Sulfuric Acid Research Articles

Studies on Effect of Sulphuric Acid Attack on Concrete Made with Colloidal Silica as Replacement and Addition to Cement

Studies on Effect of Sulphuric Acid Attack on Concrete Made with Colloidal Silica as Replacement and Addition to Cement

Sputter Deposited Crystalline MoO2 Films as a High-Capacity and Stable Electrode Material for Supercapacitors: Mechanistic/Electrochemical Insights

In this work, we have optimized and fabricated pristine molybdenum dioxide (MoO2) electrodes over the Silicon (Si) substrate and examined the impact of various ion-loaded aqueous electrolytes on their electrochemical behavior. The sputtered electrodes exhibited a high crystalline structure and a very low resistivity. These highly conductive electrodes were tested in three different aqueous electrolytes (acidic, neutral, and alkaline) to establish a relation between the electrode and the nature of the electrolyte to achieve optimal electrochemical performance and cyclability. The electrochemical kinetics showed that the charge storage mechanism was unique for all the electrolytes. The capacitive current was dominant in the neutral electrolyte, whereas it was diffusive dominant in alkaline and 70% capacitive in the acidic electrolyte. Our findings indicated that the MoO2@Si electrode exhibited superior electrochemical activity in an acidic electrolyte. The electrode showed a voltage window of 0.6 V with an areal capacity of 24 mF/cm2 at 0.1 V/s scan rate. Moreover, the electrode also demonstrated excellent cyclability and capacitance retention (∼145%) till 5000 cycles. These results highlighted that the binder-free MoO2@Si electrode showed outstanding electrochemical activity and stability, which makes it suitable for sulfuric acid electrolyte-based energy storage systems.

Features of the crystal structure and surface of superprotonic conductor caesium hydrogen sulfate phosphate.

The crystal structure of superprotonic conductor caesium hydrogen sulfate phosphate [Cs4(HSO4)3(H2PO4)] have been analyzed using neutron diffraction methods. Additionally, its structure and surface layers have been investigated using atomic force microscopy. From the diffraction data obtained, Fourier syntheses of neutron scattering densities were calculated, and the localization of hydrogen atoms and the parameters of three types of hydrogen bonds in the crystal structure were accurately determined. Correlation of surface characteristics of samples obtained by atomic force microscopy with their crystal structure is shown.

Evaluation of sugar content and bioethanol production of Ethiopian local varieties “Nech Tinkish” and “Hawaye” sweet sorghum (Sorghum bicolor (L.))

Diversifying the use of climate-smart crops such as sweet sorghum has the potential to solve integrated food, bioenergy, feed, and land management problems. The study’s purpose is to quantify the sugar content of Nech Tinkish (v1) and Hawaye (v2) Ethiopian sweet sorghum varieties and investigate the interaction effect of fermentation parameters to determine their capacity for ethanol production. Sweet sorghum varieties were analyzed to determine their difference in °Brix content by extracting their juices. The juice was clarified using milk lime. Its total soluble sugars, total carbohydrates, and reducing sugars were determined using a digital refractometer, phenol sulfuric acid, and 3,5-dinitrosalicylic acid, respectively. A completely randomized factorial was employed to evaluate ethanol production capacity, and the ethanol content was estimated using a potassium dichromate solution. The °Brix results revealed that v2 had a higher sugar concentration than v1. Additionally, the estimated carbohydrate content of the juice ranged from 37.402 to 157.641 g/L. The estimated reducing sugar also varied from 4.644 to 33.412 g/L. Therefore, the estimated reducing sugar showed the hydrolysis of sweet sorghum juice by invertase and sulfuric acid produced more fermentable sugars. Fermentation at 30 °C with pH 4.5 incubated for 4 days yields the highest ethanol, and v2 yields higher (15.31%) ethanol, compared to v1 produced 14.85%. This study showed a basis for the existence of two sugar-rich climate smart sweet sorghum varieties with an extraordinary amount of sugar used as a source of biofuel and food simultaneously in a single plot of land.

