Sulfuric Acid Research Articles

Spontaneous Molecular Bromine Production in Sea-Salt Aerosols.

Bromine chemistry is responsible for the catalytic ozone destruction in the atmosphere. The heterogeneous reactions of sea-salt aerosols are the main abiotic sources of reactive bromine in the atmosphere. Here, we present a novel mechanism for the activation of bromide ions (Br-) by O2 and H2O in the absence of additional oxidants. The laboratory and theoretical calculation results demonstrated that under dark conditions, Br-, O2 and H3O+ could spontaneously generate Br and HO2 radicals through a proton-electron transfer process at the air-water interface and in the liquid phase. Our results also showed that light and acidity could significantly promote the activation of Br- and the production of Br2. The estimated gaseous Br2 production rate was up to 1.55×1010 molecules cm-2 ⋅ s-1 under light and acidic conditions; these results showed a significant contribution to the atmospheric reactive bromine budget. The reactive oxygen species (ROS) generated during Br- activation could promote the multiphase oxidation of SO2 to produce sulfuric acid, while the increase in acidity had a positive feedback effect on Br- activation. Our findings highlight the crucial role of the proton-electron transfer process in Br2 production; here, H3O+ facilitates the activation of Br- by O2, serves as a significant source of atmospheric reactive bromine and exerts a profound impact on the atmospheric oxidation capacity.

Development of an Enhanced Method for Copper Extraction from Sulfuric Acid Solutions

Development of an Enhanced Method for Copper Extraction from Sulfuric Acid Solutions

Stability Prediction of Oxidative Active Species in Electrolytic Sulfuric Acid

Stability Prediction of Oxidative Active Species in Electrolytic Sulfuric Acid

Assessment of the Impact of Pretreatment of Spent Coffee Grounds with Diluted Sulfuric Acid on the Efficiency of Methane and Lactic Acid Fermentation

Lignocellulosic materials are composed of three major biocomponents such as cellulose, hemicellulose and lignin, which form a compact lignocellulosic complex. Characterized by high caloric content, lignocellulosic biomass, including coffee grounds, is a valuable energy source that can be efficiently used in various bioconversion and biotransformation processes. Due to the high consumption of coffee in the world, there is an increasing amount of coffee grounds, which is a rich waste and at the same time a valuable secondary raw material, and its use fits perfectly into a closed-loop economy. Coffee grounds biomass contains polysaccharides, mainly mannans, proteins, lipids, polyphenols, which will allow the development of different biorefinery strategies, the creation of new value-added products with reduced waste generation. The research describes the pre-treatment of coffee grounds with dilute sulfuric acid to evaluate the effect of acid concentration, hydrolysis time on biogas yield, including methane and lactic acid biosynthesis during anaerobic fermentations. A yield of 381.12 mL of CH4/g-VS methane was obtained, accounting for 72.48% of the total biogas composition. It was found that the most efficient sample in terms of substrate pre-treatment for lactic acid biosynthesis was coffee grounds after 90 min hydrolysis with 1.5% H2SO4 at 121 °C.

Cluster-dynamics-based parameterization for sulfuric acid–dimethylamine nucleation: comparison and selection through box and three-dimensional modeling

Abstract. Clustering of gaseous sulfuric acid (SA) enhanced by dimethylamine (DMA) is a major mechanism for new particle formation (NPF) in polluted atmospheres. However, uncertainty remains regarding the SA–DMA nucleation parameterization that reasonably represents cluster dynamics and is applicable across various atmospheric conditions. This uncertainty hinders accurate three-dimensional (3-D) modeling of NPF and the subsequent assessment of its environmental and climatic impacts. Here we extensively compare different cluster-dynamics-based parameterizations for SA–DMA nucleation and identify the most reliable one through a combination of box model simulations, 3-D modeling, and in situ observations. Results show that the parameterization derived from Atmospheric Cluster Dynamic Code (ACDC) simulations, incorporating the latest theoretical insights (DLPNO-CCSD(T)/aug-cc-pVTZ//ωB97X-D/6-311++G(3df,3pd) level of theory) and adequate representation of cluster dynamics, exhibits dependable performance in 3-D NPF simulation for both winter and summer conditions in Beijing and shows promise for application in diverse atmospheric conditions. Another ACDC-derived parameterization, replacing the level of theory with RI-CC2/aug-cc-pV(T+d)Z//M06-2X/6–311++G(3df,3pd), also performs well in NPF modeling at relatively low temperatures around 280 K but exhibits limitations at higher temperatures due to inappropriate representation of SA–DMA cluster thermodynamics. Additionally, a previously reported parameterization incorporating simplifications is applicable for simulating NPF in polluted atmospheres but tends to overestimate particle formation rates under conditions of elevated temperature (>∼300 K) and low-condensation sink (<∼3×10-3 s−1). Our findings highlight the applicability of the new ACDC-derived parameterization, which couples the latest SA–DMA nucleation theory and holistic cluster dynamics, in 3-D NPF modeling. The ACDC-derived parameterization framework provides a valuable reference for developing parameterizations for other nucleation systems.

