FTIR Research Articles

Influence of physico-chemical properties of hydroxypropyl methylcellulose on quetiapine fumarate release from sustained release matrix tablets

Quetiapine fumarateis a typical antipsychotic with a short half-life of 6 h and is administered multiple times daily. In this study, a copolymer for controlled delivery of quetiapine fumarate will be developed. In order to prevent side effects and improve patient compliance, hydroxypropyl methylcellulose K15M (HPMC K15M) was included in the formulation of the quetiapine fumarate oral sustained-release tablets at a concentration of 10–30%. A series of analytical methods were used to determine the characteristics of the prepared hydrogels, including Fourier transform-infrared spectroscopy, Differential scanning calorimetry, X-ray diffraction, and Scanning electron microscope. At two different pH values (1.2 and 6.8), swelling and release studies were conducted. A variety of release kinetic models was used to study drug release mechanisms. A non-Fickian diffusion mechanism released hydrogels prepared from quetiapine fumarate. It was found that swelling was increased by increasing the amount of HPMC K15M. Compared to the other batches (10–20%), the produced tablets with 30% HPMC K15M content had a better release profile after 20 h of dissolution. Because of the effective matrix complex’s limited solubility in water, the drug diffuses through the gel layer at a steady rate rather than dissolving quickly.

An Investigation of RNA Methylations with Biophysical Approaches in a Cervical Cancer Cell Model

RNA methylation adds a second layer of genetic information that dictates the post-transcriptional fate of RNAs. Although various methods exist that enable the analysis of RNA methylation in a site-specific or transcriptome-wide manner, whether biophysical approaches can be employed to such analyses is unexplored. In this study, Fourier-transform infrared (FT-IR) and circular dichroism (CD) spectroscopy are employed to examine the methylation status of both synthetic and cellular RNAs. The results show that FT-IR spectroscopy is perfectly capable of quantitatively distinguishing synthetic m6A-methylated RNAs from un-methylated ones. Subsequently, FT-IR spectroscopy is successfully employed to assess the changes in the extent of total RNA methylation upon the knockdown of the m6A writer, METTL3, in HeLa cells. In addition, the same approach is shown to accurately detect reduction in total RNA methylation upon the treatment of HeLa cells with tumor necrosis factor alpha (TNF-α). It is also demonstrated that m1A and m6A methylation induce quite a distinct secondary structure on RNAs, as evident from CD spectra. These results strongly suggest that both FT-IR and CD spectroscopy methods can be exploited to uncover biophysical properties impinged on RNAs by methyl moieties, providing a fast, convenient and cheap alternative to the existing methods.

Chemical properties of peat micro particles modified asphalt.

This study investigated the chemical properties of peat microparticles modified asphalt (Pt.M.A.). The originality of the study resides in the examination of the chemical characteristics of peat microparticles (Pt.) modified asphalt (Pt. M.A.) utilising FTIR, SEM, SFE, and XRD methodologies. This encompasses Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), surface free energy (SFE), and X-ray diffraction (XRD). Initially, FTIR examined the functional groups of both unaltered and altered asphalt binders. The SEM images reveal improved compatibility, showcasing superior diffusion of the modifier across the asphalt. A further critical factor is that improved adhesion properties, according to the SFE study, indicate that modified binders generally offer more SFE compared to unmodified binders. The XRD measurements revealed a semi-crystalline structure in the Pt. modifier and an amorphous structure in the basal asphalt binder. The integration of Pt. into the asphalt cement resulted in modifications to the phases of both constituents, culminating in the emergence of a new semi-crystalline phase inside the modified asphalt binder. These data suggest that peat microparticles (Pt.) can improve the efficacy of asphalt binders by enhancing compatibility, adhesion, and resistance to ageing.

A semiconducting supramolecular Co(II)-metallogel based resistive random access memory (RRAM) design with good endurance capabilities.

