Sulfuric Acid Research Articles

Formulation of a carbon-based solid acid catalyst from groundnut husk for the esterification of oleic acid

In this research, a biochar was prepared from groundnut husk and sulphuric acid. The biochar wassulphonated with chlorosulphonic acid to give a carbon-based sulphonated solid acid catalyst (SAC). The catalyst was characterised by N2 adsorption and desorption at 77K after degassing overnight under vacuum at 250˚ C, scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectroscopy, and total acid density measurement. The results of the acid density measurement showed that the sulphonated biochar has a relatively high acid density of 3.2 mmol/g, while that of the non-sulphonated counterpart is 0.56 mmol/g. Comparison of the percentage conversion of oleic acid by esterification with methanol and butanol was carried out under three different conditions, viz: without catalyst, with the non-sulphonated biochar and with the sulphonated biochar, under the same experimental conditions of 5% catalyst weight percent (based on weight of acid), acid-methanol mole ratio of 1:12, reaction temperature of 70 oC, and five hours reaction time. Up to 91.6% percentage conversion of oleic acid to methyl oleate and 86.4% for butyl oleate were achieved, proving the effectiveness of the sulphonated biochar in catalysing the esterification reaction of oleic acid with methanol and butanol. The results of this study are expected to provide insights into the development of sustainable and cost-effective solid acid catalysts for the synthesis of oleate esters and other value-added materials from renewable feedstocks.

Long-term durability of iron-rich geopolymer concrete in sulphate, acidic and peat environments

This study assesses the behaviour of iron-rich type F fly ash geopolymer concretes (GC) exposed to simulated sulphate, acidic, and peat environments, typical of those encountered in tropical peatlands. GC and Portland cement (PC) concrete of comparable strengths were exposed to a range of simulated solutions for 18 months, including 5 % magnesium sulphate (MgSO4), 5 % sodium sulphate (Na2SO4), 1 % and 3 % sulfuric acid (H2SO4) and peat. The GC generally outperformed PC in all conditions. The GC showed a significant increase in strength in the first year, along with enhanced durability properties. Microstructural analysis indicated a decrease in total porosity and pore size. This was attributed to continuing geopolymerization leading to the foration of additional N-A-S-H gel, which filled the pores and solidified the concrete matrix. However, compressive strength decreased at 18 months due to crack propagation caused by drying shrinkage. In Na2SO4, GC attained an 8.9 % and 6.3 % increase in compressive strength at 12 and 18 months, respectively, again attributed to ongoing geopolymerization. GC exposed to MgSO4 exhibited a significant decrease in compressive strength of approximately 11 % at 12 months and 19.8 % at 18 months, attributed to the formation of lower-strength M-A-S-H from reaction between MgSO4 and N-A-S-H gel. After 12 months GC exposed to 1 % and 3 % H2SO4 demonstrated a decrease in compressive strength of approximately 1.2 % and 4.5 %, respectively, together with 2 % and 3 % mass loss. Chemical and microstructural data confirmed this strength reduction due to the vulnerability of N-A-S-H to when exposed to H2SO4. GC exposed to peat solution exhibited a 1.25 % increase in compressive strength at 12-month, but a decrease of 11.3 % at 18-month. Microstructural analysis observed a reduction in Na+ within GC matrix, and the presence of gypsum. The reduction in pore sizes and total porosity suggested generation of zeolite crystalline material was contributing to the pore filling.

Designing bipolar anodizing towards white anodic aluminum oxide (AAO)

Obtaining white anodic aluminum oxide (AAO) is a major challenge in the surface finishing industry. The present work presents a cost-effective route to design light-scattering morphologies through submicrometric hollows homogeneously dispersed in the depth of the oxide layer, created by localized hydrogen evolution. To this end, cathodic steps are added in alternance with anodic steps in a bipolar pulse anodizing process performed in 2 M sulfuric acid. The mechanisms of nucleation and growth of the targeted hollows within the AAO are highlighted by combining in situ electrochemical measurements and high magnification SEM observations. The aesthetic performances in terms of white color, evaluated by reflectance spectroscopy in comparison with a white reference, are directly related to the size, shape and distribution of the hollows, controlled by both the parameters of the cathodic step and the thickness of the unit anodic oxide layers.

