Precipitation pH Research Articles

Recovery and Size-Tuning of Amorphous Silica from Geothermal Scales in Batangas, Philippines

Scale deposits in geothermal power plants are well-known potential sources of minerals. Extensive research in mineral recovery is crucial due to the considerable variability in scale composition and geochemistry based on location. Geothermal scales from Batangas, Philippines, were used to synthesize size-modified amorphous silica (SiO2) via sol-gel method. Initial analyses employing x-ray fluorescence spectroscopy (XRF), total dissolved solids (TDS), electrical conductivity (EC), and pH measurements confirmed that the scale is rich in silica and salts at neutral pH. Then, the effect of varying scale concentration, precipitation pH, and aging time on the particle size distribution of recovered amorphous silica were investigated. Dynamic light scattering (DLS) for particle size analysis (PSA) revealed that the sample with 2.5% (w/v) scale precursor in NaOH and precipitated until pH 10 had the lowest average cumulant diameter (1.66 μm). Moreover, the synergy of precipitation pH and aging time was found to significantly affect the polydispersity index and cumulative diameter of precipitated SiO2 based on 23 factorial ANOVA at 0.05 significance level. X-ray diffractometry (XRD), Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) confirmed that the precipitates were amorphous SiO2 with spherical morphology. This study proves the viability of utilizing geothermal scales from Batangas, Philippines for the synthesis of amorphous SiO2 with controlled particle size, which is a potential filler for composite materials.

An improved representation of aerosol in the ECMWF IFS-COMPO 49R1 through the integration of EQSAM4Climv12 – a first attempt at simulating aerosol acidity

Abstract. The atmospheric composition forecasting system used to produce the Copernicus Atmosphere Monitoring Service (CAMS) forecasts of global aerosol and trace gas distributions, the Integrated Forecasting System (IFS-COMPO), undergoes periodic upgrades. In this study we describe the development of the future operational cycle 49R1 and focus on the implementation of the thermodynamical model EQSAM4Clim version 12, which represents gas–aerosol partitioning processes for the nitric acid–nitrate and ammonia–ammonium couples and computes diagnostic aerosol, cloud, and precipitation pH values at the global scale. This information on aerosol acidity influences the simulated tropospheric chemistry processes associated with aqueous-phase chemistry and wet deposition. The other updates of cycle 49R1 concern wet deposition, sea-salt aerosol emissions, dust optics, and size distribution used for the calculation of sulfate aerosol optics. The implementation of EQSAM4Clim significantly improves the partitioning of reactive nitrogen compounds, decreasing surface concentrations of both nitrate and ammonium in the particulate phase, which reduces PM2.5 biases for Europe, the US, and China, especially during summertime. For aerosol optical depth there is generally a decrease in the simulated wintertime biases and for some regions an increase in the summertime bias. Improvements in the simulated Ångström exponent are noted for almost all regions, resulting in generally good agreement with observations. The diagnostic aerosol and precipitation pH calculated by EQSAM4Clim have been compared to ground observations and published simulation results. For precipitation pH, the annual mean values show relatively good agreement with the regional observational datasets, while for aerosol pH the simulated values over continents are quite close to those simulated by ISORROPIA II. The use of aerosol acidity has a relatively smaller impact on the aqueous-phase production of sulfate compared to the changes in gas-to-particle partitioning induced by the use of EQSAM4Clim.

Optimization of struvite from sewage sludge ash as phosphorus source.

Phosphorus is an essential macronutrient for crop production. Struvite precipitation and reuse from phosphorus-rich sewage sludge are cost-effective measures to improve phosphorus utilization efficiency and decrease its negative environmental impact. In this study, the objectives were to optimize the phosphorus extraction (using sulfuric acid) and recovery (as struvite) processes and determine the most appropriate process conditions using RSM. This was done by evaluating the effect of different parameters such as acid concentration (mol/l) (0.02 to 0.8), H2SO4/ISSA ratio (liquid/solid) (20 to 150ml/g), and time (0.5 to 4h) for leaching tests and N: P ratio (1 to 2), Mg: P ratio (1 to 2), and pH (8 to 11) for struvite precipitation. The optimization of the factors affecting PO43--P extraction from SSA by acidic leaching showed that applying 0.5mol/l H2SO4 and 57ml/g L/S ratio at 2h achieved the highest PO43--P extraction (99.8%). The extraction of phosphorus also leached heavy metals; however, using a cation exchange resin, it was possible to effectively remove heavy metals from P-rich solutions. The optimal phosphorus recovery as struvite (98.5%) was achieved at the lowest pH and N/P ratio, while an increase in Mg/P ratio from 1 to 2 positively affected phosphorus recovery. The obtained struvite had a high content 94.6%, and the heavy metal content in struvite was lower than the value of standard, so that the obtained struvite sample can be used as fertilizer.