A highly efficient approach for synthesizing a supramolecular metallogel of Co(II) ions, denoted as CoA-TA, has been established under room temperature and atmospheric pressure conditions. This method employs the metal-coordinating organic ligand benzene-1,3,5-tricarboxylic acid as a low molecular weight gelator (LMWG) in DMF solvent. A comprehensive analysis of the mechanical properties of the resulting supramolecular Co(II)-metallogel was conducted through rheological investigation, considering angular frequency and thixotropic study. The hierarchical rocky network structure of the supramolecular Co(II)-metallogel was unveiled using field emission scanning electron microscopy (FESEM). Transmission electron microscopic (TEM) analysis showed rod-shaped structures via low-magnification high angle annular dark field (HAADF) bright field scanning transmission electron microscopic (STEM) imaging, while energy dispersive X-ray (EDX) elemental mapping confirmed its primary chemical constituents. The formation mechanism of the metallogel was examined via fourier transform infrared spectroscopy (FTIR) spectroscopy. The nature of the synthesized CoA-TA metallogel was affirmed through powder X-ray diffraction (PXRD) analysis. Furthermore, this study involved fabrication of Schottky diode structures in a metal-semiconductor-metal geometry based on cobalt(II) metallogel (CoA-TA), enabling observation of charge transport behavior. Remarkably, a resistive random access memory (RRAM) device utilizing cobalt(II) metallohydrogel (CoA-TA) demonstrated bipolar resistive switching at room temperature and under ambient conditions. The switching mechanism was investigated, revealing the formation and rupture of conductive filaments between metal electrodes that govern the resistive switching behavior. This RRAM device exhibited an impressive ON/OFF ratio (~ 414) and exceptional endurance over 5000 switching cycles. These structures offer great potential for diverse applications such as non-volatile memory design, neuromorphic computing, flexible electronics and optoelectronics. Their advantages lie in their fabrication process, reliable resistive switching behavior and overall performance stability.

New Copper(I) oxide biocatalyst based on functionalized olive stone for the synthesis of 1,4-disubstituted-1,2,3-triazoles under very mild conditions

An efficient methodology for coating silanized olive stone with copper(I) oxide has been described and fully characterized using various techniques, including X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR-ATR), X-ray fluorescence (XRF), electronic microscopy, thermogravimetric analysis (TGA), moisture content, electrophoretic mobility and particle size distribution. The applicability of this new biocatalyst in the 1,3-dipolar cycloaddition click reaction between alkynes and azides has been demonstrated leading to the obtention of a great variety of 1,4-disubstituted-1,2,3-triazoles with good to excellent conversions. The new biocatalyst showed promising features in terms of recyclability and industrial or biomedical application. It could be recycled up to five times with minimal loss of catalytic activity when synthezing compound 3a-3n. Additionally, it was effective in the multi-gram scale synthesis of compounds 3b and 3e, which were tested for the first time in cells, specifically on the human fibroblast-derived M1 cell line, demonstrating that these compounds are non-cytotoxic and thus suitable for potential uses in biomedicine.

Extraction, characterization and antioxidative potentials of UV-screening compound, mycosporine-like amino acids from epilithic cyanobacterium Lyngbya sp. HKAR - 15.

Mycosporine-like amino acids (MAAs) are a unique class of UV-screening bioactive molecules with potent antioxidants and photoprotective properties, synthesized by various species of cyanobacteria in different habitats. The cyanobacterial biofilms play a crucial driver in the development of ecological communities. The current study examined the existence of the photoprotective MAAs in a novel epilithic cyanobacterium Lyngbya sp. strain HKAR-15 isolated from cyanobacterial biofilms on the rock surface. The isolated MAAs were identified, purified and characterized using UV-Vis spectroscopy, HPLC (High-Performance Liquid Chromatography), ESI-MS (Electrospray Ionization-Mass Spectrometry), FTIR (Fourier Transform Infrared Spectroscopy) and NMR (Nuclear Magnetic Resonance). The compounds were recognized as palythine (retention time (RT): 2.7min; UV λmax: 320nm; m/z: 245.02) and porphyra-334 (RT: 3.6min; UV λmax: 334nm; m/z: 347.1). FTIR spectroscopy analyses also revealed the presence of functional groups of both compounds. NMR spectroscopy analyses confirmed the presence of both palythine and porphyra-334. The UV-induced production of both MAAs was visualized under ultraviolet radiation (UVR) in contrast to the photosynthetically active radiation (PAR). The MAAs (palythine and porphyra-334) had a significant dose-dependent free radical scavenging capacity. The findings show that MAAs perform a dynamic role in the survival and photoprotection of cyanobacteria in hostile environments under high solar UV irradiances. These photoprotective compounds may have various biotechnological applications as well as role in the development of natural sunscreens.

