Molar Ratio Research Articles

Effect of magnetron sputtering power on the properties of the AlO X monolayer and AlO X /MgF2 bilayer anti-reflection films

The AlO X monolayer anti-reflection (MLAR) films and the AlO X /MgF2 bilayer anti-reflection (BLAR) films were deposited on high-purity glasses with magnetron sputtering. We investigated the influences of sputtering power on the O/Al molar ratio, microstructure, and optical properties of the AlO X MLAR films and AlO X /MgF2 BLAR films. The results showed that a too high or a too low sputtering power was detrimental to the preparation of the high-quality films, which could only be obtained when the sputtering power was 115 W. However, the sputtering power did not affect the crystallinity of the films, all of which were amorphous. When the sputtering power was 115 W, the high-purity AlO X MLAR film exhibited an O/Al molar ratio of 2.27:1, a refractive index of 1.426, and an average transmittance (T avg: average transmittance of the quartz glass deposited the film, hereinafter the same) of 94.03% within 300–1100 nm wavelength range. The T avg of AlO X /MgF2 BLAR film with a power of 115 W was 94.99%, which was 1.92% higher than that of the glass substrate. And it improved the cell’s photoelectric conversion efficiency (PCE) by 3.19%.

PET Imaging of Differentiated Thyroid Cancer with TSHR-Targeted [89Zr]Zr-TR1402.

Thyroid cancer is the most common endocrine cancer, with differentiated thyroid cancers (DTCs) accounting for 95% of diagnoses. While most DTC patients are diagnosed and treated with radioiodine (RAI), up to 20% of DTC patients become RAI refractory (RAI-R). RAI-R patients have significantly reduced survival rates compared to patients who remain RAI-avid. This study explores [89Zr]Zr-TR1402 as a thyroid-stimulating hormone receptor (TSHR)-targeted PET radiopharmaceutical for DTC. [89Zr]Zr-TR1402 was synthesized with a molar activity of 25.9 MBq/nmol by conjugating recombinant human TSH (rhTSH) analogue TR1402 to chelator p-SCN-Bn-deferoxamine (DFO) in a molar ratio of 3:1 (DFO/TR1402) and radiolabeling with 89Zr (t1/2 = 78.4 h, β+ = 22.7%). As TSHR is absent in commonly available DTC-derived cell lines, TSHR was reintroduced via stable transduction by delivering a lentivirus containing the full-length coding region of the human TSHR gene. Receptor-mediated uptake of [89Zr]Zr-TR1402 was evaluated in vitro in stably transduced TSHR+ and wild-type TSHR- DTC cell lines. In vivo PET imaging was performed on Days 1-3 postinjection in male and female athymic nude mice bearing TSHR+ and TSHR- xenografts, along with ex vivo biodistribution on Day 3 postinjection. In vitro uptake of 1 nM [89Zr]Zr-TR1402 was significantly higher in TSHR+ THJ529T (P < 0.0001) and FTC133 (P < 0.01) cells than in TSHR- THJ529T and FTC133 cells. This uptake was shown to be specific in both TSHR+ THJ529T (P < 0.0001) and TSHR+ FTC133 (P < 0.0001) cells by blocking uptake with 250 nm DFO-TR1402. In vivo PET imaging showed accumulation of [89Zr]Zr-TR1402 in TSHR+ tumors, which was the highest on Day 1. In the male FTC133 xenograft model, ex vivo biodistribution confirmed a significant difference (P < 0.001) in uptake between FTC133+ (1.3 ± 0.1%ID/g) and FTC133- (0.8 ± 0.1%ID/g) tumors. A significant difference (P < 0.05) in uptake was also seen in the male THJ529T xenograft model between THJ529T+ (1.8 ± 0.6%ID/g) and THJ529T- (0.8 ± 0.4%ID/g) tumors. The in vitro and in vivo accumulation of [89Zr]Zr-TR1402 in TSHR-expressing DTC cell lines support the continued preclinical optimization of this approach.

