Ammonium Sulfate Research Articles

Additive Water Uptake of the Mixtures of Urban Atmospheric HULIS and Ammonium Sulfate

AbstractThe hygroscopicity of atmospheric aerosols affect the global climate and human health. However, the hygroscopic behavior of mixtures of inorganic salts and organics in atmospheric aerosols have not been well characterized for ambient complex organic mixtures. Here, the hygroscopic growth of humic‐like substances (HULIS), which represent the complexity of organic aerosol compounds, from urban aerosols and their mixtures with ammonium sulfate were investigated with measurements from a hygroscopicity tandem differential mobility analyzer and model analyses. The Zdanovskii–Stokes–Robinson (ZSR) relationship, which assumes that the water uptake of each component is additive, was examined for the mixtures. The dependence of the hygroscopicity parameters (κ) of the mixtures on the volume fraction of HULIS is generally represented by the ZSR relationship with the deviations of κ on average of 16% (4%–27% in different mixing ratios), and 0.03 (0.02–0.04) on absolute basis. An assumption of asphericity for the dry particles reduced the deviations (14%). Approximations for the surface tension depression by surfactants and surface‐bulk partitioning were predicted to account for the deviations to a small extent. Furthermore, a thermodynamic model for simplified compound systems showed that the non‐ideality of the solutions potentially explained the deviations from the ZSR relationship. The results of this study support the use of the ZSR relationship for organic‒inorganic mixtures as a practical approximation in atmospheric models, provide a guide for the uncertainty associated with this approximation, and suggest directions for future studies.

Nitrogen migration and transformation characteristics of the soil in karst areas under the combined application of oxalic acid and urea inhibitors

ObjectiveWe investigated the horizontal migration and transformation of nitrogen in soil with oxalic acid and inhibitors (e.g., nitrification inhibitors, DMPP, urease inhibitors, and NBPT) under different soil water contents to provide a basis for the efficient utilization of nitrogen fertilizer in agricultural production in karst areas.MethodsFour nitrogen fertilizers (e.g., ammonium bicarbonate, ammonium sulfate, ammonium chloride, and urea) were applied separately and combined with oxalic acid, DMPP, and NBPT. The ammonium and nitrate nitrogen contents in the different soil layers were measured. The soil columns were cultured through an indoor soil column simulation at water content levels of 30%, 40%, and flooded (50%) for 30 days.ResultsAmmonium bicarbonate with inhibitors increased soil NH4+-N content by 15.42–21.12%. Ammonium sulfate with oxalic acid or NBPT increased soil NH4+-N content by 27.56–52.25% at 30% and 40% moisture content treatments, compared to ammonium sulfate alone. Urea with DMPP application significantly increased soil NH4+-N content by 11.93–14.87% at 40% water content and flooded conditions. In all treatments, the NH4+-N content in the soil treated with 30% water content of ammonium chloride with oxalic acid was the highest. The NH4+-N content showed a decreasing trend with an increase in the water content. The NO3−-N content in soil treated with ammonium bicarbonate and DMPP was higher than that treated with other nitrogen fertilizers at 30% moisture. The NO3−-N content decreased with increased water content. Under all treatments, ammonium chloride with oxalic acid had the highest percentage of soil NH4+-N and soil soluble inorganic nitrogen at 30% water content, with 55.29% and 55.97%, respectively.ConclusionAmong the nitrogen fertilizer treatments, the soil NH4+-N content increased in ammonium bicarbonate with DMPP or NBPT, ammonium sulfate with oxalic acid or NBPT, and urea with DMPP. The four nitrogen fertilizers with DMPP increased the soil NO3−-N content. Nitrogen fertilizer combined with oxalic acid and inhibitors could effectively improve the effective use of nitrogen fertilizer.