Molecular level analysis of the influence of natural biomaterials on aviation flame retardant performance

The use of natural biomaterials in flame retardant formulations as sustainable alternatives has gained significant interest in recent years. Given the high-risk environment in which airplanes operate, aviation safety remains a top priority. Flame retardants (FRs) are crucial for preventing or reducing the spread of flames in flammable materials used in aircraft construction and interior furnishings, thus mitigating fire risks. This study aims to analyze the molecular-level influence of natural biomaterials on aviation flame retardant performance, with a focus on lignin. Lignin, a natural polymer derived from plant cell walls, offers an environmentally friendly alternative to conventional synthetic flame retardants. Lignin-based composites can be applied to various aircraft components, such as wings and fuselage. The study employs Fourier Transform Infrared Spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and Nuclear Magnetic Resonance (NMR) to investigate the molecular interactions of these biomaterials. Additionally, to assess thermal stability and degradation, Thermo-gravimetric Analysis (TGA) is utilized. The results indicate that lignin enhances flame retardancy by promoting the formation of a protective char layer and improving thermal stability. This research also provides insights into the molecular mechanisms underlying lignin’s effectiveness as a flame retardant and explores its potential in developing high-performance aircraft flame retardants.

Standardization of FTIR-Based Methodologies for Microplastics Detection in Drinking Water: A Meta-Analysis Indeed and Practical Approach

The detection of microplastics (MPs) in drinking water presents significant environmental and public health challenges. This study comprises two stages: a meta-analysis aimed at standardizing Fourier Transform Infrared Spectroscopy (FTIR) methods for MP detection, followed by the practical implementation of these findings in the laboratory. The review of studies conducted from 2019 to 2023 identifies 0.45 μm cellulose nitrate filters and Nile red staining as the most effective techniques for fluorescent detection. Experimental results demonstrate the superior retention capabilities of cellulose nitrate filters and the uniformity of Nile red staining. This dual approach not only optimizes water treatment processes but also enhances the accuracy of MP detection. The findings contribute to improved water quality management and public health protection by establishing robust protocols for MP analysis.

Non-standard adhesives for wood-based composites: powder adhesives and bicomponent fibers

Powder adhesives and bicomponent fibres are widely used for composite manufacturing; mainly, they are used for glueing fibres during non-woven production. However, in the woodworking industry, they are rarely used. This study aims to investigate the possibility of powder adhesive and bicomponent fibres utilisation for gluing wood. For this purpose, epoxy-polyester powder adhesive and polyester (PES) bicomponent fibres were selected, and one-component moisture-curing polyurethane adhesive was used as a reference. The selected wood species were spruce, beech, oak and wenge. The differences between powder adhesive- and bicomponent fibre-glued wood joints were observed using scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDX). Mechanical properties of glued wood joints were characterised by tensile shear strength and modelled using finite element modelling (FEM). The adhesives were further characterised using Fourier-transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC). The wood joints produced by all combinations of selected wood species and adhesives were comprehensively characterised. The highest values of tensile shear strength were reached by powder epoxy-polyester adhesive (14.85 MPa), whereas joints bonded by bicomponent fibres (5.19 MPa) reached lower values than reference samples.

