Addition Of Acetate Research Articles

Study on the Thermal Safety of 3,7‐Dinitro‐1,3,5,7‐Tetraazabicyclo[3.3.1]nonane Synthesized by Nitrolysis of Hexamine

AbstractThe thermal flow curves of the nitrolysis for the synthesis of 3,7‐dinitro‐1,3,5,7‐tetraazabicyclo[3.3.1]nonane (DPT) from hexamine in the presence of different amounts of acetic anhydride were obtained using reaction calorimetry. The maximum heat release rates during the feeding process, the corresponding maximum adiabatic temperature rises, and the Maximum Temperature of the Synthesis Reaction (MTSR) were determined, respectively. The thermal stability of the reaction product DPT and the reaction mixture was analyzed, and data on their thermal decomposition characteristics were obtained. The thermal decomposition kinetic model was utilized to simulate the stability under adiabatic conditions. TD24 (The temperature corresponding to the time required to reach the maximum reaction rate under adiabatic conditions for 24 hours) of the reaction mixture was calculated as 69.65°C. According to the thermal hazard parameters of the reaction, the process's hazard level under various acetic anhydride addition conditions was determined to be level 5 using the cooling failure scenario method.

Insight into the impact of air flow rate on algal-bacterial granules: Reactor performance, hydrodynamics by Computational Fluid Dynamics (CFD) and microbial community analysis

This study evaluated the impact of air flow rates on nitrogen removal and the formation of algal-bacterial granules in domestic wastewater treatment, revealing that sodium acetate addition and aeration shifted the microbial community composition. Two separate feedings and the addition of external organic carbon significantly enhanced inorganic nitrogen removal efficiency (over 90 %), which might have contributed to the increased microbial diversity and the relative abundance of denitrifiers such as Acinetobacter. This study also demonstrates that the higher air flow rate (0.5 LPM) resulted in higher nitrification rates (up to 6.4 mg N/L/h) and produced smaller and denser granules. The higher air flow rate also led to the increasing relative abundances of nitrogen-related genera (such as Nitrospira) and the decreasing relative abundances of cyanobacteria and Chlorella. Computational Fluid Dynamics (CFD) simulations revealed that mechanical mixing predominantly generated shear force. Increasing the air flow rate from 0.2 LPM to 0.5 LPM only yielded a 12 % increment in the volume-averaged strain rate, suggesting diminishing returns from higher air flow rates in terms of shear force enhancement. Moreover, the decrease in total abundance of grazers and pathogens along with the operation, including Chytridiomycetes, Sessilida, and Operculariidae, might result from the shear force and the decrease of Chlorella spp.. This study underscores the critical roles of aeration and carbon source management in optimizing the performance and microbial ecology of algal-bacterial systems in wastewater treatment while minimizing energy inputs.

Study on the mechanism of SAR1B in sodium acetate promoting milk fat synthesis.

Acetate can promote milk fat synthesis in dairy cow mammary epithelial cells (BMECs). In this study, gene function analysis was used to explore the role of Ras family secretion-related GTP binding protein 1B (SAR1B) in milk fat synthesis of BMECs and its role and molecular mechanism in acetate-promoted milk fat synthesis. We found that the synthesis of lipid droplets and triglycerides was inhibited, and the expression levels of key genes and proteins in milk fat synthesis such as FASN and ACC were decreased in SAR1B knockout, which was reversed by overexpression of SAR1B. Addition of sodium acetate in BMECs can promote the expression of SAR1B, and SAR1B plays an important role in the synthesis of milk fat promoted by sodium acetate. We further investigated the underlying mechanism of SAR1B upregulation by sodium acetate, and found that sodium acetate could affect SAR1B expression through the positive regulation of SAR1B gene promoter activity by C/EBPβ and PPARγ. In conclusion, the results suggest that SAR1B can promote milk fat synthesis in BMECs, while C/EBPβ and PPARγ play important roles in sodium acetate to promote the expression of SAR1B.

