Residual Products Research Articles

Resolving electrochemical incompatibility between LATP and Li-metal using tri-layer composite solid electrolyte approaches for solid-state Li-metal batteries

Due to its excellent air stability, low cost, and high ionic conductivity, Li1.3Al0.3Ti1.7(PO4)3 (LATP) has emerged as a viable option for solid-state lithium batteries (SSLBs). However, the irreversible reactivity between LATP and the Li-metal anode severely restrict its electrochemical performances. Herein, a tri-layer composite solid electrolyte (t-CSE1) comprised of LATP, PVDF-HFP, SN, and LiTFSI as the middle layer and Al-LLZO, PVDF-HFP, SN, and LiTFSI as the top and bottom layers is prepared to solve these prominent limitations since Al-LLZO is stable towards Li metal anode. As a result, the lithium plating-stripping lifetimes for the Li||Li symmetry cell is prolonged from 550 to 1950 h at 0.1 mA cm−2 without any residual redox products. In addition, the as-prepared t-CSE1 exhibited excellent ionic conductivity (ca. 6.46 × 10−4 S cm−1 at room temperature), high lithium-ion transference number (ca. 0.69) and remarkable mechanical strength (ca. 12.82 MPa). Furthermore, the Li||LiFePO4 (Li||LFP) full cell achieved significantly improved long cycle performances of 500 cycles with 80.31 % capacity retention and 99.93 % average coulombic efficiency at 0.2C. Moreover, the Li||LFP full cell showed 85.53 % capacity retention and 99.95 % coulombic efficiency after 200 cycles at 0.5C at room temperature. Thus, this study gives an insight into how to prevent the electrochemical incompatibility between LATP and Li metal for SSLBs.

Joule heat assisting electrochemical degradation of polyethylene microplastics melted on anode

Polyethylene (PE) microplastics (MPs) in water was rapidly degraded using a “Joule heat assisting electrochemical degradation” strategy. In a tailor-made reactor, PE MPs were captured by anode, being softened or even melted by the interface Joule heat, enabling direct electron transfer and making the maximum use of short-lived active species. Within a few hours, above 99 % of PE MPs (∼ 1 g·L−1) vanished, and residual solid products with higher carbonyl index (CI) and O/C ratio inclined to combine, avoiding creating more harmful nanoplastics (NPs), just leaving a few low-threatening soluble products with unsaturated carbon chains. Compared with SO42- and S2O82-, the presence of Cl- water matrix could facilitate the chain-scission degradation and make solid products fusion more significant. After proposing a novel MPs degradation mechanism and verifying the universality of this novel strategy by degrading other five kinds of MPs. Subsequently, a techno-economic analysis was conducted.

Hydrothermal liquefaction of composite household waste to biocrude: the effect of liquefaction solvents on product yield and quality.

The hydrothermal liquefaction (HTL) of composite household waste (CHW) was investigated at different temperatures in the range of 240-360 °C, residence times in the range of 30-90 min, and co-solvent ratios of 2-8 ml/g, by utilising ethanol, glycerol, and produced aqueous phase as liquefaction solvents. Maximum biocrude yield of 46.19% was obtained at 340 °C and 75 min, with aqueous phase recirculation ratio (RR) of 5 ml/g. The chemical solvents such as glycerol and ethanol yielded a biocrude percentage of 45.18% and 42.16% at a ratio of 6 ml/g and 8 ml/g, respectively, for 340 °C and 75 min. The usage of co-solvents as hydrothermal medium increased the biocrude yield by 35.30% and decreased the formation of solid residue and gaseous products by 19.82% and 18.74% respectively. Also, the solid residue and biocrude obtained from co-solvent HTL possessed higher carbon and hydrogen content, thus having a H/C ratio and HHV that is 1.01 and 1.23 times higher than that of water as hydrothermal medium. Among the co-solvents, HTL with aqueous phase recirculation resulted in higher carbon and energy recovery percentages of 9.36% and 9.78% for solid residue and 52.09% and 56.75% for biocrude respectively. Further qualitatively, co-solvent HTL in the presence of obtained aqueous phase yielded 33.43% higher fraction of hydrocarbons than the pure water HTL and 7.70-17.01% higher hydrocarbons when compared with ethanol and glycerol HTL respectively. Nitrogen containing compounds, such as phenols and furfurals, for biocrudes obtained from all HTL processes, were found to be present in the range of 8.30-14.40%.