Design and synthesis of glycofullerene derivatives as novel photosensitizer for potential application in PDT to treat cancer

Cancer is one of the most aggressive diseases known to humanity, characterized by low survival rates and poor prognoses. Currently, platinum-based anticancer drugs and traditional photosensitizers used in photodynamic therapy (PDT) are the most widely employed treatment modalities. However, the platinum-based medications, particularly cisplatin, the most commonly used agent, have several drawbacks. These drawbacks may include systemic toxicity, which can manifest as nephrotoxicity, neurotoxicity, ototoxicity, or emesis during treatment. Such side effects can severely impair patients and significantly diminish the overall effectiveness of therapeutic interventions. In contrast, photodynamic therapy does not present these disadvantages. PDT offers numerous benefits, including reduced long-term morbidity, minimal systemic toxicity, low invasiveness, negligible drug resistance, and temporal and geographic selectivity, all of which enhance patients' quality of life. Consequently, the search for novel, effective, and practical photosensitizers is essential. Fullerenes possess unique physicochemical properties that make them highly suitable as photosensitizers. In this study, we developed a comprehensive and straightforward synthesis for two water-soluble sugar fullerene derivatives, designated as 12 and 13. Multiple analytical techniques, including 1H NMR, 13C NMR, high-resolution mass spectrometry (HRMS), Fourier-transform infrared spectroscopy (FT-IR), and ultraviolet–visible (UV–Vis) spectroscopy, collectively confirmed the chemical structures of these derivatives and validated their successful synthesis. Upon exposure to white light irradiation at an intensity of 2.5J/cm2, compound 13 demonstrated significant biological activity against three distinct tumor cell lines: HepG2, MKN45, and RPMI 4788, with IC50 values of 5.65 μM, 2.43 μM, and 1.82 μM, respectively. This study establishes a foundation for the development of innovative clinical photosensitizers.

Paper‐based sensors for real‐time cure monitoring in the production of glass fiber‐reinforced phenol‐formaldehyde composites for aerospace interiors

AbstractThe aerospace industries demand for advanced materials necessitates stringent quality control measures, particularly for composite structures to ensure optimal curing and structural integrity. Traditional methods like differential scanning calorimetry (DSC) and dynamic mechanical analysis, while useful, are limited to laboratory settings. This study explores the use of a printed paper‐based sensor for real‐time cure monitoring of glass fiber‐reinforced phenol‐formaldehyde (PF/GF) prepregs. The sensor, composed of a cellulose paper substrate with screen‐printed electrodes, offers flexibility, ease of integration, and cost‐effectiveness compared to commercial polymer‐based dielectric sensors. Real‐time monitoring with the printed paper‐based sensor was conducted at temperatures ranging from 130 to 180°C, both with and without pressure, and validated against DSC and Fourier‐transform infrared (FTIR) spectroscopy. The results showed a strong correlation between real‐time monitoring and the DSC prediction model, as well as FTIR spectroscopy. Notably, the real‐time monitoring revealed a shorter curing cycle on the production line than the predicted cure kinetic model, which is crucial for large‐scale production, such as fabricating honeycomb panels for aircraft interiors. This research underscores the importance of innovative sensor technologies in improving quality control and manufacturing efficiency in aerospace composites.Highlights Cure Monitoring of PF‐based prepregs was carried out using paper‐based sensor. Sensor offered reproducibility and seamless integration in composites. Sensor data showed a strong correlation with DSC and FTIR spectroscopy results. Paper sensors enable online monitoring of composite in aerospace manufacturing.

Eco-friendly high microporosity low temperature plasma exposed activated carbon from coconut shell for nano hybrid supercapacitors

Abstract This study looked at the structural, chemical, and electrochemical properties of coconut shell activated carbon (CSAC) before and after plasma treatment. Structural analysis using x-ray diffraction (XRD) demonstrated that plasma treatment improves graphitic structure by plans at (002) and (101) for higher angles. Chemical investigation utilizing Fourier-transform infrared spectroscopy (FTIR) revealed an increase in hydroxyl groups and carboxylic content following plasma treatment, which enhances electrochemical performance. Raman spectroscopy revealed a drop in the ID/IG ratio from 1.00 to 0.90, indicating enhanced graphitic order. Scanning electron microscopy (FESEM) showed that plasma treatment improves surface shape, while elemental analysis assessed the high carbon content (76.56% by weight). Contact angle measurements showed a decrease from 114° to 65°, showing improved hydrophilicity after treatment. Electrochemical investigation shows that the plasma-treated CSAC had a maximum specific capacitance of 1612 F g−1, compared to 729 F g−1 for the untreated CSAC, and a total capacitance of plasma treated1685 F/g are untreated 1400 F g−1. A Type II+III pattern on the isotherms implied capillary condensation in mesopores. The plasma treatment indicated improved porosity and potential adsorption capacity by increasing the specific surface area and decreasing the average pore width. The cyclic stability tests indicated that the plasma-treated CSAC retained 94% capacitance and 98% coulombic efficiency after 3000 cycles, which is superior to the untreated CSAC’s 92% capacitance retention and 95% coulombic efficiency. This reveals that plasma-treated CSAC has significantly improved performance and stability, making it an excellent alternative for high-performance and cost-effective energy storage applications.