Different organic carbon sources affect microalgal growth and extracellular polymeric substances synthesis to trigger biomass flocculation process

The addition of organic carbon sources into the culture medium represents an effective strategy for microalgae cultivation. However, its influence on the subsequent flocculation process remains poorly understood. In this study, four representative organic carbon sources were supplemented to microalgal cultures with the aim of evaluating their potential to enhance biomass accumulation, optimize fatty acid composition and improve phototolerance. The results demonstrated that the addition of ethanol, sodium acetate, glucose and fructose to the cultures resulted in extracellular protein contents of 90.9, 125.7, 67.5 and 46.0 mg/g, respectively, compared to 36.8 mg/g observed in the control culture with pure BG-11 medium. The addition of organic carbon sources led to alterations in protein content and the composition ratio of charged groups within the extracellular polymeric substances of microalgae, which in turn influenced the flocculation process. This study provides valuable insights into the selection of appropriate organic carbon sources for promoting microalgal growth and clarifies the flocculation mechanisms under various carbon utilization strategies.

Improving the performance of polyvinylidene fluoride (PVDF)-based proton exchange membranes with the addition of cellulose acetate for direct methanol fuel cells

Improving the performance of polyvinylidene fluoride (PVDF)-based proton exchange membranes with the addition of cellulose acetate for direct methanol fuel cells

Utilization of Cassava Peel Waste for Renewable Electrical Energy Production Using Joule Thief Series with Microbial Fuel Cell Technology (Addition of Yeast and Acetate)

Utilization of Cassava Peel Waste for Renewable Electrical Energy Production Using Joule Thief Series with Microbial Fuel Cell Technology (Addition of Yeast and Acetate)

THE EFFECTS OF NaClO2 AND H2O2 AS BLEACHING AGENTS IN THE SYNTHESIS OF CELLULOSE ACETATE FROM OIL PALM EMPTY FRUIT BUNCH

Indonesia is one of the largest palm oil-producing countries in the world. The results of palm oil processing produce a lot of waste, such as oil palm empty fruit bunches (OPEFB). The utilization of OPEFB in Indonesia is minimal, so it needs further development. OPEFB has a very high α-cellulose content, so that it can be used as raw material for manufacturing cellulose acetate. Making cellulose acetate from OPEFB consists of three main steps: delignification, bleaching, and acetylation. This study aims to compare the effects of the concentration of NaClO2 or H2O2 in the bleaching process on the physical properties of cellulose acetate from OPEFB. In the delignification process, 100 mesh-sized OPEFB powder is reacted with 5% sodium hydroxide (NaOH) at 100oC for 2 hours. The residue from deliglinfication was washed using distilled water until pH 7, filtered using filter paper, and dried using an oven at 50oC. The next step is the bleaching process using NaClO2 or H2O2 with concentration variations (1%, 2%, 3%, 4% and 5%). The bleaching process was carried out at 90oC for 1.5 hours. After filtration, the bleached residue was washed using distilled water until pH 7, filtered using filter paper, and dried using an oven at 50oC. After the bleaching process, α-cellulose powder was produced. The next step is acetylation, containing three main steps. The first step is the reaction between α-cellulose powder with acetic acid (CH3COOH) and sulfuric acid (H2SO4) at 40oC for 1.5 hours to perform activation. The second step is the addition of anhydrous cellulose in a ratio of 1:10 and mixed at 40oC for 1.5 hours. The third step is the addition of distilled water, acetic acid, and sodium acetate (CH3COONa) at 40oC for 5 minutes. Then, followed by filtration, the residue was washed using distilled water and methanol until pH 7 and dried at 50oC. The best result is using NaClO2 as a bleaching agent with a concentration of 2%, resulting in cellulose acetate yielding 98.85%, density of 1.954 g/mL, and L value of 91.897 for colorimetric test results. The density and L-value were close to commercial cellulose acetate (Sigma Aldrich). From the results of FTIR analysis, it can be concluded that the acetylation of α-cellulose into cellulose acetate has been successful, as evidenced by the formation of carbonyl groups (C=O).

Propyl acetate protects intestinal barrier during parenteral nutrition in mice and Caco-2 cells.