Effects of polymer matrix and temperature on pyrolysis of tetrabromobisphenol A: Product profiles and transformation pathways

Plastics are crucial constituents in electronic waste (e-waste) and part of the issue in e-waste recycling and environmental protection. However, previous studies have mostly focused on plastic recovery or thermal behavior of flame retardants, but not both simultaneously. The present study simulated the process of e-waste thermal treatment to explore tetrabromobisphenol A (TBBPA) pyrolysis at various temperatures using polystyrene (PS), polyvinyl chloride (PVC), and e-waste plastics as polymer matrices. Pyrolysis of TBBPA produced bromophenol, bromoacetophenone, bromobenzaldehyde, and bromobisphenol A. Co-pyrolysis with the polymer matrices increased emission factors by 1 − 2 orders of magnitude. The pyrolytic products of TBBPA, TBBPA+PS, and TBBPA+PVC were mainly low-brominated bisphenol A, while that of TBBPA in e-waste plastics was consistently bromophenol. Increasing temperature drove up the proportions of gaseous and particulate products, but lowered the relative abundances of inner wall adsorbed and residual products in pyrolysis of pure TBBPA. In co-pyrolysis of TBBPA with polymer matrix, the proportions of products in different phases were no longer governed solely by temperature, but also by polymer matrix. Co-pyrolysis of TBBPA with PS generated various bromophenols, while that with PVC produced chlorophenols and chlorobrominated bisphenol A. Transformation pathways, deduced by ab initio calculations, include hydrogenation-debromination, isopropylphenyl bond cleavage, oxidation, and chlorination.

Salivary levels of eluents during Invisalign™ treatment with attachments: an in vivo investigation

BackgroundThe aim of the present study was to investigate qualitatively and quantitatively the elution of substances from polyester-urethane (Invisalign™) aligners and resin composite attachments (Tetric EvoFlow) in vivo.MethodsPatients (n = 11) treated with the aligners and attachments (16 per patient, without other composite restorations) for an average of 20 months, who were planned for attachment removed were enrolled in the study. Patients were instructed to rinse with 50 mL of distilled water upon entry and the rinsing solution was collected (before removal). Then, the attachments were removed with low-speed tungsten carbide burs for adhesive residue removal, a thorough water rinsing was performed immediately after the grinding process to discard grinding particle residues, and subsequently, after a second water-rinsing the solution was collected for analysis (after removal). The rinsing solutions were analyzed for targeted (LC-MS/MS: Bis-GMA, DCDMA, UDMA, BPA) and untargeted (LC-HRMS: screening of leached species and their degradation products) compounds.ResultsTargeted analysis revealed a significant reduction in BPA after attachment removal (4 times lower). Bis-GMA, DCDMA, UDMA were below the detection limit before removal but were all detectable after removal with Bis-GMA and UDMA at quantifiable levels. Untargeted analysis reviled the presence of mono-methacrylate transformation products of Bis-GMA (Bis-GMA-M1) and UDMA (UDMA-M1), UDMA without methacrylate moieties (UDMA-M2), and 4-(dimethylamino) benzoic acid (DMAB), the degradation product of the photo-initiator ethyl-4-(dimethylamino) benzoate (EDMAB), all after attachment removal. Several amino acids and endogenous metabolites were also found both before and after removal.ConclusionsElevated levels of BPA were traced instantaneously in patients treated with Invisalign™ and flowable resin composite attachments for the testing period. BPA was reduced after attachment removal, but residual monomers and resin degradation products were found after removal. Alternative resin formulations and attachment materials may be utilized to reduce eluents.

