Search Results (324)

Neodymium-doped bioactive wollastonite–tricalcium phosphate (W-TCP:Nd) coatings were fabricated by combining dip-coating and laser floating zone (LFZ) techniques to investigate the dependence of optical emission on polarization. Structural and spectroscopic analyses were performed on both longitudinal and transversal sections of the coating to assess the effects of directional solidification on luminescence and vibrational behavior. Micro-Raman spectroscopy revealed that the coating exhibited sharp, well-defined peaks compared to the W-TCP:Nd glass, confirming its glass-ceramic nature. New Raman modes appeared in the longitudinal section, accompanied by red and blue shifts in some bands relative to the transversal section, suggesting the presence of anisotropic stress and orientation-dependent crystal growth. Optical emission measurements showed that while the ⁴F_3/2→⁴I_11/2 transition near 1060 nm was nearly polarization independent, the ⁴F_3/2→⁴I_9/2 transition around 870–900 nm exhibited strong polarization dependence with notable Stark splitting. The relative intensity and spectral position of the Stark components varied systematically with the rotation of the emission polarization. These findings demonstrate that directional solidification induces polarization-dependent optical behavior, indicating potential applications for polarization-sensitive optical tracking and sensing in bioactive implant coatings. Full article

Airborne micro- and nanoplastic particles (MNPs) are increasingly recognized as a potential occupational exposure hazard, yet substance-specific workplace data remain limited. This study quantified airborne MNP concentrations during polyester microfiber production using a correlative SEM–Raman approach that enabled chemical identification and size-resolved particle characterization. The aerosol mixture at the workplace was dominated by sub-micrometer particles, with PET—handled onsite—representing the main process-related MNP type, and black tire rubber (BTR) forming a substantial background contribution. Across both sampling periods, total MNP particle number concentrations ranged between 6.2 × 10⁵ and 1.2 × 10⁶ particles/m³, indicating consistently high particle counts. In contrast, estimated MNP-related mass concentrations were much lower, with PM₁₀ levels of 12–15 µg/m³ and PM_2.5 levels of 1.3–1.6 µg/m³, remaining well below applicable occupational exposure limits and near or below 8 h-equivalent WHO guideline values. Comparison with earlier workplace and indoor studies suggests that previously reported concentrations were likely underestimated due to sampling strategies with low efficiency for small particles. Moreover, real-time optical measurements substantially underestimated particle number and mass in this study, reflecting their limited suitability for aerosols dominated by small or dark particles. Overall, the data show that workplace MNP exposure at the investigated site is driven primarily by very small particles present in high numbers but low mass. The findings underscore the need for substance-specific, size-resolved analytical approaches to adequately assess airborne MNP exposure and to support future development of MNP-relevant occupational health guidelines. Full article

Understanding the molecular mechanisms of protein–nanoparticle interactions is crucial for enabling the development of new applications in biomedicine and nanotechnology. Ubiquitin, an important and structurally small functional protein, plays a central role in numerous cellular processes. Therefore, in the current study, we focused on the few-layer graphene (FLG)–Ubiquitin complexes formed by exfoliating FLG structures using only water. Optical spectroscopic techniques (Raman, FT-IR, UV-Vis and circular dichroism) were employed to investigate these complexes on the molecular level. Overall, both CD and FT-IR data reveal that the formation of the FLG–Ubiquitin complexes occurred without inducing disordered structures in the protein. Based on the existence of a blue shift (hypsochromic shift) in the UV-Vis data, the presence of a single tyrosine and two phenylalanine residues in ubiquitin enables the detection of FLG-induced micro-environmental changes, particularly influencing the protein’s β-sheet and α-helix structures. The CD spectral results and CDPro quantitative estimations are in line with ATR FT-IR results, confirming the absence of disordered structure formation while altering the protein’s chirality. UV-Vis and CD spectroscopy results revealed concentration-dependent trends consistent with FLG–protein interactions that preserve the overall protein structure. This study has potential applications in both academic research and practical usage, particularly in biomedicine and nanotechnology specifically for FLG. Full article

