Fourier Transform Infrared Spectrometer Research Articles

The critical role of organic matter for cadmium-lead interactions in soil: Mechanisms and risks

Understanding the interaction mechanisms between complex heavy metals and soil components is a prerequisite for effectively forecasting the mobility and availability of contaminants in soils. Soil organic matter (SOM), with its diverse functional groups, has long been a focal point of research interest. In this study, four soils with manipulated levels of SOM, cadmium (Cd) and lead (Pb) were subjected to a 90-day incubation experiment. The competitive interactions between Cd and Pb in soils were investigated using Fourier transform infrared spectrometer (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and X-ray adsorption near-edge structure (XANES) analysis. Our results indicate that Pb competed with Cd for adsorption sites on the surface of SOM, particularly on carboxyl and hydroxyl functional groups. Approximately 22.6 % of Cd adsorption sites on humus were occupied by Pb. The use of sequentially extracted exchangeable heavy metals as indicators for environment risk assessments, considering variations in soil physico-chemical properties and synergistic or antagonistic effects between contaminants, provides a better estimation of metal bioavailability and its potential impacts. Integrating comprehensive contamination characterization of heavy metal interactions with the soil organic phase is an important advancement to assess the environmental risks of heavy metal dynamics in soil compared to individual contamination assessments.

One-Pot Preparation of Layered Double Hydroxide-Engineered Boric Acid Root and Application in Wastewater.

Heavy metals and organic pollutants are prevalent in water bodies, causing great damage to the environment and human beings. Hence, it is urgent to develop a kind of adsorbent with good performance. Anion interlacing layered double hydroxides (LDHs) are a promising adsorbent for the sustainable removal of heavy metal ions and dyes from wastewater. Using aluminum chloride, zinc chloride and ammonium pentaborate tetrahydrate (NH4B5O8 · 4H2O, BA) as raw materials, the LDHs complex (BA-LDHs) of B5O8- intercalation was prepared by one-step hydrothermal method. The BA-LDHs samples were characterized by a X-ray powder diffractometer (XRD), scanning electron microscope (SEM), Fourier transform infrared spectrometer (FT-IR) and the Brunauer-Emmett-Teller (BET) method. The results showed that B5O8- was successfully intercalated. Adsorption experimental results suggested that BA-LDHs possess a maximum adsorption capacity of 18.7, 57.5, 70.2, and 3.12 mg·g-1 for Cd(II), Cu(II), Cr(VI) and Methylene blue (MB) at Cs = 2 g·L-1, respectively. The adsorption experiment conforms to the Langmuir and Freundlich adsorption models, and the kinetic adsorption data are well fitted by the pseudo-second-order adsorption kinetic equation. The as-prepared BA-LDHs have potential application prospects in the removal of heavy metals and dyes in wastewater. More importantly, they also provide a strategy for preparing selective adsorbents.

Keratin hydrolysate as a chrome exhaust aid and keratin filler in leather processing: A cleaner technology approach for tannery solid waste management and leather manufacturing

Hair burning unhairing and dampening of tannery wastes during the hair-saving unhairing process are becoming significant problems in the tanning industry. Therefore, this research article focuses on the extraction of keratin hydrolysate (KH) and its application as a chrome exhaust aid and keratin filler in leather manufacturing process. The structure, morphology and functional groups of the extract were examined using X-Ray Diffractometer (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectrometer (FTIR), respectively. To study and contrast the degree of improvement in chromium uptake, the KH solution was applied both before tanning on the pickled pelt and after tanning during basification. The thermal stability, physical strength characteristics and organoleptic properties of the leathers obtained were characterized. Furthermore, the environmental impact of the tanning system was assessed through a comparative analysis of the spent liquors. Finally, experimental retanning process was conducted to replace the commercial protein filler (Celatan F: 50, 75, and 100 %) with KH solution, with concurrent processing of control leather using conventional chrome tanning agent at 6 % dosage of chromium. The FTIR analysis of the extract confirmed the presence of alkyl side chains of amino acids as well as carboxylic, amide, carboxyl group and aldehyde functional groups at 1400-1700 cm−1,3,303.46 cm−1,3270 cm−1 and 2752 cm−1, respectively. XRD spectrum showed two diffraction peaks at 2 theta values of 9.36° and 21.16°, respectively. Leathers with improved mechanical strength, organoleptic properties and thermal stability were obtained with 100 % substitution of Celatan F at pH 6 and 10 % chromium dosage. It was also discovered that the shrinkage temperature of the experimental leather was enhanced to more than 105 °C. Environmental impact evaluation on the spent liquor showed that the complete replacement of Celatan F with KH solution brought about a notable decrease in COD and TDS in the spent liquor. The extraction and application of tannery hair waste-based keratin hydrolysate as an efficient, environmentally friendly chrome exhaust aid and keratin filler has been attempted and established in this research article.