Efficient glycosylation and in vitro neuroprotective evaluation of abundant prenylflavonoid in hops

Structurally unique isopentenyl flavonoids are extremely low in natural plant species, and their cumbersome chemical pathways, scarcity of donors, and poor stability have severely hindered their application scenarios. Xanthohumol (XN), an isopentenyl chalcone, is a unique and abundant herbal efficacy substance in hops (Humulus upulus L.), which is an herb with a variety of clinical benefits. However, 90% of XN is left behind in the production of hop residue, resulting in a waste of natural resources. The poor water solubility and low bioavailability of XN also limit its wide application. Combined biotransformation strategies can greatly enhance the added value of resource materials and become one of the important means for the sustainable utilization of traditional Chinese medicine resources. In this study, an extreme microbial screening strategy for efficient bioconversion of phrenylflavonids is established to achieve Bacillus zanthoxyli GQ8 obtained from brewer's dregs and a non-aqueous biosynthesis system of xanthohumol glycosides (XNG, substrate concentration of 0.5 g/L, conversion rate of 73.2%) is constructed by GQ8. With HT22 cell model of H2O2-induced oxidative damage and BV2 cell model of LPS-induced neuroinflammation, XNG showed little cytotoxicity and exhibited better anti-inflammatory and antioxidant effects compared with the original compound. Our experimental results firstly provide a high-efficiency biotransformation strategy for glycosylation of XN with bacteria and provide a support that prenylflavonoid glycoside derivatives have remarkable biological activity and show better development potential.

The EBI2 receptor is coexpressed with CCR5 in CD4 + T cells and boosts HIV-1 R5 replication.

CCR5, a G protein-coupled receptor (GPCR), is used by most HIV strains as a coreceptor. In this study, we looked for other GPCR able to modify HIV-1 infection. We analyzed the effects of one GPCR coexpressed with CCR5, EBI2, on HIV-1 replicative cycle. We identified GPCR expressed in primary CD4 + CCR5 + T cells by multi-RT-qPCR. We studied GPCR dimerization by FRET technology. Cell lines expressing EBI2 were established by transduction with HIV vectors. HIV-1 entry was quantified with virions harboring β-lactamase fused to the viral protein vpr, early and late HIV-1 transcriptions by qPCR, NFkB nuclear activation by immunofluorescence and transfection, and viral production by measuring p24 concentration in culture supernatant by ELISA. We showed that EBI2 is naturally expressed in primary CD4 + CCR5 + T cells, and that CCR5 and EBI2 heterodimerize. We observed that this coexpression reduced viral entry by 50%. The amount of HIV reverse transcripts was similar in cells expressing or not EBI2. Finally, the presence of EBI2 induced the translocation of NFkB and activated HIV-1 genome expression. Globally, the result was a drastic HIV-1 R5, but not X4, overproduction in EBI2 -transduced cells. EBI2 expression in CD4 + CCR5 + cells boosts HIV-1 R5 productive infection. As the natural ligand for EBI2 is present in blood and lymphoid tissues, the constant EBI2 activation might increase HIV replication in CD4 + T cells. It might be of interest to test the effect of EBI2 antagonists on the residual viral production persisting in patients aviremic under treatment.

Optimization of Biodiesel Production Process Using MoO3 Catalysts and Residual Oil: A Comprehensive Experimental 23 Study.