Two folding screens by futurist artist Giacomo Balla (1871–1958) in the collection of the Kröller-Müller Museum (the Netherlands) were investigated: Paravento con linea di velocità (1916–1917) and Paravento (1916/1917–1958). The screens are painted on both sides, the first on four canvases, stretched onto two wooden strainers and framed with painted wooden strips, and the second on wooden panels set into four painted stiles. In the past, damages on Paravento con linea di velocità were restored by conservators, while Paravento was probably first reworked by the artist himself and later restored by conservators. Yellowed varnish and discolored retouches on both screens led to a wish for treatment. The aim of this research was to gain insight into the painting techniques, layer buildup, pigments, binders, and varnishes of the two artworks. This information supported the decision making for treatment, and it broadens the knowledge on the materials used by Balla. Up to now, only a few published studies deal with the technical examination of paintings by this artist. Both folding screens were subjected to technical photography (UV, IR photography, and X-ray) and were examined with portable point X-ray fluorescence (pXRF) and Raman spectroscopy. Moreover, samples were taken. Cross-sections were studied with optical microscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), attenuated total reflection Fourier-transform infrared (ATR-FTIR) imaging, and micro-Raman spectroscopy. Loose samples were examined with SEM-EDX, FTIR and micro-Raman spectroscopy, and pyrolysis gas chromatography mass spectrometry (Py-GC/MS). For Paravento con linea di velocità, all pigments and fillers of the painted canvases are compatible with the dating of the screen (1916–1917), but they differ from those on the frame. Here, rutile, in combination with various pigments, among which are blue copper phthalocyanine (PB15) and other synthetic organic pigments, was found. This indicates that the frame has been painted later, likely after the Second World War. The composition of the binders differs as well. Drying oil and pine resin have been used on the canvases, explaining the smooth and glossy appearance and solvent-sensitivity of the paint. On the frame, oil with some alkyd resin was identified. The provenance of the screen before 1972 is not clear, nor when the frame was made and painted and by whom. The results for Paravento indicate that the palettes of the two sides—painted in different styles—are comparable. Mainly inorganic pigments were found, except for the dark red areas, where toluidine red (PR3) is present. pXRF showed high amounts of zinc; cross-sections revealed that zinc white is present in the lower layers. These pigments are compatible with the dating of the screen (1916–1917). In many of the upper paint layers though, except for some green, dark red, and black areas, rutile has been identified. This indicates that these layers were applied later, likely after the Second World War. Since this folding screen was used by the artist and his family until his death in 1958, it seems likely that Balla himself reworked the screen. Full article

An optical levitation system in a vacuum is an efficient system to investigate the dynamics of isolated micro- and nanoparticles. However, the motion and stability of the trapped particles in this system can be affected by the internal temperature, which remains a challenge to measure. Conventional methods are constrained by material specificity or lack the capability for direct temperature measurement. Here, we demonstrate the application of Raman thermometry for non-contact temperature detection of an optically levitated fused silica sphere in vacuum. In addition, the experimental results reveal a linear increase in particle temperature with laser power, consistent with photothermal theory. The integration of Raman thermometry with the optical levitation system enables high-precision thermal sensing at the microscale, offering significant potential for applications in precision metrology and fundamental physics. Full article

An in-depth study of the genetic mechanisms of graphite in shear zones is crucial for understanding crustal weakening and the origins of inorganic carbon. This research focuses on mylonitic marble (MM) and cataclastic marble (CM) from the Tongyuanpu shear zone of Eastern China. The occurrences, nanostructures, carbon sources, and genesis of graphite were systematically investigated through micro- to ultra-microscale analysis. The results reveal that the MM contains two graphite varieties: C-foliation-aligned bands and stylolite-derived serrated aggregates. Both exhibit strong Z-axis LPO, indicating a deformation temperature below 200 °C. In contrast, the CM features individual graphite particles within fragmented grains. Near-ideal graphite structures are characterized in both types; however, a higher TOC content and a greater graphitization degree are observed in the CM. Raman thermometry indicates metamorphic peak temperatures of 588–673 °C (MM) and 540–682 °C (CM), with the former showing a significant discrepancy from the EBSD results. The δ¹³C_ORG values (−12.21‰ to −8.06‰) suggest fluid-derived carbon sources. We propose that reduction reactions involving high-temperature metamorphic fluids supplied the essential carbon source. Ductile shearing accelerated the graphitization of these carbonaceous materials through the accumulation of local strain energy, while subsequent brittle deformation with frictional sliding further facilitated structural transformation. Full article

