Raman Spectroscopy Techniques Research Articles

Evaluation of Ilex guayusa and Piper marginatum Extract Cytotoxicity on Human Dental Pulp Mesenchymal Stem Cells.

Amelogenesis imperfecta is a hereditary disorder affecting dental enamel. Among its phenotypes, hypocalcified AI is characterized by mineral deficiency, leading to tissue wear and, consequently, dental sensitivity. Excessive fluoride intake (through drinking water, fluoride supplements, toothpaste, or by ingesting products such as pesticides or insecticides) can lead to a condition known as dental fluorosis, which manifests as stains and teeth discoloration affecting their structure. Our recent studies have shown that extracts from Colombian native plants, Ilex guayusa and Piper marginatum, deposit mineral ions such as phosphate and orthophosphate into the dental enamel structure; however, it is unknown whether these extracts produce toxic effects on the dental pulp. To assess cytotoxicity effects on human dental pulp stem cells (hDPSCs) exposed to extracts isolated from I. guayusa and P. marginatum and, hence, their safety for clinical use. Raman spectroscopy, fluorescence microscopy, and flow cytometry techniques were employed. For Raman spectroscopy, hDPSCs were seeded onto nanobiochips designed to provide surface-enhanced Raman spectroscopy (SERS effect), which enhances their Raman signal by several orders of magnitude. After eight days in culture, I. guayusa and P. marginatum extracts at different concentrations (10, 50, and 100 ppm) were added. Raman measurements were performed at 0, 12, and 24 h following extract application. Fluorescence microscopy was conducted using an OLIMPUS fv1000 microscope, a live-dead assay was performed using a kit employing a BD FACS Canto TM II flow cytometer, and data analysis was determined using a FlowJo program. The Raman spectroscopy results showed spectra consistent with viable cells. These findings were corroborated using fluorescence microscopy and flow cytometry techniques, confirming high cellular viability. The analyzed extracts exhibited low cytotoxicity, suggesting that they could be safely applied on enamel for remineralization purposes. The use of nanobiochips for SERS effect improved the cell viability assessment.

Label-Free Fiber-Optic Raman Spectroscopy for Intravascular Coronary Atherosclerosis and Plaque Detection.

The rupture of atherosclerotic plaques remains one of the leading causes of morbidity and mortality worldwide. The plaques have certain pathological characteristics including a fibrous cap, inflammation, and extensive lipid deposition in a lipid core. Various invasive and noninvasive imaging techniques can interrogate structural aspects of atheroma; however, the composition of the lipid core in coronary atherosclerosis and plaques cannot be accurately detected. Fiber-optic Raman spectroscopy has the capability of in vivo rapid and accurate biomarker detection as an emerging omics technology. Previous studies demonstrated that an intravascular Raman spectroscopic technique may assess and manage the therapeutic and medication strategies intraoperatively. The Raman spectral information identified plaque depositions consisting of lipids, triglycerides, and cholesterol esters as the major components by comparing normal region and early plaque formation region with histology. By focusing on the composition of plaques, we could identify the subgroups of plaques accurately and rapidly by Raman spectroscopy. Collectively, this fiber-optic Raman spectroscopy opens up new opportunities for coronary atherosclerosis and plaque detection, which would assist optimal surgical strategy and instant postoperative decision-making. In this paper, we will review the advancement of label-free fiber-optic Raman probe spectroscopy and its applications of coronary atherosclerosis and atherosclerotic plaque detection.