Characterisation of finger millet (Eleusine coracana) starch isolated by conventional and ultrasound‐assisted starch isolation methods

SummaryStarch is a versatile biomaterial with a wide range of applications across various industrial sectors. Therefore, starch isolation methods play a crucial role in fulfilling the demand for high‐quality starch required for different applications. Waxy maize starch is the most used starch for different food applications. It is isolated using an alkaline extraction method and available in the market at a high price. The traditional process of starch isolation involves labour‐intensive and costly downstream processing that leads to exploring cost‐effective isolation methods for various food applications. Finger millet (Eleusine coracana) is an underutilised cereal crop composed of 65–70% of starch. In the present study, the starch from finger millet is isolated using conventional and ultrasound‐assisted isolation methods to fulfil the current requirement. The isolated finger millet starch was characterised by morphological structure obtained by scanning electron microscopy (SEM), X‐ray diffractogram (XRD), infrared spectrum obtained by Fourier transform infrared spectrometer (FT‐IR), differential scanning calorimetry (DSC) analysis, and rheological analysis. The SEM images confirmed the reduced particle size and uniform grain size distribution in the starch isolated using ultrasound‐assisted isolation. The relative crystallinity of starch isolated using ultrasound‐assisted isolation method (69.05 ± 0.57%) was higher compared to other conventional isolation methods (57.18 ± 0.70%, 67.66 ± 1.00%, and 68.34 ± 0.33% for distilled water soaking, alkali soaking, and sodium bisulphite soaking, respectively). The FTIR analysis confirmed no significant changes in the functional group of starch with respect to different isolation methods. Thermal and rheological analysis of isolated starch using ultrasound‐assisted isolation indicated the lowest gelatinisation enthalpy (45.38 ± 1.67 J/g) and showed the lowest loss factor indicating the most elastic behaviour, respectively.

A new strategy to prepare ammonium aluminum carbonate hydroxide using plasma electrolytic oxidation in electrolyte containing carbon nanotubes

In this work, a plasma electrolytic oxidation (PEO) technique was used to prepare ammonium aluminum carbonate hydroxide (AACH) in an electrolyte containing carbon nanotubes (CNTs). CNTs were also involved in the composite coating on the surface of 6063 aluminum alloy. The formation mechanism of AACH and effects of CNTs on the microstructure and corrosion behavior of the PEO coatings were investigated. The surface morphology, pore distribution, phase composition, functional groups and electrochemical characteristics of the PEO composite coatings were examined using scanning electron microscopy (SEM), Image Pro software, X-ray diffractometer (XRD), Fourier transform infrared spectrometer (FT-IR) and electrochemical workstations, respectively. Results showed that the rod-like AACH was generated around the discharge channel by reacting between ammonia, carbon dioxide and AlOOH under transient high temperature and high pressure environment with the presence of CNTs. The surface micropores of the composite coatings were enlarged due to the excellent electrical conductivity of CNTs. With the by addition of CNTs of 1.5 g/L, the self-corrosion current of the coating was the smallest, and the polarization resistance Rp was larger than that of 1.0 g/L and 2.0 g/L CNTs.