Dissolution process and mechanism of montmorillonite in oxalic acid and sulfuric acid media at various pH levels

The dissolution of silicate minerals plays a crucial role in many natural geological processes. In order to better comprehend the reaction mechanisms and dissolution characteristics of montmorillonite in different acidic systems, the effects of interfacial reactions of montmorillonite with oxalic and sulfuric acid solutions at various pH levels on the ionic dissolution, crystal structure, and micro-morphology were studied, and the morphology of aluminum and saturation index of secondary mineral were simulated. It was shown that the dissolution amounts of Mg2+, Al3+ and Si4+ in montmorillonite structure decreased with the increase of pH value, which reflected the dependence of montmorillonite dissolution on the pH value of solution. The dissolution percentages of Mg2+, Al3+ and Si4+ after the reaction of montmorillonite with oxalic acid solution were greater than those in sulfuric acid solution, and the highest dissolution rate of Al3+, indicated that both ligands and protons attacked the surface sites of montmorillonite and accelerated the dissolution of ions. Moreover, oxalate ligands exerted specific binding effects on Al3+ ions. While reacting with oxalate and sulfate, the tetrahedral, octahedral and interlayer cations of montmorillonite exhibited the non-stoichiometric and inconsistent dissolution. The oxalate ligands have a strong complexation effect on Al3+, so that Al3+ in oxalate solution exists in the form of aluminum oxalate complex, which reduces the effective concentration of Al3+ in solution and promotes the dissolution of Al3+ in montmorillonite structure. The Mg2+ ions settled at octahedral substitution sites possessed weak stability, while those from the interlayer featured strong interlayer interchangeability, demonstrating the dissolution percentage up to 10.85 % and 8.62 % even in oxalic and sulfuric acid solutions at pH of 6.5. All secondary mineral phases in the solution were undersaturated, making the montmorillonite dissolution difficult to balance. Montmorillonite has a high cation exchange capacity, which makes it have a strong buffer capacity to exogenous acids. This study helps to explain the dissolution process of montmorillonite in inorganic and organic acid solutions at different pH value.

Sulfuric acid solvolysis of cellulose in a butanol-1/benzene mixture for isolating cellulose nanocrystals

The absence of a universal method for isolating cellulose nanocrystals (CNCs) has prompted researchers to explore alternative approaches to traditional sulfuric acid hydrolysis. In this study, the authors continue their previous research by investigating CNC synthesis through cellulose solvolysis in an alcoholic environment. The CNCs were successfully obtained utilizing controlled sulfuric acid solvolysis of sulfate cellulose in a butanol-1/benzene mixture. The highest CNC yield (over 60 %) was achieved at strictly controlled acid-to-benzene ratios in a butanol-1/benzene/sulfuric acid reaction mixture, with a significant reduction in the optimal acid concentration. The study also analyzes the physicochemical properties of the isolated CNCs. No surface alkylation of the synthesized CNCs was observed during the cellulose solvolysis in the butanol-1/benzene mixture. Besides, the properties of these CNCs closely resembled those obtained through traditional sulfuric acid hydrolysis. The paper also discusses the potential mechanism of cellulose solvolysis in the process of CNC production.

Enhanced corrosion inhibition performance of 5-amino-3‑bromo-1-methylindazole on copper in sulfuric acid environments

The corrosion inhibitor 5-amino-3‑bromo-1-methylindazole (ABMI) with multiple substituents can effectively protect the copper substrate. According to the electrochemical experiment results, at 298 K, 3 mM ABMI may suppress copper corrosion by 92.1 %. Furthermore, going from 298 K to 308 K raises the temperature at which 3 mM ABMI may continue to suppress corrosion with an efficiency exceeding 90 %. The weight loss test, SEM, AFM, and XRD data all reveal that the presence of ABMI efficiently prevents the corrosion media from dissolving the copper substrate. The ΔGads0 value of ABMI is −32.97 kJ/mol, demonstrating that it works on the metal/solution interface through physical adsorption and chemisorption. The results of molecular dynamics modeling and quantum chemical computation show that ABMI adsorbs to the metal superficies in a nearly parallel way, minimizing the exposure area among the metal superficies with the medium with corrosive substances and providing the best possible protection for copper.

Proton Transport Scenarios in Sulfuric Acid Explored via Ab Initio Molecular Dynamics Simulations.

