Molar Ratio Research Articles

Fluorophilic Sigma(σ)-Lock Self-Healable Copolymers.

Although F-containing molecules and macromolecules are often used in molecular biology to increase the binding with Lewis acidic groups by introducing favorable C-F dipoles, there is virtually no experimental evidence and limited understanding of the nature of these interactions, especially their role in synthetic polymeric materials. These studies elucidate the molecular origin of inter- and intra-chain interactions responsible for self-healing of F-containing copolymers composed of pentafluorostyrene and n-butyl acrylate units (p(PFS/nBA). Guided by dynamic surface oscillating force (SOF) and spectroscopic measurements supported by molecular dynamics (MD) simulations, these studies show that the reformation ofσ-σorbitals in -C-F of PFS and CH3CH2- of nBA units enables the recovery of entropic energy viaflouorophilic-σ-lockvan der Waals forces when PFS/nBA molar ratios are ~50/50. The strength of these interactions determined experimentally for self-healable PFS/nBA compositions is in the order ~0.3 kcal/mol which primarily comes fromflouorophilic-σ-lock(~70%) contributions. These interactions are significantly diminished for non-self-healable counterparts. Strongly polarized -C-Fσorbitals create lateral dipolar forces enhancing the affinity towards -C-H orbitals, facilitating energetically favorable interactions. Entropic recovery driven by non-covalent bonding offers a valuable tool in designing materials with unique functionalities, particularly self-healable batteries or otherenergy storage devices.

Modeling Zinc Absorption in the Adult Population of Colombia: Insights for Nutritional Evaluation and Intervention Strategies.

Zinc is a vital trace element, yet its deficiency is common in various populations. This study addresses the gap in understanding zinc intake and its relationship with key nutritional parameters in a Colombian population. We analyzed data from 12,987 individuals, focusing on the daily intake of zinc, phytate, protein, and calcium, and used the phytate/zinc molar ratio as an input parameter in the Miller et al. (2013) model. This model was employed to estimate the total absorbed zinc (TAZ) and the fractional absorption of zinc (FAZ). Our findings highlight a general trend towards insufficient intake compared to the standards of the Institute of Medicine (IOM) and Colombia, with a significant percentage of the population falling below the estimated average requirement (EAR) and recommended daily allowance (RDA) for zinc, underscoring the need for targeted nutritional strategies. Our study contributes to a broader understanding of zinc nutrition and public health implications in Colombia, providing a basis for future dietary guidelines and health interventions.

"Dissolve-on-Demand" 3D Printed Materials: Polymerizable Eutectics for Generating High Modulus, Thermoresponsive and Photoswitchable Eutectogels.

Solvent-free photopolymerization of vinyl monomers to produce high modulus materials with applications in 3D printing and photoswitchable materials is demonstrated. Polymerizable eutectic (PE) mixtures are prepared by simply heating and stirring various molar ratios of N-isopropylacrylamide (NIPAM), acrylamide (AAm) and 2-hydroxyethyl methacrylate (HEMA). The structural and thermal properties of the resulting mixtures are evaluated by 1D and 2D NMR spectroscopy as well as differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). UV photocuring kinetics of the PE mixtures are evaluated via in situ photo-DSC and photorheology measurements. The PE mixtures cure rapidly and display storage moduli that are orders of magnitude greater than equivalent copolymers cured in an aqueous medium. The versatility of these PE systems is demonstrated through the addition of a photoswitchable spiropyran acrylate monomer, as well as applying the PE formulation as a stereolithography (SLA)-based 3D printing resin. Due to the hydrogen-bonding network in PE systems, 3D printing of the eutectic resin is possible in the absence of crosslinkers. The addition of a RAFT agent to reduce average polymer chain length enables 3D printing of materials which retain their shape and can be dissolved on demand in appropriate solvents. This article is protected by copyright. All rights reserved.