Microwave and ultrasound-assisted green protocols for 5-methylthiazole induced Betti bases: molecular docking, in-silico pharmacokinetics, and anticancer activity studies

ABSTRACT Herein, we describe an efficient one-pot three-component microwave and ultrasound-endorsed approaches for synthesizing distinct 5-methylthiazole induced Betti bases (5-methyl-thiazol-2-ylamino-aryl-benzylnapthols) employing silica sulfuric acid (SSA, silica-OSO3H) as an active heterogeneous acid catalyst. The title compounds produced in good yields (86–95%) from naphthalen-2-ol, 5-methylthiazol-2-amine, and assorted aryl aldehydes; and structurally characterized by spectral and elemental analyses. A comprehensive comparative study of conventional, ultrasonic, and microwave-irradiated synthetic routes has been achieved by optimizing various reaction parameters. These new protocols provide several advantages, including the use of an inexpensive, non-toxic, and reusable catalyst. Additionally, they benefit from mild reaction conditions, short reaction times, and simple workup and purification procedures, thereby increasing their practicality. Furthermore, the synthesized compounds were evaluated for their anticancer potency against A-549 (lung cancer) and A-498 (kidney cancer) cell lines, with scaffold IVa demonstrating excellent (GI50 < 10 µg/mL) inhibitory activity against A-549. Additionally, molecular docking was performed to investigate potential binding interactions between ligands and proteins. Scaffold IVa exhibited the best docking with cancerous target proteins 1M17 (−8.9 kcal/mol) and 1M14 (−7.2 kcal/mol), thereby supporting our bio-activity studies.

The behaviour of charged particles (ions) during new particle formation events in urban Leipzig, Germany

Abstract. Air ions are electrically charged particles in air. They are ubiquitous in the natural environment and affect the Earth's radiation budget by accelerating the formation and growth of new aerosol particles. Despite this, few datasets exist exploring these effects in the urban environment. A neutral cluster and air ion spectrometer was deployed in Leipzig, Germany, to measure the number size distribution of charged particles from 0.8 to 42 nm, between 27 July and 25 August 2022. Following previous analyses, charged particles were classified into small (0.8–1.6 nm), intermediate (1.6–7.5 nm), and large (7.5–22 nm) fractions by mass diameter, and their mean concentrations (sum of positive and negative polarities) during the campaign were 405, 71.6, and 415 cm−3, respectively. The largest peaks in intermediate and large ions were explained by new particle formation (NPF), with intermediate ions correlating well with sulfuric acid dimer. Smaller morning and evening peaks were coincident with black carbon concentrations and attributed to primary emissions. NPF events, observed on 30 % of days, coincided with intense solar radiation and elevated sulfuric acid dimer. Small charged particles were primarily associated with radioactive decay and highest during the early hours, and they are unrelated to primary emissions or NPF. The apparent contributions of charged particles to 3 and 7.5 nm particle formation rates were 5.7 % and 12.7 %, respectively, with mean growth rates of 4.0 nm h−1 between 3–7.5 nm and 5.2 nm h−1 between 7.5 and 22 nm. The ratio of charged to total particle formation rates at 3 nm suggests a minor role for charged particles in NPF. We conclude that NPF is a primary source of &gt; 3 nm ions in our data, with primary emissions being the major source in the absence of NPF.

Poly(3,4-ethylenedioxythiophene)-Coated Vanadium-Doped MnO2 Nanorods for High-Performance Flexible Aqueous Zinc-Ion Battery Cathode.