Observing super-coarse carbonaceous aerosol particles containing chloride in a tropical savanna climate at an agro-forest site in Thailand.

Coarse aerosol particles containing chloride in tropical forests are significant for understanding biogeochemical cycles and atmospheric processes, with implications for environmental health and climate change mitigation. This study explored the sources of super-coarse carbonaceous aerosol particles containing chloride in a tropical savanna climate. Aerosol samples were collected from an agro-forest site in Thailand during the dry season and analyzed using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and Fourier-transform infrared (FTIR) spectroscopy. By examining the morphology and elemental compositions of individual aerosol particles, along with employing Positive Matrix Factorization (PMF) and backward trajectory analysis, potential sources were identified. The findings revealed two primary sources for the super-coarse aerosol particles: a mixture of biomass burning smoke and inorganic salts (likely from saline soil and sea salt), as well as halophilic fungal spores. FTIR analysis indicated the presence of compounds linked to biomass burning and clay minerals, influenced by prevailing northeast and southeast winds. Recommendations for future research include continued monitoring, correlation with meteorological parameters, and the application of transmission electron microscopy (TEM) for more detailed visualization and confirmation of aerosol sources.

Expansion in low calcium fly ash-based geopolymer concrete: chemical factors influenced by silica fume and NaOH concentration

Geopolymer technology offers a sustainable alternative to energy-intensive cement production, potentially reducing dependence on natural resources and mitigating environmental impact. Silica fumes (SF) are mostly used to enhance the fresh, hardened, and durable performance of geopolymers. However, their influence on geopolymerization may result in the expansion of the geopolymer mortar (GPM) due to reaction with alkaline liquid. In this study, the effect of NaOH concentration, particle size and dosage of SF, alkaline liquid-to-binder ratio, Na2SiO3-to-NaOH ratio, and sand-to-binder ratio on the expansion behavior of a low calcium fly ash (FA)-based GPM was investigated. FA-based GPMs were tested using two distinct SFs with varying particle sizes (SF1 = 9.5 µm and SF2 = 16.2 µm) and two varying dosages of SF (2.5% and 5%). Physical observations of GPMs revealed that NaOH concentration, particle size and dosage of SF are crucial factors that significantly impact the expansion which is concomitant with a reduction in compressive strength. Analytical techniques such as X-ray diffraction (XRD), Rietveld analysis, Fourier transform infrared spectroscopy (FTIR), and Thermo Gravimetric Analysis (TGA) were employed to comprehensively investigate reaction product(s) that led to the expansion of such GPMs. The chemical analysis confirmed the presence of excess analcime in the mortars fabricated by blending SF1 and FA at 12 M NaOH concentration. This study is the first to report the expansion of low calcium FA-based GPMs blended with a SF of particle size 9.5 µm. These findings emphasize the significance of selecting the appropriate SF particle size to prevent expansion and ensure optimal compressive strength in geopolymer applications.