The study aimed to utilize MoO3 catalysts, produced on a pilot scale via combustion reaction, to produce biodiesel from residual oil. Optimization of the process was conducted using a 23 experimental design. Structural characterization of the catalysts was performed through X-ray diffraction, fluorescence, Raman spectroscopy, and particle size distribution analyses. At the same time, thermal properties were examined via thermogravimetry and differential thermal analysis. Catalytic performance was assessed following process optimization. α-MoO3 exhibited a monophasic structure with orthorhombic phase, whereas α/h-MoO3 showed a biphasic structure. α-MoO3 had a larger crystallite size and higher crystallinity, with thermal stability observed up to certain temperatures. X-ray fluorescence confirmed molybdenum oxide predominance in the catalysts, with traces of iron oxide. Particle size distribution analyses revealed polymodal distributions attributed to structural differences. Both catalysts demonstrated activity under all conditions tested, with ester conversions ranging from 93% to 99%. The single-phase catalyst had a long life cycle and was reusable for six biodiesel production cycles. The experimental design proved to be predictive and significant, with the type of catalyst being the most influential variable. Optimal conditions included α-MoO3 catalyst, oil/alcohol ratio of 1/15, and a reaction time of 60 min, resulting in high biodiesel conversion rates and showcasing the viability of MoO3 catalysts in residual oil biodiesel production.

The Relationship of Hot Work Climate on Physiological Response in Traditional Clover Leaf Oil Refining Workers

In the clove leaf oil refining process which uses steam, it produces a hot temperature residue which affects clove leaf oil refinery workers. Exposure to a hot working climate can have an impact on human physiological responses such as an increase in body temperature, pulse rate, blood pressure and weight loss. as a result of producing quite a lot of sweat fluid. This research aims to investigate the physiological responses of clove leaf oil refinery workers to exposure to a hot working climate. In the clove leaf oil refining process, which utilizes steam, the production of hot temperature residue affects the workers. Exposure to such conditions can lead to various physiological responses, including increased body temperature, pulse rate, blood pressure, and weight loss due to significant sweating. Employing a quantitative research design with a cross-sectional analytical approach, data were collected from all 22 workers using a total sampling technique. The primary data collected were subjected to analysis using paired simple t-tests and the Pearson correlation test to explore relationships between variables. The findings reveal significant increases in physiological responses post-work, including elevated body temperature, pulse rate, systolic and diastolic blood pressure, and a reduction in body weight. The obtained p-values for all variables were <0.05, indicating statistically significant differences between pre-work and post-work conditions. Furthermore, the Pearson correlation test analysis between heat stress data and post-work physiological responses, including body temperature, pulse rate, systolic and diastolic blood pressure, as well as body weight, revealed moderate to strong correlations (r). These results underscore the detrimental impact of hot working climates on the physiological well-being of clove leaf oil refinery workers. Such findings highlight the urgent need for implementing appropriate measures to mitigate heat-related health risks in occupational settings, safeguarding the health and safety of workers.

Charge-solvated versus protonated salt forms of cyclodepsipeptide toxins in electrospray: Dissociation of alkali-cationized forms enables straightforward sequencing of cereulide.

Bacillus cereus is responsible for foodborne outbreaks worldwide. Among the produced toxins, cereulide induces nausea and vomiting after 30 min to 6h following the consumption of contaminated foods. Cereulide, a cyclodepsipeptide, is an ionophore selective to K+ in solution. In electrospray, the selectivity is reduced as [M + Li]+; [M + Na]+ and [M + NH4]+ can also be detected without adding corresponding salts. Two forms are possible for alkali-cationized ions: charge-solvated (CS) that exclusively dissociates by releasing a bare alkali ion and protonated salt (PS), yielding alkali product ions by covalent bond cleavages (CBC) promoted by mobile proton. Based on a modified peptide cleavage nomenclature, the PS product ion series (b, a, [b + H2O] and [b + CnH2nO] [n = 4, 5]) are produced by Na+/Li+/K+-cationized cereulide species that specifically open at ester linkages followed by proton mobilization promoting competitive ester CBC as evidenced under resonant collision activation. What is more, unlike the sodiated or lithiated cereulide, which regenerates little or no alkali cation, the potassiated forms lead to an abundant K+ regeneration. This occurs by splitting of (i) the potassiated CS forms with an appearance threshold close to that of the PS first fragment ion generation and (ii) eight to four potassiated residue product ions from the PS forms. Since from Na+/Li+-cationized cereulide, (i) the negligible Na+/Li+ regeneration results in a higher sensibility than that of potassiated forms that abundantly releasing K+, and (ii) a better sequence recovering, the use of Na+ (or Li+) should be more pertinent to sequence isocereulides and other cyclodepsipeptides.