The increasing prevalence of orthopedic disorders and technological advances have significantly improved the design and functionality of orthopedic implants, fostering the growth of the orthopedic implant market. Polyetheretherketone (PEEK) has emerged as a promising alternative to the gold standard of metallic implants due to its favorable biocompatibility and mechanical properties, comparable to those of bone tissue. However, its chemical inertness results in poor osseointegration. This study investigates femtosecond (fs) laser-induced micro- and nanoscale surface modifications of PEEK, aiming to develop surface modifications potentially favorable for bioactivity enhancement of the as-created transient cellular scaffolds. Various texturing designs were fabricated by precisely controlling the laser parameters applied (laser beam power P = 20–80 mW, hatch spacing dx = 45–100 µm, scanning velocity V = 3.44–32 mm/s). The resulting morphologies were characterized by SEM, EDX, XRD, micro-Raman, 3D profilometry, water contact angle measurements, and evaluated for preliminary biological response. The main achievement of the research indicates that the hierarchical topography created by fs laser microprocessing significantly increased surface morphology, which may subsequently provide surface conditions supporting successful osseointegration. These findings demonstrate the feasibility of femtosecond laser structuring as a promising, reproducible, and environmentally friendly method for sustainable surface biofunctionalization of PEEK in orthopedic applications. Full article

Ionic liquid (IL)-based electrolytes have garnered significant interest for enhancing lithium-ion battery (LIB) safety due to their non-flammability, thermal stability, high conductivity, and broad electrochemical stability. We propose novel pyrrolinium-based ionic liquids to enhance lithium-ion mobility and address safety concerns in LIBs. This study investigated LiTFSI in [Pyr13] [FSI] ionic liquid for Li-ion batteries. The cyclic stability and rate performance of single-layer full cells with commercial graphite anode and NMC532 cathode were examined for the electrolyte required per cell and compared to those using a carbonate electrolyte (LP30). Electrolytes containing LiTFSI/[Pyr13] [FSI] exhibited satisfactory rate performance and stable cycling for 100 cycles. The reversible capacity was maintained at over 22 mAh for a cycle period of 100 cycles with an electrolyte loading of 161.8 µL/cm². These electrolytes exhibited the highest oxidation stability, surpassing 5.3 V compared to that of the Li⁺/Li reference electrode. Long cycle life of up to 1000 cycles was conducted, showing 80% capacity retention. Post-mortem analysis using scanning electron microscopy (SEM) and micro-Raman spectroscopy allowed observation of LiTFSI/ [Pyr13] [FSI] effects on cathode and anode active particle stability, and reduced formation of secondary reactions between the IL and battery electrodes. Full article

Graphene-based nanomaterials, including graphene oxide (GO) and graphene quantum dots (GQDs), exhibit exceptional properties, which might facilitate the functional modification of TiO₂ nanotubes (NTs) for enhanced rapid osseointegration. This study investigated the effects of GO/GQD-deposited TiO₂-NTs on cell proliferation, osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells (BMSCs), and early osseointegration in male 6-week-old Sprague Dawley (SD) rats. TiO₂-NTs (control group) were fabricated on titanium substrates via anodic oxidation. GO and GQDs were electrochemically deposited onto the TiO₂-NTs using cyclic voltammetry with 0.5 mg/mL GO and 0.1 mg/mL GQD dispersions to form NT-GO and NT-GQDs. In vitro assays evaluated cell adhesion, proliferation, and osteogenic differentiation. Implants were randomly inserted into one femoral epiphysis of nine rats (n = 3), and osseointegration was evaluated using micro-computed tomography and sequential fluorescence labeling at 2, 4, and 6 weeks post-implantation. Statistical analysis was conducted using ANOVA. Cyclic voltammetry successfully synthesized NT-GO and NT-GQDs, with Raman spectra confirming D and G bands. Both NT-GO and NT-GQDs exhibited superior cell adhesion, proliferation, and enhanced osteogenic differentiation compared with TiO₂-NTs. Notably, the NT-GQDs significantly promoted new bone formation in vivo. The integration of graphene nanomaterials onto TiO₂-NTs improves biocompatibility and accelerates osteogenesis, suggesting a promising strategy for enhancing osseointegration in orthopedic and dental implants. Full article

