Glucagon-like peptide-1 analog liraglutide reduces fat deposition in chicken adipocytes.

Previously, we reported that glucagon-like peptide-1 (GLP-1) and its analog liraglutide could inhibit fat de novo synthesis in the liver and reduce abdominal fat accumulation in broiler chickens. Nevertheless, the impact of GLP-1 on adipocyte fat deposition remains enigmatic. This study aimed to investigate the effects of GLP-1, via its analog liraglutide, on chicken chicken adipocytes in vitro. Chemical assays, quantitative real-time polymerase chain reaction (qRT-PCR), and western blot were employed to assess the proliferation, differentiation, and fat deposition of chicken adipocytes. Our findings indicated that liraglutide significantly suppressed cell proliferation and promoted preadipocyte differentiation in comparison to the control group. This was evidenced by elevated triglyceride (TG) content and upregulated mRNA expression of lipogenesis-related enzymes, such as acetyl-CoA carboxylase (ACC) and fatty acid synthase (FAS), as well as regulators including peroxisome proliferator-activated receptor γ (PPARγ), sterol regulatory element binding protein-1 (SREBP1) and CCAAT/enhancer binding protein α (CEBPα). In mature adipocytes, liraglutide attenuated fat deposition by inhibiting fat de novo synthesis, evidenced by decreased mRNA expression of ACC, FAS, PPARγ, C/EBPα, and SREBP1, and concurrent upregulation of phosphorylated AMP-activated protein kinase (p-AMPK) and phosphorylated ACC (p-ACC). This resulted in reduced accumulation of lipid droplets and TG content in mature adipocytes. Collectively, our findings indicate that liraglutide suppresses the proliferation of preadipocytes, enhances their differentiation, and concurrently inhibits de novo lipogenesis in mature adipocytes. This observation offers profound insights into the mechanisms that underlie liraglutide's anti-adipogenic effects, which could have significant implications for the treatment of obesity in broiler chickens.

Regulator DegU can remarkably influence alkaline protease AprE biosynthesis in Bacillus licheniformis 2709.

Alkaline protease AprE, produced by Bacillus licheniformis 2709 is an important edible hydrolase, which has potential applications in nutrient acquisition and medicine. The expression of AprE is finely regulated by a complex transcriptional regulation system. However, there is little study on transcriptional regulation mechanism of AprE biosynthesis in Bacillus licheniformis, which limits system engineering and further enhancement of AprE. Here, the severely depressed expression of aprE in degU and degS deletion mutants illustrated that the regulator DegU and its phosphorylation played a crucial part in AprE biosynthesis. Further electrophoretic mobility shift assay (EMSA) in vitro indicated that phosphorylated DegU can directly bind to the regulatory region though the DNase I foot-printing experiments failed to observe protected region. The plasmid-mediated overexpression of degU32 (Hy) obviously improved the yield of AprE by 41.6 % compared with the control strain, which demonstrated the importance of phosphorylation state of DegU on the transcription of aprE in vivo. In this study, the putative binding sequence of aprE (5'-TAAAT……AAAAT…….AACAT…TAAAA-3') located upstream -91 to -87 bp, -101 to -97 bp, -195 to -191 bp, -215 to -211 bp of the transcription start site (TSS) in B. licheniformis was computationally identified based on the DNA-binding sites of DegU in Bacillus subtilis. Overall, we systematically investigated the influence of the interplay between phosphorylated DegU and its cognate DNA sequence on expression of aprE, which not only contributes to the further AprE high-production in a genetically modified host in the future, but also significantly increases our understanding of the aprE transcription mechanism.

Association of urine glyphosate levels with renal injury biomarkers in children living close to major vegetable-producing regions in China.