Copper sulfide precipitation from alkaline monosodium glutamate solutions

Recent studies of metal leaching using monosodium glutamate have shown promising results of this being an alternative to conventional leaching reagents. However, limited information is available covering the treatment of leaching solutions and the final recovery of metals. In this regard, this article presents an experimental study on the precipitation of copper from glutamate solutions using sodium hydrosulfide (NaHS), as a simple and efficient route for the processing of leaching solutions from this new system. Synthetic pregnant leach solutions (PLS) with varying copper total concentrations [CuT] and glutamate concentrations were used. The effects of [CuT], [CuT]:[NaHS] molar ratio and glutamate concentration on the particle size distribution and copper recovery were investigated. The results revealed that higher [CuT] led to smaller particle sizes, with the P90 decreasing from 106 µm to 60.7 µm and 73.2 µm for Cu concentrations of 1 g/L, 2.5 g/L, and 5 g/L, respectively. The [CuT]:[NaHS] molar ratio reduced the P90 particle size, from 60.7 µm to 56.4 µm and 7.44 µm as the molar ratio increased from 1:0.8 to 1:1 and 1:1.2, respectively. Copper recovery from glutamate solutions increased with higher molar ratios, achieving values of 70.95 %, 88.24 %, and 99.55 % for molar ratios of 1:0.8, 1:1, and 1:1.2, respectively, agreeing with copper recovery values of other chemical systems. The glutamate concentration had minimal impact on particle size but affected copper recovery, with a decrease from 88.24 % to 85.83 % when increasing the glutamate concentration from 0.5 M to 1 M. X-ray diffraction (XRD) analysis confirmed the presence of pure covellite with hexagonal phase in the precipitates. These findings contribute to understanding copper precipitation dynamics from glutamate solutions using NaHS and have implications for optimizing copper recovery processes in the perspectives of the advent of alkaline leaching of copper ores.

Layered carbon encapsulated CuOx nanopaticles for selective hydrogenation of furfural to furfuryl alcohol

Furfuryl alcohol (FOL) is commercially available by selective hydrogenation of furfural (FAL). A variety of catalysts have been developed for such purpose, among which Cu-based catalysts show superior catalytic performance. However, copper nanoparticles with complex valence states are easy to agglomerate during hydrogenation reaction, which might have a negative influence on the catalytic performance. The carbon coating is an efficient strategy to prevent the sintering of Cu-based catalysts. Herein, a strategy based on the thermal decomposition of Cu-EDTA complex was designed to prepare carbon encapsulated Cu-based catalysts. The prepared catalysts were applied in the selective hydrogenation of FAL to FOL in the batch reactor. The results showed that a nearly quantitative conversion of FAL with a selectivity of 98.7 % towards FOL was achieved using CuOx@NC-150 (molar ratio of Cu: Na4EDTA·4H2O=2:1; obtained by oxidative activation at 150 °C) under 140 °C, 3 MPa in 4 h. The performance was comparable to that of the commercial CuCr2O4 catalyst under the identical conditions. In addition, the developed carbon encapsulated Cu-based catalysts exhibited a slightly better stability than CuCr2O4 catalyst in terms of FOL yield in five consecutive cycles. XPS and XAES characterizations implied that the presence of a suitable surface ratio of Cu+/(Cu++Cu0) of the prepared catalyst may contribute to the selective hydrogenation of FAL to FOL.