Mechanistic insights into the foaming properties of potato proteins based on protein composition, colloidal state, and air-water interfacial properties

Potato proteins have been shown to be suitable alternatives for animal proteins in food foam formulations but their ability to form and stabilize foam is mechanistically ill-understood. The present study aimed to better understand the foaming properties of a protein fraction isolated from potato trimmings, a by-product from the potato industry. This was achieved by comparing the properties of these in-house isolated proteins to those of commercial and highly purified potato proteins. Protein isolates (53.8 ± 4.7 g/100 g dry weight) were produced from trimmings by alkaline solubilization (pH 9.0) and isoelectric precipitation (pH 4.0). The foaming properties of the in-house isolate at pH 3.0 and 7.0 were better than those of a blend of commercial potato proteins with similar relative amounts of patatin and protease inhibitors as the in-house isolate. Notably, this was the case despite the fact that more proteins were insoluble in the in-house isolate than in the commercial potato protein suspensions. Patatin and protease inhibitors were further shown to both contribute considerably to the formation and stabilization of foams. Interestingly, a beneficial effect on foam stability was found when patatin and protease inhibitors of various colloidal sizes were present. Additionally, impurities in the in-house isolates likely contributed to their superior foaming properties. In conclusion, a protein-rich fraction with good foaming properties can be recovered from potato trimmings. Mechanistic insights were gained into the foaming properties of potato protein (mixtures). This research also highlighted the importance of assessing protein colloidal state when investigating plant protein structure-function relationships.

Magnesium recovery from brackish water desalination brine and valorization in fertilizer production

The generated brine from the desalination unit hurts the environment. In this work, we try to valorize the nanofiltration and reverse osmosis brine generated from a hybrid desalination unit of treated wastewater located in Tunisia by magnesium recovery and reuse it as a cheap resource for fertilizer production. The brine was first purified by calcium removal. The pH of calcite precipitation was 11.32 and 9.78 using brine NF and brine RO respectively. After that, the filtrate was used to produce brucite. The pH of brucite precipitation was 11.3 and 9.74 for NF and RO brine respectively. 55 % of magnesium was recovered from NF brine and 65.5 % from RO respectively. To obtain a 100 % recovery rate of magnesium for brucite precipitation, the optimal molar alkaline reagent/Mg ratio was 5.5 and the pH was 11.9. The brucite was dissolved in sulfuric acid, then the Epsomite fertilizer was extracted with pure ethanol. The highest weight of epsomite was obtained for a volume ratio of acid/ ethanol of 0.8:3.5. The second fertilizer produced using brine magnesium was struvite. It was obtained for pH 9 and 11 using H2NH4PO4 acid and wastewater as a source of ammonia and phosphate respectively. 90 % and 50 % of magnesium recovery were obtained for the first and the second cases respectively. The infrared spectrum and X-ray diffractogram confirmed the brucite, epsomite, and struvite production using brine magnesium.

Effect of reagent addition and aging by microwave on the structure of layered double hydroxides

A series of MgAl-layered double hydroxides (MgAl-LDHs) were prepared by variable pH precipitation. The addition of the metal (M) containing solution to the base (B=NaOH) solution, either rapidly (r) or dropwise (d), led to the obtention of the MBr and MBd samples, respectively. In the other hand, by inverting the order of the added solution (pH increase methodology), BMr and BMd were obtained. The BMd sample was microwave aged at 80 °C, 150 °C and 220 °C for 45 min. The results of powder X-ray diffraction showed that rapid precipitation produces more crystalline LDHs than those obtained by dripping. The crystallinity of BMd was improved by microwave aging. All precipitation conditions produced nanoparticles with an average size of around 27.5 nm, which increased almost 5-fold with the microwave treatment. Precipitation by increasing pH gave LDHs with low pore volume, which increased during the heat treatment. Nevertheless, the specific surface area decreased significantly with aging temperature due to the increase in particle size.