Glyphosate (GLY)-based herbicides exposure contributes to renal dysfunction in experimental conditions, but the effects on humans are rarely reported. Biomonitoring is practically relevant for evaluating the association of urine GLY levels and renal damage in children living close to vegetable-cultivating regions. In this study, we collected the first-morning void urine samples of 239 healthy children (aged 3-12, 48.12 % boys) living near major vegetable-producing regions in March-May and August 2023 in Shandong Province, China. Urine levels of GLY and kidney injury-associated biomarkers were determined using ELISA kits to assess their correlation. GLY was detected in 92.05 % of urine samples (220 out of 239 participants) and the geometric concentration (GM) was 7.429 µg/L (range: 0.625 to 38.267 µg/L). Binary logistic regression and multivariate regression analysis revealed GLY detectability and levels positively correlated with home ventilation and self-producing vegetable intake of the subjects, as well as sampling periods. Moreover, a statistically significant concentration association with urine GLY was found for kidney injury-associated biomarkers (NGAL and KIM-1) (R2 = 0.923 and 0.855, respectively). Additionally, risk assessment revealed that the maximum value of probable daily intake was 0.150 mg/kg bw/day, accounting for 30.1 % of the established Acceptable Daily Intake of GLY. This study unveils a positive correlation between continuous GLY-based herbicide exposure and renal injury biomarkers of children. A large-scale epidemiological study is warranted for comprehensively assessing the effects of GLY-based herbicides on kidney function of the entire public.

Grape seed-derived procyanidin inhibits glyphosate-induced hepatocyte ferroptosis via enhancing crosstalk between Nrf2 and FGF12.

BACKGROUND: Glyphosate (GLY) exposure induces hepatocyte ferroptosis through overproduction of reactive oxygen species, regarded as an important contributor to liver damage. Grape seed-derived procyanidin (GSDP) has been reported to be an effective antioxidant, but whether and, if any, how GSDP can attenuate GLY-induced liver injury via inhibiting ferroptosis is unclear. PURPOSE: The current study aimed to investigate the hepato-protective effects and possible mechanisms of GSDP. METHODS: GLY-induced liver damage mice model was established to explore the hepatoprotective roles of GSPE in vivo. Subsequently, bioinformatics methodology was used to predict the key pathways and factors related to the action targets of GSPE against hepatocyte ferroptosis. Finally, we explored the roles of nuclear factor E2 related factor 2 (Nrf2) and fibroblast growth factor 21 (FGF21) in blunting GLY-induced liver damage via suppressing ferroptosis in vitro. RESULTS: GSDP exerts hepato-protective effects in vivo and in vitro through reduced oxidative stress and inhibited ferroptosis, which was related to the activation of Nrf2. Bioinformatics analysis showed an interaction between Nrf2 and FGF21. Furthermore, Nrf2 inhibition reduced FGF21 expression in the mRNA and protein levels. Fgf21 knockdown suppressed Nrf2 expression level, but recombinant FGF21 protein increased Nrf2 expression and promoted Nrf2 translocation into nucleus, suggesting a crosstalk between Nrf2 and FGF21. Intriguingly, the decreased levels of Nrf2 and FGF21 compromised the protective roles of GSDP against GLY-induced hepatocyte ferroptosis. CONCLUSION: These findings suggest that GSDP attenuates GLY-caused hepatocyte ferroptosis via enhancing the interplay between Nrf2 and FGF21. Thus, GSDP may be a promising natural compound to antagonize ferroptosis-related damage.

Glyphosate-triggered hepatocyte ferroptosis via suppressing Nrf2/GSH/GPX4 axis exacerbates hepatotoxicity.