Cryoradiolysis of oxygenated cytochrome P450 17A1 with lyase substrates generates expected products

When subjected to γ-irradiation at cryogenic temperatures the oxygenated complexes of Cytochrome P450 CYP17A1 (CYP17A1) bound with either of the lyase substrates, 17α-Hydroxypregnenolone (17-OH PREG) or 17α-Hydroxyprogesterone (17-OH PROG) are shown to generate the corresponding lyase products, dehydroepiandrosterone (DHEA) and androstenedione (AD) respectively. The current study uses gas chromatography–mass spectrometry (GC/MS) to document the presence of the initial substrates and products in extracts of the processed samples. A rapid and efficient method for the simultaneous determination of residual substrate and products by GC/MS is described without derivatization of the products. It is also shown that no lyase products were detected for similarly treated control samples containing no nanodisc associated CYP17 enzyme, demonstrating that the product is formed during the enzymatic reaction and not by GC/MS conditions, nor the conditions produced by the cryoradiolysis process.

Regolith mapping using airborne gamma-ray spectrometry in central Brazil

In deeply weathered terrains, with high geological diversity and scarce outcrops, the lateritic regolith features support mineral research. Predictive regolith mapping uses spatial modeling and airborne gamma-ray spectrometric data to locate weathered residual products, such as the ferruginous lateritic duricrusts found in tropical regions. Although the regolith materials exhibit qualitative similarities in their gamma-ray spectrometric responses in RGB (KThU) images, the Boolean and fuzzy approaches highlighted differences that allows for mapping the regolith weathering residual products on a wide geodiversity protoliths. Two inference systems were used, one identified the ferruginous lateritic duricrusts and oxisols derived from the felsic/pelitc and mafic rocks types (TP test procedures), and the other identified solely those derived exclusively from mafic rocks (TPM test procedures). Cutoff values for the conjunction eTh/K ∩ eU/K ∩ eTh ∩ K (TP-4) using Boolean logic, provided the most accurate regolith map (accuracy = 95%) among the various tests carried out and indicate that in 28.6% of the total study area, there are lateritic duricrust and oxisols relative to rocks, saprolites, mottled horizons and other soils type. The eTh cutoff value > 4.4 ppm was used to exclude mafic rocks and associated soils, and the K value < 1.3% to exclude rocks with eTh/K and eU/K values similar to the lateritic duricrusts and oxisols. For mapping the lateritic duricrusts derived exclusively from the mafic rocks the conjunction of eTh ∩ eU/K ∩ eTh/K ∩ K ∩ eU (TPM-3) fuzzified by the large membership function was the most efficient. The eU variable with values < 1.21 ppm helps improve the effectiveness of this procedure. The generated predictive map indicated that in about ∼12% (657.9 km2) of the total study area, there are lateritic duricrusts and oxisols derived from mafic rocks. Therefore, a successful method of mapping vast areas from complicated lateritic regolith mosaic derived from a large geodiversity is to apply specific plugins for data fuzzification, supported by observations from field outcrops.