Sulfuric acid (H2SO4), a highly reactive reagent containing intrinsic protonic charge carriers, has been studied via ab initio molecular dynamics simulations. Specifically, we explore the solvation shell structure of the protonic defects, H1SO4- and H3SO4+, as well as the underlying proton transport mechanisms in both the neat and hydrated H2SO4 solutions. Our findings reveal a significant contraction of the dynamic hydrogen-bonded network around the protonic defects, which resembles features seen in water. The simulations provide estimates of the structural relaxation time scales for proton release from both the covalent O-H bonds (∼23 ps) and the hydrogen bonds (∼0.4 ps). In contrast to water, our analysis of the proton transfer scenarios in sulfuric acid reveals correlated events mediated by the formation of longer (up to four) hydrogen-bonded Grotthuss chains.

Effect of thermochemical treatment of sewage sludge on its phosphorus leaching efficiency: Insights into leaching behavior and mechanism

Thermochemical conversion, including hydrothermal processing, pyrolysis and incineration, has become a promising technology for sewage sludge (SS) treatment and disposal. Furthermore, acid leaching is considered as an effective method to recover phosphorus (P) from SS and its thermochemical treatment products. This study has investigated the potential of P reclamation from SS and its thermochemical derivatives, including hydrochar (HC), biochar (BC), and SS incinerated ash (SA). Comparative analyses of physicochemical properties of these derivatives revealed a decrease in hydroxyl and aromatic groups and an increase in aliphatic and oxygen-containing functional groups in HC and BC. Leaching experiments using 1 M sulfuric acid (H2SO4) and 1 M oxalic acid (C2H2O4) suggested that H2SO4 slightly outperformed C2H2O4 in terms of P leaching efficiency. HC achieved 79.1 % optimal leaching efficiency in 60 min using H2SO4, while BC, SS, and SA required 360 min to achieve comparable efficiency. SS and BC reached optimal leaching efficiency at 74.1 % and 76.2 % in H2SO4, while SA achieved 80.9 % in C2H2O4. Importantly, HC and SA are more favorable for P extraction using acid leaching, whereas BC tends to be a potential P carrier. Time-dependent kinetics revealed a two-stage leaching process, i.e., fast and slow reaction stages. Shrinking core model indicates product layer diffusion as the primary rate-limiting step in both stages. Overall, these fundamental insights play an important role in practical P recovery through acid leaching of SS derived residues after thermochemical treatment.

Electrochemical, thermodynamic and DFT studies of Fomitopsis pinicola as green corrosion inhibitor for carbon steel in sulfuric acid

In this work, the methanolic extract of Fomitopsis pinicola has been evaluated as a green corrosion inhibitor for the dissolution of 1018 carbon steel in 0.5 M sulfuric acid. For this, gravimetric tests and electrochemical methods such as potentiodynamic polarization curves, linear polarization resistance (LPR) and Electrochemical Impedance Spectroscopy (EIS) techniques were used. These tests were aided with Infrared and GC–MS analytical techniques. In addition to this, theoretical calculation with the use of the density functional theory (DFT) technique has been used to correlate the electronic extract properties and its inhibitory capacity. Weight loss results have shown an inhibitor efficiency of 85 % with the addition of 400 ppm. Thermodynamic parameters have shown that Fomitopsis pinicola extract is physically adsorbed onto the steel following a Langmuir adsorption isotherm. Potentiodynamic polarization curves showed that the extract behaves as a mixed type of corrosion inhibitor inducing the formation of a protective film onto the steel surface. In the presence of the Fomitopsis pinicola extract, a more resistive film obtained the highest polarization resistance value when 400 ppm of extract was used. In addition to this, as the concentration of the extract increased the charge transfer resistance and the double electrochemical layer capacitance decreased. GC–MS results indicated that main compounds contained in the Fomitopsis pinicola extract were Dehydrergosterol, Hydrazino-acetic acid ethyl ester, and Phthalic acid, di (2-propylpentyl) ester, whereas theoretical calculations showed that the highest EHOMO and lowest ELUMO values correspond to Dehydrergosterol and the Phthalic acid, which are the responsible for the extract inhibitory properties.