Sb-loaded MnOx/TiO2/CNTs catalysts for selective catalytic reduction of NOx: insight to the SO2 and H2O tolerance

Purpose This paper aims to synthesize and test Mn-Sb/TiO2-CNT catalysts with different Sb/Mn molar ratios to be used in NH3-SCR reaction. Design/methodology/approach A series of Sb-loaded carbon nanotubes (CNTs)-based Mn/TiO2 catalysts were prepared by the incipient wetness co-impregnation method and tested for the selective catalytic reduction (SCR) of NOx with NH3. Findings The Sb-loaded Mn/TiO2-CNTs catalyst outperformed other catalysts and presented the highest activity in the temperature regime of 100–400°C. The catalyst loaded with Sb also showed good SO2 and H2O resistance and exhibited better thermal stability. A stepwise study of SO2 addition evidenced that Mn-Sb/TiO2-CNTs catalyst exhibited better SO2 resistance than the base catalyst Mn/TiO2, where the Sb doping greatly inhibited the sulphating of active phase of the catalyst. Originality/value In Sb-loaded catalysts, the formed SOx species fused with SbOx instead of MnOx. This favoured interaction of SO2 with SbOx successfully prevents the MnOx from being sulphated by SO2 which substantially improves the SO2 tolerance of Sb-loaded catalysts.

Structural characterization of extracellular polysaccharides from Phellinus igniarius SH-1 and their therapeutic effects on DSS induced colitis in mice

Phellinus igniarius is a valuable medicinal and edible mushroom, and its polysaccharides exhibit excellent anti-inflammatory activity. During liquid fermentation to produce P. igniarius mycelia, the fermentation liquid is often discarded, but it contains extracellular polysaccharides. To better utilize these resources, P. igniarius SH-1 was fermented in a 100 L fermenter, and PIPS-2 was isolated and purified from the fermentation broth. The structural characteristics and anti-inflammatory activity of PIPS-2 were determined. PIPS-2 had a molecular weight of 22.855 kDa and was composed of galactose and mannose in a molar ratio of 0.38:0.62. Structural analysis revealed that the main chain of PIPS-2 involved →2)-α-D-Manp-(1 → 3)-β-D-Galf-(1→, and the side chains involved α-D-Manp-(1 → 6)-α-D-Manp-(1→, α-D-Manp-(1 → 3)-α-D-Manp-(1→, and α-D-Manp-(1. PIPS-2 alleviated the symptoms of dextran sodium sulfate (DSS)-induced colitis in mice, improved the imbalance of inflammatory factors and antioxidant enzymes, and increased short-chain fatty acid contents. Combining the intestinal flora and metabolite results, PIPS-2 was found to regulate the abundance of Firmicutes, Lachnospiraceae_NK4A136_group, Proteobacteria, Bacteroides, and many serum metabolites including hexadecenal, copalic acid, 8-hydroxyeicosatetraenoic acid, artepillin C, and uric acid, thereby ameliorating metabolite related disorders in mice with colitis. In summary, PIPS-2 may improve colitis in mice by regulating the gut microbiota and metabolites.

Chemical insights into plasma-assisted dry reforming of methane in a nanosecond discharge

The present study explores the chemical kinetics of plasma-assisted dry reforming of methane (340 K, 30 Torr) in a flow reactor activated by a nanosecond pulsed dielectric barrier discharge (DBD). Experiments are conducted with the inlet CO2/CH4 mol ratios varying from 0.4 to 2.8 in CH4/CO2/Ar mixture. Synchrotron vacuum ultraviolet photoionization mass spectrometry (SVUV-PIMS) is employed for detailed species measurement of the ions, radicals, and molecules in this system. Eight ions are observed, including CH3+, O+, CH4+, Ar2+, CO+, C2H4+, Ar+, and CO2+. The identification of several intermediate species and products are achieved based on the photoionization efficiency (PIE) spectra, such as methyl radical (CH3), water (H2O), acetylene (C2H2), carbon monoxide (CO), ethylene (C2H4), formaldehyde (CH2O), methanol (CH3OH), ketene (CH2CO), and acetone (CH3COCH3). Species mole fraction profiles as a function of inlet CO2 concentrations are obtained. The present work provides a unique dataset and enriches our understanding of the kinetics of plasma-assisted dry reforming of methane. A kinetic mechanism incorporating plasma reactions and combustion reactions is developed for this system, and its prediction performance of the product selectivity is validated against the experimental data. The main reaction pathways for the consumption of CH4 and CO2 and the formation of products and intermediates are indicated based on the rate of production (ROP) analysis. The ionic reactions are predominant for CH4 consumption, leading to CH4+ and CH5+, while CH4 reactions with electrons and Ar* contribute to CH2 and CH3 formation. CO2 mainly reacts with electrons and Ar*, producing CO, and can also undergo reactions with CH4+ and CH5+, forming HCO2+. The principal formation pathways for H2, CO, CH2O, and CH3OH are discussed. A competition between the discharge pathways and oxygen-containing pathways in CH4/CO2/Ar plasma is proposed.