Manganese-based aqueous zinc-ion batteries (AZIBs) are considered promising cathode materials for large-scale energy storage applications due to their low cost and high safety. However, the primary constraints on achieving high specific capacity and cycling stability are the inherent low conductivity and suboptimal structural stability of the AZIB cathodes. Herein, we report a high-performance poly(3,4-ethylenedioxythiophene) (PEDOT)-coated vanadium-doped MnO2 nanorod (NR) electrode for AZIBs. First, vanadium-doped MnO2 (V-MnO2) NRs were synthesized by a simple hydrothermal synthesis method. The V-MnO2 NRs were further encapsulated with a nanolayer of PEDOT through an in situ polymerization process, which was subsequently treated with sulfuric acid to achieve a smooth surface. The V doping creates oxygen vacancies within the MnO2, allowing for the rapid embedding and diffusion of Zn2+. The PEDOT nanolayer greatly enhances the conductivity and structural stability of the V-MnO2. Benefiting from the unique features, an optimal composite NRs electrode exhibits a high specific capacity of 250 mAh g-1 at 0.4 A g-1, a high energy density (388 Wh kg-1 at 151 W kg-1), and excellent stability over 5000 cycles at 3 A g-1. In addition, the flexible pouch cell assembled with the electrode shows good stability under bending. Given the positive outcomes, the material holds great potential for use as a cathode in next-generation flexible energy storage systems.

PSLBII-4 The effect of standardized ileal digestible sulfur amino acid intake during late gestation on gilt whole-body nitrogen retention and subsequent litter performance

Abstract Gestating gilts [n = 27; body weight (BW) = 158 ± 5.5 kg] were used to determine the effect of standardized ileal digestible (SID) sulfur amino acid (SAA) intake during late gestation on whole-body nitrogen (N) retention and subsequent litter performance. Gilts were assigned to one of two experimental diets that provided SAA at 60 or 200 % of estimated requirements during late gestation (0.29 and 0.92 % SID SAA, respectively; n = 15 and 12, respectively; Table 1 and 2). Each gilt received 2.53 kg of the assigned diet between gestation d 90 and farrowing; standard lactation and nursery diets were provided to gilts after farrowing and offspring after weaning, respectively. Gilt whole-body N balance was determined between d 107 and 109 of gestation using total urine collection and fecal grab-sampling. After farrowing, litters were standardized to 13 piglets and were not offered creep feed. Whole-body N retention was greater in gilts fed the diet containing 0.92 vs. 0.29 % SID SAA in late gestation (27.2 vs. 19.3 ± 1.8 g/d; P &amp;lt; 0.05; Table 3), but the number of piglets born alive, litter birth weight, subsequent piglet growth rates, and litter size at weaning were not different between treatment groups. The post-weaning growth performance of offspring was also not influenced by maternal dietary treatment in late gestation (Table 4). At farrowing, the post-absorptive plasma concentration of Cys tended to be less (P = 0.072) and taurine was greater (P &amp;lt; 0.01) for gilts fed 0.92 vs. 0.29 % SID SAA in late gestation; however, there were no differences in plasma SAA metabolites concentrations for gilts at weaning or offspring at birth (Table 5. At weaning, offspring from gilts fed 0.92 % SID SAA had greater plasma homocysteine (P &amp;lt; 0.05) and plasma Cys concentrations (tendency; P = 0.072) vs. offspring from gilts fed 0.29 % SID SAA in late gestation. Three weeks after weaning, plasma taurine concentration was less (P &amp;lt; 0.05) for offspring from gilts fed 0.92 vs. 0.29 % SID SAA in late gestation (Table 6). Six weeks after weaning, plasma glutathione concentration tended to be less (P = 0.057) for offspring from gilts fed 0.92 vs 0.29 % SID SAA in late gestation. When SAA were fed below estimated requirements during late gestation, whole-body N retention was reduced, but fetal growth appeared to be maintained, likely at the expense of maternal N retention. Such divergences in dietary SAA supply in late gestation had no effect on subsequent offspring growth performance, but it appeared that offspring SAA metabolism was impacted until at least 6 wk after weaning. The influence of differences in sulfur AA metabolites on offspring performance beyond the nursery phase remains unknown. Therefore, carry-over effects of maternal SAA supply in late gestation should be considered when developing feeding recommendations for gestating gilts.