Effect of Milk Sources on Whey Protein and Fractions of Casein

Aim: Milk from Cow, Buffalo and goat was used for the study of isolation and fractionation of casein and whey proteins. Buffalo and goat milk were subjected to physicochemical attribute studies and a detailed protein profile namely total protein, casein fractions α-, β- and κ casein and whey protein were separated by urea fractionation method. The aim of this study was to compare various casein fractions isolated from cows, Buffalo and Goat milk. The method of separating casein into its fractions is based on the solubility of the individual components in urea the solution. The separation of casein fractions was carried out in dissolving molar concentration of urea and the yield of fractions and total protein percentages were calculated. Buffalo and goat milk have comparatively higher total protein and whey protein content as compared to cow milk. Maximum whey proteins found in goat milk (20.58%) whereas cow milk had the lowest whey protein (19.29%). Among casein fractions, α fraction (16.64%) was found maximum in Buffalo milk followed by cow (14.92%) and goat milk (5.42%). The goat milk showed the highest level of β casein (17.81%) whereas, the lowest concentration of β casein was found in cow milk (9.38%). Study Design: A significant contribution to the total milk production of India comes from buffalo milk and goat milk. Despite that, Buffalo milk and goat milk are not being utilized for many products because of difference in composition of different species milk and their inherent problems associated in the production of products. Place and Duration of Study: Karnataka Veterinary Animal and Fisheries Sciences University (KVAFSU), Dairy Science College, Hebbal, Bangalore Karnataka, India Materials: The Goat milk samples were collected from Sinchana Goat and Sheep farm, Marenahalli village (Bengaluru Rural Dist) and Buffalo milk was obtained from Country Delight Pvt. Ltd., J. P. Nagar, Bengaluru, Karnataka. Cow milk used in this investigation was collected from SEDP, Dairy Science College, Hebbal, Bengalore.. All the glassware used was soaked in chromic acid solution, repeatedly washed with water, rinsed with distilled water and dried before use. For microbiological analysis dried test tubes, conical flasks, pipettes were cotton plugged and sterilized in a hot air oven. The chemicals and reagents used in this study were mainly of analytical grade procured from Prince Laboratory Company Pvt. Limited, Bangalore. The protein molecular weight markers used for the electrophoretic study were procured from Bangalore Genei Pvt. Ltd. Methodology: Standard urea fractionation method adopted by Hipp et al was used for isolation and fractionation of caseins. Skim milk was prepared by subjecting whole milk for centrifugation, the skim milk obtained was acidified using 1 % hydrochloric acid at 200 C to obtain casein precipitate. Obtained whole casein was dissolved in 3.3 M urea at pH 7.5 and adjusted to pH 4.6 which precipitates the bulk of α casein and leaving k-caseins into soluble filtrates. Again the supernatant was adjusted to pH 4.9 diluted to 1.0 M urea and warmed to 300 C precipitating the β-caeisn. Further, addition of ammonium sulphate was used to isolate k-casein from the precipitate. Results: The sources of protein had a significant influence on the total casein, casein fractions and whey protein content of different species. The highest quantity of total caseins (34.30g/l) and whey protein (8.87 g/l) were observed in buffalo milk followed by cow (28.52 g/l) and lowest was observed in goat milk (28.45 g/l). Total protein, casein and whey protein contents were greatly affected by the source of milk. Conclusion: The significant effect of source of milk on total protein, casein, its fractions and their yield was observed. highest yield of casein (54.31%) was observed in cow milk than buffalo milk (48.95 %) and lower yield was found in goat milk. Amongst the three species, highest per cent of β casein was noted in goat milk (54.05 %) followed by buffalo (36.03%) and cow milk (34.14%). Recommendation: Rasagulla will be consumed universally by all age groups globally. Thus, the consumption of Rasagulla helps in providing overall nutritional requirements. However, the study has been conducted on a pilot scale. Moreover, commercial production may necessitate huge cost on enzymatic modification of proteins and separation peptides for value addition.

Влияние КАС-32, жидких и твердых комплексных удобрений на урожайность и показатели качества зерна яровой пшеницы в условиях Предгорий Салаира при ее возделывании по технологии No-till