A computationally efficient parameterization of aerosol, cloud and precipitation pH for application at global and regional scale (EQSAM4Clim-v12)

A computationally efficient parameterization of aerosol, cloud and precipitation pH for application at global and regional scale (EQSAM4Clim-v12)

Evaluation of the functional properties of a protein isolate from Arthrospira maxima and its application in a meat sausage

Arthrospira maxima is a microalga that has been collected in Lake Texcoco in the Valley of Mexico since pre-Hispanic times and has been a traditional food source due to its high biomass production and protein content (50–60 %), making it promising for protein extraction. In this context, a protein isolate was obtained from powdered biomass of Arthrospira maxima (PbAm) by alkaline solubilization (pH 11) and isoelectric precipitation (pH 4.2). Arthrospira maxima protein isolate (AmPI) presented higher protein content (82.58 %) and total amino acids compared to PbAm. Functional properties of AmPI were evaluated in comparison with PbAm and soy protein isolate (SPI). Protein extraction resulted in a significant increase in protein solubility (PS) and foaming capacity (FC) of up to 87.78 % and 238.10 %, respectively. Emulsifying capacity (EC) of AmPI was superior to that of PbAm and SPI in pH range 5–7. Inclusion of AmPI as a partial substitute for SPI in the formulation of meat sausages was evaluated by implementing four treatments: T1 (15 % AmPI, 85 % SPI), T2 (10 % AmPI, 90 % SPI), T3 (5 % AmPI, 95 % SPI) and T4 (0 % AmPI, 100 % SPI). Although the texture attributes remained unchanged, a significant reduction in color parameters was observed as the concentration of AmPI increased. An inclusion of 15 % AmPI significantly enhanced the nutritional quality of meat sausages. Results highlight the excellent properties of AmPI, confirming Arthrospira maxima as a promising protein source in the food industry.

A comprehensive comparative study of ultrasound-alkaline and thermal-alkaline hydrolysis of duck feather

Feathers, as a byproduct of the poultry industry, present a significant source of keratinous waste. Conventional methods have been widely used to extract keratin from feathers; however, they are associated with limitations such as high operational costs and environmental concerns. It is, therefore, crucial to develop cost-effective and time-efficient methods for extracting keratin on a large scale. In recent years, ultrasound-assisted alkaline hydrolysis has emerged as a promising and sustainable approach for efficient keratin recovery. This study compares the hydrolysis time, yield, and chemical properties of keratin extracted from feathers using ultrasound-assisted alkaline hydrolysis and thermal alkaline hydrolysis (hot plate method). The influence of factors such as particle size, alkali concentration, liquid-to-solid ratio, reactor geometry, temperature of keratin colloid upon precipitation, precipitation pH, and precipitating acid was investigated. Favorable conditions for ultrasound-assisted alkaline hydrolysis were found to be 3% NaOH, a 10:100 (w/v) solid-to-liquid ratio, using a cylindrical vessel, and an ultrasonic energy density of 360 kJ/L, with pH adjustment to 4.5 using citric acid after cooling to room temperature. This method outperformed the thermal approach, yielding 70% keratin in 25 min, compared to 23% in 90 min using a hot plate, due to the exothermic effect of cavitation. The results provide valuable insights into the potential of ultrasound-assisted alkaline hydrolysis as an eco-friendly and cost-effective approach to address the management of keratinous waste and enhance the overall recovery of keratin.