Glyphosate (GLY) exposure has been reported to damage organs in animals, in particular the liver, due to increased reactive oxygen species (ROS). Ferroptosis is defined as a new type of cell death that is characterized by the increase of ROS. The purpose of this study was to elucidate whether the relationship between ferroptosis and GLY-induced hepatotoxicity is of significance to enlarge the knowledge about GLY toxicity and consequences for human and animal health. To this end, in this study, we investigated the role of ferroptosis in GLY-induced hepatotoxicity both in vivo and in vitro. The results showed that GLY exposure triggered ferroptosis in L02 cells, but pretreatment with ferroptosis inhibitor ferrostatin (Fer-1) rescued ferroptosis-induced injury, thereby indicating that ferroptosis plays a key role in GLY-induced hepatotoxicity. Moreover, N-acetylcysteine, a glutathione (GSH) synthesis precursor, reversed GLY-triggered ferroptosis damage, thus indicating that GSH exhaustion may be a prerequisite for GLY-triggered hepatotoxicity. Mechanistically, GLY inhibited GSH biosynthesis via blocking the phosphorylation and nuclear translocation of Nrf2, which resulted in GSH depletion-induced hepatocyte ferroptosis. In a mouse model, GLY exposure triggered ferroptosis-induced liver damage, which can be rescued by pretreatment with Fer-1 or tBHQ (a specific agonist of Nrf2). To our knowledge, this is the first study to reveal that GLY-triggered hepatocyte ferroptosis via suppressing Nrf2/GSH/GPX4 axis exacerbates hepatotoxicity, which expands our knowledge about GLY toxicity in animal and human health.

Transcriptome analysis reveals the mechanisms of hepatic injury caused by long-term environmental exposure to atrazine in juvenile common carp (Cyprinus carpio L.).

Atrazine (ATZ) is the second most commonly used herbicide worldwide, resulting in the pollution of water bodies and affecting the economic benefits of aquaculture. ATZ is known to cause liver damage in the common carp, Cyprinus carpio L., one of the most widely cultivated fish in China, but the underlying mechanisms are poorly understood. In this study, juvenile common carp Cyprinus carpio L. were exposed to three different environmental levels (0.4, 0.8, and 1.2 µg/L) of ATZ for 12 weeks and changes in the liver transcriptomes between the high-dose group and the control group were analyzed. The data showed that different levels of ATZ exposure caused hepatotoxicity in juvenile carp, shown by biochemical parameters and histopathological changes. Comparative transcriptomics showed that high-dose ATZ exposure led to alterations in the expression of various lipid metabolism-related gene changes, including genes associated with metabolic pathways, fatty acid metabolism, and fatty acid elongation. Furthermore, a connection network analysis of the top 100 differentially expressed genes (DEGs) showed a variety of associations between high-dose ATZ-induced liver damage and the principal DEGs, indicating the complexity of hepatotoxicity induced by ATZ. In conclusion, the molecular mechanisms underlying ATZ-triggered hepatotoxicity in juvenile carp are primarily related to impaired lipid metabolism.

Synthesis, physicochemical characterization, antibacterial activity, and biocompatibility of quaternized hawthorn pectin.

Quaternized polysaccharides are considered as potential antimicrobial materials due to their antimicrobial activity, biodegradability, biocompatibility, and water solubility. In this work, hawthorn pectin (HP) was obtained by ultrasound­sodium citrate assisted extraction, quaternized hawthorn pectin (QHP) derivatives (namely: QHP-1, QHP-2, QHP-3, and QHP-4) with different degree of substitution were produced using (3-Chloro-2-hydroxypropyl) trimethylammonium chloride under alkaline conditions. The structure, properties, and morphology of HP and QHP were characterized by FTIR, XRD, 1H NMR, high-performance gel permeation chromatography (HPGPC), thermal analysis, and SEM. The results of FTIR and 1H NMR demonstrated that the quaternary ammonium modification was successful, and the degree of substitution (DS) of derivatives was calculated through elemental analysis. The determination of the minimum inhibitory concentrations and biofilm inhibition assay exhibited that QHP has a certain inhibitory effect on Escherichia coli and Staphylococcus aureus. Acceptable values of QHP were obtained in cytotoxicity assay on human keratinocytes.

Characterization of edible film fabricated with HG-type hawthorn pectin gained using different extraction methods.