Strong and tough semi-crystalline poly(aryl ether nitrile) with low coefficient of thermal expansion

The crystallization of poly(aryl ether nitrile) (PEN) has an essential impact on improving heat resistance, mechanical properties, chemical resistance, and dielectric properties. However, during the synthesis process, high crystallinity PEN is prone to precipitate out, which makes it difficult to carry out the synthesis reaction, which poses a significant challenge to synthesizing high crystallinity and high molecular weight PEN. In this work, hydroquinone (HQ) as the main phenolic monomer and 4,4’-biphenol (BP) as the second phenolic monomer were used to solve the technical difficulties in synthesis by copolymerization. The crystalline PEN with high molecular weight and significant crystallinity was obtained by regulating the molar ratio of BP to HQ. The effects of isothermal heat treatment on its crystalline, mechanical, and thermal properties were investigated. The influence laws of molecular chain structure and heat treatment process on the properties of PEN films were revealed. Among them, when the isothermal treatment temperature was 270 °C and the HQ: BP was 85:15, the mechanical strength reached 130 MPa, and the elongation at break could be up to an astonishing 50%. Besides, the CTE value from 50 °C ∼ 150 °C is 40.84 ppm/ °C, which is lower than most thermoplastics. Therefore, PEN with the HQ to BP molar ratio of 85:15 is suitable for large-scale production, providing new crystalline plastic specifications for high-performance special engineering plastics. A crystal bridge-tie chain model is summarized by the properties of HQ/BP-PEN films under different crystallization conditions, which provides an idea for preparing stiff and tough films.

Phosphorus recovery via struvite crystallization in batch and fluidized-bed reactors: Roles of microplastics and dissolved organic matter

Struvite crystallization, a promising technology for nutrient recovery from wastewater, is facing considerable challenges due to the presence of emerging contaminants such as microplastics (MPs) ubiquitously found in wastewater. Here, we investigate the roles of MPs and humic acid (HA) in struvite crystallization in batch and fluidized-bed reactors (FBRs) using synthetic and real wastewater with a Mg:N:P molar ratio of 1:3:(1–1.3) at an initial pH of 11. Batch reactor (BR) experiment results show that MPs expedited the nucleation and growth rates of struvite (e.g., the rate of crystal growth in the presence of 30 mg L−1 of polyethylene terephthalate (PET) was 1.43 times higher than that in the blank system), while HA hindered the formation of struvite. X-ray diffraction and the Rietveld refinement analysis revealed that the presence of MPs and HA can result in significant changes in phase compositions of the reclaimed precipitates, with over 80 % purity of struvite found in the precipitates from suspensions in the presence of 30 mg L−1 of MPs. Further characterizations demonstrated that MPs act as seeds of struvite nucleation, spurring the formation of well-defined struvite, while HA favors the formation of newberyite rather than struvite in both reactors. These findings highlight the need for a more comprehensive understanding of the interactions between emerging contaminants and struvite crystallization processes to optimize nutrient recovery strategies for mitigating their adverse impact on the quality and yield of struvite-based fertilizers. Environmental ImplicationThe presence of microplastics in wastewater poses a significant challenge to struvite crystallization for nutrient recovery, as it accelerates nucleation and growth rates of struvite crystals. This can lead to changes in the phase compositions of the reclaimed precipitates, with implications for the quality and yield of struvite-based fertilizers. Additionally, the presence of humic acid hinders the formation of struvite, favoring the formation of other minerals like newberyite. Understanding the interactions between emerging contaminants and struvite crystallization processes is crucial for optimizing nutrient recovery strategies and mitigating the environmental impact of these contaminants on water quality and struvite-based fertilizers.