A systematic study of solvation structure of asymmetric lithium salts in water

Aqueous electrolytes are promising in large-scale energy storage applications due to intrinsic low toxicity, non-flammability, high ion conductivity, and low cost. However, pure water’s narrow electrochemical stability window (ESW) limits the energy density of aqueous rechargeable batteries. Water-in-salt electrolytes (WiSE) proposal has expanded the ESW to over 3 V by changing electrolyte solvation structure. The limited solubility and WIS electrolyte crystallization have been persistent concerns for imide-based lithium salts. Asymmetric lithium salts compensate for the above flaws. However, studying the solvation structure of asymmetric salt aqueous electrolytes is rare. Here, we applied small-angle x-ray scattering (SAXS) and Raman spectroscope to reveal the solvation structure of imide-based asymmetric lithium salts. The SAXS spectra show the blue shifts of the lower q peak with decreased intensity as the increasing of concentration, indicating a decrease in the average distance between solvated anions. Significantly, an exponential decrease in the d-spacing as a function of concentration was observed. In addition, we also applied the Raman spectroscopy technique to study the evolutions of solvent-separated ion pairs (SSIPs), contacted ion pairs (CIPs), and aggregate ions (AGGs) in the solvation structure of asymmetric salt solutions.

Characterization of rice cultivars using Raman spectroscopy and multivariate analysis

Rice is a widely consumed cereal known for its high carbohydrate content and the presence of essential nutritional elements such as proteins and lipids. The previous Raman spectroscopy (RS) studies on whole brown rice kernel have only been able to partially reveal nutritional content. This study employs RS to accurately assess the nutritional profiles of forty rice cultivars in powdered form, facilitating their characterization. The combination of RS and advanced chemometric techniques enables the discrimination of rice cultivars based on key biochemical attributes, including amylose and starch content, aromatic properties, protein content, and total antioxidant capacity, resulting in an impressive accuracy rate of 73%. Significant observations in the fingerprint region included specific Raman spectral features associated with glucose ring stretching at ∼478 cm−1 and indicative stretching vibrations for glycosidic bonds and amylose structures at ∼409 cm−1, ∼439 cm−1, ∼521 cm−1, and ∼868 cm−1. Furthermore, prominent spectral bands associated with amino acids such as phenylalanine (∼1004 cm−1, ∼1580 cm−1, ∼1606 cm−1), tryptophan (∼872 cm−1, ∼1360 cm−1, ∼1543 cm−1, ∼1620 cm−1), and tyrosine (∼853 cm−1, ∼1176 cm−1, ∼1556 cm−1) were observed. Additionally, characteristic peaks related to protein content, carotenoids, and amino acids were identified at ∼1084 cm−1, ∼1111 cm−1, ∼1162 cm−1, ∼1263 cm−1, ∼1310 cm−1, and ∼1404 cm−1. These findings underscore the potential of RS as a fully automated, rapid, and accurate tool for evaluating the nutritional content of rice cultivars.

Mirror Plane Effect of Magnetoplumbite-Type Oxide Restraining Long-Chain Polysulfides Disproportionation for High Loading Lithium Sulfur Batteries.

A facile solid-state approach is employed to synthesize a novel magnetoplumbite-type oxide of NdMgAl11O19, which integrates spinel-stacking layers (MgAl2O4) with Nd-O6 mirror plane structures. The resulting NdMgAl11O19 exhibits remarkable catalytic activity and conversion efficiency during the sulfur reduction reaction (SRR) in lithium-sulfur batteries. By employing the 2D projection mapping technique of in situ confocal Raman spectroscopy and electrochemical technique, it is discovered that the exposed mirror plane structure of Nd-O6 can effectively suppress the undesiring disproportionation reaction (S8 2-→S6 2-+1/4 S8) of long-chain lithium polysulfides at the initial stages of sulfur reduction, thereby promoting the positive process of sulfur to lithium sulfide. This not only mitigates the issue of sulfur shuttle loss but also significantly improve the kinetics of the conversion process. Leveraging these advantages, the NdMgAl11O19/S cathode delivered an impressive initial capacity of up to 1398 mAh g-1 at an electrolyte/sulfur (E/S) ratio of 5.1µL mg-1 and a sulfur loading of 2.3mg cm-2. Even when the sulfur loading is increased to 10.02mg cm-2, the cathode retained a reversible areal capacity of 10.01 mAh cm-2 after 200 cycles. This mirror engineering strategy provides valuable and universal insights into enhancing the efficiency of cathodes in Li-S battery.