In this study, four HG-type pectins were obtained using hydrochloric acid extraction (HA-HP), citric acid extraction (CA-HP), ultrasonic-assisted extraction (UA-HP), and microwave-assisted extraction (MA-HP). Four pectin films (HA-HPF, CA-HPF, UA-HPF, and MA-HPF) were prepared by a solution casting method, respectively. Compared to four pectins, the asymmetric COO - vibrational peak of UA-HPF, HA-HPF, and CA-HPF were blue-shifted (1604-1606 cm-1), while was red-shifted (1611 cm-1) in MA-HPF. The crystallinity was greater for HA-HPF and CA-HPF than UA-HPF and MA-HPF. Four pectin films all had relatively homogeneous surface morphology. CA-HPF had the best mechanical properties and oxygen barrier performance, HA-HPF had the best transparency. UA-HPF had the lowest hydrophilicity and water vapor permeability. MA-HPF had the best thermal stability. Our study shows that different physicochemical properties of HG-type pectins can influence the physicochemical properties of films. The difference of these properties gives the resulting film different possibilities for application.

Construction of an alkaline protease overproducer strain based on Bacillus licheniformis 2709 using an integrative approach.

Bacillus licheniformis 2709 is a potential cell factory for the production of alkaline protease AprE, which has important value in industrial application but still lacks sufficient production capacity. To address this problem, we investigated the effects of the secretory viscous materials on the synthesis of AprE, which might seriously affect the industrial fermentation. Furthermore, an iterative chromosomal integration strategy at various chromosomal loci was implemented to achieve stable high-level expression of AprE in B. licheniformis 2709. The host was genetically modified by disrupting the native pgs cluster controlling the biosynthesis of viscous poly-glutamic acid identified in the study by GC/MS, generating a mutant with significantly higher biomass and better bioreactor performance. We further enhanced the expression of alkaline protease by integrating two additional aprE expression cassettes into the genome, generating the integration mutant BL ∆UEP-3 with three aprE expression cassettes, whose AprE enzyme activity in shake flasks reached 25,736 ± 997 U/mL, which was 136% higher than that of the original strain, while the aprE transcription level increased 4.05 times. Thus, an AprE high-yielding strain with excellent fermentation traits was engineered, which was more suitable for bulk-production. Finally, the AprE titer was further increased in a 5-L fermenter, reaching 57,763 ± 1039 U/mL. In summary, genetic modification is an enabling technology for enhancing enzyme production by eliminating the unfavorable characteristics of the host and optimizing the expression of aprE through iterative chromosomal integration. We believe that the protocol developed in this study provides a valuable reference for chromosomal overexpression of proteins or bioactive molecules in other Bacillus species.

Two Birds One Stone: Facile and Controllable Synthesis of the Ag Quantum Dots/Reduced Graphene Oxide Composite with Significantly Improved Solar Evaporation Efficiency and Bactericidal Performance.

Interfacial solar evaporation (ISE) is an environmentally friendly and promising water treatment strategy. However, the bactericidal performance of an ISE system during the evaporation process is usually ignored, which may result in potential water safety hazards. In this study, a facile method is presented for the controllable synthesis of Ag quantum dots (QDs)/rGO to simultaneously achieve efficient solar evaporation and evaporated water disinfection. The size of the Ag nanoparticles (NPs) rather than the loading amount is the factor that considerably affects the solar evaporation efficiency and the bactericidal performance. Under 1 sun of irradiation (1 kW·m2), the evaporation rate and solar evaporation efficiency of Ag QDs/rGO are as high as 2.11 kg·m2·h-1 and 94.0%, respectively. Based on E. coli and S. aureus, the bactericidal activity of Ag QDs/rGO in the evaporation process is qualitatively and quantitatively characterized; no bacteria could be detected in the evaporated water. Furthermore, various water samples, including acidic water, alkaline water, dye water, and seawater, are selected to verify the solar evaporation performance of Ag QDs/rGO. When considering complex water samples, the as-prepared material maintains a high evaporation efficiency and an excellent purification effect, indicating attractive potential for various practical applications.

Transcriptome based functional identification and application of regulator AbrB on alkaline protease synthesis in Bacillus licheniformis 2709.