Gut microbiota dysbiosis induces intestinal barrier damage during parenteral nutrition (PN). However, the underlying mechanisms remain unclear. This study aimed to investigate gut microbiota dysbiosis, luminal short-chain fatty acids, and autophagy in a mouse model and how these short-chain fatty acids regulate autophagy. Eight-week-old male specific-pathogen-free mice were randomly divided into a Chow group (standard diet and intravenous normal saline infusion) and a PN group (continuous infusion of PN nutrient solution) for 7 days. Caco-2 cells were also treated with intestinal rinse solutions from Chow and PN mouse models. Compared with the Chow group, the PN group exhibited increased Proteobacteria and decreased Firmicutes, correlating with decreased propyl acetate. In the PN group, intestinal tissue exhibited elevated adenosine monophosphate-activated protein kinase (AMPK) phosphorylation, LC3II protein levels, and Atg3 and Atg7 messenger RNA levels. P62 protein levels were decreased, indicating an increase of autophagy flux in the PN group. In the Caco-2 cell model, cells treated with PN solution plus propyl acetate exhibited increased Claudin-1 and occluding along with decreased interleukin-6 and tumor necrosis factor α compared with those treated with PN solution alone. Propyl acetate addition inhibited the AMPK-mammalian target of rapamycin (mTOR) pathway, mitigating the excessive autophagy induced by the PN intestinal rinse solution in Caco-2 cells. PN led to a significant reduction in propyl acetate levels in the intestine, excessive activation of autophagy, and barrier dysfunction. Propyl acetate inhibited excessive autophagy via the AMPK/mTOR signaling pathway and protected the intestinal barrier during PN.

Response of anammox to organics with different degradation characteristics and exposure time: Performance, sludge characteristics and bacterial community

The effects of typical organic compounds including easily degradable organic matters sodium acetate, yeast and methanol, and refractory organic matter (ROM) humic acid on anaerobic ammonium oxidation (anammox) systems in short-term and medium-term exposure time were studied. During short-term experiments, nitrogen removal activity (NRA) was inhibited at sodium acetate level of 150 mg L−1 total organic carbon (TOC) and methanol level of 30–150 mg L−1 TOC, but humic acid and yeast (≤150 mg L−1 TOC) enhanced nitrogen removal in anammox systems. The greatest NRA of 30.10 mg TN g−1 VSS h−1 was recorded at yeast level of 90 mg L−1 TOC. In medium-term experiments, organics significantly inhibited the nitrogen removal ability. As a ROM, humic acid enhanced sludge aggregation and biological diversity, but decreased the bioactivity and extracellular polymeric substances levels. Due to the endogenous denitrification, the relative abundance of anammox bacteria (AnAOB) was decreased. Candidatus Kuenenia is still dominant in sludge with methanol and humid acid, but AnAOB are not dominant due to the addition of sodium acetate and yeast. This research would be beneficial for the full-scale application of the anammox process in treating real wastewater with organics and ammonia.

Sodium Acetate Enhances Neutrophil Extracellular Trap Formation via Histone Acetylation Pathway in Neutrophil-like HL-60 Cells.

Neutrophil extracellular trap formation has been identified as a new cell death mediator, termed NETosis, which is distinct from apoptosis and necrosis. NETs capture foreign substances, such as bacteria, by releasing DNA into the extracellular environment, and have been associated with inflammatory diseases and altered immune responses. Short-chain fatty acids, such as acetate, are produced by the gut microbiota and reportedly enhance innate immune responses; however, the underlying molecular mechanisms remain unclear. Here, we investigated the effects of sodium acetate, which has the highest SCFA concentration in the blood and gastrointestinal tract, on NETosis by focusing on the mechanisms associated with histone acetylation in neutrophil-like HL-60 cells. Sodium acetate enhanced NETosis, as shown by fluorescence staining with SYTOX green, and the effect was directly proportional to the treatment duration (16-24 h). Moreover, the addition of sodium acetate significantly enhanced the acetylation of Ace-H3, H3K9ace, and H3K14ace. Sodium acetate-induced histone acetylation rapidly decreased upon stimulation with the calcium ionophore A23187, whereas histone citrullination markedly increased. These results demonstrate that sodium acetate induces NETosis via histone acetylation in neutrophil-like HL-60 cells, providing new insights into the therapeutic effects based on the innate immunity-enhancing effect of dietary fiber.