Synergy between Fe-Co oxide catalysts supported over HZSM-5 for direct conversion of methane to methanol

The direct conversion of methane to methanol over iron and cobalt oxide based composite catalysts supported over HZSM-5 was carried out in a fixed-bed micro reactor under changing process parameters and catalyst compositions. The prepared catalysts were well characterized by various techniques including N2 adsorption desorption, X-ray diffraction (XRD), Fourier transformed infrared spectroscopy (FTIR), pyridine FTIR, X-ray photoelectron spectroscopy (XPS), UV–vis spectroscopy and temperature programmed reduction (H2-TPR). The characterization results revealed the presence of various reducible iron and cobalt oxide species depending on the Fe/Co molar ratio and total metal oxide loading. Moreover, the XPS and UV–vis spectroscopic results also confirmed the variation of Fe2+/Fe3+ and Co2+/Co3+ species depending on the Fe-Co molar ratio which had strong influence on the performance of the composite catalysts. It was found that the cobalt species favours the formaldehyde formation whereas the iron species promotes the formic acid formation in their respective pure supported oxide catalysts. However, the synergistic effect of iron and cobalt oxide in equimolar ratio in composite catalysts appeared as effective for achieving highest yield of methanol. The methanol selectivity was also influenced by the alteration of various studied process parameters. The higher reaction temperature favoured the overoxidation of methanol to CO2 whereas the methanol selectivity increased with increasing the methane to oxygen ratio. The lattice to adsorbed oxygen ratio also had strong influence on the activity of composite catalysts and methanol selectivity. The highest methanol yield of 1.87% was achieved at the methane conversion of 42.81 % with the 20Fe1Co1Z catalyst at 873 K reaction temperature with CH4/O2 ratio of 2:1 and WHSV of 1030 ml hr−1 gcat−1.

Unlocking Direct Lithium Extraction in Harsh Conditions through Thiol-Functionalized Metal-Organic Framework Subnanofluidic Membranes.

Metal-organic framework (MOF) membranes with high ion selectivity are highly desirable for direct lithium-ion (Li+) separation from industrial brines. However, very few MOF membranes can efficiently separate Li+ from brines of high Mg2+/Li+ concentration ratios and keep stable in ultrahigh Mg2+-concentrated brines. This work reports a type of MOF-channel membranes (MOFCMs) by growing UiO-66-(SH)2 into the nanochannels of polymer substrates to improve the efficiency of MOF membranes for challenging Li+ extraction. The resulting membranes demonstrate excellent monovalent metal ion selectivity over divalent metal ions, with Li+/Mg2+ selectivity up to 103 since Mg2+ should overcome a higher energy barrier than Li+ when transported through the MOF pores, as confirmed by molecular dynamics simulations. Under dual-ion diffusion, as the Mg2+/Li+ mole ratio of the feed solution increases from 0.2 to 30, the membrane Li+/Mg2+ selectivity decreases from 1516 to 19, corresponding to the purity of lithium products between 99.9 and 95.0%. Further research on multi-ion diffusion that involves Mg2+ and three monovalent metal ions (K+, Na+, and Li+, referred to as M+) in the feed solutions shows a significant improvement in Li+/Mg2+ separation efficiency. The Li+/Mg2+ selectivity can go up to 1114 when the Mg2+/M+ molar concentration ratio is 1:1, and it remains at 19 when the ratio is 30:1. The membrane selectivity is also stable for 30 days in a highly concentrated solution with a high Mg2+/Li+ concentration ratio. These results indicate the feasibility of the MOFCMs for direct lithium extraction from brines with Mg2+ concentrations up to 3.5 M. This study provides an alternative strategy for designing efficient MOF membranes in extracting valuable minerals in the future.

