Spectroscopy Analysis Research Articles

Characterization, biological activity, and anticancer effect of green-synthesized gold nanoparticles using Nasturtium officinale L.

BackgroundNanostructured materials used have unique properties and many uses in nanotechnology. The most striking of these is using herbal compounds for the green synthesis of nanoparticles. Among the nanoparticle types used for green synthesis, gold nanoparticles (AuNPs) are used for cancer therapy due to their stable structure and non-cytotoxic. Lung cancer is the most common and most dangerous cancer worldwide in terms of survival and prognosis. In this study, Nasturtium officinale (L.) extract (NO), which contains biomolecules with antioxidant and anticancer effects, was used to biosynthesize AuNPs, and after their characterization, the effect of the green-synthesized AuNPs against lung cancer was evaluated in vitro.MethodsUltraviolet‒visible (UV‒Vis) spectrophotometry, scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), multiple analysis platform (MAP), and Fourier transform infrared (FT-IR) spectroscopy analyses were performed to characterize the AuNPs prepared from the N. officinale plant extract. Moreover, the antioxidant activity, total phenolic and flavonoid contents and DNA interactions were examined. Additionally, A549 lung cancer cells were treated with 2–48 µg/mL Nasturtium officinale gold nanoparticles (NOAuNPs) for 24 and 48 h to determine the effects on cell viability. The toxicity of the synthesized NOAuNPs to lung cancer cells was determined by the 3-(4,5-dimethylthiazol-2-il)-2,5-diphenyltetrazolium bromide (MTT) assay, and the anticancer effect of the NOAuNPs was evaluated by apoptosis and cell cycle analyses using flow cytometry.ResultsThe average size of the NPs was 56.4 nm. The intensities of the Au peaks from EDS analysis indicated that the AuNPs were synthesized successfully. Moreover, the in vitro antioxidant activities of the NO and NOAuNPs were evaluated; these materials gave values of 31.78 ± 1.71% and 31.62 ± 0.46%, respectively, in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay at 200 g/mL and values of 25.89 ± 1.90% and 33.81 ± 0.62%, respectively, in the 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assay. The NO and NOAuNPs gave values of 0.389 ± 0.027 and 0.308 ± 0.005, respectively, in the ferrous ion reducing antioxidant capacity (FRAP) assay and values of 0.078 ± 0.009 and 0.172 ± 0.027, respectively, in the copper ion reducing antioxidant capacity (CUPRAC) assay. When the DNA cleavage activities of NO and the NOAuNPs were evaluated via hydrolysis, both samples cleaved DNA starting at a concentration of 25 g/mL in the cell culture analysis, while the nanoformulation of the NO components gave greater therapeutic and anticancer effects. We determined that the Au nanoparticles were not toxic to A549 cells. Moreover, after treatment with the half-maximal inhibitory concentration (IC50), determined by the MTT assay with A549 cells, we found that at 24 and 48 h, while the necrosis rates were high in cells treated with NO, the rates of apoptosis were greater in cells treated with NOAuNPs. Notably, for anticancer treatment, activating apoptotic pathways that do not cause inflammation is preferred. We believe that these results will pave the way for the use of NOAuNPs in in vitro studies of other types of cancer.ConclusionIn this study, AuNPs were successfully synthesized from N. officinale extract. The biosynthesized AuNPs exhibited toxicity to and apoptotic effects on A549 lung cancer cells. Based on these findings, we suggest that green-synthesized AuNPs are promising new therapeutic agents for lung cancer treatment. However, since this was an in vitro study, further research should be performed in in vivo lung cancer models to support our findings and to explain the mechanism of action at the molecular level.