The purpose of research is to study the influence of different combinations of UAN-32 with the addition of ammonium sulfate, liquid and solid complex (JCU, ammophos, diammofoska, sulfoammophos) fertile-zers on the formation of basic quality indicators and grain yield of spring wheat when cultivating the crop using the no-till system. In the conditions of the Salair Foothills in the Tselinny District on leached chernozems of medium humus in 2020–2022. Research was carried out on the local pre-sowing application of different combinations of fertilizers. The highest yield is ensured by the application of UAN-32 150 kg/ha with 60 kg/ha ammonium sulfate and 100 kg/ha ammophos (N88P52S14) and according to the UAN-32 option 150 kg/ha + liquid fertilizers 100 kg/ha + sulfoammophos 100 kg/ha (N92P57S22): respectively 7.03–7.24 t/ha (average for 2 years) and 6.66–6.69 t/ha (average for 3 years). For all combinations of applied fertilizers, the protein content increases from 9.3 to 10.9–11.3 %, and gluten – from 18.8 to 24.1–26.4 %. Under the influence of fertilizers, the grain belongs to the 3rd class in terms of gluten, while under the control it is of the 4th class. The increase in yield is due to improved nutritional regimes in the soil and an increase in their consumption by spring wheat, especially nitrogen and sulfur. Local application of the studied combinations of UAN-32, liquid fertilizers, ammonium sulfate and complex fertilizers in all years ensured an increase in the grain yield of spring soft wheat of the Buran variety by 25.9–34.2 % on average over 2 years and by 41.8–47.6 % on average over 3 years with a payback of 1 kg of a.v. fertile¬zers, respectively, 5.8–12 kg and 11.3–13.8 kg of grain.

Thermogravimetry as a research tool for the development of an ammonium sulphate roasting process for selective metal extraction from minerals

AbstractThe ammonium sulphate roasting process involves reacting mineral-bearing materials with ammonium sulphate via a solid–solid roasting process and subjecting the resulting roast residue to aqueous leaching. This process enables the simultaneous, non-selective co-extraction of strategic metals from the starting materials. However, effective separation of the extracted metals is often mandatory to produce quality products of high purity. In this study, the combined application of thermogravimetric analysis, X-ray powder diffraction and inductively coupled plasma optical emission spectrometry confirmed the non-selectivity of the process when applied to a South African diamond mine residue residue roasted with ammonium sulphate in a 1:2 mass ratio (m/m) at 450 °C for 2 h, with magnesium, iron and aluminium being co-extracted into water-soluble metal sulphates. Thermogravimetry was then applied to develop a multi-step, multi-temperature selective roasting process using mixtures of pure commercial metal sulphate salts. The first step of the modified process successfully separated iron and aluminium sulphates from magnesium-sulphates in the roast residues by thermally decomposing soluble iron and aluminium sulphates into insoluble oxides via calcination at 750 °C for 2 h. This temperature was lower than the one at which magnesium sulphates convert into magnesium oxide. In the second and final step, iron and aluminium were recovered from the oxide minerals via solid–solid re-roasting with ammonium sulphate at 450 °C for 1 h, causing the oxides to revert back to their water-soluble sulphate forms. The effectiveness of the modified process was subsequently verified using a diamond mine residue, showing that the soluble iron and aluminium contents in the magnesium-bearing leachate could be reduced by over 90%.

Sulfur availability minimizes nitrate leaching losses in vulnerable agricultural soils

Despite the critical need for nitrogen (N) in cropping systems, excessive N fertilizer application has severe environmental consequences. The synergistic interaction between sulfur (S) and N in plant nutrition could be exploited to increase N utilization, thereby maximizing N recovery and reducing losses. In a three-year study at six locations across three countries (USA, Ghana, and Mali), we evaluated the effect of S availability on N leaching losses from N fertilizer application using corn as the study crop. The study consisted of three S sources (micronized elemental sulfur [MES], untreated elemental sulfur [ES], and ammonium sulfate [AS]); five S application rates [(i) site-specific recommended S rate (SR), (ii) ¼ of the recommended S rate (25%_SR) (iii) ½ of the recommended S rate (50%_SR), (iv) ¾ of the recommended S rate (75%_SR); and (v) 1¼ of the recommended S rate (125%_SR)]; and a single N application rate (site-specific recommended N rate). Regardless of the S source, N recovery progressively increased with increasing S application rate. For the AS and MES sources, leachate nitrate concentration from the treatments with S application ≥ SR was statistically similar to that of the background concentrations, and the highest concentrations occurred with the treatment with no S application. Thus, for environmental stewardship, a critical look into S application in cropping systems is a necessity due to its synergistic interaction with N. In addition to improving productivity and enhancing efficient recovery of applied N fertilizers, S availability will minimize nitrate leaching commonly associated with application of N fertilizers.