Synthesis of High‐Sodium‐Content Oxythiosilicate Glass Electrolytes Via Sodium Polysulfide

AbstractSulfide glass electrolytes with high ionic conductivities and formabilities are key materials for practical use in all‐solid‐state sodium secondary batteries. Both sealing and quenching are considered to be necessary for producing high‐alkali‐content sulfide glass electrolytes. In this study, the glass‐forming ability of sodium thiosilicate glasses is enhanced by adding a small quantity of SiO2. Consequently, high‐sodium‐content oxythiosilicate glass is synthesized without sealing and quenching processes under Ar atmosphere. The prepared Na4SiS4·0.200SiO2 (molar ratio) glass exhibits ionic conductivity of 4.0 × 10−5 S cm−1 at 25 °C, surpassing that of Na4SiS4 glass. The Na4SiS4·0.200SiO2 glass shows high reduction stability to sodium metal. The all‐solid‐state Na metal/Na4SiS4·0.200SiO2 glass/Na2.88Sb0.88W0.12S4/TiS2 cell shows a reversible capacity of 140 mAh g−1 for 5 cycles. The amount of H2S gas generated in Na4SiS4·0.0830SiO2 and Na4SiS4·0.200SiO2 glasses is one‐tenth that of the Na4SiS4 glass, suggesting increased chemical stability to humidity by incorporating oxygen in the structure. High‐sodium‐content oxythiosilicate glass with high ionic conductivity, high chemical stability against humidity, and high reduction stability is successfully prepared under ambient pressure without sealing and quenching processes.

A new laboratory‐based method to experimentally induce diagenetic modifications in human bone tissue using archaeological gravesoils

AbstractThe conditions of the burial environment trigger microstructural modifications and physical‐chemical changes in the bone, such as chemical dissolution, increase of crystallinity, chemical exchanges, collagen degradation and changes in porosity, hence to reproduce these patterns is a challenging task. This work presents a new method to accelerate the diagenetic processes in the laboratory. Artificial aging is obtained by immersion at 80°C in “enriched” solutions derived from the leaching of gravesoils, maintaining the same pH, for 1 month, on modern bones collected from an autopsy. Two distinct solutions from two graves of the necropolis of Travo (IT) (7th–8th century AD) were adopted. The induced damage patterns, on the bone microstructure and the organo‐mineral fraction, have been compared with those observed on buried skeletal elements from the same graves, by providing a multi‐analytical approach (BSE‐SEM, EMPA, FT‐IR, MP‐AES). Bioapatite parameters, such as crystallinity index and Ca/P molar ratio, evolved similarly and, in some cases, reached the same values of buried bones. Conversely, in the absence of microbial activity, the organic fraction better survived the artificial aging. For the same reason, the porosity due to bioerosion was absent in the artificially aged samples, whereas the biological pores and the post‐mortem fractures exhibited the same histomorphology. It is believed that the opportunity of reproducing the diagenetic changes by replicating the chemical environment of the burial site at the laboratory scale is of great interest to forensic science and archaeology (e.g., to reconstruct the burial environment).

Construction of Z‐scheme 1T/2H‐MoS2/CdS for improving photocatalytic degradation of antibiotic residues

Abstract1T/2H‐MoS2/CdS composite was effectively prepared by a two‐step hydrothermal method, which greatly improved the photocatalytic degradation efficiency of tetracycline hydrochloride and photocatalytic cycle stability compared with pristine 1T/2H‐MoS2. The highest photodegradation efficiency of 70.8% is achieved when the molar ratio of 1T/2H‐MoS2 to cadmium sulfide is 1:4. The capture experiment indicates that hydroxyl radical (⋅OH) and superoxide radical (⋅O2−) play a role in the photocatalytic degradation process. A Z‐type heterojunction may be formed on the 1T/2H‐MoS2/CdS composite based on a series of analyses, which improves the photocatalytic performance effectively via expanding the range of light response and promoting the separation of photogenerated electrons and holes. This work provides an alternative to constructing novel Z‐scheme photocatalysts with high performance in the absence of noble metals.