Improved hydrogen production in immobilized Chlamydomonas reinhardtii cells with inhibited inter-photosystem electron transfer

The production of molecular hydrogen (H2) by microalgae holds great promise, and immobilization techniques offer potential for further advancement in this field. The current study focuses on investigating the positive impact of immobilization on maintaining the stability and activity of photosystem II (PSII) over incubation time, with the aim of enhancing H2 production potential in green microalgae Chlamydomonas reinhardtii. For this purpose, immobilized cells within alginate beads were treated with small concentrations of 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone (DBMIB) inhibitor to induce the partial inhibition of inter-photosystem electron transport, recently reported as a novel approach for sustaining microalgal H2 production. A comparative analysis of fluorescence decay kinetic changes and EPR spectroscopy of the cell beads revealed the superior capacity of immobilization for sustaining PSII stability and activity in batch culture over time. Treatment of the cell beads with 3.5 μM DBMIB led to sustained H2 production yielding over 200 μmol H2/mg Chl within 3 weeks, with an average H2 production rate of approximately 10 μmol/mg Chl per day, both of which were roughly twice as high as those observed in free cells treated with DBMIB. Our findings underscore the significance of integrating immobilization with a proven and effective method for H2 production, thereby enhancing its sustainability and productivity.

Investigating the expansion behavior of silicon nitride nanopores

Nanopores are a single-molecule detection platform that has attracted more and more researchers’ attention, but so far there is still a lack of systematic research on their stability. In this study, we investigated the mechanism behind the expansion behavior of solid-state nanopores and its effect on the electrical properties of nanopores. Through the analysis of electron energy loss spectroscopy, it was found that the expansion process of nanopores is accompanied by the loss of silicon elements. Three nanopore expansion models can well explain the differential impact of silicon element loss in different regions on the electrical properties of nanopores. Molecular dynamics simulations analyzed the differences in nanopore conductivity and expansion rate corresponding to different expansion models from the perspective of single-atom loss. Finally, we demonstrated that chemical modification can isolate direct contact between the nanopore wall and the solution, thereby greatly delaying the expansion behavior of solid-state nanopores.

Machine learning and artificial intelligence: enabling the clinical translation of atomic force microscopy-based biomarkers for cancer diagnosis

The influence of biomechanics on cell function has become increasingly defined over recent years. Biomechanical changes are known to affect oncogenesis; however, these effects are not yet fully understood. Atomic force microscopy (AFM) is the gold standard method for measuring tissue mechanics on the micro- or nano-scale. Due to its complexity, however, AFM has yet to become integrated in routine clinical diagnosis. Artificial intelligence (AI) and machine learning (ML) have the potential to make AFM more accessible, principally through automation of analysis. In this review, AFM and its use for the assessment of cell and tissue mechanics in cancer is described. Research relating to the application of artificial intelligence and machine learning in the analysis of AFM topography and force spectroscopy of cancer tissue and cells are reviewed. The application of machine learning and artificial intelligence to AFM has the potential to enable the widespread use of nanoscale morphologic and biomechanical features as diagnostic and prognostic biomarkers in cancer treatment.

Li-Si alloy pre-lithiated silicon suboxide anode constructing a stable multiphase lithium silicate layer promoting Ion-transfer kinetics

Enhancing the initial Coulombic efficiency (ICE) and cycling stability of silicon suboxide (SiOx) anode is crucial for promoting its commercialization and practical implementation. Herein, we propose an economical and effective method for constructing pre-lithiated core–shell SiOx anodes with high ICE and stable interface during cycling. The lithium silicon alloy (Li13Si4) is used to react with SiOx in advance, allowing for improved ICE of SiOx without compromising its reversible specific capacity. The pre-lithiated surface layer contains uniform multiphase lithium silicates (L2SiO3, Li4SiO4, and Li2Si2O5) in the nanoscale. This multiphase lithium silicate layer exhibits mechanical robustness against variation of micro-stress, which can act as a buffer layer to relieve volume variation. In addition, analysis of dynamic electrochemical impedance spectroscopy (dEIS) and distribution of relaxation time (DRT) confirm that the multiphase lithium silicate layer enhances Li-ion diffusion kinetics and contributed to constructing stable SEI. As a result, the optimal L10-850 anode shows a high ICE of 85.3 %, together with a high specific capacity of 1771.5mAh mg−1. This work gives a perspective strategy to modify SiOx anodes by constructing a pre-lithiated surface layer with practical application potentials.