Synthesis of Low-Silicon X-Type Zeolite from Lithium Slag and Its Fast Exchange Performance of Calcium and Magnesium Ions.

Without the addition of silicon and aluminum sources, a pure-phase KNaLSX zeolite was successfully synthesized from the residue (lithium slag), which was produced from spodumene in the production process of lithium carbonate. The KNaLSX samples were characterized by an X-ray Diffractometer (XRD), Scanning Electron Microscope (SEM), X-ray Fluorescence Spectrometer (XRF), Thermogravimetric Differential Thermal Analysis (TG-DTA), Fourier Transform Infrared Spectrometer (FT-IR), and N2 adsorption measurement. The ion exchange capacity and the ion exchange rate of calcium and magnesium ions were measured as used for a detergent builder, and the results were compared with the standard zeolites (KNaLSX and 4A). The experimental results show that the pure-phase KNaLSX synthSynthesis and characterization of co-crystalline zeolite composite of LSX/esized from lithium slag has a SiO2/Al2O3 ratio of 2.01 with a grain size of 3~4 μm, which is close to the commercial KNaLSX sample of a SiO2/Al2O3 ratio of 2.0. The BET-specific surface area of KNaLSX is 715 m2/g, which is larger than the low-silicon X-type zeolite (LSX) synthesized from waste residue reported in the literature. The ion exchange rate constant of calcium and magnesium ions in KNaLSX is 5 times and 3 times that of 4A zeolite, respectively. KNaLSX also has a high ion exchange capacity for magnesium ion of 191 mgMgCO3/g, which is 2 times than that of 4A zeolite, and a high ion exchange capacity for calcium ion of 302 mgCaCO3/g, which meets the first-grade standard of zeolite for detergent builders in China. The work provides the basis for high-value resource utilization of lithium slag and the development of a detergent builder for rapid washing.

Synthesis of platinum-nickel nanoparticles supported by carbon and titanium oxide structures for efficient and enhanced formic acid oxidation

In this study, Platinum Nickel (PtNi) nanoparticles was synthesized using the chemical reduction method and functionalized multi-walled carbon nanotube (f-MWCNT) was synthesized by handling multi-walled carbon nanotube (MWCNT) with weak acid using the arc discharge method. To be evaluated in formic acid oxidation, f-MWCNT supported by PtNi (PtNi@f-MWCNT) and titanium oxide (TiO2) supported by PtNi (PtNi@TiO2) catalysts were synthesized using chemical reduction method. The comparison of PtNi, PtNi@f-MWCNT, and PtNi@TiO2 catalysts obtained in the study for formic acid oxidation is presented and their characterizations were carried out by X-ray Diffraction (XRD), Transmission Electron Microscope (TEM), and Fourier Transform Infrared Spectrometer (FTIR). According to TEM results; PtNi, PtNi@f-MWCNT, and PtNi@TiO2 particle sizes were found to be 12.00 nm, 7.37 nm, and 5.38 nm, respectively. According to the CV results obtained for formic acid oxidation, the anodic peak peaks for PtNi, PtNi@f-MWCNT, and PtNi@TiO2 were 61.20 mA.cm−2, 80.17 mA.cm−2 and 65.07 mA.cm−2, respectively. These results showed that the addition of f-MWCNT and TiO2 support exhibited 1.30 and 1.06 times higher electrocatalytic activity for formic acid oxidation and higher resistance to CO poisoning with If/Ib ratios of 0.97 and 1.48, respectively. With the long-term stability tests obtained, it was observed that the f-MWCNT-supported catalyst showed approximately 9 times more current at the end of 5000 s and provided faster charge transfer with EIS. These findings demonstrated that a more cost-effective catalyst with high electrocatalytic activity was synthesized by obtaining f-MWCNTs from MWCNTs using the arc discharge method. It has also been revealed that TiO2 and f-MWCNT supports exhibit very high potential for fuel cell applications.