The widespread and excessive use of plastic in our daily life has led to serious microplastic pollution in the atmosphere, water, and soil. These microplastics can enter freshwater systems and pose significant risks to the ecosystem and human health via the food chain. This environmental problem deserves proper investigation and mitigation strategies. In this study, the abundance, morphology, color, size and polymer composition of microplastics in surface water of Feiyun River Basin were systematically studied by means of field sampling, microscopy and laser micro-Raman spectroscopy. The result showed that microplastic abundance ranged from 3.7 to 36.4 items/L, with an average of 11.0 ± 2.39 items/L. These microplastics were mainly particles, followed by fragments and fibers, with white, black, and blue being the most common colors. Most of the particles were smaller than 0.1 mm (57%), and a laser micro-Raman spectrometer was used to identify the polymer types of the microplastics. The results showed that the main polymer types identified were PET, PP, and PS. Risk assessment based on PLI, PHI, and PERI indices indicated a low ecological risk of microplastics in the study area. These findings provide further insight into the sources and distribution of microplastics in local watersheds and support future assessments of riverine transport of microplastics to estuarine and marine environments. Full article

Akaganeite is the most destructive corrosion product in a rust layer, and it accelerates the corrosion rate of steel in certain atmospheres. Until now, considerable controversy has existed regarding the conditions required for its formation and its mechanism of formation. In this work, the formation of akaganeite in the specific corrosion process, which was atmospheric corrosion induced by NaCl deliquescence, was investigated through simulated experiments in a laboratory setting. Stereoscopic microscopy and scanning electron microscopy were employed to characterize the morphologies of the corrosion products, which could illuminate the morphological features of the electrolyte induced by the NaCl particles. The constituents of rust in a single droplet were analyzed by micro-Raman spectroscopy, and the components of the corrosion phases on a macroscopic scale were analyzed by XRD. The results indicate that the deliquescence of NaCl particles caused droplets to form around them, and atmospheric corrosion occurred in each droplet independently. Akaganeite can form during atmospheric corrosion induced by NaCl particles in the early stage within 12 h. The initial corrosion products, lepidocrocite and magnetite, increase the amount of akaganeite formed. The amount of salt deposited also plays an essential role in the formation of akaganeite on a macroscopic scale. Full article

Freshwater bead-cultured pearls (FWBCPs) from Zhuji, China, have gained significant market prominence due to their large size, unique pearl luster, and diverse color. This study systematically investigated the mineral compositions and organic color-related compounds of twelve representative freshwater cultured pearls through a multi-analytical approach integrating Fourier transform infrared spectroscopy (FTIR), Laser Raman spectroscopy (LRS), ultraviolet–visible spectroscopy (UV-Vis), cathodoluminescence (CL), micro-infrared spectroscopy, and differential thermal–thermogravimetric analysis (TGA-DTA). Key findings reveal that FWBCPs from Zhuji primarily consist of aragonite, organic matter and adsorbed water, occasionally containing vaterite. No obvious correlation was observed between the mineral compositions and the quality of the pearls. Raman spectra exhibit characteristic bands of polyenes near 1525 cm⁻¹ (attributed to the stretching vibration of C=C, ν₁) and near 1131 cm⁻¹ (attributed to the stretching vibration of C-C, ν₂). The different colors are formed by various polyenes with the exact position of the characteristic bands determined by the concentrations of C=C in the polyenes. FWBCPs and freshwater non-bead-cultured pearls (FWNBCPs) exhibit essentially the same mineral compositions and organic color-related compounds, but can be distinguished from each other based on their internal structures. These results advance the understanding of freshwater pearl formation mechanisms and establish a scientific foundation for quality evaluation in the gemological industry. Full article