Alginate-based bio-nanocomposite reinforced with poly(2-hydroxypropyl methacrylamide) and magnetite graphene oxide for delivery of etoposide and photothermal therapy

Recently, bio-nanocomposite nanogels/hydrogels composed of natural polymers and carbon-based nanomaterials are attracting increasing attention in the fields of nanomedicine and bioengineering due to their unique properties. In this study, we propose the creation of an innovative multifunctional bio-nanocomposite based on alginate graft copolymer with poly(2-hydroxypropyl methacrylamide) (SA-g-PHPM) and magnetite graphene oxide (mGO) loaded with etoposide (EPS) for drug delivery and photothermal therapy (PTT). The SA-g-PHPM/mGO bio-nanocomposite was synthesized using an emulsion method and exhibited favorable physicochemical properties. The structural functionalities and surface morphology of the SA-g-PHPM/mGO bio-nanocomposite were comprehensively characterized using spectroscopic techniques, including FT-IR, XRD, UV, DLS, TEM/FE-SEM, and AFM analyses. Under near-infrared (NIR) irradiation (808 nm, 1 Wcm-2, 10 min), the SA-g-PHPM/mGO bio-nanocomposite demonstrated the ability to effectively induce a temperature increase exceeding 29 °C. Additionally, exposure to NIR light and magnetic field led to an increased release of EPS whereas an increment in percentage of mGO caused a decreased EPS release. Notably, the synergistic effects of chemotherapy, light-triggered drug release, and PTT collectively contributed to a significant enhancement in lung cancer (H1299) cell death. In conclusion, our findings suggest that the developed SA-g-PHPM/mGO/EPS bio-nanocomposite serves as an efficient vehicle for multimodal therapy in lung cancer.

Lignans and phenols with potential anti-inflammatory effect from the stems of Mallotus paxii Pamp

Phytochemical investigation of the stems of Mallotus paxii Pamp. led to the isolation and identification of four new compounds, including three neolignans (1–3) and one phenol (13), along with eight known neolignans (4–12) and one known phenol (14). Their structures were determined by spectroscopic methods, including NMR, MS and ECD analyses. Bioassay demonstrated that malloapelin A (4) exhibited a most potent anti-inflammatory activity to NO release with IC50 value of 21.32 μM. Furthermore, malloapelin A (4) markedly decreased the secretion of TNF-α, iNOS, and NF-κB and inhibited the expression of COX-2 and NF-κB/p65 in LPS-induced RAW264.7 cells in a dose-dependent manner.

The applicability of the SERS technique in food contamination testing – The detailed spectroscopic, chemometric, genetic, and comparative analysis of food-borne Cronobacter spp. strains

Microorganisms assigned as Cronobacter are Gram-negative, facultatively anaerobic, bacteria widely distributed in nature, home environments, and hospitals. They can also be detected in foods, milk powder, and powdered infant formula (PIF). Additionally, as an opportunistic pathogen, Cronobacter may cause serious infections, sometimes leading to the death of neonates and infants. Thus, it is essential to test food products for the presence of Cronobacter spp. The currently used standard described in ISO 22964:2017 is a laborious method that could be easily replaced by surface-enhanced Raman scattering (SERS).Here, we demonstrate that SERS allows the identification of food-borne bacteria belonging to Cronobacter spp. based on their SERS spectra. For this purpose, twenty-six Cronobacter strains from different food samples were analyzed. Additionally, it was shown that it is possible to differentiate them from other closely related pathogens such as Salmonella enterica subsp. enterica, Escherichia coli, or Enterobacter spp. The SERS results were supported by principal component analysis (PCA), as well as and sequencing of 16S rRNA, rpoB and fusA genes. Last but not least, it was demonstrated that the cells of Cronobacter sakazakii may be easily separated from PIF using an appropriate filter, microfluidic chip, and dielectrophoresis (DEP) technique.

Palladium‐N‐heterocyclic Carbene Complexes: Synthesis, Characterization and Catalytic Application of C−H Activation for Carboxaldehyde Derivatives

AbstractA series of palladium‐N‐heterocyclic carbene complexes (2 a‐e) were synthesized from corresponding N‐heterocyclic carbene precursors (1 a‐e) in good yields. The structural analysis of all novel compounds was done by spectroscopic methods and elemental analysis was also performed to evaluate the purity of the complexes. Further confirmations of complexes 2 a‐d were provided by X‐ray crystallography technique. Under optimized reaction conditions, the catalytic activity of the palladium‐N‐heterocyclic carbene complexes was reviewed by direct arylation of furan‐2‐carboxaldehyde and 1‐methylpyrrole‐2‐carboxaldehyde with varied aryl halides. This arylation showed productive and selective reaction at the C5‐position of heteroaryl derivatives.