Bioethanol Production from Spirulina (Arthrospira platensis) by Microwave-Assisted Acid Hydrolysis Pretreatment

The world's high consumption of fossil energy increases carbon dioxide (CO2) emissions. The depletion of fossil fuel sources, combined with rising CO2 emissions, has prompted intensive research into renewable energy sources. Bioethanol is an environmentally friendly energy source that has the potential to reduce reliance on gasoline. Bioethanol is produced through the fermentation of monosaccharides. The first and second generations of bioethanol are derived, respectively, from food crops, agricultural waste, and plantations, while the third generation is derived from algae. However, the third generation bioethanol research is still being conducted intensively to develop an optimal process. Macro/microalgae are low-level plants that have the potential to become raw materials for bioethanol. Arthrospira platensis, a spirulina species, is a microalgae with a high carbohydrate content. Apart from that, this type of microalgae is easy to cultivate and grow. This research aims to determine the reducing sugar content which are monosaccharides produced from acid hydrolysis using a microwave at a temperature of 100 °C for 60 – 120 minutes with 0.2 M H2SO4 as the solvent. The hydrolysate obtained was then fermented anaerobically with Saccharomyces cerevisiae in a shaking water bath. The High Performance Liquid Chromatography (HPLC) test was carried out to identify the reducing sugar groups in the hydrolysate. Moreover, the solid content of the biochar remaining from the hydrolysis process was analyzed using Fourier-Transform Infrared Spectrometer (FTIR). From the test results, it was found that the highest concentration of D-glucose (1.19 g/L) occurred at 90 minutes of the hydrolysis. In addition, the hydrolysis of microalgae was also carried out with 0.3 M H2SO4 solvent for 90 minutes. The hydrolysate was then fermented for 96 hours. From the distillation process, it was obtained a bioethanol yield of 2.89%.

The dyeing properties of alginate/lyocell blended fabric with reactive dyes

The difficulties in dyeing have significantly limited the application of alginate fibers in the field of textile industry. This study aimed to provide a dyeing method suitable for alginate fibers with reactive dyes. The results showed that alginate fibers could be successfully dyed with Reactive Red 195, Reactive Blue 19, and Reactive Yellow 145. Scanning Electron Microscope (SEM), Fourier Transform Infrared Spectrometer (FTIR), and fiber strength were investigated and found that dyed alginate fibers can keep their original structure and physical properties well. Colorfastness was also evaluated, which proved that dyed alginate fibers could maintain their color after soap washing, rubbing, and solarization to some extent. In order to further explore the applicability of the dyeing method, alginate fibers and lyocell were blended at 20/80 ratio to make yarns, knitted into weft plain fabrics, and carried out in the same way. The leveling property of dyed blended fabrics was good, for there was almost no color difference in naked eye observation. The washing and light fastness of blended fabrics were excellent, up to 4–5, while the rubbing fastness was slightly poor due to the fibrination of lyocell possibly. The weight loss rate of alginate fibers was less than 5%, which once again confirmed the dyeing method has less damage to alginate fibers. In addition, tensile strength of dyed blended fabrics was improved. This study can provide a new reference for alginate fiber dyeing.

Synergy of devulcanized rubber and rock asphalt for asphalt modification

Rock asphalt (RA) has gradually been recognized as a green and efficient asphalt modifier. However, the weakness of low-temperature performance and fatigue resistance for RA modified asphalt limited its application and popularization in asphalt pavement. To overcome the above shortcomings, this study aimed to synergistically apply devulcanized rubber powder (DRP) with American rock asphalt (ARA) for asphalt modification. Multiple experiments such as dynamic shear rheology (DSR) and bending beam rheology (BBR) were conducted to evaluate the rheological properties and road performance of composite modified asphalt (CMA). Cigar tube test (CTT) was applied to assess storage stability of CMA. In addition, Fourier transform infrared spectrometer (FTIR) and microscopic test (MT) were used to investigate the modification mechanisms. The results showed that CMA modified by DRP and ARA exhibited comparable storage stability, low-temperature performance and rutting resistance as SBS modified asphalt. ARA tended to cause aging problems of asphalt, but the addition of DRP effectively improved the aging resistance performance of modified binder blends, especially long-term aging resistance. The mixing of DRP, ARA and base asphalt is a physical process without chemical reactions. Even though the ash in ARA slightly lowered its storage stability, it significantly improved dispersion and homogenous interface of DRP in asphalt.