Voltammetric Investigation of Paracetamol Detection in Acidic Conditions by Using Cork-Modified Carbon Paste Electrodes

Developing new products that satisfy performance and durability expectations while also addressing environmental concerns is possible through the reuse of residues produced by industrial processes, aiming to fulfill the principles of circular economy. In this study, we improved the performance of a carbon paste sensor by incorporating untreated (RC) and regranulated/thermally treated (RGC) cork, which are considered biomass residues from the cork industry. We explored the electroanalytical behavior of paracetamol in sulfuric acid solutions using cyclic voltammetry and differential pulse techniques. The cork-modified carbon paste sensors showed greater sensitivity towards paracetamol. Both modified sensors allowed for an excellent resolution in distinguishing the voltammetric responses of paracetamol in sulfuric acid, showing for both an increase in peak currents compared to the unmodified carbon paste electrode. The quantification of paracetamol without interference has proved to be a feasible operation for the RC- and RGC-modified carbon paste sensors; notably, the first showed the most favorable limits of detection (LD = 2.4112 µM) and quantification (LQ = 8.0373 µM) for paracetamol in the sulfuric acid solution, performing significantly better than the second (LD = 10.355 µM, and LQ = 34.518 µM). Finally, the practical utility of the proposed sensors was assessed by analyzing paracetamol in pharmaceutical samples, obtaining satisfactory results that were in line with those obtainable using high-performance liquid chromatography.

Poly(ether-ether-ketone) copolymers featuring sulfonyl moieties for organic solvent nanofiltration membranes

Poly(ether-ether-ketone) (PEEK) is an attractive material for membrane fabrication due to its exceptional thermal and chemical stability. However, traditional PEEK processing necessitates the use of harsh chemicals, such as sulfuric acid because of its limited solubility in organic solvents. To overcome this limitation, copolymers offer a solution by enhancing solubility and subsequently improving membrane characteristics such as permeability and selectivity. Herein, three novel copolymers – PEEK with various contents of SO2 and CH3 – were developed and used in membranes for the separation of polar and non-polar solvents. The chemical structure of the copolymers was tailored by varying the monomer ratio between 0.25 and 0.75 for CH3 and SO2 containing monomers. Diamine–crosslinked PEEK copolymer membranes were prepared using a green solvent (TamiSolve). The effects of the polymer structure, the dope solution rheology, and membrane properties together with separation performance were studied. The resulting membranes demonstrated a permeance for acetonitrile ranging from 7.4 to 8.2 L m−2 h−1 bar−1 with molecular weight cutoffs of 839–915 g mol−1. Molecular dynamic simulations were conducted to explore the interaction between the copolymers and nine different organic solvents. Our findings underscore the significance of copolymer design in achieving tailored membrane properties for diverse separations.

Chicken meal is not an appropriate reference protein for estimating protein quality of ingredients used in extruded diets intended for dogs.

The indicator amino acid oxidation (IAAO) method has been used to determine metabolic availability (MA) of amino acids in feedstuffs for pigs, humans, and preliminarily for cats. Peas are a commonly used protein source in grain-free extruded dog diets. However, peas have a poor sulfur amino acid (AA) ratio (methionine [Met]:cysteine) with Met being the first limiting AA. Furthermore, little is known about the MA of Met in peas fed to dogs. Therefore, our objective was to compare the MA of Met in peas to chicken meal (CM), as a gold-standard reference protein. The study was done as a replicated 5 × 5 complete Latin square design. Ten neutered male mixed-breed dogs (1.5 years old; 26.0 kg ± 2.4kg body weight; BW) fed to maintain ideal BW received all dietary treatments: BAS: lamb-based diet (deboned lamb and lamb meal) providing Met at 50% of its requirement (0.27g/100g dry matter [DM]), CHK: CM and lamb-based diet, and PEA: ground dried pea and lamb-based diet both providing Met at 68% of its requirement (0.35 and 0.37g/100g DM, respectively). Two other treatments were created by blending BAS with PEA (BAP) and the BAS with CHK (BAC) to create diets with Met at 59% of requirement (0.32 and 0.31g/100g DM, respectively). This resulted in three graded levels of Met for both CM and peas to allow for a slope-ratio assay approach to quantify MA with the BAS diet as the common first point. All other AAs were provided to meet at least 120% of the AAFCO recommendations for adult dogs. The BAS diet, with supplemental DL-Met, was fed for a 2-wk wash-in period. After 2 d of diet adaptation IAAO was performed. Dogs were fed 13 small meals where meal 6 contained a priming dose (9.4mg/kg BW) of L-[1-13C]-phenylalanine (Phe; 99%) as well as a constant dose (2.4mg/kg BW) in meals 6-13. Breath samples were collected and enrichment of 13CO2 was measured using isotope-ratio mass spectrometry to calculate the rate of Phe oxidation (F13CO2 umol/kg BW/h). Oxidation was analyzed via SAS using PROC GLIMMIX with dog and period as random effects, and diet, %Met, and their interaction as fixed effects. Unexpectedly, the slope of Phe oxidation, in response to increasing Met intake, from CM was 31% of that of peas, indicating a lower MA for Met in CM as compared to peas. This finding may be due to damage of AAs during rendering. At this time, CM in extruded diets is not an acceptable reference protein to determine MA of AAs in dogs, and the MA of Met from peas cannot be confidently assessed.