Transformation of Silicate Ions into Silica under the Influence of Acid on the Structure of Serpentinite

The process of transformation of the silicate components of the crystal lattice structure of chrysotile during its quantitative interaction with aqueous solutions containing various stoichiometrically required amounts of sulfuric acid (SRA H2SO4) calculated with respect to the magnesium content in the composition of chrysotile is investigated. It has been shown by IR spectroscopic, X-ray phase, thermal and chemical methods of investigation and analysis that, with quantitative interactions of chrysotile and sulfuric acid, first of all, the “brucite layer” of the molecular structural structure of chrysotile is exposed to acid at SRA H2SO4 = 0.1–0.3. As a result of ion exchange processes, acidic silanol (≡Si–O–H) or disilanol (=Si=(O–H)2) bonds are formed. These acid groups form one-dimensional silicate chains with transverse bridges (≡Si–O–Si≡), where the angles (Si–O–Si = 180°C) straighten, which are recorded in the IR spectra in the region of characteristic absorption of 1220–1250 cm−1 silica. The association of the resulting acid groups into silicate chains, dimers, and trimers with transverse bridges, leads to the appearance of colloidal silica particles in the system, which cause some inhibition of the dissolution of layered magnesium hydrosilicate in sulfuric acid solutions containing H2SO4˃ 0.3 SRA.

Leaching behaviour of limonite ores from Lapaopao, Southeast Sulawesi, Indonesia: Effect of mineralogy and acid types

An atmospheric leaching study of limonite ores from Lapaopao, Southeast Sulawesi, using hydrochloric acid (HCl), nitric acid (HNO<sub>3</sub>), and sulfuric acid (H<sub>2</sub>SO<sub>4</sub>) has been performed. The objectives of this study were to analyze the effect of ore mineralogy and acid types on the dissolution behavior of minerals and the leaching rate of Ni and Co at atmospheric pressure conditions. Mineralogical analysis was carried out using optical microscopy, scanning electron microscopy (SEM), and X-ray diffractometry (XRD), while the ore's chemical composition was determined by using X-ray fluorescence spectrometry (XRF) and atomic absorption spectrophotometry (AAS). Mineralogically, the limonite ores are dominated by goethite, followed by gibbsite, talc, and lizardite, with less amounts of hematite and quartz. Analysis results of solid residues revealed that mineral dissolution order was determined as follows: goethite > lizardite > gibbsite> hematite > talc> quartz. The results of the leaching experiment exhibited that the order of leaching rates of Ni in the three ores samples using three different acids were found as follows: Ore-1 > Ore-2 > Ore-3. Comparison of HCl, HNO<sub>3</sub>, and H<sub>2</sub>SO<sub>4</sub> as the lixiviants for the leaching of limonite ores demonstrated that HCl was the most reactive acid, followed by HNO<sub>3</sub> and then H<sub>2</sub>SO<sub>4</sub>. This might be due to the differences in mineralogical nature and reactivities of acids during the leaching process.

Physicochemical Properties of Cellulose Nanocrystals Extracted from Postconsumer Polyester/Cotton-Blended Fabrics and Their Effects on PVA Composite Films