Phytochemical Investigation and Characterization of Azadirachta Indica-Mediated Silver Nanoparticles and Their Potential as Antibacterial and Antidiabetic Agents

In this study, we report the synthesis of silver nanoparticles (AgNP’s) by reducing silver ions from a solution of silver nitrate with an aqueous extract from Azadirachta indica. Using silver ions as the catalyst, nanoparticles were formed in 8[Formula: see text]min without the use of toxic chemicals. As evidenced by UV-vis spectroscopy, a broad surface plasmon resonance spectrum at 225[Formula: see text]nm was detected, which indicates the colloidal solution of silver nanoparticles is stable and produces silver nanoparticles. As revealed by the fourier transform-infrared spectrometer (FTIR) analysis, the flower extract contained a variety of biomolecules that acted as capping and reducing agents for the synthesis of AgNPs. As determined by X-ray diffraction (XRD), silver nanoparticles displayed a crystalline structure and ranged in size from 18 to 39[Formula: see text]nm. In addition to these findings, transmission electron microscopy (TEM) images showed that the silver nanoparticles were spherical and rod-shaped, as confirmed by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDAX). A variety of pathogenic bacteria, such as Klebsiella pneumoniae, Escherichia coli, Bacillus subtilis and Staphylococcus aureus, were tested against AgNP’s antibacterial properties. A significant inhibition zone was observed for Escherichia coli when AgNPs were applied at different concentrations. Silver nanoparticles were shown to have antidiabetic effects through a diphtheria assay with inhibition rates ranging from 31.09% to 83.33% for concentrations of 50–250[Formula: see text][Formula: see text]g/mL. As researchers seek natural sources of compounds with potential health benefits, silver nanoparticles were also investigated for their antioxidant properties.

Tilted fiber Bragg grating sensor based on surface plasmon resonance and electrospinning for glucose detection

A tilted fiber Bragg grating (TFBG) sensor based on surface plasmon resonance (SPR) with electrospinning nanofibers was proposed for the precise detection of glucose. In this design, a 50 nm thick gold film was deposited on the surface of a 10° TFBG. Polyacrylonitrile (PAN) nanofibers were wrapped around the sensor through electrospinning, subsequently serving as a scaffold for the immobilization of glucose oxidase (GOD). Within the dynamic range of 100–500 mg/dL glucose concentrations, the sensor exhibited good response and worked effectively. The experimental results show that the sensitivity and limit of detection (LOD) of the sensor are 12.42 pm/(mg/dL) and 100 mg/dL. Furthermore, the structural characterization was carried out using atomic force microscopy (AFM), scanning electron microscopy (SEM), and Fourier transform infrared spectrometer (FTIR). This sensor exhibits outstanding stability and high sensitivity, providing a new method for diabetes detection.

Combining metabolomics and transcriptomics to analyze key response metabolites and molecular mechanisms of Aspergillus fumigatus under cadmium stress