Large-scale cultivation of Synechocystis sp. PCC6803 for the production of Poly(3-hydroxybutyrate) and its potential applications in the manufacturing of bulk and medical prototypes

Polyhydroxyalkanoates (PHAs) are biopolymers produced by microorganisms under nutrient limiting conditions and in the presence of excess carbon source. PHAs have gained popularity as a sustainable alternative to traditional plastics. However, large scale production of PHAs is economically challenging due to the relatively high costs of organic carbon. Alternative options include using organisms capable of phototrophic or mixotrophic growth. This study aimed at the production of poly(3-hydroxybutyrate) P(3HB), a type of PHA, at pilot scale using the freshwater cyanobacterium Synechocystis sp. PCC6803. First, to identify optimal conditions for P(3HB) production from Synechocystis sp. PCC6803, different supplemental carbon source concentrations and salinity levels were tested at laboratory scale. The addition of 4 g/L acetate with no added NaCl led to P(3HB) accumulation of 10.7 % dry cell weight on the 28th day of cultivation. Although acetate additions were replicated in an outdoor 400 L serpentine photobioreactor, P(3HB) content was lower, implying uncontrolled conditions impact on biopolymer production efficiency. An optimized P(3HB) extraction methodology was developed to remove pigments, and the biopolymer was characterized and subjected to 3D printing (fused deposition modelling) to confirm its processability. This study thus successfully led to the large-scale production of P(3HB) using sustainable and environmentally friendly cyanobacterial fermentation.

(Invited) Luminescent InP Quantum Dots: They're Not Just Like CdSe

Time-resolved photoluminescence (PL) and transient absorption (TA) spectroscopy have been used to elucidate the electron and hole dynamics in high quality InP/ZnSe/ZnS quantum dots (QDs) at room temperature. These dynamics depend critically on the overall In:P ratio. Stoichiometric QDs (those having an In:P ratio close to unity), have PL quantum yields of > 90% and exhibit dynamics that are very simple: both electron and hole relaxation to the bandedge is fast compared to the ~ 40 ps time-correlated photon-counting instrument response and the PL follows a single exponential decay having a time constant of about 26 ns. However, QDs having an In:P ratio greater than about 1.1 maintain PL quantum yields > 90%, but show much more complicated PL kinetics. In the non-stoichiometric QDs, a significant fraction of the PL exhibits a slower risetime. The PL rises over a range of timescales varying from close to the instrument response to approximately 2.0 ns. The time constant of the slowest component increases with increasing InP core size and the fraction of the PL that has the slow risetime increases with excess indium in the particle. The slow risetime is absent in the TA results, indicating that the slow dynamics may be assigned to relaxation in the valence band. The risetime increases with the thickness of the ZnSe shell, varying from < 40 ps for the thinnest (1.1 nm) to about 2.0 ns for the thickest (2.7 nm) ZnSe shells. In addition to the slow risetime, the QDs having excess indium show a significant long-lived (>100 ns) decay component. The magnitude and time constant of this slow decay also increases with ZnSe shell thickness.These results suggest that holes are transiently trapped at sites associated with indium dopants in the ZnSe shell. The trapped hole has negligible overlap with the conduction band electron, making this an optically dark state. The holes are in an equilibrium between the shell traps and the valence band, giving rise to the delayed emission. Several possible assignments of the trapping species can be considered, and a substitutional indium adjacent to a zinc vacancy, In3+/VZn 2-, is the most likely. This assignment is consistent with the observation that trapping occurs only when the QD has excess indium and is supported by experiments showing that the addition of zinc oleate or acetate decreases the extent of trapping, presumably by filling some of the vacancy traps. Further experiments show that addition of alkyl carboxylic acids causes increased trapping, presumably by the formation of zinc oleate, thereby creating additional zinc vacancies. Chloride ion is a common impurity in the synthesis of InP/ZnSe/ZnS QDs and the possibility of In3+/Cl- impurities acting as the hole trap can be also considered. However, additional experimental data on InP/ZnSe/ZnS QDs synthesized in the absence of chloride show the same PL risetimes and delayed emission, eliminating this possibility. Density functional theory calculations further corroborate assignment of the trapping species to In3+/VZn 2-. These calculations show that either a single In2+ ion or an In2+-In3+ dimer is much too easily oxidized to form the reversible traps observed experimentally, while In3+ is far too difficult to oxidize. However, a zinc vacancy adjacent to a substitutional indium is calculated to have its highest occupied orbitals about 1 eV above the top of the valence band of bulk ZnSe, in the appropriate energy range to act as reversible traps for quantum confined holes in the InP valence band.