Seed pretreatment using design of engineering approach for regulating <em>Humulus lupulus</em> seed germination in different media

Humulus lupulus, a plant of commercial benefit, has been widely explored for its therapeutic applications. Plant propagation via seeds is one of the major challenges due to seed dormancy and low germination. The physical dormancy of the seed caused by a hard seed coat makes seeds impervious to water. Different types of methods have been reported to break the seed dormancy. The present study emphasizes the optimized chemical method of seed pretreatment for regulating the germination efficiency in three different media namely, Murashige and Skoog (MS), Hoagland’s media and Leafy 200®. The study explores the interaction between two variables viz., acid treatment time and concentration of sulphuric acid, on germination of Humulus lupulus seeds using the Design of Experiment (DOE) approach. The results showed a higher germination rate in MS media and Leafy200® media (100%) seed germination percentage with respect to Hoagland’s media. The result demonstrates the synergistic role of seed pretreatment and media on the seed germination efficiency. The scanning electron microscopy (SEM) analysis of the seeds pretreated with acid revealed small perforations on the seed coat ranging between 5-15 µm. Furthermore, the elemental analysis of the seed coat surface by Energy Dispersive X-ray (EDX) revealed a substantial decrease in carbon and oxygen (%) and the presence of calcium, magnesium, and sulfur. The results indicate the acid hydrolysis of organic constituents on the seed surface enabling changes in seed porosity. Additionally, factors such as pretreatment and media play a pivotal role in regulating seed germination.

Study on performance deterioration and life prediction of reed straw-recycled brick aggregate concrete after freeze-thaw cycle

The current rate of carbon dioxide emissions poses a significant threat to global climate, making it increasingly important and urgent to lead the carbon-intensive construction industry to achieve carbon neutrality. Currently, the most practical method involves reusing waste materials. In this study, waste red bricks were used to replace 75 % of natural aggregates in concrete, and three different forms of reed stalks (including reed straw ash, reed straw strips, and reed straw powder) were added to prepare the recycled reed straw brick aggregate concrete (RSAC). Freeze-thaw tests were carried out for 25, 50, 75, and 100 cycles in water and sodium sulfate solution to establish a freeze-thaw deterioration model and perform life prediction. The results showed that the degree of freeze-thaw deterioration of the specimens in sulfuric acid solution was small, and the degree of deterioration of reed powder concrete (RSAC-F) and reed ash concrete (RSAC-H) was more serious than reed strip concrete (RSAC-T) and additive-free concrete (RSAC-0). After 100 water freeze-thaw cycles, the strength losses of the specimens were 21.55 %, 21.7 %, 18.71 %, and 20.54 %, and the relative dynamic elastic modulus losses were 6.11 %, 7.25 %, 4.39 %, and 5.79 %, and the mass losses were 1.79 %, 2.04 %, 1.4 %, and 1.5 %. The fitting results showed that the predicted values of the parabolic model and two-parameter Weibull distribution damage model were closer to the experimental values, and the fitting rates are both greater than 90 %. The life prediction results show that the freeze-thaw resistance of the four types of reed-brick aggregate recycled concrete can reach more than 80 years in southern China, meeting the durability requirements, and the RSAC-T and RSAC-0 group concrete could also be used in projects with lower frost resistance requirements in the north region of China.