The co-cultivation of fungi with microalgae facilitates microalgae harvesting and enhances heavy metal adsorption. However, the mechanisms of fungal tolerance to cadmium (Cd) have not yet been studied in detail. In this study, functional groups of fungi were analyzed under Cd stress using Fourier transform infrared spectrometer (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), and transmission electron microscope (TEM) to explore their morphology. Confocal laser scanning microscope (CLSM) was used to characterize the changes in the content of extracellular polysaccharides and proteins, and a decrease in the ratio of glutathione (GSH) to oxidized glutathione (GSSG) was monitored. The GSH and GSSG contents in mycelium were 7.4 and 7.9 times higher than that in the control, respectively. After 72 h of Cd treatment, the fungal extracellular polysaccharide and extracellular protein contents increased by 16 and 11.4 mg/g, respectively, compared to the control. This provided several functional groups for the complexation of Cd ions to enhance fungal Cd tolerance. The metabolomic and transcriptomic results revealed a total of 358 differential metabolites after 20, 48, and 72 h in the positive and negative ion modes, and the number of differential metabolites specific to each group was 104, 14, and 89, respectively. There were 927, 1167, and 1287 up-regulated genes, and 1301, 1480, and 1683 down-regulated genes at 20, 48, and 72 h, respectively. Energy metabolism, amino acid metabolism, and the ABC transport system are the key metabolic pathways for tolerance enhancement and heavy metal detoxification in fungi. The expression of S-cysteinosuccinic acid was significantly up-regulated after Cd stress and associated with enhanced fungal tolerance and resistance to Cd.

Development of novel composite materials containing rice bran wax and waste polyethylene for neutron shielding applications

Neutrons are utilized in diverse fields, such as physics, biology, chemistry, geology, agriculture, medicine, mining, military, and space research. Neutrons interacting with human tissues and cells can cause harm to soft tissues, such as the cornea, and alter cell functionality, leading to the cessation of cell proliferation and resulting in cell/tisssue damage or cancers. Effective protective materials are necessary to enable the safe use of neutrons in these applications. In this study, several samples of novel types of composites were prepared by blending rice bran wax (RBX) with recycled polyethylene (rPE) at five different ratios ranging from 0% to 50%. The RBX in the composites enhances their neutron absorption capacities and while the rPE in the composites reduce their costs. Several essential fast neutron shielding parameters, such as half-value layer, effective removal cross-section, mean free path, and neutron transmission ratio, were calculated with Monte Carlo simulation GEANT4 code. Absorbed dose amount by the samples were determined using a241Am-9Be neutron source. The theoretical and experimental values of the shielding capacities of the novel composites were compared with those of paraffin and traditional concrete. Compared with the reference samples, the new RBX composite samples had higher neutron radiation absorption capacities. The functional groups of the RBX and rPE were identified using Fourier transform infrared (FTIR) spectrophotometry (Bruker Vertex 70v FTIR spectrometer with the attenuated total reflection (ATR) module) in the spectral area of 400–4000 cm−1 with 32 scans. The thermal chareteristics of the samples were determined with the differential scanning calorimeter Mettler-Toledo/DSC1/700. The developed composite materials are useable as protective material against neutron radiation in radiation settings, such as radiotherapy rooms, within and outside nuclear power plants, as well as in settings involving the storage or transportation of radioactive waste.

Synthesis and evaluation of oleic acid‐derived hyperbranched polyester as an efficient plasticizer for PVC

AbstractIn response to the health and environmental concerns associated with the plasticizer dioctyl phthalate (DOP), this research explores the utilization of methyl oleate (MO) derived from plant oil, 1,2,4‐Benzeneticarboxylic anhydride (TMA) and isobutyric anhydride (IA) as a precursor for synthesizing a hyperbranched polyester named IA‐MO‐TMA. This polyester serves as an alternative plasticizer for Polyvinyl chloride (PVC). The chemical structure of IA‐MO‐TMA was thoroughly characterized using Fourier Transform Infrared Spectrometer (FTIR) and nuclear magnetic resonance hydrogen spectra, and its molecular weight was assessed. The PVC film, plasticized with IA‐MO‐TMA, underwent comprehensive testing using techniques such as differential scanning calorimetry, scanning electron microscopy, and thermogravimetric analysis. Notably, the glass transition temperature (Tg) of the plasticized PVC film exhibited a significant reduction from 75°C to −6.7°C. The plasticized film demonstrated an elongation at break of 318.1%, a tensile strength of 19.2 MPa, and a plasticizing efficiency of 109.9%. Moreover, the use of IA‐MO‐TMA as a plasticizer increased the initial decomposition temperature of PVC film from 235.6 to 264.1°C. Additionally, the extraction rate of IA‐MO‐TMA in petroleum ether was found to be 35.6% lower than that of DOP.