Physicochemical and functional characteristics of a gourd (Cucurbita argyrosperma Huber) seed protein isolate subjected to high-intensity ultrasound

The impact of high-intensity ultrasound (HIU, 20 kHz) on the physicochemical and functional characteristics of gourd seed protein isolate (GoSPI) was studied. GoSPI was prepared from oil-free gourd seed flour through alkaline extraction (pH 11) and subsequent isoelectric precipitation (pH 4). The crude protein concentration of GoSPI ranged from 91.56 ± 0.17 % to 95.43 ± 0.18 %. Aqueous suspensions of GoSPI (1:3.5 w/v) were ultrasonicated at powers of 200, 400, and 600 W for 15 and 30 min. Glutelins (76.18 ± 0.15 %) were the major protein fraction in GoSPI. HIU decreased the moisture, ash, ether extract, and nitrogen-free extract contents and the hue angle, available water and a* and b* color parameters of the GoSPI in some treatments. The L* color parameter increased (7.70 %) after ultrasonication. HIU reduced the bulk density (52.63 %) and particle diameter (39.45 %), as confirmed by scanning electron microscopy, indicating that ultrasonication dissociated macromolecular aggregates in GoSPI. These structural changes enhanced the oil retention capacity and foam stability by up to 62.60 and 6.84 %, respectively, while the increases in the solvability, water retention capacity, and emulsifying activity index of GoSPI were 90.10, 19.80, and 43.34 %, respectively. The gelation, foaming capacity, and stability index of the emulsion showed no improvement due to HIU. HIU altered the secondary structure of GoSPI by decreasing the content of α-helices (49.66 %) and increasing the content of β-sheets (52.00 %) and β-turns (65.00 %). The electrophoretic profile of the GoSPI was not changed by HIU. The ultrasonicated GoSPI had greater functional attributes than those of the control GoSPI and could therefore be used as a functional food component.

The effect of ultrasound on the extraction and foaming properties of proteins from potato trimmings

High-intensity ultrasonication is an emerging technology for plant protein isolation and modification. In this study, the potential of temperature-controlled ultrasonication to enhance the recovery of functional proteins from potato trimmings was assessed. Different ultrasound energy levels [2000–40,000 J/g fresh weight (FW)] were applied during protein extraction at pH 9.0. True protein yields after ultrasonication significantly increased (up to 91%) compared to conventional extraction (33%). Microstructural analysis of the extraction residues showed more disrupted cells as ultrasonication time increased. Ultrasound treatments (10,000 and 20,000 J/g FW) increased the protein yield without affecting the foaming and air-water interfacial properties of protein isolates obtained after isoelectric precipitation (pH 4.0). However, proteins obtained after extended ultrasonication (40,000 J/g FW) had significantly slower early-stage adsorption kinetics. This was attributed to ultrasound-induced aggregation of the protease inhibitor fraction. In conclusion, ultrasonication shows potential to help overcome some challenges associated with plant protein extraction.

The Influence of Substrate and Strain on Protein Quality of Pleurotus ostreatus

Background: The effect of substrate and strain on the nutritional and functional properties of mushroom flours and protein concentrates (PCs) has not thoroughly been investigated. Methods: The proteins of P. ostreatus flours (strains AMRL144 and 150) were isolated following alkaline extraction (pH 12) and isoelectric precipitation (pH 4) as it was determined by the solubility curves. The protein quality of the flours and PCs were evaluated by determining the protein solubility index (PSI) and their functional properties, such as water (WAC) and oil absorption capacity (OAC), foam capacity (FC), foam stability (FS) and emulsion stability (ES). The amino acid (AA) composition of the flours was determined by reversed-phase liquid chromatography after protein hydrolysis and o-phthalaldehyde derivatization. Results: The PSIs of the flours and PCs of P. ostreatus were comparable to those of soy protein flours and protein concentrates. The highest AA concentration was found for both strains when cultivated on the barley and oat straw (BOS) substrate, showing a similar trend as the protein content. A principal component analysis (PCA) indicated an impact of the strain on the functional properties. Conclusions: Both strains can produce high quality proteins especially when cultivated on wheat straw (WS). The FS was positively correlated with the P. ostreatus strain AMRL150 whereas the FC was positively correlated with AMRL144.