Production of greenhouse gases by logging residue in boreal clear-cut forests

AbstractForest deadwood is an important carbon reserve, estimated to contain 8% of the total forest carbon. This type of woody debris is recognized as a source of carbon dioxide (CO2), as the carbon is released back into the atmosphere by microbial decomposition. Production of methane (CH4) and nitrous oxide (N2O) has also been reported. In managed forests, logging residues form a major source of fine deadwood, but its role in the greenhouse gas exchange of forest ecosystems is poorly understood. We studied the greenhouse gas production of spruce and birch left-over fine woody debris and estimated the residence time of these residues at 18 spruce-dominated boreal forest sites in Central Finland. The study areas consisted of clear-cut forest stands, totally covering approximately 47 hectares, with logging residue ages varying between 0 and 10 years. The research was carried out over eight months from May to December 2019. We observed that CO2 dominated the greenhouse gas production of the logging residues, with the production being regulated by air temperature, tree species, residue age, and wood moisture. Emission of CO2 continued throughout the research period with a clear seasonal pattern. Production of CH4 and N2O was also observed, but not in climatically-relevant amounts. Deadwood half-life was estimated at 18 years for spruce and 9 years for birch. Our study demonstrates that logging residues form a mid-term carbon reserve and suggests that global warming could reduce the lifetime of the residues as a result of elevated and temperature-dependent CO2 release in the studied Myrtillus type forest stands.

Clinical and molecular significance of flow cytometric analysis for reactive oxygen species production and residual p67phox expression in p67phox-deficient chronic granulomatous disease.

Chronic granulomatous disease (CGD) is a primary immunodeficiency disease caused by molecular defects in nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. p67phox-CGD is an autosomal recessive CGD, which is caused by a defect in the cytosolic components of NADPH oxidase, p67phox, encoded by NCF2. We previously established a flow cytometric analysis for p67phox expression, which allows accurate assessment of residual protein expression in p67phox-CGD. We evaluated the correlation between oxidase function and p67phox expression, and assessed the relevancy to genotypes and clinical phenotypes in 11 patients with p67phox-CGD. Reactive oxygen species (ROS) production by granulocytes was evaluated using dihydrorhodamine-1,2,3 (DHR) assays. p67phox expression was evaluated in the monocyte population. DHR activity and p67phox expression were significantly correlated (r = 0.718, p < 0.0162). Additionally, DHR activity and p67phox expression were significantly higher in patients carrying one missense variant in combination with one nonsense or frameshift variant in the NCF2 gene than in patients with only null variants. The available clinical parameters of our patients (i.e., age at disease onset, number of infectious episodes, and each infection complication) were not linked with DHR activity or p67phox expression levels. In summary, our flow cytometric analysis revealed a significant correlation between residual ROS production and p67phox expression. More deleterious NCF2 genotypes were associated with lower levels of DHR activity and p67phox expression. DHR assays and protein expression analysis by using flow cytometry may be relevant strategies for predicting the genotypes of p67phox-CGD.

Contribution of arbuscular mycorrhizal fungi to the bioavailability of micronutrients (iron and zinc) in millet accessions.

Micronutrient deficiencies, particularly iron (Fe) and zinc (Zn) deficiencies, are prevalent public health issues in developing countries, with children under 5 years old and breastfeeding women being the most affected in Senegal. Agronomic approaches, including soil fertilization and microbial biotechnology, are used to alleviate these deficiencies, yet challenges persist due to poor nutrient availability in staple food crops like pearl millet (Pennisetum glaucum L.). This study aimed to assess the contribution of one arbuscular mycorrhizal fungal (AMF) strain, Glomus mosseae, to the bioavailability of micronutrients (zinc and iron) in pearl millet biomass. Four pearl millet accessions from the National Laboratory for Research on Plant Production (LNRPV) collection were inoculated with G. mosseae obtained from the Common Microbiology Laboratory (LCM), with four replications. Gaussian regression tests were employed to analyze the data and determine correlations between AMF concentration and micronutrient bioavailability. The results indicate that the combination of Glomus mosseae inoculation and organic residual products improved growth parameters and micronutrient absorption in pearl millet accessions. Analysis revealed significantly greater iron, zinc, phosphorus, and potassium contents in the foliar biomass of mycorrhizal pearl millet plants compared to non-mycorrhizal plants (control). Inoculation with AMF facilitated micronutrient absorption, particularly iron and zinc, not only in roots but also in aerial parts of the plants. These findings suggest that incorporating AMF and organic residual products in millet cultivation could be a viable strategy for enhancing plant development and increasing iron and zinc contents in varieties. Further research is needed to elucidate the mechanisms underlying AMF-mediated nutrient uptake and optimize their use in agricultural practices.