The utilisation of cotton waste as precursors in the synthesis of nanocrystalline cellulose has gained significant attention. This approach suggests a sustainable solution to address the growing concern of textile waste accumulation while simultaneously producing a valuable material. The main aim of this study is to examine the properties of cellulose nanocrystals (CNCs) obtained from postconsumer polyester–cotton waste and assess the effect of different fabric structures on the extraction and these properties. To acquire nanocellulose, a thorough decolourisation pretreatment process was utilised, which involved the treatment of polyester–cotton waste with sodium dithionite and hydrogen peroxide. Consequently, the postconsumer material was then treated with an acid hydrolysis method employing a 64% (v/v) sulphuric acid solution at 50 °C for 75 min, resulting in the formation of CNCs with average yield percentages ranging from 38.1% to 69.9%. Separation of the acid from the CNC was facilitated by a centrifugation process followed by dialysis against deionised water. Uniform dispersion was then achieved using ultrasonication. A variety of analytical techniques were employed to investigate the morphological, chemical, thermal, and physical properties of the isolated CNCs. Among these techniques, attenuated total reflection-Fourier-transform infrared spectroscopy (ATR-FTIR), energy-filtered transmission electron microscopy (EF-TEM), thermogravimetric analysis (TGA), and X-ray diffraction (XRD) were utilised to analyse the CNCs. The findings indicated that the separated CNCs exhibited a rod-shaped morphology, measuring between 78 and 358 nm in length and 5 and 16 nm in diameter, and also exhibited high crystallinity (75–89%) and good thermal stability. The extracted CNCs were mixed with polyvinyl alcohol (PVA) and glycerol to assess their reinforcing effect on plastic films. The prepared composite film exhibited improved mechanical properties and thermal stability. Incorporating CNCs led to a 31.9% increase in the tensile strength and a 42.33% rise in the modulus of elasticity. The results from this research proved that CNCs can be extracted from postconsumer mixed fabrics as a potential solution to effectively address the mounting concerns surrounding waste management in the textile industry and also provide avenues for enhancing the qualities of eco-friendly composite films.

Sulfide oxidation by members of the Sulfolobales

Abstract The oxidation of sulfur compounds drives the acidification of geothermal waters. At high temperatures (>80°C) and in acidic conditions (pH <6.0), oxidation of sulfide has historically been considered an abiotic process that generates elemental sulfur (S0) that, in turn, is oxidized by thermoacidophiles of the model archaeal order Sulfolobales to generate sulfuric acid (i.e., sulfate and protons). Here, we describe five new aerobic and autotrophic strains of Sulfolobales comprising two species that were isolated from acidic hot springs in Yellowstone National Park (YNP) and that can use sulfide as an electron donor. These strains significantly accelerated the rate and extent of sulfide oxidation to sulfate relative to abiotic controls, concomitant with production of cells. Yields of sulfide-grown cultures were ∼2-fold greater than those of S0-grown cultures, consistent with thermodynamic calculations indicating more available energy in the former condition than the latter. Homologs of sulfide:quinone oxidoreductase (Sqr) were identified in nearly all Sulfolobales genomes from YNP metagenomes as well as those from other reference Sulfolobales, suggesting a widespread ability to accelerate sulfide oxidation. These observations expand the role of Sulfolobales in the oxidative sulfur cycle, the geobiological feedbacks that drive the formation of acidic hot springs, and landscape evolution.

PVDF-HFP-based polymer inclusion membrane functionalized with D2EHPA for the selective extraction of bismuth(III) from sulfate media

This study is the first application of a PVDF-HFP-based polymer inclusion membrane incorporating the poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and di(2-ethylhexyl)phosphoric acid (D2EHPA) as the base polymer and extractant for the extraction of bismuth(III), respectively. It is demonstrated that the PIM comprised of 60 wt% PVDF-HFP and 40 wt% D2EHPA is the most effective in the extraction of bismuth(III) from feed solution containing 20 mg L−1 bismuth(III) and 0.2 mol L−1 sulfate adjusted to pH 1.4. The extracted bismuth(III) ions are back-extracted quantitatively to the receiving solution containing 1 mol L−1 sulfuric acid. The stoichiometry experiments reveal that the Bi: D2EHPA ratio in the bismuth(III) extracted complex is 1:6, and D2EHPA is dimer. Moreover, it is shown that the studied PIM has high selectivity in the extraction of bismuth(III) over other interfering ions such as Mo(VI), Cr(III), Al(III), Fe(III), Ni(II), Zn(II), Cd(II), Co(II), Cu(II), and Mn(II). The interference of Fe(III) is also eliminated by masking with fluoride, leading finally to a nearly pure extraction of bismuth(III).