Ion Exchange Processes for CO2 Mineralization Using Industrial Waste Streams: Pilot Plant Demonstration and Life Cycle Assessment

AbstractAn attractive technique for removing CO2 from the environment is sequestration within stable carbonate solids (e. g., calcite). However, continuous addition of alkalinity is required to achieve favorable conditions for carbonate precipitation (pH>8) from aqueous streams containing dissolved CO2 (pH<4.5) and Ca2+ ions. In this study, a pH‐swing process using ion exchange was demonstrated to process 300 L of produced water brine per day for CO2 mineralization. Proton titration capacities were quantified for aqueous streams in equilibrium with gas streams at various concentrations of CO2 (pCO2=0.03–0.20 atm) and at various flow rates (0.5–2.0 L min−1). Energy intensities for the process were determined to be between 30 and 65 kWh per tonne of CO2 sequestered depending on the composition of the brine stream. A life cycle assessment was performed to analyze the net carbon emissions of the technology which indicated a net CO2 reduction for pCO2≥0.12 atm (−0.06–−0.39 kg CO2e per kg precipitated CaCO3) utilizing calcium‐rich brines. The results from this study indicate the ion exchange process can be used as a scalable method to provide alkalinity necessary for the capture and storage of CO2 in Ca‐rich waste streams.

Selective removal of Fe(Ⅲ) from HNO3 leach liquor of saprolitic laterite ore: Precipitation efficiency, hydrolysis mechanism, and removal strategy

HNO3 leach liquor of saprolitic laterite ore contains Fe3+, Al3+, Sc3+, Ni2+, Co2+, Mg2+, etc. Efficient removal of Fe3+ while reducing the loss of valuable metals is the key to solution purification. In this paper, a detailed study was carried out on the removal of Fe3+ by hydrolysis precipitation. First, thermodynamic calculations were conducted to analyze the precipitation pH changes and possible hydrolysis products at different temperatures. Subsequently, the experimental results show that more than 99 % Fe can be removed via low-temperature hydrolysis at 25–80 ℃ and pH = 3.0–3.5, but over 40 % Al and 30 % Sc also precipitate together, causing valuable metals losses. Differently, under high-temperature conditions (180 ℃, pH = 1.0, 0.5 h), 99.49 % of Fe can be selectively removed as Fe2O3 product, while other valuable metals hardly precipitate. It was found that the low-temperature Fe removal residue exhibits irregular agglomeration and uneven particle size, and contains 9.48 % NO3– and 25.86 % Fe. The high-temperature Fe removal residue presents a nanoscale spherical shape with uniform particle size and only contains 0.087 % NO3–, and the Fe content is up to 69.07 %. Finally, the Fe3+ hydrolysis mechanism was analyzed and an efficient Fe removal process from the HNO3 system including pH adjustment of leach liquor, selective Fe removal at high temperature, flash evaporation to recover free HNO3, and solid–liquid separation to obtain Fe2O3 products was proposed.

Isolation and Characterization of Indigenous Ureolytic Bacteria from Mindanao, Philippines: Prospects for Microbially Induced Carbonate Precipitation (MICP)

Microbially induced carbonate precipitation (MICP), a widespread phenomenon in nature, is gaining attention as a low-carbon alternative to ordinary Portland cement (OPC) in geotechnical engineering and the construction industry for sustainable development. In the Philippines, however, very few works have been conducted to isolate and identify indigenous, urease-producing (ureolytic) bacteria suitable for MICP. In this study, we isolated seven, ureolytic and potentially useful bacteria for MICP from marine sediments in Iligan City. DNA barcoding using 16s rDNA identified six of them as Pseudomonas stutzeri, Pseudomonas pseudoalcaligenes, Bacillus paralicheniformis, Bacillus altitudinis, Bacillus aryabhattai, and Stutzerimonas stutzeri but the seventh was not identified since it was a bacterial consortium. Bio-cementation assay experiments showed negligible precipitation in the control (without bacteria) at pH 7, 8, and 9. However, precipitates were formed in all seven bacterial isolates, especially between pH 7 and 8 (0.7–4 g). Among the six identified bacterial species, more extensive precipitation (2.3–4 g) and higher final pH were observed in S. stutzeri, and B. aryabhattai, which indicate better urease production and decomposition, higher CO2 generation, and more favorable CaCO3 formation. Characterization of the precipitates by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS) and attenuated total reflectance Fourier transform spectroscopy (ATR-FTIR) confirmed the formation of three carbonate minerals: calcite, aragonite, and vaterite. Based on these results, all six identified indigenous, ureolytic bacterial species from Iligan City are suitable for MICP provided that the pH is controlled between 7 and 8. To the best of our knowledge, this is the first report of the urease-producing ability and potential for MICP of P. stutzeri, P. pseudoalcaligenes, S. stutzeri, and B. aryabhattai.