SN 2021wvw: A Core-collapse Supernova at the Subluminous, Slower, and Shorter End of Type IIPs

We present detailed multiband photometric and spectroscopic observations and analysis of a rare core-collapse supernova, SN 2021wvw, that includes photometric evolution up to 250 days and spectroscopic coverage up to 100 days postexplosion. A unique event that does not fit well within the general trends observed for Type IIP supernovae, SN 2021wvw shows an intermediate luminosity with a short plateau phase of just about 75 days, followed by a very sharp (∼10 days) transition to the tail phase. Even in the velocity space, it lies at a lower velocity compared to a larger Type II sample. The observed peak absolute magnitude is −16.1 mag in r-band, and the nickel mass is well constrained to 0.020 ± 0.006 M ⊙. Detailed hydrodynamical modeling using MESA+STELLA suggests a radially compact, low-metallicity, high-mass red supergiant progenitor (M ZAMS = 18 M ⊙), which exploded with ∼0.2 × 1051 erg s−1 leaving an ejecta mass of M ej ≈ 5 M ⊙. Significant late-time fallback during the shock propagation phase is also seen in progenitor+explosion models consistent with the light-curve properties. As the faintest short-plateau supernova characterized to date, this event adds to the growing diversity of transitional events between the canonical ∼100 days plateau Type IIP and stripped-envelope events.

A composite laser ablation diagnosis method based on multiple spectroscopic and imaging analyses

This study proposes a novel diagnostic approach for target ablation to comprehensively elucidate the physical mechanisms of laser ablation in aluminium alloys and stainless steel, precisely measure sample temperatures, and predict the ablation state. The method utilizes a spatially weighted emissivity model in conjunction with multispectral thermometry techniques to analyze spatial variations in temperature and emissivity distributions, facilitating the evaluation of target ablation status. Through a series of experiments, temperature data obtained using an enhanced weighted radiative spectral inversion technique were compared with temperatures recorded by thermal imaging cameras, confirming the effectiveness and accuracy of the weighted radiative spectral inversion method in multispectral thermometry. Additionally, a detailed examination of laser ablation in aluminium alloys and stainless steel was conducted to elucidate the underlying damage mechanisms. This refined approach establishes a solid groundwork for further investigation into the characteristics and dynamic Evolution of laser-damaged regions.

Macrocyclic anti-inflammatory diterpenes from the South China Sea soft coral Sinularia erecta and their isolation by combined column chromatography

Eleven new macrocyclic casbane-type diterpenes, namely sinueracasbanones E–O (1–11), have been isolated from the South China Sea soft coral Sinularia erecta using combined column chromatography. The structures of new compounds were elucidated by extensive spectroscopic data analysis, the modified Mosher's method, X-ray diffraction analysis and quantum mechanical calculation methods. In bioassay, compounds 2, 5, 10 and 11 displayed interesting anti-inflammatory activities by the inhibition of lipopolysaccharide (LPS)-induced tumor necrosis factor (TNF)-α protein release with half maximal inhibitory concentration (IC50) values of 15.6, 7.1, 13.7 and 6.6 µM, respectively.

Advanced exploration of rare metal mineralization through integrated remote sensing and geophysical analysis of structurally-controlled hydrothermal alterations