Optimization of Ammonia Nitrogen Removal and Recovery from Raw Liquid Dairy Manure Using Vacuum Thermal Stripping and Acid Absorption Process: A Modeling Approach Using Response Surface Methodology

Dairy manure adds a substantial amount of nitrogen to wastewater due to its high levels of associated nutrients. Removal and recovery of ammonia nitrogen (NH3-N) from raw liquid dairy manure (RLDM) is greatly valued. This study was focused on the vacuum thermal stripping–acid absorption (VTS-AA) process for NH3-N from RLDM, followed by modeling and optimization. Using the response surface methodology (RSM)-based central composite design (CCD) approach, the critical operational parameters of the vacuum thermal stripping process, including temperature (50–70 °C), pH (9–11), vacuum pressure (35–55 kPa), and treatment time (60–90 min), were optimized. With the specified parameters set at temperature 69.9 °C, pH 10.5, vacuum pressure 53.5 kPa, and treatment time 64.2 min, the NH3-N removal efficiency attained was 98.58 ± 1.05%, aligning closely with the model prediction. Furthermore, the recovered ammonium sulfate ((NH4)2SO4) closely matched their commercial counterparts, confirming the effectiveness of the VTS-AA process in recovering NH3-N from RLDM. The distinct advantage of the employed technology lies in the concurrent energy demand reduction achieved by introducing a vacuum system. These findings contribute valuable insights into the practical implementation of the VTS-AA process for treating raw dairy manure, particularly in large-scale operational contexts.

Environmental transport of excess nitrogen fertilizer in peach orchard: Evidence arising from 15N tracing trial

In pursuit of high fruit yield, overwhelming amount of nitrogen (N) fertilizer was unreasonably applied in orchard, resulting in lower fertilizer N uptake and higher environmental loss. It is crucial to propose appropriate fertilization timing and optimal N management by clarifying fruit tree N uptake pattern in orchard systems. Here, a 15N isotope enrichment trial was conducted in peach orchard to assess the transport of applied synthesized fertilizer-N to the plant and environment in the Taihu Lake region. Ammonium sulfate ((NH4)2SO4, 10.12 atom % 15N), as the N source, was applied with four split applications at 382.5 kg N ha−1 during one plant growth cycle. Results showed N deriving from fertilizer (NDFF) accounted for 24.5% in leaves and 38.4% in fruits, respectively. During the annual growth cycle, the applied fertilizer-N uptake and utilization was higher in reproductive growth stage than vegetative growth stage. After harvest, 28.8% of applied fertilizer-N was absorbed by peach tree, 9.5% was lost to the environment through surface runoff, ammonia (NH3) volatilization and nitrous oxide (N2O) emission, 29.6% was retained in the 0–160 cm soil profile, the remaining 32.1% was unaccounted N including N leaching and N loss from the N removal progress. Generally, more applied fertilizer-N moved to the environment in high N input peach orchard. In order to promote optimal N management, the applied fertilizer-N rate should be reduced by 30% and emphasized on fertilization at the reproductive growth period according to tree N uptake pattern.

Modulating the Activity and SO2 Resistance of α-Fe2O3 Catalysts for NH3-SCR of NOx via Crystal Facet Engineering.

The development of Fe-based catalysts for the selective catalytic reduction of NOx by NH3 (NH3-SCR of NOx) has garnered significant attention due to their exceptional SO2 resistance. However, the influence of different sulfur-containing species (e.g., ferric sulfates and ammonium sulfates) on the NH3-SCR activity of Fe-based catalysts as well as its dependence on exposed crystal facets of Fe2O3 has not been revealed. This work disclosed that nanorod-like α-Fe2O3 (Fe2O3-NR) predominantly exposing (110) facet performed better than nanosheet-like α-Fe2O3 (Fe2O3-NS) predominantly exposing (001) facet in NH3-SCR reaction, due to the advantages of Fe2O3-NR in redox properties and surface acidity. Furthermore, the results of the SO2/H2O resistance test at a critical temperature of 250 °C, catalytic performance evaluations on Fe2O3-NR and Fe2O3-NS sulfated by SO2 + O2 or deposited with NH4HSO4 (ABS), and systematic characterization revealed that the reactivity of ammonium sulfates on Fe2O3 catalysts to NO(+O2) contributed to their improved catalytic performance, while ferric sulfates showed enhancing and inhibiting effects on NH3-SCR activity on Fe2O3-NR and Fe2O3-NS, respectively; despite this, Fe2O3-NR showed higher affinity for SO2 + O2. This work set a milestone in understanding the NH3-SCR reaction on Fe2O3 catalysts in the presence of SO2 from the aspect of crystal facet engineering.