VIBRATIONAL AND X-RAY MEASUREMENTS OF La2Ti2O7 UNDER HIGH PRESSURE CONDITION

The present study focuses on investigating the impact of high-pressure conditions on the crystal structure and vibration spectra of the perovskite-like layered compound La2Ti2O7. To this end, X-ray diffraction and Raman spectroscopy techniques were employed to observe the behavior of the compound under pressure levels up to 30 GPa. The neutron diffraction at ambient pressure confirms that the structure of La2Ti2O7 is monoclinic P21. The results indicate that when the pressure attains 17.3 GPa, the original monoclinic phase of P21 symmetry undergoes a phase transition to the monoclinic phase of P2 symmetry. The observed pressure-induced phase transitions in La2Ti2O7 are associated with anomalous changes in both the unit cell parameters and the vibrational modes. Additionally, the study obtained the baric dependences of lattice parameters, unit cell volume and vibration frequencies, which were used to calculate the bulk modules for the initial and pressure-induced phases of La2Ti2O7.

Probing molecular spectral functions and unconventional pairing using Raman spectroscopy

An impurity interacting with an ultracold Fermi gas can form either a polaron state or a dressed molecular state, the molaron, in which the impurity forms a bound state with one gas particle. This molaron state features rich physics, including a negative effective mass around unitarity and a first-order transition to the polaron state. However, these features have remained so far experimentally inaccessible. In this work we show theoretically how the molaron state can be directly prepared experimentally even in its excited states using Raman spectroscopy techniques. Initializing the system in the ultrastrong coupling limit, where the binding energy of the molaron is much larger than the Fermi energy, our protocol maps out the momentum-dependent spectral function of the molecule. Using a diagrammatic approach we furthermore show that the molecular spectral function serves as a direct precursor of the elusive Fulde-Ferell-Larkin-Ovchinnikov phase, which is realized for a finite density of fermionic impurity particles. Our results pave the way to a systematic understanding of how composite particles form in quantum many-body environments and provide a basis to develop new schemes for the observation of exotic phases of quantum many-body systems. Published by the American Physical Society 2024

Synthesis and characterization of pristine CuO and Mg/CuO nanostructures for their anti-breast cancer and photocatalytic degradation applications: Experimental and DFT investigations

The present manuscript emphasizes the versatility of Mg-doped CuO nanostructures for environmental remediation (photocatalytic degradation of pollutants) and biomedical applications (anticancer activity) thus highlighting their potential impact in addressing societal and health challenges. The primary focus of the manuscript is the synthesis, characterization, and applications of Mg-doped CuO nanostructures. In order to meet this purpose, pure and Mg doped CuO nanostructures were synthesized using the solid-state reaction method and ball milling techniques. To characterize the prepared samples, X-ray diffraction, transmission electron microscopy, UV-Visible, photoluminescence, and Raman spectroscopy techniques were utilized. A profusion of structural defects and the reduction in crystallite size have been observed in CuO nanomaterial’s due to the dopant's complete incorporation into the CuO lattice. Additionally, the band gap of CuO has been observed to decrease as a result of Mg doping. Density functional theory was employed to simulate the effect of Mg on the properties of CuO. The efficiency of photocatalytic degradation aided by sunlight against methylene blue increased from 50.8 % to 89.5 %. MCF-7, a cell line representing human breast adenocarcinoma, was utilized to assess the cytotoxicity of Mg/CuO samples. CuO nanoparticles enriched with Mg are viable biocompatible anti-cancer agents and prospective photocatalyst for the removal of environmental pollutants from aqueous solutions, according to the findings of this study.

Assessment of acoustic shock wave resistance of SiO2 (α-cristobalite): A potential material for aerospace and defense industry applications

In the present research article, the acoustic shock wave-resistant efficiency of silica microparticles (SiO2-α-cristobalite)) has been experimentally evaluated in terms of structural, optical and morphological stability against the impact of shock waves. The required SiO2 particles were synthesized by a hydrothermal method which was subjected to a different number of shock pulses such as 200,400 and 600 with Mach number 2.2. Shocked samples’ structural, morphological and optical stabilities have been evaluated by utilizing a powder X-ray diffractometer (PXRD), Ultraviolet–Diffuse reflectance spectrometer (DRS) while the surface morphological analysis has been scrutinized by the field emission scanning electron microscopic technique (FESEM) and transmission electron microscopy (TEM). X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy techniques are utilized to evaluate oxidation states and crystallographic structural stability. The above-mentioned analytical techniques provide convincing proofs whereby the synthesized SiO2 particles are authentically proven to possess outstanding structural, optical and morphological stability against the impact of shock waves. The implicated experimental results and the arguments strongly suggest that the SiO2 particles are suitable candidates for aerospace and defense industry applications due to their outstanding shock wave-resistant properties.