Controllable preparation of carbon nanofiber membranes for enhanced flexibility and permeability

The electrospinning-produced carbon nanofiber membranes (CNFM) have been applied in many fields for their three-dimensional porous networks, however, the natural fragility impedes their practical applications. Introducing plasticizers into carbon fibers has been proven an efficient way to increase the flexibility of CNFM but the extent is limited. This work explored dual plasticizers strategy to improve the flexibility of CNFM. The addition of zinc acetate and tetraethyl orthosilicate leads to bigger carbon nanofibers and higher mean pore diameters. They can be transformed into SiO2 and ZnO nanoparticles that embed in the carbon fibers, and act as plasticizers to inhibit stress diffusion. The Young's modulus of the optimal SZCNFM-2.0-1.5-700 is 31.0 MPa, which is lower than single plasticizer can reduce. The mechanism of dual plasticizers collaboratively improving the flexibility of SZCNFM was proved based on the characterization results. The SZCNFM-2.0-1.5-700 with well flexibility also revealed high permeability, for instance, the gravity-induced cyclohexane flux is 486.67 L m−2 h−1. Furthermore, the SZCNFM-2.0-1.5-700 requires only half the time compared to the commercial filter membrane when separating the same amount of Pd@CN suspension in the suction filter.

Reduction of c-type cytochromes by Fe(II)-ligand under oxic conditions: Roles of Fe(II)-heme complexation and reactive oxygen species

Microbial Fe(II) oxidation is mainly mediated by the outer-membrane proteins that contain c-type cytochromes (c-Cyts), and the widespread Fe(II)-oxidizing bacteria are usually subjected to fluctuations between oxic and anoxic conditions. However, it remains unclear how oxygen affects the redox dynamics of c-Cyts by Fe(II), particularly in the presence of organic ligands that are widely distributed in the environment. Here, the reduction of a model heme-containing c-Cyts by Fe(II) was investigated in the absence and presence of organic ligands (i.e., citrate and acetate) at pH 5.5 under anoxic and oxic conditions. The kinetic results showed that c-Cyts reduction was enhanced by citrate and acetate under anoxic conditions, and the enhancement by citrate was more pronounced than that by acetate. The speciation calculation and cyclic voltammetry results suggested that the proportions of Fe(II)-Citrate complexes were much higher than those of Fe(II)-Acetate complex, but the addition of acetate and citrate caused minor changes in redox potential of Fe(II)/Fe(III) species. Further analysis using quantum chemical computation demonstrated that the formation of Fe(II)-Heme complexes via lateral binding to the carboxyl group of c-Cyts was more stable than those via replacing the S-linked axial ligand of heme, with the recombination energy with Heme ranking as Fe(II)-Citrate < Fe(II)-Acetate < Fe(II). Therefore, the stronger complexation of Fe(II)-Citrate and its lower recombination energy with c-Cyts drive the enhanced c-Cyts reduction under anoxic conditions. By contrast, the c-Cyts reduction by Fe(II) and Fe(II)-ligand was inhibited under oxic conditions. The electron spin resonance characterization indicated that both O2−• and OH• radicals were produced in the system of c-Cyts with Fe(II) or Fe(II)-ligand under oxic conditions and the signals were higher with Fe(II)-ligand than those with Fe(II). These reactive oxygen species were proposed to enable a re-oxidation of the c-Cyts that was reduced by Fe(II) or Fe(II)-ligand, causing an inhibitory effect on the observed c-Cyts reduction and forming more reactive oxygen species. Our findings shed light on the important roles of Fe(II)-ligand-heme complexation and reactive oxygen species in the interaction between Fe(II) and c-Cyts, which deepen the understanding of microbial/enzymatic Fe(II) oxidation under oxic conditions at the molecular level.