Bacillus licheniformis 2709 is the major alkaline protease producer, which has great potential value of industrial application, but how the high-producer can be regulated rationally is still not completely understood. It's meaningful to understand the metabolic processes during alkaline protease production in industrial fermentation medium. Here, we collected the transcription database at various enzyme-producing stages (preliminary stage, stable phase and decline phase) to specifically research the synthesized and regulatory mechanism of alkaline protease in B. licheniformis. The RNA-sequencing analysis showed differential expression of numerous genes related to several processes, among which genes correlated with regulators were concerned, especially the major differential gene abrB on enzyme (AprE) synthesis was investigated. It was further verified that AbrB is a repressor of AprE by plasmid-mediated over-expression due to the severely descending enzyme activity (11,300 U/mL to 2695 U/mL), but interestingly it is indispensable for alkaline protease production because the enzyme activity of the null abrB mutant was just about 2279 U/mL. Thus, we investigated the aprE transcription by eliminating the theoretical binding site (TGGAA) of AbrB protein predicated by computational strategy, which significantly improved the enzyme activity by 1.21-fold and gene transcription level by 1.77-fold in the mid-log phase at a cultivation time of 18 h. Taken together, it is of great significance to improve the production strategy, control the metabolic process and oriented engineering by rational molecular modification of regulatory network based on the high throughput sequencing and computational prediction.

Facile Deflagration Synthesis of Hollow Carbon Nanospheres with Efficient Performance for Solar Water Evaporation.

Solar water evaporation is a promising and environment-friendly approach to relieve global water scarcity issues. Currently, many reports show that the voids and porous structure are beneficial to the absorption of solar energy to generate water steam. Herein, carbon nanospheres with central cavity structures are rationally designed by the one-step NaN3/fluorinated graphite deflagration method. The Na clusters derived from NaN3 deflagration are not only provided as the hollow templates but also react with fluorinated graphite to release heat, further boosting the formation of hollow carbon nanospheres (HCSs). Benefiting from the diversity of carbon nanomaterials, rough surface, unique hollow structures, and numerous micron/submicron holes, the light absorption ability, heat localization, and water supply capacity of HCSs have been significantly enhanced. Because of these advantages, the HCS-3 exhibits an excellent water evaporation efficiency of 92.7% at 1 kW m-2, which is much higher than that of carbon nanospheres, graphene oxide, and even most of the previous carbon materials. In addition, we demonstrated that the HCSs have a long-term stability and high efficiency of production of drinkable water and purifying various types of wastewater, including seawater, strong acid/alkaline water, and water containing dyes. To sum up, the deflagration synthetic technology as a facile and ultrafast process can be a new insight for future photothermal material design.

Ionic liquid derived Fe, N, B co-doped bamboo-like carbon nanotubes as an efficient oxygen reduction catalyst.

Iron-nitrogen (Fe-N) co-doped carbon nanomaterials are promising catalysts for oxygen reduction reaction (ORR) with outstanding catalytic activity at low cost. Here, we demonstrate a facile bottom-up strategy to fabricate Fe, N, B co-doped bamboo-like carbon nanotubes using ionic liquid as dopant source. We show that the synergistic effect of Fe, N, B in the mesoporous carbon structure can derive excellent ORR activity, for which the FeNB/C-800 catalyst delivers an onset potential of 0.97 V (vs. reversible hydrogen electrode, RHE), a half-wave potential of 0.81 V (vs. RHE) and a high limiting current density (5.59 mA cm-2), comparable to a commercial Pt/C. The catalyst also shows good methanol tolerance as compared to Pt/C catalyst. This work highlights a bottom-up strategy for creating ternary Fe, N, B sites on carbon nanotubes using boron-containing ionic liquid precursor.

In Situ Synthesized MEMS Compatible Energetic Arrays Based on Energetic Coordination Polymer and Nano-Al with Tunable Properties.