Varying precipitation conditions allow directing the composition and physical properties of soy protein concentrates.

Soy protein concentrates (SPCs) are common food ingredients. They typically contain 65% (w/w) protein and ∼30% (w/w) carbohydrate. SPCs can be obtained with various protein precipitation conditions. A systematic study of the impact of these different protein precipitation protocols on the SPC protein composition and physical properties is still lacking. Here, SPCs were prepared via three different protocols, that is, isoelectric (pH 3.5-5.5), aqueous ethanol (50%-70% [v/v]), and Ca2+ ion (5-50mM) based precipitations, and analyzed for (protein) composition, protein thermal properties, dispersibility, and water-holding capacity. SPCs precipitated at pH 5.5 or by adding 15mM Ca2+ ions had a lower 7S/11S globulin ratio (∼0.40) than that (∼0.50) of all other SPC samples. Protein in SPCs obtained by isoelectric precipitation denatured at a significantly higher temperature than those in ethanol- or Ca2+ -precipitated SPCs. Precipitation with 50%-60% (v/v) ethanol resulted in pronounced denaturation of 2S albumin and 7S globulin fractions in SPCs. Additionally, increasing the precipitation pH from 3.5 to 5.5 and increasing the Ca2+ ion concentration from 15 to 50mM caused a strong decrease of both the dispersibility of the protein in SPC and its water-holding capacity at pH 7.0. In conclusion, this study demonstrates that the SPC production process can be directed to obtain ingredients with versatile protein physicochemical properties toward potential food applications. PRACTICAL APPLICATION: This study demonstrates that applying different protein precipitation protocols allows obtaining SPCs that vary widely in (protein) composition and physical properties (such as protein dispersibility and water-holding capacity). These varying traits can greatly influence the suitability of SPCs as functional ingredients for specific applications, such as the production of food foams, emulsions, gels, and plant-based meat alternatives. The generated knowledge may allow targeted production of SPCs for specific applications.

Predicting Cyanide Degradability and Destruction Using Artificial Neural Networks: A Case Study in West Azerbaijan, Iran”

ABSTRACT The presence of cyanide compounds in soil can lead to the formation and evaporation of hydrogen cyanide (HCN), while some of these compounds can undergo conversion by microorganisms present in the soil. However, high concentrations of cyanide can be toxic to soil microorganisms. During the gold extraction of mines, sodium cyanide (NaCN) solution is commonly used which results in a significant amount of cyanide waste that is regarded as an environmental pollutant. Previous studies have proposed physical, chemical, and biological methods to eliminate cyanide, but they have not achieved optimal efficiency. Unfortunately, the potential of artificial intelligence (AI) in this domain has been overlooked. Artificial Neural Network (ANN) models, specifically the multilayer perceptron (MLP) and simple linear regression, can significantly enhance and expedite the cyanide remediation process due to their remarkable predictive capabilities. In this study, an MLP and simple linear regression were employed to predict the biodegradation procedures of cyanide in soil. The study focused on cyanide waste generated by gold extraction factories and utilized environmental factors such as initial waste cyanide concentration, pH, soil and environmental temperature, humidity, chloride concentration, alkaline, electrical conductivity, precipitation, evaporation intensity, cyanide concentration, and initial pH as input data for the artificial neural network. The results of the MLP model revealed that electrical conductivity is the most influential factor in predicting the cyanide rate and initial pH of the waste soil. Conversely, the results of the simple linear regression indicated that the variables with the greatest impact on cyanide concentration are electrical conductivity (0.881), time (0.862), and alkalinity (0.724). By leveraging AI techniques such as ANN, this study demonstrates the potential for improved cyanide remediation. The integration of environmental factors and predictive models can contribute to more effective strategies for addressing cyanide pollution in soil.

A probe into the acid deposition mitigation path in China over the last four decades and beyond.