Phosphoric acid-activated metakaolin-based geopolymer: Optimizing P/A molar ratio to solidify Cs+ and Sr2+ in nuclear waste

Phosphoric Acid-activated Metakaolin-based Geopolymer (PAMG) is an efficient solidified material. This paper reports the effect of the H3PO4 to Al2O3 (P/A) molar ratio on the hydration, phase assemblage, morphology, and compressive strength of PAMG and the solidification of simulated radionuclides Sr and Cs by PAMG. The hydration behavior and microstructure of PAMG were investigated using isothermal calorimetry, X-ray diffraction (XRD), and scanning electron microscope (SEM). The impacts of Cs and Sr on the leaching behavior and microstructure of PAMG were assessed using atomic absorption spectrum (AAS), SEM, and energy dispersion spectrum (EDS). The results indicate that the compressive strength of PAMG increases and then decreases as the P/A ratio increases. The highest compressive strength reaching 98.1 MPa after 28 days of curing, was observed at a P/A molar ratio of 1.8. The addition of Cs and Sr resulted in a decrease in the compressive strength of PAMG, with Sr showing a more significant reduction in PAMG's compressive strength. However, PAMG still exhibited a high efficiency in solidifying simulated nuclides Cs and Sr, with 42 days leaching rates of 3.7 × 10−5 cm/d and 5.0 × 10−6 cm/d, respectively. These results indicate the huge potential of PAMG in solidifying nuclides.

Magnetic iron‐oxide coffee husk and khat waste biochar nanocomposites for removal of methylene blue from aqueous solution

AbstractWastewater from the textile and dyeing industries contains hazardous dyes. This study aims to determine the effectiveness of magnetic biochar nanocomposites synthesized from khat leftovers (KLs) and coffee husks (CHs) in removing methylene blue (MB) from wastewater. Magnetic biochar nanocomposites were synthesized by pretreating 25 g of biomass with a 12.5 mmol mixture of FeS and FeCl3 at a 1:1 molar ratio, followed by pyrolyzing at 300°C for 1 h. The resulting products were analyzed using X‐ray diffraction, Fourier transform infrared, scanning electron microscope, and Brunauer‐Emmett‐Teller. The results showed that the adsorbents are amorphous, and the activated biochars, are more porous and contain various functional groups such as C‐O, C = C, O‐H, C‐H, and Fe‐O. When 0.2 g of pristine biochars of CH and KL were applied to 20 mL aqueous solutions containing 20 mg/L of MB at pH 7.5 and 25°C, they removed 44.73% and 75.26% of MB, respectively. However, the resulting nanocomposites exhibited a maximum removal efficiency of 99.10% and 99.23% with magnetic iron oxide‐CH biochar nanocomposite (Fe3O4‐CHBNC) and magnetic iron oxide‐KL biochar nanocomposite (Fe3O4‐KLBNC), respectively, with maximum adsorption capacities of 51.02 and 78.13 mg/g. The reusability study also showed removal efficiencies of 77.57% and 83.49% up to six‐cycle reuse.

Reduction of an Ilmenite Concentrate by Using a Novel CO2/CH4 Thermal Plasma Torch

Plasma technology has emerged as a very helpful tool in a variety of sectors, notably metallurgy. Innovators and scientists are focused on the problem of finding a more ecologically friendly way of extracting titanium and iron metal from natural ilmenite concentrate for industrial applications. A direct current (DC) plasma torch operating at atmospheric pressure is used in this study to describe a decarbonization process for reducing an ilmenite concentrate. The plasma gases employed in this torch are CO2 and CH4. The molar ratio of the gases may be crucial for achieving a satisfactory reduction of the ilmenite concentrate. As a result, two molar ratios for CO2/CH4 have been chosen: 1:1 and 2:1. During torch operation, a thin layer of graphite is formed on the cathode to establish a protective barrier, prolonging the cathode’s life. The material was analyzed using X-ray diffraction (XRD) and scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS). The output gases were analyzed using mass spectrometry (MS). In addition, a thermodynamic analysis was performed to predict the development of thermodynamically stable phases. An economic assessment (including capital expenditures (CAPEX) and operating expenditures (OPEX)) and a carbon balance were developed with the feasibility of the piloting in mind.

An eutectic Mixture in the Tetrabutylammonium Bromide-Octanol System: Macroscopic and Microscopic Points of View.