Design, development, and performance of a versatile graphene epitaxy system for the growth of epitaxial graphene on SiC.

A versatile graphene epitaxy (GrapE) furnace has been designed and fabricated for the growth of epitaxial graphene (EG) on silicon carbide (SiC) in diverse growth environments ranging from high vacuum to atmospheric argon pressure. Radio-frequency induction enables heating capabilities up to 2000 °C, with controlled heating ramp rates achievable up to 200 °C/s. The details of critical design aspects and temperature characteristics of the GrapE system are discussed. The GrapE system, being automated, has enabled the growth of high-quality EG monolayers and turbostratic EG on SiC using diverse methodologies, such as confinement-controlled sublimation (CCS), open configuration, polymer-assisted CCS, and rapid thermal annealing. This showcases the versatility of the GrapE system in EG growth. Comprehensive characterizations involving atomic force microscopy, Raman spectroscopy, and low-energy electron diffraction techniques were employed to validate the quality of the produced EG.

Gaining insights into the responses of individual yeast cells to ethanol fermentation using Raman tweezers and chemometrics

Saccharomyces cerevisiae is the most common microbe used for the industrial production of bioethanol, and it encounters various stresses that inhibit cell growth and metabolism during fermentation. However, little is currently known about the physiological changes that occur in individual yeast cells during ethanol fermentation. Therefore, in this work, Raman spectroscopy and chemometric techniques were employed to monitor the metabolic changes of individual yeast cells at distinct stages during high gravity ethanol fermentation. Raman tweezers was used to acquire the Raman spectra of individual yeast cells. Multivariate curve resolution-alternating least squares (MCR-ALS) and principal component analysis were employed to analyze the Raman spectra dataset. MCR-ALS extracted the spectra of proteins, phospholipids, and triacylglycerols and their relative contents in individual cells. Changes in intracellular biomolecules showed that yeast cells undergo three distinct physiological stages during fermentation. In addition, heterogeneity among yeast cells significantly increased in the late fermentation period, and different yeast cells may respond to ethanol stress via different mechanisms. Our findings suggest that the combination of Raman tweezers and chemometrics approaches allows for characterizing the dynamics of molecular components within individual cells. This approach can serve as a valuable tool in investigating the resistance mechanism and metabolic heterogeneity of yeast cells during ethanol fermentation.

Modification of WS2 thin film properties using high dose gamma irradiation

The tunability of the transition metal dichalcogenide properties has gained attention from numerous researchers due to their wide application in various fields including quantum technology. In the present work, WS2 has been deposited on fluorine doped tin oxide substrate and its properties have been studied systematically. These samples were irradiated using gamma radiation for various doses, and the effect on structural, morphological, optical and electrical properties has been reported. The crystallinity of the material is observed to be decreased, and the results are well supported by x-ray diffraction, Raman spectroscopy techniques. The increase in grain boundaries has been supported by the agglomeration observed in the scanning electron microscopy micrographs. The XPS results of WS2 after gamma irradiation show evolution of oxygen, carbon, C=O, W–O and SO4 −2 peaks, confirming the addition of impurities and formation of point defect. The gamma irradiation creates point defects, and their density increases considerably with increasing gamma dosage. These defects crucially altered the structural, optical and electrical properties of the material. The reduction in the optical band gap with increased gamma irradiation is evident from the absorption spectra and respective Tauc plots. The I–V graphs show a 1000-fold increase in the saturation current after 100 kGy gamma irradiation dose. This work has explored the gamma irradiation effect on the WS2 and suggests substantial modification in the material and enhancement in electrical properties.