Efficient Separation of Re (VII) and Mo (VI) by Extraction Using E-1006–Ammonium Sulfate Aqueous Two-Phase System

Aqueous two-phase extraction (APTE) stands out as an environmentally friendly technique for the separation of metal ions. The separation of Re (VII) and Mo (VI) in an aqueous solution was investigated using a novel aqueous two-phase system (ATPS) consisting of isodecanol polyoxyethylene ether (E-1006), ammonium sulfate, and water. A phase diagram of this system was developed, and the effects of pH, temperature, extraction time, the concentrations of E-1006 and (NH4)2SO4, and metal ions on the separation of Re (VII) and Mo (VI) were examined. The results show that at pH 7.0, Mo (VI) had almost transformed into the (NH4)2SO4-rich phase, while Re (VI) was extracted into the E-1006-rich phase. The increase in temperature induces a transition of Mo (VI) to the salt-rich phase, which is unfavorable for the extraction of Re (VII). The increase in the concentrations of E-1006 and (NH4)2SO4 has a positive effect on the separation of rhenium and molybdenum. Overall, the ATPS consisting of 200 g/L of E-1006, 200 g/L of (NH4)2SO4, and water yields an extraction efficiency of 97.2% for Re and a high separation factor of 2700 for Re (VII) and Mo (VI) from a mixture of 0.1 g/L of Re (VII) and 5 g/L of Mo (VI) at pH 7.0 and 323.15 K. Separation studies of the simulated leaching solution show that the extraction efficiency for Re (VI) is 99.1% and the separation factor of Re (VII) and Mo (VI) is 5100.

N-Alkyl-1,2,4-triazole–Borane Complexes as High-Density Hypergolic Materials

AbstractHydrazine and its derivatives have served as a conventional bipropellant fuel for several decades. However, their extremely acute toxicity and carcinogenicity, high volatility, and environmental impact have attracted significant attention. In order to synthesize green bipropellant fuels with high density, high specific impulse, and good thermal stability, three novel N-alkyl-1,2,4-triazole–borane complexes were successfully synthesized by reacting alkylated 1,2,4-triazole coordinated with sodium borohydride in the presence of ammonium sulfate. During the droplet test with white fuming nitric acid, there was a relatively short ignition delay time of 98 ms. Additionally, these hypergolic fuels possessed a high density exceeding 1.10 g cm–3, and the specific impulse is ranging from 187 to 199 s, and the highest decomposition temperature reaches 153.4 °C. These results demonstrate their great potential as hypergolic fuels or hypergolic ionic liquid additives in the field of hypergolic materials.

Evaporating crystallization effect of ammonium sulfate at atmospheric pressure under the action of ultrasound

Ultrasound enhanced evaporating crystallization has been proposed to solve the problems of low crystallization yield and uneven particle size in the evaporating crystallization process of ammonium sulfate solution at atmospheric pressure. The effects of key operating parameters, including the ultrasound power, stirring speed, pH value, and ultrasound time, on the yield of ammonium sulfate product and the duration of solid–liquid transformation time are studied. The results show that the ultrasound crystallization can increase the ammonium sulfate yield by 52.9 %, reduce the solid–liquid transformation time of ammonium sulfate by 10 %, and obtain ammonium sulfate products with higher crystallinity and more uniform particle size. Ultrasound promotes the crystallization of ammonium sulfate by enhancing the transfer of heat in the solution and reducing the supersolubility of the ammonium sulfate solution from 937.5 g/L to 833.33 g/L. This study provides experimental justification for the use of ultrasound in atmospheric evaporative crystallization.