Optimizing Biocompatibility and Gene Delivery with DMAEA and DMAEAm: A Niacin-Derived Copolymer Approach.

Gene therapy is pivotal in nanomedicine, offering a versatile approach to disease treatment. This study aims to achieve an optimal balance between biocompatibility and efficacy, which is a common challenge in the field. A copolymer library is synthesized, incorporating niacin-derived monomers 2-acrylamidoethyl nicotinate (AAEN) or 2-(acryloyloxy)ethyl nicotinate (AEN) with N,N-(dimethylamino)ethyl acrylamide (DMAEAm) or hydrolysis-labile N,N-(dimethylamino)ethyl acrylate (DMAEA). Evaluation of the polymers' cytotoxicity profiles reveals that an increase in AAEN or DMAEA molar ratios correlates with improved biocompatibility. Remarkably, an increase in AAEN in both DMAEA and DMAEAm copolymers demonstrated enhanced transfection efficiencies of plasmid DNA in HEK293T cells. Additionally, the top-performing polymers demonstrate promising gene expression in challenging-to-transfect cells (THP-1 and Jurkat cells) and show no significant effect on modulating immune response induction in ex vivo treated murine monocytes. Overall, the best performing candidates exhibit an optimal balance between biocompatibility and efficacy, showcasing potential advancements in gene therapy.

Trans-catena-Poly[[(bis-(µ-N,N′-bis[(pyridin-3-yl)methyl]ethanediamide))-diaqua-cadmium(II)] bis(nitrate) tetrahydrate)

The reaction between cadmium nitrate tetrahydrate and N,N′-bis(pyridin-3-ylmethyl)oxalamide (L) in a 1:3 molar ratio in a water/acetonitrile (1:6 v/v) mixture afforded single crystals of compound 1 suitable for X-ray diffraction analysis. Compound 1 consists of the coordination polymer (CP) [[Cd(L)2(OH2)2](NO3)2·4H2O]∞, in which CdII ions are bridged by neutral L antiperiplanar N-ligands in a wavy ribbon fashion developed along the c-axis. Two trans-disposed water molecules complete the pseudo-octahedral coordination geometry of the metal ion. The crystal packing of 1 revealed the interplay between π–π stacking interactions and an intricate hydrogen-bonded network involving oxalamides, nitrates, and water molecules. The donor properties of L and the intermolecular interactions in compound 1 are interpreted based on hybrid-DFT calculations.

Catalytic Dechlorination of Three Organochlorides by Recyclable Nano-Palladium-Engineered Natural Sponge with Formic Acid

Catalytic dechlorination of organic chlorides by palladium (Pd) with HCOOH represents one of the most effective and promising techniques for environmental remediation. In this study, we adopted alkaline-modified porous natural sponge as support of a Pd nanocatalyst (Pd@M-Sponge) and HCOOH as a hydrogen source for the hydrodechlorination of florfenicol (FF), o-chlorophenol (o-CP), and p-chlorophenol (p-CP). Favorable conversion efficiency of FF, o-CP, and p-CP was achieved at 25 °C and atmospheric pressure attributed to the small diameter and high catalytic reactivity of the prepared Pd NPs, in addition to the slight internal mass transfer limitation of the prepared Pd@M-Sponge. High reaction rate constants were obtained even in the conditions of a low molar ratio of HCOOH to p-CP (10:1) and a high concentration of p-CP (500 mg/L). The prepared catalyst also demonstrated superior recyclability without any obvious decrease in catalytic reactivity in 20 successive p-CP dechlorination cycles. This work provides an ideal recyclable and cost-effective catalyst based on renewable and biocompatible natural material for the catalytic hydrodechlorination of chlorinated organic pollutants with formic acid and a new view for the exploration and designing of highly reactive and stable catalysts for hydrodechlorination.