Arone-containing cyclomatrix-type polyphosphazene hybrid microspheres for epoxy resin: Enhancing fire safety and mechanical properties

Arone-containing cyclomatrix-type polyphosphazene hybrid microspheres (PZK) were synthesized to enhance both the fire safety and mechanical performance of epoxy resin (EP). The chemical structure and micro-morphology of PZK were characterized using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy, and X-ray photoelectron spectroscopy. Subsequently, PZK was employed in fabricating EP thermosets. Thermal properties of the PZK modified EP thermosets were comprehensively assessed through thermalgravimetric analysis (TGA) and dynamic mechanical analysis. The results indicate that PZK endowed EP with enhanced char yield and storage modulus, attributed to its exceptional thermal stability and distinctive microsphere structure. Additionally, with only a 1.5% loading of PZK, EP achieved a UL-94 V-1 rating during vertical flame testing, accompanied by an increased limiting oxygen index of 28.3%. Additional analysis with a cone calorimeter demonstrated that the addition of PZK markedly reduced the peak heat release rate, total heat release, fire growth rate, and total smoke production of EP, indicating notable efficacy in suppressing heat and smoke release. Char residue and pyrolysis products were analyzed using SEM, TG-FTIR, and pyrolysis gas chromatography-mass spectrometry, revealing that PZK effectively inhibits the release of combustible gases from EP during thermal decomposition. The expected generation of Ph—O• radicals from arone units in PZK suggested a gaseous free radical trapping mechanism. The phosphazene framework played a crucial role in forming condensed-phase char due to its exceptional thermal stability. Consequently, PZK exhibited a typical biphasic flame-retardant mechanism for EP. Notably, the study observed that the introduction of PZK simultaneously enhances the tensile strength, flexural strength, and modulus of EP, with a particularly significant improvement observed in impact strength. This research expands the scope of investigation into the preparation and flame-retardant application of cyclomatrix-type polyphosphazene hybrid microspheres in polymers.

Effects of statins beyond lipid-lowering agents in ART-treated HIV infection.

Antiretroviral therapies (ART) have reduced human immunodeficiency virus (HIV) infection-associated morbidity and mortality improving the life of people with HIV (PWH). However, ART lead to residual HIV production, which in conjunction with microbial translocation and immune dysfunction contributes to chronic inflammation and immune activation. PWH on ART remain at an increased risk for cardiovascular diseases (CVDs) including myocardial infarction and stroke; which in part is explained by chronic inflammation and immune activation. Lifestyle factors and certain ART are associated with dyslipidemia characterized by an increase of low-density lipoprotein (LDL), which further contributes in the increased risk for CVDs. Lipid-lowering agents like statins are emerging as immune modulators in decreasing inflammation in a variety of conditions including HIV. The international randomized clinical trial REPRIEVE has shed light on the reduction of CVDs with statin therapy among PWH. Such reports indicate a more than expected benefit of statins beyond their lipid-lowering effects. Bempedoic acid, a first-in-class non-statin LDL-lowering drug with immune modulatory effects, may further aid PWH in combination with statins. Herein, we critically reviewed studies aimed at lipid-lowering and immune-modulating roles of statins that may benefit aging PWH.