Effect of the Atmosphere on the Properties of Aluminum Anodizing

This study aims to quantify the effect of process parameters on the anodizing of Al6061 aluminum. To achieve this, studies on layer thickness, the porosity of the anodized surface, electrochemical techniques, X-ray diffraction, grain size estimation, and statistical analysis were conducted for three different atmospheres (without air, air, and oxygen). Parameter levels were established as follows: temperature (30 °C, 45 °C, and 60 °C), time (20 min, 40 min, and 60 min), electrolyte concentration (0.5 M), voltage (9 V), and current intensity (0.600 A). A 33 experimental design (three factors, three levels) was proposed, and mathematical models were obtained using general factorial design. The experimental design was used to determine the three most important variables in the optimal condition. A total of 27 tests were conducted using sulfuric acid electrolytic solutions, of which 12 samples were selected by the factorial design method, which simultaneously evaluates the effects of factors and their interactions in a single experiment. Measurement of porosity and oxide layer thickness was performed using scanning electron microscopy. The purity of the anodic layer formed was characterized using X-ray diffraction techniques with a vertical goniometer X-ray diffractometer. The electrochemical behavior is presented through potentiodynamic polarization curves for the anodic layer. A general factorial design and an analysis of variance (ANOVA) were conducted to establish the significant factors for layer thickness, grain size, and reaction rate. Finally, the best results and their parameters for each response are presented.

A Kinetic Study of Silver Extraction from End-of-Life Photovoltaic Panels through Gold-REC1 Process

Recycling materials from end-of-life devices and products is becoming increasingly a fundamental activity for the sustainable development of nations. With the return from the market of immense quantities of photovoltaic panels at the end of their life, it is essential to foresee processes for recovering and valorizing all the raw materials present in them to avoid wasting important flows of raw materials. This research introduces a novel process aimed at the recovery of silver and silicon from end-of-life photovoltaic panels. The leaching efficiency and kinetics of ground cake powder in sulfuric acid, ferric sulfate, and thiourea were investigated in the leaching system. In particular, the influences of significant parameters, including particle size, leaching temperature, and stirring rate, on the extraction kinetics were analyzed using the shrinking core model. The results showed silver dissolving mechanisms, in which more than 90% of silver recovery at 60 min of reaction time and 99% at 120 min was achieved (120 rpm, 53–125 µm, and 40 °C). The significant effect of the leaching temperature suggests that the process is under the control of the chemical reaction. Moreover, these results were confirmed by the regression analysis of the experimental data with the shrinking core model. It can be concluded that this newly proposed process, called Gold-REC1, allows the recovery of Ag and Si (solid residue from the process) with extremely high yields and rapid kinetics. The obtained results can provide fundamental data for developing end-of-life photovoltaic recycling on an industrial scale.

Comparative Study of Adsorbents for Treatment of Industrial Effluent

Water contaminated with various impurities is considered as wastewater and industrial wastewater obtainedfrom industries is known as effluent. The industrial effluent adversely affects the aquatic ecosystems,deteriorate human health, and degrades overall environmental quality. Treatment of such effluent withadsorbent is one of the most efficient and cost-effective method. In the present study, industrial effluent wastreated with various bio-adsorbents obtained from orange peels, cotton, neem tree bark. Effect of adsorptionon parameters like pH, COD, BOD, TDS and TSS were determined and their results were compared withcommercial grade activated charcoal. For majority of the parameters, the effectiveness of adsorbent varied as:activated charcoal > tree bark-based adsorbent > cotton-based adsorbent > orange peels-based adsorbent.Effect of pretreatment- acid treatment- was also examined for cotton and tree bark-based adsorbent.Phosphoric acid was proven to be better acid for pretreatment in comparison with sulfuric acid. For tree barkbased adsorbent treated with phosphoric acid, % removal for COD, BOD, TDS and TSS were 46.5 %, 57.06%, 35.51% and 90.43% respectively

The Testing Results of ACORGA, LIX Extractants and CR60 Crud Mitigation Reagent Influence during SX-EW Copper Extraction