Near-infrared photothermal lens as microfluidic analyzer for determination of phosphate in food and biological samples

In this work, photothermal lens spectrophotometer (PTLS) with crossed-beam configuration pumped by a laser diode (850 nm) was used for determination of soluble phosphorus exists mainly in the form of orthophosphate (PO43−) in nonalcoholic beverage and human blood serum samples. The determination was carried out after complexation reaction between blue molybdenum and phosphate in aqueous solution. UV–vis spectrophotometry was used by measuring absorption in the near infrared region (815 nm) for optimizing the complex formation time, concentrations of reducing agent and sulfuric acid. The UV–vis absorption measurements showed that the calibration curve was obtained in the concentration ranges of 0.5–80 mg L−1 with a linear correlation coefficient of 0.98 and a detection limit of 0.2 mg L−1. Then, PTLS at a wavelength of 850 nm after optimizing the device conditions (flow rate, excitation laser power and interrupting frequency) was used for phosphate determination. The calibration curve in the concentration range of 11–1000 µg L−1 has a correlation coefficient of 0.98 and a detection limit of 4 µg L−1. The achieved detection limit was about 50 times better than NIR absorption spectrometry using a conventional 1 cm sample cell. In PTLS with the 3 μL microfluidic cell experimental detectability amount of phosphate is 33 picogram, while in UV–vis-NIR method this amount is 1.5 µg.

Surface characteristics of maraging steel during electropolishing as a function of polishing time

ABSTRACT Thermal-based machining process like EDM, Laser-assisted additive manufacturing process degrades the surface integrity of the component. Therefore, a post-polishing method is required to improve the surface integrity as well as the performance of the component. A gyroscope, made of maraging steel, fabricated by EDM, is utilised in space industry and has poor surface integrity, which affects its performance. Thus, electropolishing (EP), a non-conventional polishing process, is used for the above said problem as it possesses several advantages over other polishing methods. There are very few literatures available for EP of maraging steel. The present manuscript is the preliminary analysis for the electrolyte (Ortho-phosphoric acid, sulphuric acid and hydrochloric acid) and its effect on maraging steel with respect to time. The surface characteristics such as surface roughness and surface reflectivity, along with surface elemental composition, have been evaluated. With increase in time, maximum improvement in surface roughness and surface reflectivity is 61.23% and 70%, respectively. It can be concluded that the selected electrolyte gives a promising improvement in the surface characteristics of maraging steel.

Experimental research on chemisorption energy storage performance for industrial waste heat recovery and conversion

This study investigates a solid chemisorption energy storage system utilizing a multi-component chloride salt composite adsorbent with a mass ratio of NH4Cl, CaCl2, MnCl2, and expanded natural graphite treated with sulfuric acid (ENG-TSA). The system features a shell-and-tube heat exchanger and analyzes refrigeration and heat storage performance under varying industrial low-temperature waste heat (60–110 °C) conditions, with condensation and evaporation temperatures of 0–25 °C and discharging temperatures of 40–60 °C. The results indicate that the multi-salt composite adsorbent reduces hysteresis between adsorption and desorption stages. The highest coefficient of performance (COP) and specific cooling power (SCP) were 0.461 and 328 W/kg, respectively, at an evaporation temperature of 25 °C and a charging temperature of 110 °C. Excessively long cycle times negatively affect system efficiency, with optimal performance achieved at a 40-min cycle. The findings highlight the system's effectiveness for industrial low-grade waste heat recovery, providing a solid foundation for future reactor design and material selection.

383 Performance of piglets in response to graded dietary supplementation of sulfur amino acids using either hydroxy-methionine or DL-Methionine during the post-weaning period