Investigating the Multi-Targeted Pharmacological profile of an Exopolysaccharide from Bacillus rugosus SYG20 via In Vitro Evaluation of its Antioxidant, Anti-inflammatory, Anti-diabetic, Wound Healing, and Antimicrobial Properties

IntroductionExopolysaccharides (EPSs) derived from marine microorganisms are a newly recognized reservoir of bioactive therapeutic compoundsMaterial and methodsWe isolated a high EPS-yielding bacterial strain from the Red Sea, identified as Bacillus rugosus SYG20. Its purified EPS (EPSR9) contains 45.33% uronic acid, 9.98% sulfate groups, and 5.40% N-acetyl glucosamine. The HPLC chromatogram revealed four monosaccharides - glucose, xylose, galacturonic acid, and arabinose, in a distinct molar ratio of 2:3:1:1. EPSR9 showed a wide array of bioactivities.ResultsIt displayed antioxidant activity with an IC50 of 25.6 μg/ml in the DPPH assay and a total antioxidant capacity (TAC) of 417.77μg/ml equivalent AAE and 62.67 μg/ml equivalent AAE in Ferric reducing antioxidant power (FRAP) assays. It exhibited substantial anti-inflammatory properties. The anticoagulant effect of the EPS was demonstrated by a dose-dependent increase in prothrombin time. The scratch assay resulted in a 72.66% increase in wound closure, promoting in vitro wound healing after 48 h. Anti-obesity activity was evidenced by 83.8% lipase inhibition at 1000 μg/ml with IC50 of 107.73μg/ml. EPSR9 demonstrated inhibitory effects on α-amylase with an IC50 value of 14.37μg/ml and α-glucosidase with an IC50 value of 26.73 μg/ml, highlighting its potential as an anti-diabetic agent. Then, EPS showed bactericidal properties with MBC/MIC≤2 against both G+ve and G-ve bacteria, Staphylococcus aureus , Enterococcus faecalis (MIC=3.9μg/ml), Salmonella typhi, and Helicobacter pylori.ConclusionsThe marine EPSR9 exhibited considerable potential for pharmaceutical applications as a multi-bioactive microbial metabolite. Its in vivo potency and mechanisms of action warrant further investigation.

Investigation of optimum conditions for the recovery of magnesium ammonium phosphate from human urine using the Box-Behnken design

ABSTRACT Urine from domestic wastewater greatly increases the nutritional value of wastewater. Urine has a high concentration of nutrients and minerals that can be utilized as plant growth agents, according to a chemical analysis. Due to its high phosphate, nitrogen, and potassium content, human urine can serve as a sustainable substitute for chemical fertilizers. Struvite, also referred to as MAP, can be considered as a sustainable fertilizer and it is a magnesium ammonium phosphate crystal with the chemical formula of MgNH4PO4·6H2O. Struvite may be formed from many types of wastewater, one inexpensive and reliable source for struvite formation being human urine. However, struvite formation requires an external magnesium supply due to the extremely low concentration of magnesium in human urine. In this work, magnesium ammonium phosphate was precipitated from human urine by examining the effects of Mg2+ dose, temperature, and pH on struvite crystals. Several experiments for struvite precipitation were created using the Box-Behnken design. Struvite crystals formed upon the addition of a magnesium source at 20 °C, pH 10, and a mole ratio of 1:1. The results show that the large-scale application and nutrient recovery of struvite crystals from human urine are promising.