Deterioration Mechanisms of Ultra-High-Performance Concrete Under Various Sulfuric Acid and Sulfate Attack Conditions

Deterioration Mechanisms of Ultra-High-Performance Concrete Under Various Sulfuric Acid and Sulfate Attack Conditions

Direct Measurements of Covalently Bonded Sulfuric Anhydrides from Gas-Phase Reactions of SO3 with Acids under Ambient Conditions.

Sulfur trioxide (SO3) is an important oxide of sulfur and a key intermediate in the formation of sulfuric acid (H2SO4, SA) in the Earth's atmosphere. This conversion to SA occurs rapidly due to the reaction of SO3 with a water dimer. However, gas-phase SO3 has been measured directly at concentrations that are comparable to that of SA under polluted mega-city conditions, indicating gaps in our current understanding of the sources and fates of SO3. Its reaction with atmospheric acids could be one such fate that can have significant implications for atmospheric chemistry. In the present investigation, laboratory experiments were conducted in a flow reactor to generate a range of previously uncharacterized condensable sulfur-containing reaction products by reacting SO3 with a set of atmospherically relevant inorganic and organic acids at room temperature and atmospheric pressure. Specifically, key inorganic acids known to be responsible for most ambient new particle formation events, iodic acid (HIO3, IA) and SA, are observed to react promptly with SO3 to form iodic sulfuric anhydride (IO3SO3H, ISA) and disulfuric acid (H2S2O7, DSA). Carboxylic sulfuric anhydrides (CSAs) were observed to form by the reaction of SO3 with C2 and C3 monocarboxylic (acetic and propanoic acid) and dicarboxylic (oxalic and malonic acid)-carboxylic acids. The formed products were detected by a nitrate-ion-based chemical ionization atmospheric pressure interface time-of-flight mass spectrometer (NO3--CI-APi-TOF; NO3--CIMS). Quantum chemical methods were used to compute the relevant SO3 reaction rate coefficients, probe the reaction mechanisms, and model the ionization chemistry inherent in the detection of the products by NO3--CIMS. Additionally, we use NO3--CIMS ambient data to report that significant concentrations of SO3 and its acid anhydride reaction products are present under polluted, marine and polar, and volcanic plume conditions. Considering that these regions are rich in the acid precursors studied here, the reported reactions need to be accounted for in the modeling of atmospheric new particle formation.

Synergistic corrosion inhibition of rubber seed extract with KI on cold rolled steel in sulfuric acid solution

BackgroundPlant-based inhibitor has emerged an important topic owing to the combing merits of eco-friendly, low cost, rich natural resources as well as easy preparation. Rubber seed is the agricultural waste, and is mainly composed of oil and fatty acids those contain many polar oxygen atoms, and so it can be extracted to prepare the potential corrosion inhibitor. MethodsRubber seed extract (RSE) is prepared using reflux extraction method with the extracting solvent of ethanol aqueous solution. The synergistic inhibition effect of RSE and potassium iodide (KI) on the corrosion of cold rolled steel (CRS) in 0.50 M H2SO4 solution is firstly studied by weight loss, potentiodynamic polarization (PDP) curves and electrochemical impedance spectroscopy (EIS) methods. CRS surface was thoroughly characterized using metallographic microscope, scanning electron microscope (SEM), atomic force microscope (AFM), X-ray photoelectron spectroscopy (XPS) and contact angle measurements. FTIR, UV–vis and liquid chromatography mass spectrometry (LC-MS) compositional analysis of RSE were used to analyze the efficient components in RSE. Significant findingsThe results indicate that individual RSE or KI cannot function as a successful inhibitor to prevent CRS corrosion, but the mixture of RSE/KI performs better at inhibiting, with a maximal inhibition efficacy of up to 96.4% of 200 mg L−1 RSE/100 mg L−1 KI. The synergistic coefficient of the mixture is larger than 1, indicating that a true synergism. RSE/KI can drastically retard both cathodic and anodic processes, and interfacial capacitance falls as the charge transfer resistance of CRS/solution rises. It exhibits remarkable inhibition properties when the capacitor arc grows. There is only a small corrosion response in the inhibited media, as evidenced by the variations in electrical conductivity and ultraviolet spectrum before and after immersion. The hydrophilicity and surface roughness of CRS surface is dropped as a result of the introduction of RSE/KI. A series of metallurgical microscopy, AFM, SEM or contact angle tests indicate a synergistic inhibition effect is more pronounced for RSE/KI. XPS results clearly demonstrate that elements including Fe, S, N, and I are bonded to the surface of CRS. The primary ingredients of oleic acid, polyphenols, phenylpropanoids can also produce a strong synergism with KI.