Research analysis reveals factors influencing third-phase crud formation and composition during metal extraction, including solution composition, solid suspensions, organic compounds, colloidal compounds (e.g., silicic acid), and extractant purity. Compositional analysis of copper-containing sulfuric acid solutions (1.25 g/dm3 copper) identifies principal sulfate-forming components. Copper extraction was studied using extractants LIX 984N, ACORGA M5774, and M5640 at different ratios of the organic phase to the aqueous O:A (from 1:2 to 1:10). Suppressive impact of 10 vol.% CR60 additive on third-phase crud formation during copper extraction with LIX 984N, ACORGA M5774, and M5640 is analyzed, with ACORGA M5774 being the most effective. Physicochemical analysis characterizes CR60’s active substance as poly(sodium 4-styrenesulfonate) with steel-suppression properties, and its structural formula is determined. Optimal copper extraction conditions establish ACORGA M5640’s 24% efficiency, followed by ACORGA M5774 at 15%. CR60 reduces crud formation, with 5 cm3 of ACORGA CR60 added to sulfuric acid solution reducing interfacial crud formation by 2–3 times. Optimal extraction parameters include 1:2 O:A ratio, 20 ± 5 °C temperature, 5 cm3 CR60 additive, 5 min process duration, and 1-day settling time. ACORGA M5774 (10 vol.% in kerosene) is recommended as an extractant, with 2–3 stages of countercurrent extraction.

High efficiency filtration and optimization of pelletizing performance of fine hematite concentrate using sulfuric acid filter aid: Behavior and mechanism

Following the application of anionic reverse flotation to fine low-grade hematite ore, a significant challenge emerges with elevated slurry viscosity and heightened moisture content in the resulting filter cakes. To address the challenge of dewatering during the filtration process of fine hematite concentrate, the impact of sulfuric acid filter aid dosage and filtration temperature on the filtration performance of hematite concentrate was systematically investigated in this study. In addition, the effect of sulfuric acid filter aid on the preparation of hematite pellets was also studied. The results revealed a significant decrease from 1.10 × 1010 1/m2 to 5.7 × 109 1/m2 in the specific resistance of the hematite filter cake when the sulfuric acid dosage was 1.2 g/kg and the filtration temperature was 20 °C. The mechanism underlying the enhancement of filtration performance of fine hematite concentrate by sulfuric acid was summarized. Sulfuric acid compressed the double electric layer on the surface of hematite concentrate particles, reducing the surface zeta potential and causing the aggregation of fine particles into larger ones. This led to an increase in filter cake porosity and compression of the hydration film thickness on particle surfaces, facilitating easier removal of filtrate from the filter cake. The appropriate dosage of bentonite for pelletizing was not significantly affected by sulfuric acid filter aid. Sulfuric acid improved the porosity, drying rate, and burst temperature of hematite green pellets. While the compressive strength of preheated pellets from sulfuric acid-assisted filtration of hematite concentrate showed a slight decrease, the compressive strength of roasted pellets was significantly increased.

Characterization and Cytotoxic Assessment of Bis(2-hydroxy-3-carboxyphenyl)methane and Its Nickel(II) Complex.

A condensation reaction of salicylic acid with formaldehyde in the presence of sulfuric acid led to the synthesization of the bis(2-hydroxy-3-carboxyphenyl)methane (BHCM) ligand, which was subsequently allowed to bind with nickel (II) ions. In light of the information obtained from the elemental analyses (C, H, and M), spectral (IR, MS, 1H-NMR, and UV-Vis) and thermal and magnetic measurements, the most likely structures of the ligand and complex have been identified. It has been suggested that the BHCM coordinates in a tetradentate manner with two Ni(II) ions to produce an octahedral binuclear complex. The SEM and TEM morphology of the compounds showed spherical shapes. An X-ray diffraction analysis indicated a considerable difference in the diffraction patterns between BHCM (crystalline) and Ni-BHCM (amorphous), and the Scherrer equation was used to calculate the crystallite size. Some optical characteristics were estimated from UV-Vis spectra. The ligand and its nickel(II) complex underlie the range of semiconductors. It was verified that for human lung (A-549) cancer, the BHCM compound displayed a significant barrier to the proliferation test in noncancerous cells (human lung fibroblasts, WI-38), which was also undertaken. To demonstrate the binding affinities of the chosen compounds (BHCM and Ni-BHCM) in the receptor protein's active site [PDB ID: 5CAO], a molecular docking (MD) study was carried out.