Production of highly cytotoxic and low immunogenic L-asparaginase from Stenotrophomonas maltophilia EMCC2297

L-asparaginase is an important therapeutic enzyme that is frequently utilized in the chemotherapy regimens of adults as well as pediatric patients with acute lymphoblastic leukemia. However, a high rate of hypersensitivity with prolonged use has limited its utilization. Stenotrophomonas maltophilia (S. maltophilia) EMCC2297 isolate was reported as a novel and promising source for L- asparaginase. The present study aimed at the production, purification, and characterization of L- asparaginase from S. maltophilia EMCC2297 isolate. The microbial production of L-asparaginase by the test isolate could be increased by pre-exposure to chloramphenicol at 200 µg/ml concentration. S. maltophilia EMCC2297 L-asparaginase could be purified to homogeneity by ammonium sulphate precipitation and the purified form obtained by gel exclusion chromatography showed total activity of 96.4375 IU/ml and specific activity of 36.251 IU/mg protein. SDS-PAGE analysis revealed that the purified form of the enzyme is separated at an apparent molecular weight of 17 KDa. Michaelis-Menten constant analysis showed a Km value of 4.16 × 10− 2 M with L-asparagine as substrate and Vmax of 10.67 IU/ml. The antitumor activity of the purified enzyme was evaluated on different cell lines and revealed low IC50 of 2.2 IU/ml and 2.83 IU/ml for Hepatocellular cancer cell line (HepG-2), human leukemia cancer cell line (K-562), respectively whereas no cytotoxic effect could be detected on normal human lung fibroblast cells (MRC-5). However, mice treated with native L-asparaginase showed lower IgG titre compared to commercial L-asparaginase. This study highlights the promising characteristics of this enzyme making it a valuable candidate for further research and development to be an adduct in cancer chemotherapy.

Recovery of organic acids from lactic acid-enriched fermentation broth via salting-out assisted solvent extraction

The organic acids (OAs) market has been expanding due to their versatility and wide range of uses in several industrial applications, thus prompting a transition from chemical to biological approaches to generate such high-value products. Nevertheless, downstream processes to separate OAs from the fermentation broth represent, to date, the main cost in biological OAs manufacturing. With the goal of limiting this issue, the present study investigated OAs separation from a lactic acid (LA)-rich fermentation broth through physical, i.e., using ethyl acetate (EA), and physico-chemical, i.e., using tributyl phosphate (TBP), solvent extraction. In addition, the salting-out effect of different salts on OAs recovery was investigated. Among the investigated conditions, a combination of pure TBP and 40% ammonium sulfate ensured the highest LA extraction efficiency of 65%. Besides, mixing TBP with EA (50:50) enabled to maintain the same LA extraction efficiency while reducing the process costs, limiting the toxicity of the chemicals involved, and obtaining an extracted OAs mix with lower co-metabolites, i.e. volatile fatty acids, compared to using pure TBP. Overall, solvent extraction assisted by salting-out agents were shown to be a promising method to separate OAs from a fermentation broth in liquid form, especially for fermentation processes operated at low pH.

Removal of Co(II) and various metal ions from the residue of the zinc plant through solvent extraction using both acid and neutral extractants

AbstractThe recovery of cobalt from secondary sources is a crucial issue in technology development, particularly for its numerous applications in various industries. Solvent extraction has proven an effective method for metallic ions separation from secondary sources. The main goal of this work was to study the separation of metals by solvent extraction technique from zinc plant leach waste. Initially, several extractants, including Cyanex 272, Cyanex 301, LIX 5640 H, Alamine 336, and tri‐n‐octylamine (TOA), were tested to treat the leach solution. It was discovered that the saponified extractant di‐(2‐ethylhexyl) phosphoric acid (D2EHPA) (10%) + tri‐n‐butyl phosphate (TBP) (10%) effectively eliminated interfering elements such as manganese, zinc, and iron, with extraction efficiencies of 95%, 98%, and 99.9%, respectively. To increase the concentration of cobalt in the purified solution, the cobalt recovery step was performed using various acids on the loaded organic phase. The best outcome was achieved using ammonium sulphate salt (1 M), which recovered about 50% of the cobalt present in the organic phase. The recovered cobalt was then subjected to the electrowinning process to produce cobalt metal of high purity. A cathodic current density of 100 A/m2 was determined to be the optimal current for the electrolyte solution. Lastly, scanning electron microscope (SEM) and X‐ray fluorescence (XRF) analyses were carried out to examine the structure and purity of the resulting metallic cobalt, which was found to have a purity of 99.5%.