An insight Into Surface and Diffusion Characteristics of UiO‐66@ZIF‐8 Core–Shell MOF for Asymmetric Supercapacitors with Unprecedented Energy Density

AbstractIn this study, nanosized zeolitic imidazolate framework‐8 (ZIF‐8) crystal has been produced on the universitetet i oslo‐66 (UiO‐66) metal–organic framework (MOF) to make core–shell structure using a layer‐by‐layer deposition method. In comparison to the pristine UiO‐66 and ZIF‐8, the core–shell MOF exhibits superior performance in terms of specific capacitance. This enhanced performance is attributed to its remarkable ability to facilitate the rapid diffusion of electrolyte ions through nanosized ZIF‐8 and enhance the electron transfer process involving the inner and outer metal ions within the UiO‐66@ZIF‐8 structure. Remarkably, the core–shell structure achieves an impressive specific capacitance of 588.8 F g−1 at a current density of 0.5 A g−1 using 1 m sulfuric acid (H2SO4) aqueous electrolyte. Additionally, the UiO‐66@ZIF‐8 core–shell material is demonstrated as a positive electrode, coupled with activated carbon (AC) derived from waste tissue paper serving as the negative electrode, in the fabrication of an asymmetric supercapacitor (ASC) device. At a power density of 400 W kg−1, this assembled asymmetric device delivers a notably high energy density of 53 Wh kg−1 along with a cyclic stability of 94.8% after 10 000 cycles. This study substantiates the superior performance of the UiO‐66@ZIF‐8 core–shell MOF structure as a highly effective supercapacitor electrode material, surpassing the performance of its pristine MOF counterparts.

N-Guanylurea dinitramide: Optimal synthesis process, basic properties and spectroscopic data

N-Guanylurea dinitramide (GUDN), also known as FOX-12, is indeed a fascinating organic dinitramide salt with high insensitivity and good thermal stability. It shows great promise for use in next-generation insensitive munitions. In this study, GUDN was synthesized through the nitration reaction of ammonium sulfamate salt with an acid mixture (HNO3/H2SO4) and guanylurea salts in water. The optimal conditions for this synthesis have been determined, including reaction temperature at -40 oC, the nitration reaction time of 45 minutes, and specific molar ratios of the components, which include guanylurea sulfate, ammonium sulfamate, and the mixture of sulfuric and nitric acid. Additionally, various properties and spectral data of GUDN, such as FTIR, 1H-NMR, 13C-NMR, DSC-TG, XRD, and UV-Vis, have been thoroughly studied in the referenced article.

An Incubation System for the Simulation of Ammonia Emissions from Soil Surface-Applied Slurry: Effect of pH and Acid Type

Acidification of slurry is a promising approach for reducing ammonia emissions during the application procedure. Since only a few studies have been conducted focusing on ammonia emissions during the application of liquid organic fertilizers on the soil surface, a suitable incubation system was developed to evaluate the effects of acidification under controlled conditions. This incubation system was used to measure the ammonia emissions of various liquid organic fertilizers. The substrates were acidified with sulfuric and citric acid to different pH values to determine both the influence of the pH value of the substrates and of the type of acid on the ammonia emissions. The emissions decreased with declining pH value, and the reduction in emissions compared to the initial pH of the substrate was over 86% for pH 6.5 and over 98% for pH 6.0 and below. At the same pH value, the ammonia emissions did not differ between substrates acidified with citric acid and sulfuric acid, although more than twice as much 50% citric acid was required compared to 96% sulfuric acid to achieve the same pH value. Overall, our results demonstrate that the incubation system used is suitable for measuring ammonia emissions from surface-applied liquid organic fertilizers. The system allows for the differentiation of emission levels at various pH levels and is therefore suitable for testing the effectiveness of additives for reducing ammonia emissions from liquid organic fertilizers.