An eutectic mixture of tetrabutylammonium bromide and octanol in the molar ratio 1-10 exhibited a melting point of -17°C. This system was investigated by means of infrared spectroscopy, in the liquid and in the solid state. Classical molecular dynamics was performed to study the fine details of the hydrogen bond interactions established in the mixture. Both octanol and the mixtures displayed an almost featureless far-infrared spectrum in the liquid state but it becomes highly structured in the solid phase. DFT calculations suggest that new vibrational modes appearing in the mixture at low temperatures may be related to the population of the higher energy conformers of the alcohol. Mid-infrared spectroscopy measurements evidenced no shift of the CH stretching bands in the mixture compared to the starting materials, while the OH stretching are blue shifted by a few cm-1. Consistently, molecular dynamics provides a picture of the mixture in which the hydrogen bonds (HB) of pure octanol are replaced by weaker HB formed with the TBA ion and the Br cation. Due to these interactions the ionic couple becomes more separated. In agreement with this model, the lengths of all HB are much larger than those observed in acids in previous studies.

Efficiency of magnetic zeolitic imidazolate framework-8 (ZIF-8) modified graphene oxide for lead adsorption.

Simple and efficient removal of Pb(II) ion from aqueous solution through adsorption has accelerated the development of many new composites to improve this popular method. In this study, the composites of graphene oxide (GO), zeolitic imidazolate framework-8 (ZIF-8), and magnetic materials were synthesized via coprecipitation method utilizing a different molar ratio between FeCl2 and FeCl3 of 1:0.5, 2:1, 3:1.5, and 4:2. The ZIF-8/GO was prepared via room temperature synthesis method prior to its further modification with magnetic materials for ease of separation. It was observed that the MZIF-8/GO2 of molar ratio 2:1 showed the best performance in adsorbing Pb(II) ion. As confirmed by FESEM image, it appeared to be ZIF-8 particles that have grown all over the GO platform and overlayed with Fe3O4 granular-shaped particles. The MZIF-8/GO2 successfully achieved 99% removal of Pb(II) within 10min. The optimum values obtained for the initial concentration of Pb (II) were 100mg/L, pH of 4 to 6, and adsorbent dosage used was 10mg. The Langmuir isotherm and the pseudo-second-order kinetic model were deemed suitable to evaluate the adsorption of Pb(II) using MZIF-8/GO2. Results showed that MZIF-8GO2 achieved a maximum adsorption capacity of 625mg/g of Pb(II) adsorption. All parent materials demonstrated a good synergistic effects, while exhibiting a significant contribution in providing active sites for Pb(II) adsorption. Therefore, this ternary composite of MZIF-8/GO2 is expected to be a promising adsorbent for Pb(II) adsorption from aqueous solution with an added value of ease of post phase separation using external magnetic field.

Green synthesis and photocatalytic proficiency of tunable SnO2 nanostructures: unveiling environmental-friendly strategies for sustainable water remediation

Abstract This study demonstrates a proficient and eco-friendly synthesis of SnO2 nanostructures using a hydrothermal method, without the requirement of extra surfactants. The synthesis was systematically performed by adjusting the molar ratio of stannic chloride to sodium hydroxide and varying the pH settings. It was noted that the pH value rises according to the concentration of sodium hydroxide. A comprehensive analysis was performed to characterize the resulting nanostructures, which involved studying their structural features, chemical composition, morphology, and optical properties. An X-ray diffraction (XRD) analysis showed that increasing the pH values resulted in a noticeable improvement in the crystalline structure and a decrease in the density of surface defects. The SnO2 nanostructures, synthesized using different pH settings, were subsequently assessed for their photocatalytic performance in the degradation of methylene blue (MB) dye under simulated solar irradiation. Surprisingly, the nanostructure produced at higher pH levels showed outstanding results, as 97% of the dye was broken down in just 70 minutes when exposed to simulated solar radiation. The analysis uncovered a maximum rate constant (k) value of 0.04 min−1, determined using pseudo first-order rate kinetics. In order to better understand the photodegradation process, scavenger experiments were performed to identify the active species involved. These investigations provided valuable insights into the complex mechanisms that drive the observed photocatalytic activity. This study not only enhances the progress of SnO2 nanostructures but also highlights their potential as strong and environmentally friendly materials for effective photocatalytic applications.