Characteristics of Fine Particulate Matter (PM2.5) Chemical Composition in the North Jakarta Industrial Area

Air pollution around industrial area has become a serious concern for both the public and local government. Thus, research on PM2.5 characterization is urgently needed. This study identifies the concentration and chemical characteristics of PM2.5 to provide an in-depth understanding of the composition of these particles around the largest industrial complex in North Jakarta. Sixty samples of PM2.5 were collected from residential sites around industrial areas in North Jakarta. Samples were collected on Teflon filters using a SuperSASS instrument during the period from February to July 2023, representing the wet and dry seasons. Mass concentrations of PM2.5, black carbon, and 19 chemical elements were determined. The average mass concentration of PM2.5 in the wet and dry seasons was 27.81±11.82 µg/m3 and 46.63±14.37 µg/m3, respectively. Although the concentration of PM2.5 was lower during the wet season, the concentrations of black carbon and certain elements did not decrease significantly. This shows that pollutants play an important role in both seasons in the study location. Sulfur is the most abundant element with the average concentration in the dry season (2,727.89 ng/m3) higher than in the wet season (1,983.18 ng/m3). The PM2.5 mass reconstruction results show that ammonium sulfate and black carbon have the largest portion of PM2.5 mass. The results are expected to be used as a scientific reference in studying air pollution problems in this region and assist in formulating air protection policies to reduce PM2.5 emissions.

ВЛИЯНИЕ СЕРНОГО БЕНТОНИТА НА РОСТ И ПРОДУКТИВНОСТЬ ПОДСОЛНЕЧНИКА

The research was carried out in order to study the effectiveness of the use of various new sulfur-containing fertilizers on sunflower crops in the soil and climatic conditions of the Republic of Tatarstan. Field experiments were conducted in 2023 on the basis of Agrobiotechnopark LLC (Narmonka village, Laishevsky Municipal District of the Republic of Tatarstan), laboratory analyses were carried out at the Center for Agroecological Research of the Kazan State Agrarian University. According to the research results, it was found that the introduction of 150 kg/ha of sulfur bentonite in the studied hybrids provides the growth capacity of cotyledonous leaflets by 26.3 and 29.4 %, respectively, compared with the control version of the experiment. When sulfur bentonite is applied at a dose of 150 kg/ha, the plant height of the studied Anthemis and Terramis hybrids increases by 4 and 7 cm (+3 and 5.6 %) compared with the control variant, and plant safety increases by 1.4 and 0.7 %, respectively. But the maximum values in terms of height and plant safety were obtained using the ammonium sulfate application option of 100 kg / ha, which is explained by the greater need for sunflower nitrogen than sulfur. The mass of productive seeds from one basket, depending on the hybrids studied and the fertilizers applied, ranged from 69 g in the control to 98 g in the last version of the experiment, which is 43% higher compared with the option without adding sulfur bentonite.

Ammonium Sulfate to Modulate Crystallization for High-Performance Rigid and Flexible Perovskite Solar Cells.

Perovskite solar cells (PSCs) are attracting widespread research and attention as highly promising candidates in the field of electronic photovoltaics owing to their exceptional power conversion efficiency (PCE). However, rigid or flexible PSCs still face challenges in preparing full-coverage and low-defect perovskite films, as well as achieving highly reproducible and highly stable devices. Herein, a multifunctional additive 2-aminoethyl hydrogen sulfate (AES) is designed to regulate the film crystallization and thereby form flat and pinhole-free perovskite films. It is found that the introduction of AES can effectively passivate defects, restrain charge carrier recombination, and then achieve a higher fill factor. As seen with grazing incidence wide-angle X-ray scattering (GIWAXS), this approach does not affect the crystal orientation distribution. It is observed that AES addition shows a universality across different perovskite components since the PCE is improved up to 20.7% for FA0.97MA0.03Pb(I0.97Br0.03)3-AES, 22.85% for Cs0.05FA0.95PbI3-AES, 22.23% for FAPbI2.7Br0.3-AES, and 23.32% for FAPI-AES rigid devices. Remarkably, the non-encapsulated flexible Cs0.05 (FA0.85MA0.15)0.95Pb(I0.85Br0.15)3 device with AES additive delivers a PCE of 20.1% and maintains over 97% of its initial efficiency under ambient conditions (25±5% relative humidity) over 2280h of aging.

A novel indirect ELISA for serodiagnosis of mucormycosis using antigens from Rhizopus arrhizus.