Production of Biodiesel from Crude Pittosporum resiniferum Oil Using Heterogeneous Solid Base Catalyst

ABSTRACTPittosporum resiniferum oil was extracted from the seed and the oil together with methanol was use for the production of biodiesel through transesterification process using novel solid base catalyst (K2CO3 supported on MgO). 0.6:5 (K2CO3 loaded on MgO), a 5 h calcination time, 600°C calcination temperatures were the optimum conditions under which the catalyst was prepared. FTIR, SEM, CO2‐TPD, XRD, N2 adsorption‐desorption, Hammett indicators and other techniques were used to characterize the catalyst. The molar ratio of methanol‐to‐oil, the catalyst amount, time of the reaction as well as the temperature of the reaction were examined. The study found that 16:1 methanol‐to‐oil molar ratio, 5% catalyst loading amount, a reaction time of 2.0 h, and a reaction temperature of 60°C were sufficient for a maximum yield of 97.4%. With relative high activity, the catalyst can perhaps be used again possibly for five times. The characteristics of the biodiesel produced were consistent with international standards.

Enhancing Performance and Stability of p-i-n Perovskite Solar Cells with Ag-Cu Codeposited Alloy Electrodes.

In the development of back electrodes for perovskite solar cells (PSCs), the major challenges are stability and cost. To address this, we present an innovative approach: Simultaneous evaporation of two independently controlled sources of metal materials was performed to achieve a uniform distribution of the alloy electrodes. In this study, Ag-Cu alloys (the molar ratio of Ag/Cu is 7/3) with a high-index crystal face (111) and a work function matching perovskite were prepared using a codeposition technique. These properties mitigate nonradiative carrier recombination at the interface and reduce the energy barrier for carrier migration. Consequently, compared to Ag based PSCs (22.77%), the implementation of Ag-Cu alloy (Ag/Cu is 7/3)-based PSCs resulted in a power conversion efficiency of 23.72%. In a 1500 h tracking test in ambient air, the Ag-Cu alloy (Ag/Cu is 7/3)-based PSCs maintained their initial efficiency of 86%. This can be attributed to almost no migration of elements from the Ag-Cu alloy electrode to the perovskite layer. Our work presents a vital strategy for improving the stability of PSCs and reducing the costs associated with the back electrode in PSCs.

Proposed simplified methodological approach for designing geopolymer concrete mixtures

The development of geopolymer concrete offers promising prospects for sustainable construction practices due to its reduced environmental impact compared to conventional Portland cement concrete. However, the complexity involved in geopolymer concrete mix design often poses challenges for engineers and practitioners. In response, this study proposes a simplified approach for designing geopolymer concrete mixtures, drawing upon principles from Portland cement concrete mix design standards and recommended molar ratios of oxides involved in geopolymer synthesis. The proposed methodology aims to streamline the mix design process while optimizing key factors such as chemical composition, alkali activation solution, water content, and curing conditions to achieve desired compressive strength and workability. By leveraging commonalities between Portland cement concrete and geopolymer concrete, this approach seeks to facilitate the adoption of geopolymer concrete in practical construction applications. The proposed mix design guidelines have been validated through examples for concrete cured under different conditions, including outdoor and oven curing. Future research should focus on validating the proposed methodology through experimental studies and exploring cost-effective alternatives for alkali activation solutions to enhance the feasibility and scalability of geopolymer concrete production. Overall, the proposed simplified approach holds promise for advancing the utilization of geopolymer concrete as a sustainable alternative in the construction industry.

Structural elucidation a complex galactosyl andglucosyl-rich pectin from the pericarp of immature fruits of Juglans mandshurica Maxim.