Influence of phosphorus molar ratio on the fabrication and electrochemical properties of nanorod-shaped LiFePO4 synthesized via iron powder reduction for lithium-ion battery applications

Influence of phosphorus molar ratio on the fabrication and electrochemical properties of nanorod-shaped LiFePO₄ synthesized via iron powder reduction for lithium-ion battery applications

Production and testing of mahua oil-based biodiesel synthesized through heterogeneous catalyst using experimental and numerical method.

A two-step treatment of mahua oil was conducted to synthesize mahua biodiesel using heterogeneous biomass-based catalyst derived from mahua shell. Mahua oil having higher free fatty acid (FFA) content (about 19%) was esterified to reduce the FFA content up to 1%. The esterification process was carried out using 200mL mahua oil, 5:1 molar ratio (methanol:oil), and 2.25 weight% of H2SO4 at a temperature of 60°C for 3h. Post esterification, a set of 16 experiments were created using a Box-Behnken design (BBD)-based response surface methodology (RSM) approach to conduct the transesterification of the esterified oil. Molar ratio, catalyst loading, reaction temperature, and reaction time were the four input variables chosen for the design of experiments. The optimized conditions for maximum biodiesel yield (87.7%) were found to be 14.88 molar ratio, 3.578% catalyst loading, 69.7°C reaction temperature, and 81.9min reaction time. The Diesel RK engine simulation tool which was experimentally validated for baseline diesel fuel was used for numerical simulation of mahua biodiesel. The performance, combustion, and emission behavior of mahua biodiesel analyzed using numerical simulation presented the sustainability of mahua biodiesel as an alternate fuel.

Preparation of Heterogeneous Fenton Catalysts Cu-Doped MnO2 for Enhanced Degradation of Dyes in Wastewater

Herein, a series of heterogeneous Fenton catalysts, Cu doped MnO2 (CDM), with different Cu/Mn molar ratios were prepared via a hydrothermal reaction. Meanwhile, detailed characterizations were used to study the structures of CDM, and it is amazing that the morphology of CDM changed from nanowires to nanoflowers with an increasing amount of Cu doped. Apart from this, both the specific surface area and oxygen vacancy increased obviously with the increasing Cu/Mn molar ratio. Then, the degradation of different dyes was utilized to evaluate the catalytic activity of different CDM with H2O2 used as the oxidizing agent, and the 50%-CDM with the highest content of Cu doped displayed the best catalytic activity. Herein, the degradation efficiency (D%) of Congo red (CR) solution with low concentration (60 mg/L) reached 100% in 3 min, while the D% of CR solution with a high concentration (300 mg/L) reached 99.4% after 5 min with a higher dosage of H2O2. Additionally, the 50%-CDM also displayed excellent reusability, for which the D% values were still higher than 90% after the 14th cycles. Based on the structure characteristics and mechanism analysis, the excellent catalytic capacity of 50%-CDM was due to the combined influence of large specific surface area and abundant oxygen vacancy. Thus, a promising heterogeneous Fenton catalyst was developed in this study, which proved the treatment efficiency of actual dye wastewater.