Nano-Raman spectroscopy of 2D materials

Abstract The use of nano-Raman spectroscopy to study two-dimensional (2D) systems is presented here. The nano (tip-enhanced) Raman spectroscopy technique is briefly introduced, addressing some new theoretical aspects for Raman spectroscopy in the near-field regime, including field coherence, field distribution and the relevance of atomic description and quenching effects. State-of-the-art results in graphene and transition metal dichalcogenides are presented, exploring the connection between micro- and nano-Raman metrology. Various aspects such as defects, homojunctions, twisted-bilayer structures, localized emissions at bubbles, wrinkles, and borders, as well as substrate and coherence effects are addressed in detail. The paper concludes by outlining the perspectives for nano-Raman spectroscopy in 2D systems, highlighting its potential for advancing our understanding of nanoscale phenomena and facilitating further breakthroughs in materials science and characterization.

Exploring the nanoscale: AFM-IR visualization of cysteine adsorption on gold nanoparticles

This study focuses on the adsorption process of L-cysteine (Cys), a sulfur-containing amino acid, onto monolayers of gold nanoparticles (AuNPs) prepared through distinct protocols on mica substrates. Two types of AuNPs were prepared using two different methods: the first employed a physical approach, which combined the Inert Gas Condensation (IGC) technique with the magnetron sputtering method, while the second utilized a chemical method involving the reduction of tetrachloroauric acid with trisodium citrate (TC). The characterization of AuNPs was performed using transmission electron microscopy (TEM) and atomic force microscopy (AFM), of up to 5 ± 1.3 nm for bare AuNPs obtained through vacuum techniques, and up to 12 ± 5 nm for negatively charged, citrate-stabilized TCAuNPs(−). The application of spectroscopic techniques based on the surface-enhanced effects allows for describing the adsorption process in both micro- and nanoscale systems: Cys/bare AuNPs and Cys/ TCAuNPs(−). The commonly used surface-enhanced Raman spectroscopy (SERS) technique provided insights into adsorption behaviours at the microscale level. In the case of TCAuNPs(−), an interaction involving the lone electron pair of sulfur (S) atom and metal surface, while on the bare AuNPs, S is adsorbed on the surface, but the cleavage of the SH group is not discernible. Nanoscale analysis was complemented using AFM combined with the surface-enhanced infrared absorption spectroscopy (AFM-SEIRA) technique. AFM-SEIRA map indicated the formation of hot spot which were predominantly located between aggregated TCAuNPs(−) and on specific NPs surfaces (area between NPs and gold-coated tip). Results from the SERS and AFM-SEIRA techniques were in good agreement, underscoring the comprehensive understanding achieved through the chosen experimental approach regarding the Cys interactions with layers of AuNPs.

Evaluation of structural parameters of monoclinic nanocrystalline CuO and study of sunlight-driven photocatalytic dye degradation, antimicrobial and antioxidant potential

Highly pure, crystalline and spherical-shaped Copper oxide nanoparticles (NPs) have been synthesized via facile chemical coprecipitation. Various models including the Scherrer, Monshi-Scherrer, Williamson-Hall, Size-Strain Plot and Halder-Wagner method have been applied to study the crystal structure characteristics. The lattice parameters associated with the monoclinic crystal lattice of CuO NPs were estimated to be a = 4.69 Å, b = 3.41 Å, c = 5.14 Å and β = 99.87(degree), unit cell volume V = 81.35Å3 and cell density dx = 6.49 g/cm3. The photocatalytic dye degradation proficiency at 20 mg/l CuO concentration and 120 min sunlight exposure results the order of percentage dye degradation Malachite Green (88.4%) > Crystal Violet (70.8%) > Eosin Yellow (70.2%) > Methylene Blue (54.08%) dyes. The antimicrobial activity assessment was done against the broad-spectrum pathogenic microbes unveiled the exceptional microbial controlling capability of CuO NPs. Furthermore, the antioxidant activity test demonstrated the potential free radical scavenging activity of CuO NPs with an IC50 value of 47.733 µg/ml. Highlights Synthesis of pure and spherical shaped nanocrystalline CuO was done by using low cost and facile chemical coprecipitation method. XRD, FTIR, FESEM, EDX, UV-Vis, and Raman spectroscopic techniques were used for characterization purpose. The structural and crystallographic parameters of monoclinic crystal structure of CuO NPs were evaluated successfully. The photocatalytic performance of CuO NPs follow the percentage dye degradation order as MG (88.4%) > CV (70.8%) > EY (70.20%) > MB (54.08%) after 120 minutes of sunlight exposure. CuO NPs exhibit promising antifungal activity against COVID-19 associated Pulmonary Aspergillosis (CAPA) causing pathogenic fung. CuO NPs show potential DPPH free radical scavenging activity with an IC50 value of 47.733 µg/ml.