Sulfonated graphene oxide linked with alkali metal ions membranes for proton conductivity in hydrogen production from water electrolysis

Amid technological advances, rising energy demand, and environmental concerns, countries endorse green energy solutions. Prominent among them is hydrogen production via clean water electrolysis, a key strategy for sustainable development. Herein, to address the limitations of expensive and potentially harmful Nafion membranes, we have developed a new graphene oxide (GO) series membranes (hydrophilic sulfonated GO (GO-SO3H) linked with monovalent alkali metal ions were synthesized to fabricate the membranes) to be used in water electrolysis for hydrogen production by introducing the iodide oxidation reaction (IOR) as an alternative to the traditional oxygen evolution reaction (OER). Various modifications by sulfuric acid, methanol, and different alkali metal hydroxides (LiOH, NaOH, KOH) result in membranes with distinct properties. Characterization techniques, including ATR-FTIR, SEM, AFM, XRD, water contact angle (WCA), and electrochemical impedance spectroscopy (EIS), validated the modifications, assessed membrane morphology, interlayer spacing, hydrophilicity, and electrical properties. Among the membranes, GO-SO3K stood out, exhibiting the highest proton conductivity (119.16 mS) and superior potassium ion permeability (20.382 cm/s). Importantly, all GO series membranes demonstrate excellent stability in the electrochemical system. The findings suggested that GO-SO3K holds promise as a potassium ion-conductive membrane for efficient and sustainable hydrogen production, offering a viable alternative to conventional Nafion membranes in water electrolysis applications.

Advances in the Sustainable Production of Fertilizers from Spent Zinc-Based Batteries

Wastes from spent batteries are a secondary source of raw materials. To ensure this, it is mandatory to design sustainable and low-cost processes. In the case of alkaline and zinc–carbon-based batteries, the high content of Zn and Mn makes them of interest in the development of fertilizers. The main objective of this research is to study the fertilizers production from spent zinc-based batteries, using sulfuric acid, citric acid (CIT) and glycine (GLY) solutions as leaching agents. Leaching with glycine at alkaline pHs shows a high selectivity of Zn over Mn, whereas the use of citric and sulfuric solutions leads to recoveries of Zn and Mn. Solutions with the highest Zn recoveries were tested in sand columns. Commercial ZnSO4 heptahydrate was used as a control. For sulfuric acid, two solutions (H2SO4 2M and 0.25M) were used. The elution of leached Zn and Mn in sand columns depended on the solution added. The Zn-Mn-CIT treatment showed a slight but steady increase in the leachates, reaching 70% and 75% of the total leached Zn and Mn, respectively, in the medium term. The Zn-Mn-H2SO4 2M and ZnSO4 treatments showed a similar behavior in Zn release. Both Zn-Mn-GLY and Zn-Mn-H2SO4 0.25M treatments showed similar amounts of leached Mn in the medium term (77% of total leached Mn), differing in the leached Zn. Solutions from the leaching of spent black mass batteries, especially Zn-Mn-CIT or Zn-Mn-GLY, showed promising behavior as fertilizer from the point of view of Zn and Mn availability as nutrients.