Study of the mechanism of action of cytostatic drug regimens with the addition of lysine acridone acetate in metastatic colorectal cancer

Background. One of the most common malignant tumors is colorectal cancer. Colorectal cancer is characterized by frequent metastasis to the liver, lungs, peritoneum and distant lymph nodes, and therefore its treatment is complicated. Therefore, it is urgent to search for new drugs and treatment methods based on the molecular mechanisms underlying metastatic colorectal cancer.Aim. To study the mechanism of action of cytostatic drug regimens with the addition of lysine acridone acetate to increase the effectiveness of anti-oncogenic chemotherapy in metastatic colorectal cancer.Materials and methods. We used mice of Nude line at the age of 4 weeks with inoculated tumor cells of SW837 line, which were administered chemotherapy drugs (FOLFOXIRI и FOLFOX6). On biopsy samples of liver metastases, the apoptosis level (TUNEL) and the expression of proteins CD95, p53, BCL2, histone H3, Ki-67 (immunohistochemistry) were assessed.Results. An activating effect of the studied therapeutic regimens was revealed, which was more active with the addition of lysine acridone acetate, on the development of p53-dependent apoptosis and the expression of H3K27me3 (a marker of treatment effectiveness and tumor progression) in colorectal cancer metastases in the liver of experimental mice. At the same time, the level of cancer cell proliferation (Ki-67 expression) decreased.Conclusion. Increased apoptosis in mouse liver metastases, as well as a decrease in cancer cell proliferation when using these drug regimens should be regarded as a positive therapeutic effect. A p53-dependent mechanism of apoptosis activation under the influence of appropriate treatment regimens has been revealed. Lysine acridone acetate may be preferable for clinical study.

Influence of anionic species on the low temperature pyrolysis performance of heated tobacco sheets catalyzed by sodium salts.

Development of low temperature catalytic pyrolysis technology for heated tobacco sheets is expected to increase the aroma of heated tobacco products and improve their overall smoking quality. In this study, the low temperature pyrolysis performances of heated tobacco sheets catalyzed by various anionic sodium salts were investigated using TG-DTG, Py-GC-MS technology and smoke routine chemical composition analysis. The results showed that the total weight loss between 100°C and 300°C increased by 7.8%-13.15% after adding various anionic sodium salts, among which, sodium acetate and sodium tartrate showed a relatively higher weight loss. The relative content of free hydroxyacetone, furfuryl alcohol, butyrolactone and megastigmatrienone in the pyrolysis gas increased, while the relative content of free nicotine decreased. With the change of anionic species, the catalytic decomposition ability of cellulose, lignin, and other substances may change, resulting in the distribution alteration of compounds in the pyrolysis gas. After adding sodium acetate and sodium citrate, the release of total particulate matter (TPM), glycerol, and nicotine in flue gas increased. Overall, the addition of sodium acetate and sodium citrate showed a higher low temperature pyrolysis performance of heated tobacco sheets. The research results in this paper provide data support for changing the low temperature catalytic pyrolysis performance of heated tobacco sheets by adjusting the type of anions in sodium salts.

Molecular dynamics study of free volume coalescence around nonyl ethoxylate in polyethylene with vinyl acetate‐modified branches

AbstractPolyethylene (PE) is susceptible to environmental stress cracking (ESC). In the presence of an amphiphilic compound and subjected to stress, ESC starts with cavitation followed by slow crack growth and ends with brittle fracture. In this study, we used molecular dynamics simulation to study how branch ends which were chemically modified with vinyl acetate groups affect free volume coalescence around an amphiphilic compound, nonyl ethoxylate (NE), dispersed in branched PE models. Branch ends modified with vinyl acetate significantly impact the free volume coalescence dynamics around NE. Compared with methyl branch ends, vinyl acetate branch ends show a much higher affinity, as quantified by the corresponding radial distribution functions, for the hydrophilic ethylene oxide‐segment of NE. However, this is not the case for the hydrophobic ethylene‐segment. Interestingly, vinyl acetate branch ends tend to reduce the power (amplitude) of the free volume size fluctuations around both the ethylene oxide‐ and ethylene‐segments. Indeed, the powers of the fluctuations with different PE branching characteristics decrease with increasing vinyl acetate concentration. We believe that free volume coalescence leads to cavitation and that vinyl acetate branches could inhibit cavitation, thereby crack propagation in PE. The power results seem to be consistent with the experimental observation that the addition of copolymer ethylene vinyl acetate to low‐density polyethylene improves the ESC resistance of the blend.Highlights Vinyl acetate branches reduce free volume coalescence activities. Vinyl acetate branches are attracted to the hydrophilic segment of NE. Cavitation likely starts from the free volume coalescence around NE.