Mechanical properties of poly(ethylene succinate) thin films incorporated with chemical synthesis copper oxide nanoparticles

This study investigates the synthesis and characterization of poly(ethylene succinate) (PES) thin films and their composites with copper oxide (CuO) nanoparticles. CuO nanoparticles were synthesized using a chemical synthesis method, achieving an average size of 20 nm. PES/CuO composites were prepared by incorporating CuO at various concentrations of 0, 1, 3, and 5 wt%. The thin films were produced through solution polymerization followed by casting. Mechanical testing revealed that the tensile strength of pure PES was 25 MPa, while incorporating 1 wt% CuO increased the tensile strength to 30 MPa. At 3 wt%, the tensile strength reached 35 MPa, and at 5 wt%, it peaked at 40 MPa, demonstrating a significant enhancement in mechanical properties. The elongation at break also improved, increasing from 200% for pure PES to 250% for the 5 wt% CuO composite. Characterization of the materials was performed using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) to analyze structural and morphological properties. The results confirm that the PES/CuO composites exhibit enhanced mechanical properties, indicating their potential for diverse applications in sustainable materials and biomedical fields.

Green chemistry approach to synthesize titanium dioxide nanoparticles using Fagonia Cretica extract, novel strategy for developing antimicrobial and antidiabetic therapies

Abstract This groundbreaking study explores the eco-friendly production of titanium dioxide nanoparticles (TiO2 NPs) to investigate their impact on health. TiO2 NPs were synthesized utilizing a plant extract from Fagonia cretica, acting as both stabilizers and reducers. Various techniques, including energy dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), UV-Vis, and X-ray diffraction (XRD), were employed to analyze the synthesized TiO2 NPs. FT-IR revealed functional groups crucial for nanoparticle (NP) formation. SEM confirmed the particle size of synthesized TiO2 NPs, ranging from 20 to 80 nm. XRD analysis highlighted the rutile phase crystalline structure, and EDX determined the elemental composition of TiO2 NPs. These NPs displayed potent antimicrobial properties, proving toxic to bacterial and the fungal strains at 50 µg·mL−1 concentration. Impressively, TiO2 NPs showcased significant antidiabetic effects in adult male albino mice, effectively reducing Streptozotocin-induced hyperglycemia and hypercholesterolemia by the improvement in behavior via random blood glucose, triglyceride, low density lipoproteins, high density lipoprteins, very low density lipoproteins, and GTT pathway at 100 and 200 µL. Furthermore, they exhibited a remarkable impact on human liver cancer cell lines, with a 43.2% reduction in cell viability at 100 µg·mL−1 concentration. In essence, the study highlights TiO2 NPs as a safe, natural therapeutic agent with immense potential in diabetes treatment. The MTT assay was utilized to assess their cytotoxicity and biocompatibility, affirming their promising role in healthcare.

Synthesis of Fe3O4 Derived from Acid Mine Drainage (AMD) Sludge and Catalytic Degradation of Tetracycline.

Acid mine drainage (AMD) sludge is waste generated in the process of acid mine wastewater treatment, and the use of AMD sludge to prepare Fe3O4 to activate H2O2 degradation pollutants is an effective means of resource utilization. In this study, the heterogeneous catalyst Fe3O4-based composites were synthesized by a one-step method using AMD sludge as a raw material, and the Fe3O4-based materials before and after catalysis were characterized by powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The effects of several key factors (pH values, H2O2 content, TC concentration, and Fe3O4 content) of tetracycline (TC) degradation were evaluated. The results revealed that the TC removal rate reached up to 95% within 120 min under optimal conditions (pH 3; H2O2, 5 mmol/L; TC concentration, 25 mg/L; Fe3O4 content, 1g/L). Moreover, •OH and •O2- radicals were generated during the Fenton-like degradation process, and the plausible degradation mechanism was discussed. Besides, the Fe3O4 catalyst exhibited fantastic stability after five cycles. In conclusion, this study is expected to promote the resource utilization of industrial sludge and provide a new material for the treatment of antibiotic-contaminated wastewater.

Revealing Active Sites and Reaction Pathways in Direct Oxidation of Methane over Fe-Containing CHA Zeolites Affected by the Al Arrangement.

