/Ca values and thereby might compromise its proxy application. In contrast to previously published results, this new data set shows a positive correlation between the incorporation of sulfur in the foraminifer's shell and seawater []. As the incorporation of sulfur and magnesium are positively correlated, S/Mg values of the same foraminifera may be used to improve inorganic carbon system reconstructions.

Combining different species in restoration is not always the right decision: Monocultures can provide higher ecological functions than intercropping in a desert ecosystem

Vegetation restoration in deserts is challenging due to these ecosystems' inherent fragility and harsh environmental conditions. One approach for active restoration involves planting native species, which can accelerate the recovery of ecosystem functions. To ensure the effectiveness of this process, carefully selecting species for planting is crucial. Generally, it is expected that a more diverse mix of species in the plantation will lead to the recovery of a greater number of ecosystem functions, especially when the selected species have complementary niche traits that facilitate maximum cooperation and minimize competition among them. In this study, we evaluated the planting of two native species from the hyper-desert of Taklamakan, China, which exhibit marked morpho-physiological differences: a phreatophytic legume (Alhagi sparsifolia) and a halophytic non-legume (Karelinia caspia). These species were grown in both monoculture and intercrop communities. Monoculture of the legume resulted in the highest biomass accumulation. Intercropping improved several ecosystem functions in the 50 cm-upper soil, particularly those related to phosphorus (P), carbon (C), and sulfur (S) concentrations, as well as soil enzyme activities. However, it also increased soil sodium (Na+) concentration and pH. Halophyte monocultures enhanced ecological functions associated with nitrogen concentrations in the upper soil and with P, S, C, and cation concentrations (K+, Ca2+, Mg2+, Cu2+, Fe2+, Zn2+, Co2+, Ni2+), along with enzyme activities in the deep soil. It also maximized Na+ accumulation in plant biomass. In summary, we recommend legume monoculture when the primary goal is to optimize biomass accumulation. Conversely, halophyte monoculture is advisable when the objective is to extract sodium from the soil or enhance ecosystem functions in the deep soil. Intercropping the two species is recommended to maximize the ecosystem functions of the upper soil, provided there is no salinization risk. When planning restoration efforts in desert regions, it is essential to understand the impact of each species on ecosystem function and how complementary species behave when intercropped. However, these interactions are likely species- and system-specific, highlighting the need for more work to optimize solutions for different arid ecosystems.

Adsorptive Desulfurization of Iraqi Light Naphtha Using Calcite and Modified Calcite

This study used the adsorption method to remove sulfur compounds from light naphtha fuel by using calcite and modified calcite as adsorbents. The calcite was prepared from chicken eggshells by heating and activation methods. It was modified by mixing it with commercial activated carbon as a new adsorbent. XRD and FTIR were used to characterize the adsorbents. Light naphtha fuel from the Al-Diwaniyah refinery, with a sulfur concentration of 776 ppm, was used in batch adsorption studies. Various operation conditions that affect the adsorption process were studied such as temperature (20–40 °C), weight of the adsorbent (1-3 g), and contact time (15–45 min) at constant mixing speed (300 rpm). In this study, the Minitab Program-Box-Behnken design was used to design experiments in batch adsorption studies of light naphtha, which is considered more straightforward and accurate because it shows the effect of each dependent factor on the adsorption efficiency and removal ratio. Results and analysis showed that the increase in temperature, the amount of adsorbent, and contact time would increase the removal efficiency. The analysis of adsorption equilibrium isotherms shows that the experimental data follows the Freundlich isotherm model for adsorbents. According to the results of the study, the highest removal percentages of sulfur content of light naphtha using calcite and modified calcite were 61% and 79%, respectively.

CATALYTIC ACTIVITY OF METAL-BASED IONIC LIQUIDS IN OXIDATIVE DESULFURIZATION

Effective desulfurization techniques are required due to the operational and environmental difficulties caused by sulfur compounds found in petroleum fuels. The use of Fenton catalysts in the oxidative desulfurization of petroleum fuels is examined in this work. Evaluating the viability and effectiveness of Fenton catalysts in lowering sulfur concentration while maintaining fuel quality is the main goal. Promising outcomes are found in laboratory tests using hydrogen peroxide (H2O₂) and ferrous iron (Fe³⁺) as catalysts. Fenton catalysts focus on sulfur compounds and transform them into forms that are soluble in water, making the process of separating them from the fuel easier. This procedure offers a more environmentally friendly and financially feasible desulfurization option because it works in milder circumstances than other techniques. The results provide a viable path for the development of sustainable fuel and have ramifications for greener energy sources and environmental legislation. There has been a growing interest in ionic liquids (ILs) as innovative materials for functional desulfurization. Based on their definition and fundamental structure, metal-based ionic liquids (MILs) are divided into three categories in this critical article: metal chloride MILs, metal oxide MILs, and metal complex MILs. To enhance the oxidative desulfurization (ODS) process, MILs have both the oxidation and absorption sites for intramolecular adsorption and oxidation. A noteworthy characteristic of MILs in ODS is biomimetic catalysis, which serves to enhance oxidation performance by triggering molecular oxygen. Hydrogen peroxide or oxygen combined with the available water, together with metal oxide and metal complex ions, create a Fenton-like reaction that transforms hydrophobic organic sulfur (SO2) or hydrophilic sulfoxide/sulfone (Seroxide), or sulfur acid, respectively. Promising approaches for developing environmentally friendly and highly effective desulfurization procedures for large-scale applications are also given. Keywords: supported ionic liquid catalyst (SILC), hydrogen peroxide, catalytic oxidative desulfurization, copper (I) chlorocomplexes.