Numerical analysis of a protective coating for mining industry feed chute

The selection of materials for the protective coating of a crusher’s feed chute significantly influences the mean time between failures (MTBF) and operational costs associated with the mass production of sulfuric acid at MMG/Kinsevere. Neglecting the condition of the protective coating can pose a serious challenge to production efficiency and result in increased downtime. This study focuses on enhancing industrial productivity in Sulfuric Acid production with minimal maintenance. The investigation explores the quality and type of materials used for the protective coating of the feed chute in the mining industry, particularly at MMG/Kinsevere, utilizing Ansys Fluent and SOLIDWORKS Software for analysis. The paper proposes a Ceramic protective liner for the crusher feed chute due to its superior resistance to erosion compared to other liners. Different feed chute models, constructed with materials like halogenated butyl rubber, 316 stainless steel, and ceramic, underwent analysis. The evaluation of the potential impact on the mean time between failures (MTBF) for different materials used in a protective coating, considering the rate of erosion through computational fluid dynamics (CFD) with ANSYS FLUENT software, is a central aspect of this study. The detailed modeling and simulation reveal that the ceramic material exhibits the most favorable protective coating characteristics, with an erosion rate density of 06.636753 kg/m2s, outperforming halogenated butyl rubber (3.326576 kg/m2s) and 316 stainless steel (2.186633 kg/m2s). The simulation yielded results corresponding to flow rates of 284.19 kg/s for the solid phase and 123.14 kg/s for the liquid phase.

Experimental Investigation on Shear Strength and Microstructure of Chemically Treated Sisal Fiber-Reinforced Concrete

The incorporation of sisal fiber into the concrete matrix reduces waste disposal, which has negative environmental impacts. The aim of this study was to perform an experimental investigation on shear strength and microstructure of chemically treated sisal fiber-reinforced concrete (SFRC). In order to accomplish the aim of the study, physical, shear, and mechanical properties of concrete reinforced with chemically treated sisal fiber have been performed. 0.50%, 1.00%, 1.25%, 1.50%, 1.75%, and 2.00% of sodium hydroxide (NaOH) and sulfuric acid (H2SO4) treated sisal fiber were used as an addition to the dry weight average with the help of the American Concrete Institute (ACI) mix design procedure. After the 7th and 28th days of curing, shear strength according to the ASTM D5379M standard and the mechanical properties of concrete have been conducted. For microstructural properties, scanning electron microscopy (SEM) and X-ray diffraction (XRD) were conducted after the concrete was cured for 28 days. Forty-six percent and 20% compressive strength enhancement at the 7th and 28th days of curing was compared to the control mix. Twenty-seven percent enhancement was recorded in the split tensile strength of 1.5% SFRC as compared to the control mix at 28 curing days. A shear strength of 1.5% SFRC was improved by 95% at the 7th curing days and 28% at the 28th curing days as compared to the control mix. As compared to conventional concrete, SFRC shows a denser microstructure. In addition to this, portlandite, quartz, calcium aluminum silicate, and C─S─H crystal are the available phases in the concrete matrix.

Unveiling Garlic's Arsenal: A Comprehensive Review of Antifungal and Antibacterial Cream

Garlic (Allium sativum) has long been recognized for its medicinal properties, particularly its antimicrobial effects. In this comprehensive review, we explore the therapeutic potential of garlic in the formulation of creams targeting fungal and bacterial infections. We discuss the rising prevalence of fungal infections, particularly those caused by Candida species, and the challenges they pose in healthcare settings. Furthermore, we delve into the diverse biochemical composition of garlic, including sulfur compounds, enzymes, carbohydrates, minerals, amino acids, flavonoids, and vitamins, which contribute to its antimicrobial activity. The synthesis of allicin, a key bioactive compound in garlic, and its mechanism of action against various pathogens are elucidated. Additionally, we examine the dermatological applications of topical garlic in treating fungal skin infections, wound healing, antioxidant protection, UVB shielding, and anti-aging benefits. Clinical evidence supporting the efficacy of garlic extracts in managing viral skin conditions is also discussed. Finally, we highlight the need for further research and clinical trials to fully explore garlic's therapeutic potential, safety profile, and optimal formulations, thereby enhancing patient outcomes in the management of infectious diseases.