Fusing multi-source (remote sensing and geophysical) data and diverse approaches validation in targeting hydrothermal alteration and structural anomalies enhances the potential for accurately detecting and characterizing mineralization zones. Sentinel 2 data and ASTER were processed for lithological and hydrothermal alteration mapping in the rare metal-rich Umm Naggat area (Egypt). Different image processing techniques were implemented, including false color composites, minimum noise fraction, band rationing, band math, mineral indices, relative absorption band depth, and constrained energy minimization. The rare metal-bearing Umm Naggat younger granite (NYG) pluton was lithologically discriminated and intra-differentiated to mafic-rich biotite granites, mafic-poor alkali feldspar granites, and albitized granites. Extensive hydrothermal alterations, such as albitization, ferrugination, propylitization, argillization, and phyllitization, overprint the NYG pluton. Normalized standard deviation, automatic lineament extractions, and trend analysis highlighted the key structural directions (NW, NNW, NNE, and NE) and distinguished the NYG pluton as a moderate to high structural density zone. The high structural density and intensive alteration zones are spatially associated and more localized within the NYG pluton than the surrounding rocks. Spatial overlay analysis confirmed that the hydrothermal alterations and fluid circulation systems are structurally-controlled. Furthermore, the hydrothermal alteration mapping and structural analysis outcomes were verified by combining fieldwork, slab polishing, petrographic investigations, and mineral chemistry through semi-quantitative scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS) and quantitative electron probe microanalysis (EPMA) analysis. As a result, the hydrothermal genesis of rare metal-bearing minerals (Nb-rutile, Nb-ilmenite, and columbite) close to or incorporated within alteration minerals (chlorite, muscovite, and hematite) is confirmed from the alteration zones (propylitic, phyllic, and ferruginated). In addition, biotite muscovitization and chloritization significantly contribute to the secondary rare metal enrichment. The current study emphasizes the extensive distribution of secondary rare metal-bearing minerals within the entire NYG pluton (not only limited to the northern albitized granite as depicted by previous studies), which might shed light on these hydrothermally-altered younger granites as a new potential source for Nb and Ta in Egypt.

Elevating anthocyanin extraction from mangosteen pericarp: A comparative exploration of conventional and emerging non-thermal technology

Mangosteen pericarp (MP) is abundant in bioactive compounds but is often discarded as waste, leading to environmental pollution. This study compared the extraction of dried MP using maceration and high-pressure processing (HPP). HPP at 10 min (500 MPa/20 °C) resulted in the highest ACNs, total phenolic content (TPC), total flavonoid content (TFC), and antioxidant activities. It also significantly reduced residual enzyme activities (REA) of polyphenol oxidase (PPO) and peroxidase (POD) by 33.90 % and 8.27 %, respectively. Fourier-transform infrared spectroscopy (FT-IR) analysis revealed a new wavelength at 2665.25 cm−1, and scanning electron microscopy (SEM) showed significant pore formation in MP cells, indicating cell damage. HPP-10 min enhanced the extraction of bioactive compounds, which significantly elevated the thermal stability of ACNs at 60 °C. This suggests that HPP is a promising method for extracting and preserving ACNs and other bioactive compounds from dried MP, with potential applications as natural colorants.

Integration of orange peel derived carbon quantum dots with TiO2 for enhanced photocatalytic degradation of brilliant green dye

Brilliant green (BG) dye is a non-biodegradable, highly venomous and coloured pigment. BG dye possesses remarkably high visibility even at small concentration that causes diarrhea and abdominal pain in humans when being ingested. In addition, it is harmful to living organisms and polluting aquatic environments. Hence, eliminating BG dye from contaminated water is an urgent need. In this report, a photocatalyst encompasses hydrothermally prepared titanium dioxide (TiO2) integrated with orange peel derived oxygenated carbon quantum dots (O-CQDs) was developed for effective removal of BG dye. The O-CQDs were prepared using a single step eco-friendly hydrothermal process and an intense green fluorescence was observed upon exposing the O-CQDs to far UV light irradiation (254 nm). The formation of TiO2/O-CQDs nanohybrid was confirmed through UV–Visible spectrophotometer, X-ray diffraction (XRD), Raman spectroscopy, Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM) and X-ray photoelectron spectroscopy (XPS) analyses. A random distribution of spherical shaped O-CQDs on the surface of TiO2 was clearly observed in FESEM images. The carboxyl groups present in O-CQDs not only increased interlayer spacing but also led to attachment of TiO2 effectively. The TiO2/O-CQDs nanohybrid showed 94.70 % efficiency towards photocatalytic degradation of BG dye under UV light irradiation that was ∼20 % higher than the pristine TiO2 photocatalyst. The presence of O-CQDs in the TiO2/O-CQDs nanohybrid boosted the photocatalytic degradation efficiency by enhancing UV light absorption and suppressing photo-generated electron-hole recombination. The integration of agricultural waste derived carbon with TiO2 by a facile synthesis method paves a way for large scale synthesis of TiO2/O-CQDs nanohybrid, which is anticipated to broaden its application potential in environmental remediation through photocatalytic degradation of organic compounds.