China currently has the highest acid deposition globally, yet research on its status, impacts, causes and controls is lacking. Here, we compiled data and calculated critical loads regarding acid deposition. The results showed that the abatement measures in China have achieved a sharp decline in the emissions of acidifying pollutants and a continuous recovery of precipitation pH, despite the drastic growth in the economy and energy consumption. However, the risk of ecological acidification and eutrophication showed no significant decrease. With similar emission reductions, the decline in areas at risk of acidification in China (7.0%) lags behind those in Europe (20%) or the USA (15%). This was because, unlike Europe and the USA, China's abatement strategies primarily target air quality improvement rather than mitigating ecological impacts. Given that the area with the risk of eutrophication induced by nitrogen deposition remained at 13% of the country even under the scenario of achieving the dual targets of air quality and carbon dioxide mitigation in 2035, we explored an enhanced ammonia abatement pathway. With a further 27% reduction in ammonia by 2035, China could largely eliminate the impacts of acid deposition. This research serves as a valuable reference for China's future acid deposition control and for other nations facing similar challenges.

Physiochemical and functional properties of Moringa oleifera protein obtained by isoelectric precipitation

The work investigated the effect of extraction pH (10 or 11) and precipitation pH (4 or 4.5) on the physicochemical and functional properties of Moringa oleifera protein. The physicochemical characteristics of Moringa leaf powder were analyzed using proximate quantification based on AOAC standard methods. The thermal, spectral, x-ray diffraction data were collected using the differential scanning calorimetric, Fourier transform infrared spectroscopy (FTIR), and wide-angle x-ray diffraction. The extraction at pH 10 and the precipitation process at pH 4.5 generated the highest protein content of 58.88%. Some of the functional properties of this pH combination were emulsion activity at 29.67%, emulsion stability at 50.45%, protein solubility at 32.36%, and water absorption capacity of 4.78 mL water/g. The thermal properties suggested the denaturation temperature of Moringa protein powder at 75°C, which was comparable to that previously reported plantbased protein isolate. FTIR and x-ray spectra argued the domination of amorphous protein fraction with a trace of lipid and carbohydrate. With these characteristics, protein has great potential to be used for food and drug applications.

Reducing rare earth loss by adding acetic acid in the aluminum removal process of rare earth leaching solution

The ionic-type rare earth ore, abundant in medium and heavy rare earth elements, is a strategic mineral resource. The removal of aluminum from ionic rare earth leaching solution results in over 8% loss of rare earths. Preliminary research has found that adding acetic acid (HAc) during aluminum removal process can effectively reduce the loss of rare earth elements. In this paper, through the calculation of the species distribution in the La2(SO4)3-Al2(SO4)3-HAc-H2O system, it is found that HAc forms an AlOH-Ac+ complex with aluminum ions, with a proportion of up to 70%, which will increase the initial precipitation pH of aluminum hydroxide. Furthermore, HAc and lanthanum form a LaAc2+ complex, and the proportion can reach more than 20%. Moreover, the zeta potential, FT-IR, and XPS tests of aluminum hydroxide, obtained by neutralization precipitation, revealed that the complexation of HAc and aluminum can reduce the precipitation rate of aluminum hydroxide, so that its particle size increases, the specific surface area decreases, and the van der Waals force adsorption sites are reduced. HAc can be chemically adsorbed on aluminum hydroxide, thereby increasing the zeta potential of aluminum hydroxide and ultimately reducing its electrostatic adsorption effect on rare earths. Additionally, the complexation of HAc and rare earth elements can reduce the local supersaturation of rare earth hydroxides and decline the coprecipitation of rare earth elements. Finally, under a precipitation endpoint pH of 5.2, HAc concentration of 0.006 mol/L, aluminum concentration of 0.2 g/L, rare earth concentration of 0.8 g/L, magnesium ion concentration of 0.5 g/L and magnesium oxide slurry concentration of 0.45 mol/L, the aluminum removal efficiency obtained with rare earth leaching solution reached 98.47%, and the rare earth loss efficiency was 2.62%. Compared with the control, the rare earth loss efficiency was reduced by 5.59%. This paper provides guidance for the efficient and green development of ionic-type rare earth ore.