Fe-containing zeolites are effective catalysts in converting the greenhouse gases CH4 and N2O into valuable chemicals. However, the activities of Fe-containing zeolites in methane conversion and N2O decomposition are frequently conflated, and the activities of different Fe species are still controversial. Herein, Fe-containing aluminosilicate CHA zeolites with Fe species at different spatial distances affected by the arrangement of framework Al atoms were synthesized in a one-pot manner in the presence or absence of Na. The arrangement of framework Al atoms was identified by 27Al and 29Si MAS NMR spectra and thermogravimetry-differential thermal analysis (TG-DTA) curves. Ultraviolet (UV)-vis, X-ray absorption spectroscopy (XAS), and NO adsorption fourier transform infrared spectroscopy (FTIR) spectra were adopted to analyze Fe speciation. The higher proportion of Fe species in the 6 MR of Fe-CHA zeolites in the presence of Na was confirmed by the NO adsorption FTIR spectrum. The activities of proximal and distant Fe sites in reactions including direct oxidation of methane to methanol, methanol to hydrocarbon, and N2O decomposition were compared at different temperatures to provide the corresponding active sites and reaction pathways. The distant, isolated Fe and isolated proton were more active in the direct oxidation of methane to methanol and tandem conversion of methanol to hydrocarbon reactions than the proximal, isolated Fe and paired protons, respectively. Additionally, proximal, isolated Fe sites afforded higher activity in N2O decomposition. These findings guide the design of highly active catalysts in methane oxidation, methanol to hydrocarbon, and N2O decomposition reactions, addressing energy and environmental concerns.

Potential of copper tailings as supplementary siliceous materials in the preparation of autoclaved aerated concrete

The storage of copper tailings (CT) not only consumes considerable land resources but also tends to cause a series of ecological and environmental issues. To achieve the circular economy and green industry development, CT is utilized as a supplementary siliceous material of autoclaved aerated concrete (AAC) in this study. The effects of substitution rate of CT for quartz sand are evaluated though the flow and gas-foaming properties of fresh slurry, and the physical and mechanical properties of AAC products. Meanwhile, the relationship between the macroscopic properties and hydration products is analyzed by multiple microscopic tests, including the Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). The experimental results shows that the bulk density, compressive strength and thermal conductivity of AAC incorporating CT show a trend of first decreasing and then increasing as the substitution rate of CT for quartz sand increases from 0 to 50 wt%, while the specific strength continues to decrease. When the substitution rate of CT for quartz sand is less than 40 wt%, the performances of AAC can meet the specifications of B05 A2.5 level according to Chinese national standards. These findings are closely related to the characteristics of air pore structure and the ordering, quantity and morphology of hydration products. With increasing the substitution rate of CT for quartz sand, the ordering of tobermorite gradually decreases, and its morphology transforms from plate-like to grass-like and then to needle-like, which can reduce the mechanical properties of AAC.

Photocatalytic degradation of organic dyes under sunlight using a mononuclear Zn complex-embedded-functionalized porous material.

In this study, mesoporous materials (MCM-41 and MCM-48) were synthesized and functionalized with an acid group through a post-synthetic modification method. A mononuclear Zn complex [Zn(dmp)Cl2] (dmp = neocuprine) was also prepared and incorporated into a functionalized mesoporous material. Extensive characterization of the material married was carried out using techniques such as X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) analysis, scanning electron microscopy (SEM), nuclear magnetic resonance (NMR), and Fourier-transform infrared spectroscopy (FT-IR) to evaluate the characteristics of modified materials. The characterization results revealed that the post-synthetic modification did not alter the phase purity, crystallinity, or morphology of the mesoporous materials while confirming the successful grafting of the desired sulphonic acid functionality and Zn complex. The Zn complex-grafted-functionalized mesoporous materials were then assessed for their photo-degradation using methylene blue (MB) and rhodamine B (RB). The results demonstrated exceptional photo-degradation efficiency of the modified materials under sunlight. Within 15min, 10mg/ml of dye concentration, and adsorbent dosage 0.15mg/ml and 0.1mg/ml, degradation efficiencies of 99% and 92%, were achieved for MB using M-48-S-Zn1 and M-41-S-Zn1, respectively. Similarly, 91% and 78% degradation rates were achieved within 30min for RB using the same materials. The modified mesoporous materials exhibited a remarkable degradation performance even in challenging environments, including highly acidic, basic, and salt-concentrated conditions. This highlights the versatility and robustness of the modified materials in different environmental scenarios.