Enhancing the Conductivity and Dispersion Properties of Polyaniline Using Ethyl Orange

In our research, we developed a novel one-step synthesis method for polyaniline (PANI) using the organic dye Ethyl Orange (EO). This method facilitated the formation of PANI nanorods and significantly enhanced their electrical conductivity, achieving up to 13.5 S cm−1. The structural interaction between EO and PANI was confirmed through Fourier-transform infrared (FTIR) and UV-visible (UV-Vis) spectroscopy. Notably, the inclusion of EO improved PANI's dispersion properties, resulting in a zeta potential of 34mV in water and excellent dispersibility in various organic solvents. These attributes significantly enhance the application potential of PANI nanorods, especially in protective coatings. Electrochemical impedance spectroscopy (EIS) analysis revealed that EO-PANI/WPU coatings (0.5wt% EO-PANI) exhibited exceptional electrochemical stability and corrosion resistance in a 3.5wt% NaCl solution. Specifically, the initial impedance magnitude (Zf=0.01Hz, 1010 ohms) of EO-PANI/WPU coatings was approximately two orders of magnitude higher than that of traditional WPU coatings (108 ohms). Over time, the EO-PANI coatings demonstrated higher phase angles and impedance, indicating superior electrochemical stability and protective performance.

Marine-derived magnetic nanocatalyst in sustainable ultrasound-assisted synthesis of 2,3-diphenyl-2,3-Dihydroquinazolin-4(1H)-One derivatives

This research presents a sustainable approach to fabricate iron oxide nanoparticles by employing phytochemicals derived from marine grass extract as both reducing and stabilizing agents. Formation of magnetic nanoparticles (MNPs) initially confirmed by ultraviolet–visible spectroscopy (UV–vis) showing absorption peak at 370 nm. X-ray diffraction (XRD) and transmission electron microscopy (TEM) techniques unveiled magnetic iron oxide NPs with a rod shape, an average size of 21 nm, and an inverse spinel crystal structure. The participation of organic compounds in the production and stabilization of MNPs was evidenced through Fourier transform infrared (FTIR) spectroscopy and thermogravimetric analysis (TGA). A vibrating sample magnetometer (VSM) demonstrated the magnetic properties of iron oxide NPs showing a saturation magnetization value of 21.46 emu/g. The catalytic efficiency of these marine-assisted MNPs was evaluated in a one-pot three-component reaction involving isatoic anhydride, aromatic aldehydes, and amines under ultrasonic conditions. Under optimal conditions, a low dose of 1.5 mg of biobased magnetite nanoparticles yielded dihydroquinazolin-4(1H)-One products with up to 95 % efficiency in a brief duration of 15 min at an ultrasonic power intensity of 130 W. Different directing groups were investigated, and control experiments were carried out to enhance the understanding of the reaction mechanism. The obtained results highlight the synergistic effect of marine grass-mediated magnetic nanocatalysts combined with ultrasonic-assisted synthesis in developing sustainable green methodologies in organic synthesis.

Evaluation of the reactivity of co-combustion of wheat straw and waste rubber thermolysis char