Bioassay-guided fractionation of Verbascum thapsus extract and its combination with polyvinyl alcohol in the form electrospun nanofibrous membrane for efficient wound dressing application

Verbascum thapsus (V. thpsus), family Scrophulariaceae, has considerable importance in traditional medicine worldwide because of its antioxidant and anti-inflammatory activities. V. thpsus was used in traditional medicines as a useful drug for lung disease, sore throat, wound healing, and treatment of whooping cough. The aim of this study was to extract of V. thpsus bioactive fraction using antibacterial assay guided fractionation methodology and develop a system based on electrospun nanofibrous membrane (NFM) that can be effective by releasing the extract of V. thapsus for antibacterial and wound healing applications. For this purpose, the fractionation of total extract was done using Liquid-Liquid extraction method. The selected fraction based on its anti-bacterial activity was then subjected to the silica gel column chromatography for further purification. Since electrospinning is an economical and relatively simple method to produce continuous and uniform nanofibers, and due to its high specific surface area, adjustable pore size, and flexibility, special attention has been paid to loaded the most effective fraction on PVA nanofibers for applications such as wound dressings. The obtained result showed that, the purified V. Thapsus extract has a concentration-dependent antimicrobial activity against Escherichia coli and Staphylococcus aureus. The phytochemically analyses of bioactive fraction by High-performance liquid chromatography (HPLC) proved the presence of 6 phenolic acids, 4-hydroxybenzoic acid, chlorogenic acid, caffeic acid, p-coumaric acid, ferulic acid, and flavonoid, rutin, as the major compounds. Also, physicochemical characterization of PVA-selected extract loaded electrospun nanofibrous membranes (NFM) were analyzed by scanning electron microscope (SEM), Fourier transform infrared spectrometer (FT-IR). MTT and hemolysis assays were done to affirm the biocompatibility of fabricated scaffolds. Release profile of extract loaded- NFM showed continues release of extract from mat during 90h. Moreover, the capability of these NFM in wound healing application was evaluated in-vitro and in-vivo. The cell viability test (MTT), cell adhesion images, antioxidant, antibacterial, hemolysis assays and in-vitro and in-vivo wound healing assays confirmed that fabricated NFM containing 5 % butanolic extract were the most biocompatible scaffold for wound dressing applications and accelerates the rate of wound closure. The obtained outcomes confirmed that V. thpsus/PVA NFM can be considered as promising scaffold for potential wound dressings.

Mechanism of polyaspartic acid as acid-base regulation depressant in reverse flotation separation of molybdenite and talc

The separation of talc and molybdenite through flotation has become a significant issue. The current inorganic and organic depressants demonstrate inadequate selectivity and limited efficacy in both positive flotation and reverse flotation of molybdenite. In this study, the utilization of the highly efficient green agent polyaspartic acid (PASP) as a molybdenite depressant was explored to investigate its pH-dependent acid-base depression mechanism. In the case of pH 4.0, molybdenite exhibited effective depression, talc was floated, PASP was desorbed at pH 10.0, and molybdenite was activated. In this study, the impact of electrostatic force on the adsorption process of PASP and examined the mechanism of PASP on molybdenite surface were studied by means of micro-flotation experiments, zeta potential measurements, analysis of solution chemistry, Fourier Transform Infrared Spectrometer (FT-IR) analysis, Ultraviolet–visible spectroscopy (UV–Vis) study, and X-ray photoelectron spectroscopy (XPS) detections. PASP produced chemisorption through the coordination of O or N atoms lone pair electrons with Mo2+ on the molybdenite surface. In this process, electrostatic repulsion determines whether the mineral can come into contact with PASP.