A glucosyl-rich pectin, JMMP-3 (Mw, 2.572 × 104g/mol, O-methyl % = 3.62%), was isolated and purified from the pericarp of the immature fruit of Juglans mandshurica Maxim. (QingLongYi). The structure of JMMP-3 was studied systematically by infrared spectroscopy, monosaccharide compositions, methylation analysis, partial acid hydrolysis, and 1/2D-NMR. The backbone of JMMP-3 possessed a smooth region (→ 4GalA1 →) and a hairy region (→ 4GalA1 → 2Rha1 →) with a molar ratio of 2: 5. The substitution of four characteristic side chains (R1-R4) occurs at C-4 of → 2,4)-α-Rhap-(1→, where R1 is composed of → 5)-α-Araf-(1→, R2 is composed of → 4)-β-Galp-(1 → and β-Galp-(1→, R3 is composed of α-Glcp-(1→, →4)-α-Glcp-(1 → and → 4,6)-α-Glcp-(1→, and R4 is composed of → 5)-α-Araf-(1→, β-Galp-(1→, → 4)-β-Galp-(1→, → 3,4)-β-Galp-(1→, → 4,6)-β-Galp-(1 → and → 2,4)-β-Galp-(1 → . In addition, the antitumor activity of JMMP-3 on HepG2 cells was preliminarily investigated.

Improving the catalytic activity and thermal stability of Pt-supported catalyst via modulating Ce/Zr molar ratio

The synthesis of Pt-supported catalysts with high stability faces an enormous challenge, especially for applications in high-temperature environments. Here we attempt to improve the catalytic activity and thermal stability of Pt-supported catalyst via modulating Ce/Zr molar ratio. The crystalline structure, texture and metal dispersion of the Pt/CexZr1-x samples were studied by XRD, Raman, XPS, HRTEM and H2-TPR. The results indicate that decreasing Ce/Zr molar ratio can improve the thermal stability, the reducibility of surface lattice oxygen of the catalyst, and enhance the oxygen vacancy content. On the contrary, a higher Ce/Zr molar ratio facilitates the interaction between Pt and CeO2 and inhibits the growth of Pt particles thereby maintaining high Pt dispersion. The Pt/CexZr1-x catalysts with Ce/Zr molar ratio of ∼1.0 might exhibited the best overall catalytic performance within long-term use. Ce/Zr molar ratioThe effect of the valence state of Pt on catalytic activity is greater than that of the Pt dispersion. Our findings contribute to a depth understanding of Pt/CeZr catalysts and provide insights into the design of more efficient and durable catalysts for automotive exhaust purification.

The photoluminescence studies of Gd3+/Tb3+ co-doped xerogels and nano-glass-ceramics dedicated for green-emitting devices

In this work, we reported the results of photoluminescent and structural investigations of Gd3+/Tb3+ co-doped silicate xerogels as well as derivative SiO2-LaF3 nano-glass-ceramics. with The molar ratio of appropriate acetates used during the synthesis, i.e., La(AcO)3:Gd(AcO)3:Tb(AcO)3 was fixed to x:(0.95-x):0.05. Based on XRD measurements, the crystallization of hexagonal LaF3 nanophase was verified without any admixture of GdF3 phase, even for samples with La3+:Gd3+ molar ratio ≤ 1. The optical characterization of fabricated Gd3+/Tb3+ co-doped sol-gel materials involved the registration and analysis of photoluminescence excitation (PLE) and emission spectra (PL), as well as the decay curves for the 6P7/2 (Gd3+) and the 5D4 (Tb3+) excited levels. Upon excitation at λex = 275 nm wavelength, the fabricated sol-gel samples revealed the series of emission lines assigned to the electronic transitions from both dopants, i.e., Gd3+ and Tb3+, indicating apparently the occurrence of Gd3+/Tb3+ energy transfer process (ET). The photoluminescence measurements comprehensibly proved the competitiveness between Gd3+ and Tb3+ ions to be entered into LaF3 fluoride nanocrystal lattice, formed during annealing of as-prepared xerogels. Based on the recorded PL spectra for fabricated sol-gel samples, some chromatic parameters were calculated, i.e., chromaticity coordinates (CIE), correlated color temperatures (CCT), and color purities (CP). The prepared Gd3+,Tb3+ co-doped samples are able to emit green light with CCT values in a range from 5967 K to 6291 K, and high CP reached 70%, which predispose them for use as efficient constituents for developing green-emitting devices.