Effect of B addition on the microstructure and tribological properties of laser cladding FeCoCrNiCu composite coatings

The high-entropy alloy coatings of FeCoCrNiCuBx (x = 0, 0.1, 0.3, 0.5, x values are molar ratios) were prepared on the surface of Q235 steel by laser cladding. The microstructure, microhardness, and surface energy of the FeCoCrNiCuBx coatings were investigated, and the tribological property and wear mechanism of the composite coatings at room temperature (RT) and 600 ℃(HT) were analyzed. The FeCoCrNiCu coating consists of a single FCC-type solid solution. When x = 0.3, 0.5, the composite coatings appear the Cr2B phase. The x = 0.5 (B5) coating has the lowest surface energy (27.45mN/m), which is one of the reasons it has excellent tribological properties. The tribological properties of FeCoCrNiCuBx composite coatings were improved at both RT and HT. The B5 coating has excellent tribology at both RT and HT. At RT, the wear resistance of the B5 coating (wear rate is 8.54 ×10−5 mm3/N∙m, coefficient of friction (COF) is 0.51) was improved by 54.79%, 50.89%, and 12.86% compared with x = 0(HEA), x = 0.1(B1), and x = 0.3(B3), respectively, the COF reduced by 42.69%, 41.39%, 22.73%. At HT the wear resistance of the B5 coating (wear rate is 6.69 ×10−5 mm3/N∙m, COF is 0.24) was increased by 71.53%, 52.91%, and 49.42% compared to HEA, B1, and B3, respectively, the COF reduced by 29.41%, 25.00%, 17.24%. The wear mechanisms of coatings that add B element at RT are abrasive wear and fatigue wear, and at HT are mainly oxidative wear, moderate abrasive wear and fatigue wear.B2O3 melts at HT to form a low-viscosity liquid that forms a lubricating film that isolates the contact surfaces and reduces direct contact and adhesion. This is the main reason for the excellent friction properties of B5 coating at HT.

Synthesis of ZnO and ZnO/Ag fine particles by plasma-assisted inkjet processing

Zinc oxide (ZnO) and its composite particles with controlled sizes, shapes, compositions, and physical and chemical properties are required for a wide variety of applications. In this study, we report a simple method for synthesising ZnO and ZnO/Ag composite particles via atmospheric-pressure plasma processing using inkjet droplets. Depending on the initial solution concentration, ZnO particles containing voids, with average sizes ranging from submicrons to several microns can be synthesised. Energy dispersive x-ray spectroscopy measurements of the synthesised ZnO/Ag particles suggest that the molar ratio of Ag to Zn in the initial solution was retained in the synthesised particles. A high surface-enhanced Raman scattering effect was observed in the particles synthesised from the solution with an Ag molar ratio of 50% to the total solute. The proposed method enables the synthesis of ZnO particles of various sizes, microstructures, compositions and optical properties with relatively narrow size distributions.

Recycling lithium slag into eco-friendly ultra-high performance concrete: Hydration process, microstructure development, and environmental benefits

To ascertain the viability of utilizing lithium slag (LS) in the development of eco-friendly ultra-high performance concrete (UHPC), this paper provides a detailed analysis of the effects of LS on UHPC. Specifically, the hydration and microstructural changes in UHPC containing LS (LS-UHPC) were comprehensively examined. Based on the results of isothermal calorimetry, X-ray diffraction (XRD), thermogravimetric analysis (TG), scanning electron microscopy (SEM), and mercury intrusion porosimetry (MIP), LS primarily acts as a filler, promotes nucleation, provides internal curing, and participates in the pozzolanic reaction. Significantly, the internal curing effect and the pozzolanic reaction enhanced the strength development of LS-UHPC. UHPC with 20 % LS exhibited the highest 28 d compressive strength at 134.48 MPa and presented the densest microstructure. However, approximately 4 % of the calcium hydroxide in LS-UHPC would not be involved in the pozzolanic reaction. The presence of gypsum in LS led to increased ettringite formation in LS-UHPC. Although LS extended the induction period of UHPC, it intensified the hydration degree of cement. In LS-UHPC, the molar ratio of Ca/Si of C-(A)-S-H decreased, whereas the molar ratio of Al/Si increased, implying that the dissolved aluminum from LS was incorporated into the C–S–H chains. The integration of LS not only considerably reduced the carbon emissions and energy consumption of UHPC but also optimized LS recycling. Overall, the development of a sustainable UHPC by incorporating LS is both practicable and advantageous for environmentally conscious construction practices.