Integrating energetic materials with a microelectromechanical system (MEMS) to achieve miniaturized integrated smart energetic microchips is promising. The potential applications include actuation in lab-on-a-chip devices, ignition in automobile airbags, propulsion and attitude control of micro-/nano-satellites, and miniaturized electro-explosive devices. In this work, a new type of MEMS-compatible energetic arrays was in situ realized on a copper substrate, which comprised a new energetic coordination polymer (ECP; Cu1.5C2N8O2·H2O) with tunable nanostructures and a nano-aluminum (nano-Al) covering layer. The composition, morphology, and energetic characteristics of the energetic arrays can be easily tuned by adjusting the reaction time. The maximum heat release of 1850.2 J/g in thermal analysis and the intense flame in open burning experiment proved its excellent exothermic and combustion performance. A closed-bomb experiment further revealed that the ECP@nano-Al energetic arrays supported on Cu(OH)2 nanorods had a peak pressure (5.5 MPa) and a pressure duration (0.5 s) more than twice those of nanoscale Al/CuO powder because of the introduction of gas elements (e.g., C, H, and N). A preliminary impulse experiment was also conducted through the torsion pendulum method. The displacement of the torsion pendulum in the micrometer scale proved the potential application of the energetic arrays in micropropulsion systems. Overall, this work can serve as a reference for the synthesis and applications of ECPs.

Core-Shell Structured Nanoenergetic Materials: Preparation and Fundamental Properties.

Energetic materials, including explosives, pyrotechnics, and propellants, are widely used in mining, demolition, automobile airbags, fireworks, ordnance, and space technology. Nanoenergetic materials (nEMs) have a high reaction rate and high energy density, which are both adjustable to a large extent. Structural control over nEMs to achieve improved performance and multifunctionality leads to a fascinating research area, namely, nanostructured energetic materials. Among them, core-shell structured nEMs have gained considerable attention due to their improved material properties and combined multiple functionalities. Various nEMs with core-shell structures have been developed through diverse synthesis routes, among which core-shell structured nEMs associated with explosives and metastable intermolecular composites (MICs) are extensively studied due to their good tunability and wide applications, as well as excellent energetic (e.g., enhanced heat release and combustion) and/or mechanical properties. Herein, the preparation methods and fundamental properties of the abovementioned kinds of core-shell structured nEMs are summarized and the reasons behind the satisfactory performance clarified, based on which suggestions regarding possible future research directions are proposed.

The solid phase thermal decomposition and nanocrystal effect of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) via ReaxFF large-scale molecular dynamics simulation.

The solid phase thermal decomposition and nanocrystal effect are extremely important to understand the ignition, combustion, reaction growth and buildup to detonation under shock wave action. To explore the basic mechanism at the atomic level and understand the interaction among nanocrystal lattices, molecules, and intermediates during the solid phase decomposition, ReaxFF large-scale molecular dynamics simulation at 1000-3000 K was demonstrated on the solid phase of nanocrystalline RDX with a size in the range of 5-12 nm. Based on the analysis of the RDX decay and chemical species, we found that the whole decomposition process can be divided into the solid-affected stage and the following less-condensed phase stage. From the results of NO2 diffusion and high frequency reaction statistics for the nanocrystal effect on the RDX decay, intermediate diffusion was found to be strongly associated with the chemical pathway. In addition, it was found for the first time that the thermal decomposition of RDX originates from the inside of the nanocrystal instead of its surface. Furthermore, a promising uniform energy distribution mechanism transfer by vibration inside the nanocrystalline RDX was demonstrated. The detailed information derived from this study can aid in the thorough understanding of the size effect on the chemical kinetics of nanoexplosives, especially for thermal decomposition and reaction growth.

Laser-Ignited Relay-Domino-Like Reactions in Graphene Oxide/CL-20 Films for High-Temperature Pulse Preparation of Bi-Layered Photothermal Membranes.