Flexural strength and degree of conversion of universal single shade resin-based composites

Background/purposeRecently, a group of universal single-shade resin-based composites (RBCs) has been developed to simplify the process of shade selection. Excellent mechanical and physical properties are crucial for the ultimate success and clinical longevity of restorations. Therefore, evaluating the properties of the single-shaded RBCs is imperative. This study aimed to determine the flexural strength (FS) and degree of conversion (DC) of universal single-shade RBCs. Materials and methodsIn this study, four commercial RBCs were used; three universal single-shade RBCs; Omnichroma (OC), Charisma® Diamond ONE (CD), and Vittra APS Unique (VU), and a conventional nanohybrid composite Filtek™ Z250 XT (FT) which was used as a control. Sixty composite beams and 40 composite discs were used for FS and DC, respectively. A universal test machine with a three-point bending test was used to measure the FS, whereas the DC was measured using a Fourier-transform infrared spectrometer (FTIR). Three fractured specimens from each resin composite group were qualitatively analyzed using scanning electron microscopy. ResultsANOVA was used to compare the mean values of FS and DC among the four RBCs (OC, CD, VU, and FT). Highly significant differences were observed in the mean FS and DC values (F = 673.043, p < 0.001 and F (=782.4, p < 0.0001), respectively. The highest FS was observed in the CD group, followed by FT and VU groups; the lowest value was observed in the OC group. In addition, a statistically significant difference was identified in DC values. The highest DC value was observed in VU, followed by OC and CD, and the lowest DC value was observed in FT. ConclusionUniversal single-shade RBCs demonstrated a good FS, except for OC, which exhibited a significantly low FS. The DC of the universal single-shade RBCs was higher than that of the conventional nanohybrid composite restorative material.

Performance of the silica adsorbent from snake fruit peel for removing heavy metals of Ag, Cu, Mn, and Cr in SCW

Silver crafts wastewater (SCW) typically contains environmentally harmful heavy metals, including Ag, Cu, Mn, and Cr, necessitating treatment before disposal. This study explores a promising solution using silica (SiO2) adsorbents derived from snake fruit peel through acidic activation with HCl concentrations of 2, 4, and 6 M. Qualitative analysis of the adsorbent involved Fourier-transform infrared spectrometer (FTIR) and x-ray fluorescence (XRF) techniques. XRF analysis revealed major compositions of Si (26%) and Cl (71.46%), with minor elements such as Ca (0.91%), P (0.42%), K (0.37%), Fe (0.12%), and others. FTIR analysis indicated the presence of siloxane (Si-O-Si) and silanol (Si-OH) on the adsorbent. The SiO2 adsorbent demonstrated effectiveness in removing heavy metals (Ag, Cu, Mn, and Cr) from SCW, achieving removal percentages of approximately 16.96%, 24.38%, 19.34%, and 9.82%, respectively. This research contributes to the development of an environmentally friendly approach for SCW treatment using silica adsorbents derived from agricultural waste.

Evaluation of the Effect of C9 Petroleum Resin on Rheological Behavior, Microstructure, and Chemical Properties of Styrene–Butadiene–Styrene Modified Asphalt

Understanding the modification mechanism of C9 petroleum resin (C9PR) on styrene–butadiene–styrene (SBS) polymer modified asphalt properties is of significant importance. In this paper, dynamic shear rheometer (DSR), storage stability, fluorescence morphology (FM), scanning electron microscope (SEM), Fourier transform-infrared (FTIR) spectrometer, and molecular dynamic (MD) simulation were adopted to evaluate the rheological, chemical, and microstructure molecular motion state of C9PR and SBS composite modified asphalt at different aging states. The DSR storage results indicate that the addition of C9PR could improve the high-temperature property, storage stability, and temperature susceptibility. FM and SEM results indicate that the network microstructure was enhanced and the roughness between polymer resins and virgin asphalt was improved at the microscopic scale. The MD results indicate that the heterogeneity between C9PR and SBS modified asphalt was demonstrated, and the bonding energies were enhanced with the addition of C9PR. Moreover, the FTIR results indicate that new function groups were generated in addition to C9PR. In general, the addition of C9PR is a good approach to promote high-quality polymer modified asphalt (PMA) for pavement engineering.