Low temperature method-based evaporation/spray-coating technology for wide bandgap perovskite solar cells

Years of working on perovskite solar cells (PSCs)-based tandem devices and single-junction devices have approved that low annealing temperatures can be beneficial for improving device performances. In this study, pseudo-halogen ion engineering works well in the evaporation/spray-coating method. According to our research, it is has been proven that the addition of formamidine acetate (FAAc) can effectively reduce the annealing temperature from 170 °C to 150 °C, accelerate the maturation process of the perovskite films, and broaden the annealing window. As a result, a perovskite film with homogeneous crystallization and low residual stress is achieved, leading to extended charge carrier lifetimes, elevated photoluminescence quantum yields (PLQY), reduced Urbach energies. The corresponding PSCs were prepared through evaporation/spray-coating method achieves an impressive power conversion efficiency (PCE) of 19.46%, which is the highest efficiency among wide-bandgap (WBG) PSCs fabricated by this method. And the unencapsulated devices exhibit satisfactory stability, retaining 80% of the initial PCE after 600 h of thermal aging at 60 °C and retaining 90% of the initial PCE after 1500 h of 50% humidity aging at 25 °C, respectively.

Enhanced Low-Temperature Resistance of Lithium-Metal Rechargeable Batteries Based on Electrolyte Including Ethyl Acetate and LiDFOB Additives.

To meet the demand for higher energy density in lithium-ion batteries and expand their application range, coupling lithium metal anodes with high-voltage cathodes is an ideal solution. However, the compatibility between lithium metal batteries and electrolytes affects their applicability. In this study, proposes a locally concentrated electrolyte based on ethyl acetate (EA) as the solvent, lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) as the lithium salt, and lithium difluorooxoborate (LiDFOB) as a sacrificial agent to enhance the low-temperature and high-voltage endurance of Li//Lithium cobalt oxide (LCO) batteries. The Li//LCO battery can operate within the voltage range of 3 to 4.5 V, with an initial discharge specific capacity of 174.5 mAh g-1 at 20 °C. At -40 °C, after 200 cycles, the capacity retention rate is 87.7 %. It can operate under extreme conditions of -70 °C, with a discharge specific capacity of 112.6 mAh g-1. Additionally, LCO//HC batteries using this electrolyte demonstrate excellent performance. Present work provides a new perspective for the optimization of electrolytes for low-temperature lithium-ion batteries.

A Continuous Plug-Flow Anaerobic-Multistage Anoxic/Aerobic Process Treating Low-C/N Domestic Sewage: Nutrient Removal, Greenhouse Gas Emissions, and Microbial Community Analysis

The anaerobic-multistage anoxic/aerobic (A-MAO) process has shown good potential for advanced nitrogen removal in recent years, but its greenhouse gas emissions still need to be fully explored. The effects of the influent distribution and external carbon source sodium acetate on nutrient removal, greenhouse gas emissions, and the microbial community structure in a continuous plug-flow A-MAO reactor fed with real low C/N ratio domestic sewage were investigated. The results showed that altering the allocation of carbon source resulted in average chemical oxygen demand (COD) and total nitrogen (TN) concentration in effluent reduced to 26.10 ± 4.86 and 6.65 ± 1.73 mg/L, respectively. Both operations reduced the emission rate of greenhouse gas. While the addition of external car-bon sources leaded to lower N2O emission rates and higher CO2 and CH4 emission rates. The addition of sodium acetate facilitated nitrification and denitrification processes, thereby leading to a reduction in N2O production. Meanwhile, it spurred the growth of methanogenic bacteria and heterotrophic microorganisms, thus boosting the production of CO2 and CH4. Influent distribution promoted the increase of Bacteroidota, Chloroflexi and Acidobacteriota of the reactor. The enrichment of typical hydrolytic bacteria and glycogen accumulating organisms (GAOs) increased the utilization efficiency of carbon sources in the system after the addition of sodium acetate. The significant increase of typical denitrifying bacteria (DNBs) Azospira reduced the N2O emission during heterotrophic denitrification process, which was considered to be an important functional genus for increasing nitrogen loss in this system. The rational utilization of carbon source makes the difference in metabolism function. The study provides a valuable strategy for comprehensively evaluating the pollutant removal and greenhouse gas emission reduction from the A-MAO process.