Light-ignited combustions have been proposed for a variety of industrial and scientific applications. They suffer, however, from ultrahigh light ignition thresholds and poor self-propagating combustion of typical high-energy density materials, e.g., 2,4,6,8,10,12-(hexanitrohexaaza)cyclododecane (CL-20). Here, reported is that both light ignition and combustion performance of CL-20 are greatly enhanced by embedding ε-CL-20 particles in a graphene oxide (GO) matrix. The GO matrix yields a drastic temperature rise that is sufficient to trigger the combustion of GO/CL-20 under low laser irradiation (35.6 mJ) with only 6 wt% of GO. The domino-like reduction-combustion of the GO matrix can serve as a relay and deliver the decomposition-combustion of CL-20 to its neighbor sites, forming a relay-domino-like reaction. In particular, a synergistic reaction between GO and CL-20 occurrs, facilitating more energy release of the GO/CL-20 composite. The novel relay-domino-like reaction coupled with the synergistic reaction of CL-20 and GO results in a deflagration of the material, which generates a high-temperature pulse (HTP) that can be guided to produce advanced functional materials. As a proof of concept, a bi-layered photothermal membrane is prepared by HTP treatment in an extremely simple and fast way, which can serve as a model architecture for efficient interfacial water evaporation.

Construction of Al-ZnO/CdS photoanodes modified with distinctive alumina passivation layer for improvement of photoelectrochemical efficiency and stability.

ZnO/CdS-based nanorod arrays (NRs) are an excellent class of photoanode materials, which possess high photoelectric response for solar-driven water splitting. A highly efficient photoanode system consisting of Al-doped ZnO NRs as effective electron-transfer layers and CdS as a light harvesting layer was rationally designed. Al doping increased the conductivity of ZnO NRs and simultaneously coarsened the surface of ZnO due to expansion of ZnO lattice. The rough surface favoured the growth of a CdS coating layer on it through a successive ionic layer adsorption reaction. The integrated ZnO/CdS photoanode exhibited photocurrent of 10.4 mA cm-2 at 1.23 V versus RHE (reversible hydrogen potential) and conversion efficiency of 5.75% at 0.38 V versus RHE for 60 SILAR CdS cycles. The coating of a protective Al2O3 passivation layer through the direct current magnetron sputtering technique significantly improved the stability of the electrode, and it was better than that of the conventional atomic layer deposition method.

Compartmentalizing Incompatible Tandem Reactions in Pickering Emulsions To Enable Visual Colorimetric Detection of Nitramine Explosives Using a Smartphone.

We report a visual colorimetric assay for detection of nitramine explosives such as 1,3,5-trinitro-1,3,5-triazinane (RDX) and 1,3,5,7-tetranitro-1,3,5,7-tetrazocane (HMX) using a smartphone. This assay is based on compartmentalizing incompatible tandem reactions in Pickering emulsions. The alkaline hydrolysis of RDX or HMX in one Pickering emulsion produces nitrite ions, which autodiffuse into the other Pickering emulsion to form nitrous acid. It oxidizes the 3,3',5,5'-tetramethylbenzidine (TMB) to generate yellow TMB diimine. The RGB component change of the optical images is applied to quantitatively determine the RDX and HMX at different reaction temperatures. A distinct color change occurs at RDX and HMX concentrations of 1.2 and 12 µM, respectively. The adjusted intensity increases linearly with the increase of the logarithms of the concentrations of RDX and HMX in the range of 1.2-90 µM and 12-90 µM, respectively. The limits of detection of RDX and HMX are 96 and 110 nM, respectively. Importantly, this assay is employed for the detection of RDX and HMX in real water, proving the applicability of the assay in real-world samples.

Synthesis, Characterization, and Sensitivity of a CL-20/PNCB Spherical Composite for Security.

Highly energetic materials have received significant attention, particularly 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (CL-20). However, the application of this material was limited due to its high sensitivity. It is well known that the shape, size, and structure of energetic materials (EMs) significantly influence their sensitivity. At present, there are several ways to reduce the sensitivity of CL-20, such as spheroidization, ultrafine processing, and composite technology. However, only one or two of the abovementioned methods have been reported in the literature, and the obtained sensitivity effect was unsatisfactory. Thus, we tried to further reduce the sensitivity of CL-20 by combining the above three methods. The as-prepared composite was precipitated from the interface between two solutions of water and ethyl acetate, and the composite was insensitive compared with other reported CL-20-based EMs. The H50 value for the composite ranged up to 63 cm. This approach opens new prospects for greatly reducing the sensitivity of high Ems.