Abstract Providing piglets with their precise nutritional need is critical during the stressful post-weaning period. Methionine (Met), a sulfur-containing amino acid, has a crucial role in piglet growth and health. Stressful conditions may increase Met demand due to its involvement in maintaining redox balance via downstream metabolites such as glutathione. There are different sources of supplementary Met for pigs such as DL-methionine (DL-Met) and hydroxy-methionine. The latter comes mostly as an acidic liquid form (OH-Met) and to a lesser degree as a powder calcium-salt (OH-Met-Ca). This study investigates the effect of graded levels of dietary total sulfur amino acids (TSAA) by supplementing different sources of Met on the performance and capacity of post-weaning piglets to respond to stress. Two experiments were performed. In experiment 1, post-weaning piglets [n = 90; 28 d of age; body weight (BW) = 9.13 ± 0.65 kg] were fed with either DL-Met or OH-Met-Ca to provide 80%, 100%, and 125% TSAA recommendations of NRC and performance parameters were measured for 41 d. Treatments were replicated nine times, and blocking was done according to initial BW. For experiment 2, 720 post-weaning piglets (n = 720; 28 d of age; BW = 6.84 ± 1.07 kg) from three consecutive breeding batches were fed with either DL-Met, OH-Met, or OH-Met-Ca at or above (100% or 125%) TSAA requirements of FEDNA. Performance parameters and oxidative status through various plasma indicators were measured. Treatments were replicated 12 times. Data from both experiments were analyzed separately using a mixed effect model with Met source and level as fixed effects (and their interaction in experiment 2) and blocks and batch as random effects for experiments 1 and 2, respectively. In experiment 1, piglets fed 80% of TSAA requirement showed the least average daily weight gain, while those fed OH-Met-Ca at 100% or DL-Met at 125% requirement had the greatest BW gain among the treatments (P &amp;lt; 0.01). Feed conversion ratio was best for piglets fed with OH-Met-Ca at 100% requirement, while animals fed with 80% requirement were the least efficient (P = 0.04). Contrasts showed no differences between Met sources (P ≥ 0.51) and level of TSAA (P ≥ 0.56) for any of the parameters. Meanwhile in experiment 2, there were no interactions between Met source and TSAA level (P &amp;gt; 0.10). The Met source did not affect any parameter (P ≥ 0.14). However, there was a significant decrease in daily feed intake when piglets were fed above requirements (P = 0.02), and a significant increase in the concentration of plasma glutathione peroxidase when piglets were fed at TSAA requirements (P &amp;lt; 0.05). These results suggest that post-weaning piglet performance and oxidative status can be sustained regardless of the Met source tested. Feeding healthy and unchallenged piglets with excess dietary Met may not bring extra benefits.

Correlation between preparation techniques and frictional properties of cellulose nanocrystals as additives in water-based lubricants

To explore the tribological characteristics of cellulose nanocrystals derived through various preparation techniques when utilized as additives in water-based lubricants, two types of cellulose nanocrystals (S-CNC and C-CNC) were chosen. These were produced via sulfuric acid hydrolysis and oxidation methods. The morphology and structural features were assessed through techniques such as Fourier-transform infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD), laser confocal Raman spectroscopy, elemental analysis, scanning electron microscopy (SEM), and laser particle size analysis. According to thermogravimetric analysis (TGA), the thermal stability of S-CNC is slightly superior to that of C-CNC. S-CNC exhibits liquid crystallinity when the concentration exceeds 0.5 %, whereas C-CNC does not display liquid crystallinity at any concentration tested. Further investigation was conducted on the frictional properties of the two types of CNCs using a UMT reciprocating friction tester. The results indicate that both types of CNC exhibit significant friction reduction properties at various additive concentrations, provided the addition does not exceed w=1 %. When below their respective liquid crystalline phase concentrations, the friction reduction performance of S-CNC is slightly inferior to that of C-CNC; however, when above the liquid crystalline phase concentration, the friction reduction performance of S-CNC surpasses that of C-CNC. The addition of w=0.5 % S-CNC leads to a relative reduction of 63.4 % in the friction coefficient compared to the base system. Analysis of the steel plate surface contact angle and post-wear surface suggests that the lubrication mechanism of CNC involves the adsorption of polar functional groups such as hydroxyl or carboxyl groups from the CNC structure onto the friction pair surface, forming a lubricating protective film to varying degrees. Additionally, the liquid crystalline structure of S-CNC facilitates the formation of an ordered lubricating film, further enhancing the frictional properties. These findings provide valuable insights into the application of nanocellulose crystals as lubricant additives.

Study on the behavior of AAEMs removal and the evolution of microscopic characteristics in high alkali coal under different acids

ABSTRACT In this paper, the removal behavior of alkali and alkaline earth metals (AAEMs) and the evolution of microscopic characteristics in high alkali coal under the leaching of inorganic and organic acids are studied. The results show inorganic acids have better effect on the removal of AAEMs because of their stronger ability to convert carboxylate and phenol salts into covalent carboxylic acids and phenols. Citric acid has a slightly weaker effect than inorganic acids, and oxalic acid has the least effect. The improvement of slagging characteristics is consistent with the removal ability. Sulfuric acid, hydrochloric acid and citric acid are more effective in enhancing the calorific value of coal, with an enhancement of about 0.60 MJ/kg. After leaching, the pores and cracks in the coal are developed, and the mesopores have a tendency to shift to a lower pore size range. This trend is most pronounced in citric acid leached coal and hydrochloric acid leached coal. Sulfuric acid seriously damage the surface morphology, which results in a tendency of large pore transfer in S-form coal.

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.