Durolon® polymer as a nuclear track detector: Characterization by chemical etching

This paper presents the properties of alpha particle tracks in a polymer, known as Durolon®. The study involves measurements of the time-dependent evolution of etch pit diameters and areal densities for low-energy alpha particles under various etching conditions, including different temperatures and solutions. A time-dependent model was successfully employed to describe the etch pit growth rates. Additionally, optical absorption and Raman spectroscopy techniques were applied to the samples under investigation, complementing the traditional results obtained through optical microscopy. The suitability of Durolon® polymer as a nuclear track detector is discussed based on the results obtained from the aforementioned complementary techniques. In summary, this research represents a critical step toward establishing Durolon® polymer as a viable nuclear track detector.

Effect of cobalt on CeO2 nanorod supported Pt catalyst: Structure, performance, kinetics and reaction mechanism in CO oxidation

Catalytic oxidation represents a highly efficient and extensively employed approach for the elimination of CO in exhaust gas. Rationally designing and preparing catalysts with exceptional activity and stability in the presence of H2O and SO2 at low temperatures represent crucial avenues for future advancements. In this work, a series of Pt catalysts supported on CeO2 nanorods incorporated with varying amounts of Cobalt (Co/CeO2 ratio ranging from 0 to 10 %) were prepared and evaluated for their catalytic activity in CO oxidation under both dry and wet conditions. The ultrahigh dispersion of Pt, outstanding redox properties, and abundant oxygen vacancies on the surface of Co-doped CeO2 nanorod supported Pt catalysts were revealed by XRD, TEM, Raman spectroscopy and H2-TPR techniques. The catalytic activity for CO oxidation strongly depends on the Co content and reaction conditions. Among them, Pt/Co-CeO2-5 % exhibits the highest CO oxidation performance with a T90 (the temperature to achieve 90 % conversion of CO) of 170 °C under dry conditions, which is significantly lower by 140 °C compared to T90 of Pt/CeO2. Pt/Co-CeO2-1 % demonstrates superior CO oxidation performance with a T90 of 195 °C under wet conditions, exhibiting a reduction in temperature by 65 °C compared to the T90 of Pt/CeO2. Moreover, Pt/Co-CeO2 exhibits excellent resistance to SO2 compared to Pt/CeO2. Kinetic studies, in situ DRIFT analysis and isotopic experiments demonstrated direct participation of H2O in the reaction. On the catalysts with a low Co/Ce ratio (Co/Ce < 0.03), CO readily reacts with hydroxyl groups dissociated from H2O to form carboxyl intermediates, which subsequently undergo rapid decomposition into CO2, resulting in an enhanced reaction rate of CO oxidation at low temperature.

Multi-branch attention Raman network and surface-enhanced Raman spectroscopy for the classification of neurological disorders.