Enhancement of spent coffee grounds as biofiller in biodegradable polymer composite for sustainable packaging

AbstractThis study explores the utilization of Spent Coffee Grounds (SCG), a residual product of the coffee industry, as a microfiller reinforcement in Poly‐3‐hydroxybutyrate‐co‐3‐hydroxyvalerate (PHBV) biopolymer composites at varying concentrations (1%, 3%, 5%, and 7%). Melt compounding via a twin‐screw extruder and subsequent compression molding were employed in the fabrication process. The SCG microfiller, with particle diameters ranging from 1.11 to 1.28 μm, exhibited a significant negative charge (zeta potential: −20 mV). Hydrophobicity increased up to 5% filler concentration, as indicated by higher water contact angles, but diminished at highest concentration likelihood of agglomeration of the spent coffee grounds within the biopolymer matrix. The addition of SCG enhanced overall mechanical properties, particularly at a 5% filler concentration. Field Emission Scanning Electron Microscopy (FE‐SEM) and Atomic Force Microscopy (AFM) confirmed the successful incorporation of SCG microfiller, improving structural characteristics. Schematic drawings illustrated the interphase bonding of microfiller and matrix. However, properties diminished at the highest filler content (7%) due to coffee grounds' agglomeration. Despite this, SCG incorporation enhanced functional properties, making the biopolymer composite a promising material for sustainable packaging and various applications.Highlights Enhancement of properties of spent coffee grounds in PHBV biocomposites. Characterization of Biocomposites for multifunctional properties. Fracture and 2D analysis of the tensile fractured surface of biocomposites. A promising material for sustainable and biodegradable packaging.

Study of Employee Satisfaction After Improving the Product Storage System in the Warehouse of Kerry Express Co., Ltd., Rama 7 Branch

Background and Aims: Currently, the spread of the COVID-19 virus, as a result, the e-commerce business has grown significantly. As a result, the volume of parcels that need to be delivered in the logistics system has greatly increased. When the number of products exceeds the warehouse and increases every day, the delivery of products is delayed. and not following the period It directly affects the business, causing customers to lose confidence in using the service next time. The objectives of this research were 1) to improve the storage system and increase the efficiency of picking. Dispense goods within the warehouse, 2) gain knowledge in organizing the warehouse system. Methodology: The research is quantitative. The Population is 130 employees of Kerry Express Co., Ltd., Rama 7 branch, in the parcel warehouse and delivering parcels to customers. The researcher uses a questionnaire as a data collection tool. The statistics used to analyze the data were descriptive statistics consisting of percentage, frequency, mean, and standard deviation and inferential statistics including Independent Sample t-test, One Way ANOVA, and multiple regression analysis. Results: The results found that; 1) Improving the storage system using the FIFO (First in First Out) theory can make the work more efficient based on questionnaire responses. The overall satisfaction in using the FIFO (First in First Out) theory was at the highest level. Considering this individually, it was found that the application of the FIFO system enabled your organization to solve the problem of delayed delivery with the highest average.2) Improving the working system using the FIFO (First in First Out) theory, allowing the work to work efficiently whether it is easier to work, work faster reduces work problems, and no residual product. As a result, the efficiency of goods issued within the warehouse is more efficient. Conclusion: By using the FIFO (First in First Out) theory, that is, the goods that come in first will be exported first. Therefore, the problem of residual products in the warehouse is reduced. and can work faster.

Investigation of an indigenous chalcopyrite ore leaching in ammonia solution: characterization, leaching and kinetics

ABSTRACT Chalcopyrite ore is one of the most abundant and pertinent oxidized copper minerals. In this research, the dissolution kinetics of chalcopyrite in an ammonia solution was examined. During leaching, the influences of leachant concentration, temperature, and particle diameter on the extent of copper ore dissolution were investigated. However, it was affirmed that the dissolution efficiency of chalcopyrite ore increased with decreasing particle fraction and increasing reaction temperature and ammonia concentration. About 68.6% copper ore dissolution was achieved with 2.0 mol/L NH3, 75 ºC reaction temperature, and 45 μm particle diameter within 120 minutes. The dissolution reaction mechanism was found to be described by diffusion-control with a calculated activation energy of 32.26 kJ/mol. In the XRD spectra of the residual product obtained at established conditions, CuFeS2 peaks were absent, indicating the leachability of the sample. Hence, the leach residue could serve as an important by-product for some local industries.