The co-combustion of wheat straw (WS) and waste rubber thermolysis char (WRTC) was examined with the perspective of utilizing WRTC as a high-calorific value fuel addition to agricultural biomass. The study investigated the effect of different proportions of WS-WRTC blends (10/15/25/49 wt% WRTC) and a maximum of 4 wt% binders, including potato starch and calcium oxide, on the reactivity of co-combustion and the distribution of products during the process. Thermogravimetric analysis with Fourier Transform Infrared Spectroscopy (TGA-FTIR) analyses was employed at a temperature range of 25–1000 ° C with a heating rate of 10 ° C/min. The kinetics of co-combustion were analyzed using the Fraser-Suzuki (FS) deconvolution method and a model-based kinetic modeling. The results indicate that a 10% addition of WRTC char reduces the intensity and rate of combustion and prolongs the combustion time. It was observed that the optimal addition to the blend is 25% WRCT, and it resulting in a reduction in activation energy and combustion indexes. However, it remains with no significant impact on process stability and efficiency. Kinetics of the decomposition of the WRTC25 mixture modeled by the deconvolution method indicates a 5-step reaction course, which is a combination of the characteristic combustion stages of both fuels. The main denoted functional group observed in the FTIR absorption spectra were C=O, C-O, O-H, and C-H related to the release of CO2, CO, H2O, CH4, aromatic compounds, and hydrocarbons.

Evaluation of cement-treated recycled concrete aggregates for sustainable pavement base/subbase construction

Rapid urbanization and population growth have caused a substantial rise in the generation of all kinds of waste globally. The use of recycled waste not only can replace the enormous volume of virgin materials used in construction but also alleviate environmental concerns by lowering landfilling loads. This study aims to evaluate the feasibility of using non-treated and cement-treated recycled concrete aggregates (RCA) in pavement base and subbase layers. A detailed study focused on the strength, durability and microstructural aspects of treated RCA. To fulfill this, experimental test program and analysis covered particle-size distribution, Los Angeles abrasion, aggregate impact value, modified Proctor compaction, unconfined compressive strength (UCS), weight loss under wet-dry cycles, and scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) analysis. The recycled aggregates are found to show excellent physical and mechanical characteristics in terms of abrasion and aggregate impact values. Cement treatment has shown to significantly enhance the strength and durability characteristics of RCA, rendering it suitable for pavement base/subbase layer application. RCA samples treated with a cement content of 3% and above (by weight) are found to satisfy the minimum specified unconfined compressive strength (UCS) values of 2MPa at 7 days of curing, according to the Texas Department of Transportation (TxDOT) and Austroads guidelines for pavement base and subbase layer applications. However, a relatively higher cement contents (5% and 7%) is required to meet the minimum 7-days UCS criterion of 3 and 4.5MPa for base layer applications of low- and high- volume roads, respectively, according to Indian road standards (IRC SP 72 (2015) and IRC 37(2018)). Cement-treated samples with 2% cement or above showed minimal weight loss after 12 alternate wet-dry cycles, which was well within the maximum permissible limit (14%) specified in various standards for stabilized materials. Additionally, microstructural investigations have clearly showed formation of hydration products corroborating the mechanism behind strength gain with time. Findings from this study provide references to promote the use of RCA in construction of pavement base and subbase layer, contributing towards the goal of net zero set by the United Nations.

Development and Characterisation of Myristic Acid-Paraffin Wax, Silica Fume and Zinc Oxide Cementitious Composites for Thermal Control in Buildings

This study focuses on the development of a cement-based phase change material (CBPCM) to improve thermal performance in construction applications. The CBPCM was synthesised by blending 90 wt% of myristic acid with 10 wt% of paraffin wax, absorbed into 10 wt% of silica fume to prevent leakage. Additionally, 5 wt% of zinc oxide was added to improve thermal conductivity. A leakage test conducted with 10 wt% of SF exhibited no signs of leakage during thermal cycling. Scanning electron microscopy (SEM) established the uniform dispersion of the nano-enhanced phase change material (NEPCM) within the cement. Fourier transform infrared spectroscopy (FTIR) analysis revealed no chemical structure changes after 100 thermal cycles. Thermogravimetric analysis (TGA) confirmed thermal stability in the temperature range of 74.8 to 236.64 °C with a mass loss of 6.3 wt%. The material demonstrated minimal variation in phase change temperatures and latent heats after 100 cycles. The latent heat of the CBPCM was 1.09 J/g during melting and 1.887 J/g during solidification. Incorporating NEPCM into the cement increased the thermal conductivity of the cement matrix to 0.559 W/m K. These findings underline the potential of the CBPCM for energy-efficient construction, offering enhanced thermal storage, stability, and conductivity.