Surface-enhanced Raman spectroscopy (SERS), a rapid, low-cost, non-invasive, ultrasensitive, and label-free technique, has been widely used in-situ and ex-situ biomedical diagnostics questions. However, analyzing and interpreting the untargeted spectral data remains challenging due to the difficulty of designing an optimal data pre-processing and modelling procedure. In this paper, we propose a Multi-branch Attention Raman Network (MBA-RamanNet) with a multi-branch attention module, including the convolutional block attention module (CBAM) branch, deep convolution module (DCM) branch, and branch weights, to extract more global and local information of characteristic Raman peaks which are more distinctive for classification tasks. CBAM, including channel and spatial aspects, is adopted to enhance the distinctive global information on Raman peaks. DCM is used to supplement local information of Raman peaks. Autonomously trained branch weights are applied to fuse the features of each branch, thereby optimizing the global and local information of the characteristic Raman peaks for identifying diseases. Extensive experiments are performed for two different neurological disorders classification tasks via untargeted serum SERS data. The results demonstrate that MBA-RamanNet outperforms commonly used CNN methods with an accuracy of 88.24% for the classification of healthy controls, mild cognitive impairment, Alzheimer's disease, and Non-Alzheimer's dementia; an accuracy of 90% for the classification of healthy controls, elderly depression, and elderly anxiety.

Reaction mechanism between carbon and CaO–SiO2–Al2O3–Na2O slag system during continuous casting process

The reaction behavior between the carbon and mold fluxes during the heating process is vital for a successful continuous casting process and the high billet quality. A detailed investigation combined with thermogravimetry-mass spectrometry (TG-MS), differential scanning calorimetry (DSC), X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy, and transmission electron microscopy (TEM) techniques was carried out to systematically investigate the transformation mechanistic of the macro physicochemical properties, melting behavior, viscosity, crystallization, and heat transfer performance caused by the reaction behavior. The results showed that the mold flux underwent carbonate decomposition (973–1223 K), solid reaction (1273–1573 K), and melting process (1473–1673 K) during the continuous casting process. The carbon-bearing mold flux exhibited an endothermic peak at approximately 1673 K, corresponding to a weight loss ratio of approximately 14.5% on the TG curve, confirming that carbon could react with the middle mineral phases Ca2SiO4, Ca2Al2SiO7, and Na6Ca3Si6O18 to form SiC, increasing the breaking temperature by approximately 293 K. SEM and TEM results indicated that the melting behavior was restrained by the carbon itself and the newly formed components. Besides, the addition of carbon increased the degree of polymerization of molten slag, the thickness of slag film and the proportion of small crystals in slag film, further leading to an increase in crystallization and heat transfer performances. The reaction mechanism between carbon and slag and the subsequent effects on melting point, viscosity, crystallization ratio and heat flux density were clearly understood, which is meaningful for the carbon blending process of the mold flux.

Preliminary study on the optical diagnosis of orbital rhabdomyosarcoma by Raman spectroscopy

To investigate the Raman spectral features of orbital rhabdomyosarcoma (ORMS) tissue and normal orbital tissue in vitro, and to explore the feasibility of Raman spectroscopy for the optical diagnosis of ORMS. 23 specimens of ORMS and 27 specimens of normal orbital tissue were obtained from resection surgery and measured in vitro using Raman spectroscopy coupled to a fiber optic probe. The important spectral differences between the tissue categories were exploited for tissue classification with the multivariate statistical techniques of principal component analysis (PCA) and linear discriminant analysis (LDA). Compared to normal tissue, the Raman peak intensities located at 1450 and 1655 cm−1 were significantly lower for ORMS (p < 0.05), while the peak intensities located at 721, 758, 1002, 1088, 1156, 1206, 1340, 1526 cm−1 were significantly higher (p < 0.05). Raman spectra differences between normal tissue and ORMS could be attributed to the changes in the relative amounts of biochemical components, such as nucleic acids, tryptophan, phenylalanine, carotenoid and lipids. The Raman spectroscopy technique together with PCA-LDA modeling provides a diagnostic accuracy of 90.0%, sensitivity of 91.3%, and specificity of 88.9% for ORMS identification. Significant differences in Raman peak intensities exist between normal orbital tissue and ORMS. This work demonstrated for the first time that the Raman spectroscopy associated with PCA-LDA diagnostic algorithms has promising potential for accurate, rapid and noninvasive optical diagnosis of ORMS at the molecular level.