Due to a delay in diagnosis by conventional techniques and high mortality, the development of a standardised and rapid non-culture-based technique is an unmet need in pulmonary, gastrointestinal, and disseminated forms of mucormycosis. Though limited studies have been conducted for molecular diagnosis, there are no established serologic tests for this highly fatal infection. To develop and evaluate an indirect in-house enzyme-linked immunosorbent assay (ELISA) utilising antigens of Rhizopus arrhizus for detecting anti-Rhizopus antibodies (IgG and IgM) in sera of patients with mucormycosis. We extracted both secretory and mycelial Rhizopus antigens using standardised protocols. Bradford assay was used for protein quantification. We then standardised an indirect ELISA using R. arrhizus mycelial and secretory antigens (10.0 μg/mL in bicarbonate buffer pH 9.2) for detecting anti-Rhizopus IgG and IgM antibodies in patient sera. We included patients with mucormycosis, other fungal infections, and healthy controls. Antibody index value (E-value) was calculated for each patient sample. Asparagine broth culture filtrate utilising 85% ammonium sulphate salt fractionation and mycelial homogenate grown in yeast extract peptone dextrose (YPD) broth precipitated with trichloroacetic acid (TCA) yielded a large amount of good-quality protein for the assay. We included 55 patients with mucormycosis (rhino-orbito-cerebral mucormycosis [ROCM, n = 39], pulmonary [n = 15], gastrointestinal [n = 1]), 24 with other fungal infections (probable aspergillosis [n = 14], candidiasis [n = 10]), and healthy controls (n = 16). The sensitivity of the antibody test for diagnosing mucormycosis ranged from 83.6-92.7% for IgG and 72.7-87.3% for IgM, with a specificity of 91.7-92.5% for IgG and 80-82.5% for IgM. The sera from patients with other fungal infections and healthy individuals did not show significant cross-reactivity. The detection of anti-Rhizopus IgG antibody performed significantly better in comparison to IgM-based ELISA for diagnosing both ROCM (sensitivity of 84.6% vs. 69.2%) and pulmonary cases (86.6% vs. 80.0%). More extensive studies are required to confirm our findings.

Extraction of Protein and Bioactive Compounds from Mediterranean Red Algae (Sphaerococcus coronopifolius and Gelidium spinosum) Using Various Innovative Pretreatment Strategies.

In this study, the release of proteins and other biomolecules into an aqueous media from two red macroalgae (Sphaerococcus coronopifolius and Gelidium spinosum) was studied using eight different cell disruption techniques. The contents of carbohydrates, pigments, and phenolic compounds coextracted with proteins were quantified. In addition, morphological changes at the cellular level in response to the different pretreatment methods were observed by an optical microscope. Finally, the antioxidant capacity of obtained protein extracts was evaluated using three in vitro tests. For both S. coronopifolius and G. spinosum, ultrasonication for 60 min proved to be the most effective technique for protein extraction, yielding values of 3.46 ± 0.06 mg/g DW and 9.73 ± 0.41 mg/g DW, respectively. Furthermore, the highest total contents of phenolic compounds, flavonoids, and carbohydrates were also recorded with the same method. However, the highest pigment contents were found with ultrasonication for 15 min. Interestingly, relatively high antioxidant activities like radical scavenging activity (31.57-65.16%), reducing power (0.51-1.70, OD at 700 nm), and ferrous iron-chelating activity (28.76-61.37%) were exerted by the different protein extracts whatever the pretreatment method applied. This antioxidant potency could be attributed to the presence of polyphenolic compounds, pigments, and/or other bioactive substances in these extracts. Among all the used techniques, ultrasonication pretreatment for 60 min appears to be the most efficient method in terms of destroying the macroalgae cell wall and extracting the molecules of interest, especially proteins. The protein fractions derived from the two red macroalgae under these conditions were precipitated with ammonium sulfate, lyophilized, and their molecular weight distribution was determined using SDS-PAGE. Our results showed that the major protein bands were observed between 25 kDa and 60 kDa for S. coronopifolius and ranged from 20 kDa to 150 kDa for G. spinosum. These findings indicated that ultrasonication for 60 min could be sufficient to disrupt the algae cells for obtaining protein-rich extracts with promising biological properties, especially antioxidant activity.