Contemporary murals are highly susceptible to rapid color fading due to outdoor urban exposure. This study investigates the photodegradation mechanisms affecting synthetic organic pigments (SOPs) and commercial acrylic–vinyl paints under simulated visible light exposure. Artificial aging experiments were conducted on two types of systems: (a) pigment pellets, composed of pre-fixed pigments on mineral bases, as supplied by the manufacturer, and (b) commercial paints applied on glass substrates. Both systems were aged under controlled and uncontrolled relative humidity (RH) conditions. Colorimetric analyses revealed significant color fading, particularly in pigments PR112, PO5, and PV23. Vibrational spectroscopies highlighted the reduction in pigment-related bands after aging, indicating SOPs’ vulnerability to photodegradation. In paint mock-ups, FTIR-ATR measurements indicated binder degradation and an increase in signals from inorganic fillers. A superficial layer enriched in inorganic components was investigated non-invasively by Micro Spatially Offset Raman spectroscopy (Micro-SORS) in the beamsteer modality. It highlighted a gradient of calcite to pigment with depth. These findings indicate that color fading in mural paints results from the combined degradation of both pigments and binders. Full article

While existing studies on Guatemalan jadeite have predominantly focused on green varieties, the coloration mechanisms and origin of its blue counterparts remain poorly understood. Therefore, the present study provides the first comprehensive investigation of the Guatemalan blue jadeite using an integrated analytical approach, which combines Raman spectroscopy, micro X-ray fluorescence (µ-XRF), electron microprobe analysis (EMPA), X-ray diffraction (XRD), UV-Vis spectroscopy, and Cathodoluminescence (CL) imaging on seven representative samples. The results demonstrate that these jadeites consist of two distinct phases: a primary jadeite phase (NaAlSi₂O₆) and a secondary omphacite that form by metasomatic alteration by Mg-Ca-Fe-rich fluids. Spectroscopic analysis reveals that the blue coloration is primarily controlled by Fe³⁺ electronic transitions (with characteristic absorption at 381 nm and 437 nm) coupled with Fe²⁺-Ti⁴⁺ intervalence charge transfer, supported by μ-XRF mapping showing strong Fe-Ti spatial correlation with color intensity. CL imaging documents a multi-stage formation history involving initial high-pressure crystallization (Jd-I) followed by fluid-assisted recrystallization forming Jd-II and omphacite. The detection of CH₄, CO and H₂O in the fluid inclusions by Raman spectroscopy indicates formation in a serpentinization-related reducing environment, while distinct CL zoning patterns confirm a fluid-directed crystallization (P-type) origin. These findings not only clarify the chromogenic processes and petrogenesis of Guatemalan blue jadeite but also establish key diagnostic criteria for its identification, advancing our understanding of fluid-derived jadeite formation in subduction zone environments. Full article

Beyond its renowned gemological value, diamond serves as a vital economic mineral and a unique messenger from Earth’s deep interior, preserving invaluable geological information. Since the Mengyin region is the source of China’s greatest diamond deposits, research on the diamonds there not only adds to our understanding of their origins but also offers an essential glimpse into the development of the North China Craton’s mantle lithosphere. In this article, 50 diamond samples from Mengyin were investigated using gemological microscopy, Fourier-transform infrared (FTIR) spectroscopy, Raman spectroscopy, DiamondView™, and X-ray micro-computed tomography (CT) scanning technologies. The types of Mengyin diamonds are mainly Type IaAB, Type IaB, and Type IIa, and the impurity elements are N and H. Inclusions in diamonds serve as direct indicators of mantle-derived components, providing crucial constraints on the pressure–temperature (P–T) conditions during their crystallization. Mengyin diamonds have both eclogite-type and peridotite-type inclusions. It formed at depths ranging from 147 to 176 km, which corresponds to source pressures of approximately 4.45–5.35 GPa, as determined by the Raman shifts of olivine inclusions. The discovery of coesite provides key mineralogical evidence for subduction of an ancient oceanic plate in the source region. The surface morphology of diamonds varies when they are reabsorbed by melts from the mantle, reflecting distinctive features that record subsequent geological events. Distinctive surface features observed on Mengyin diamonds include fusion pits, tile-like etch patterns, and growth steps. Specifically, regular flat-bottomed negative trigons are mainly formed during diamond resorption in kimberlite melts with a low CO₂ (X_CO2 < ~0.5) and high H₂O content. The samples exhibit varying fluorescence under DiamondView™, displaying blue, green, and a combination of blue and green colors. This diversity indicates that the diamonds have undergone a complex process of non-uniform growth. The nitrogen content of the melt composition also varies significantly throughout the different growth stages. The N3 center is responsible for the blue fluorescence, suggesting that it originated in a long-term, hot, high-nitrogen craton, and the varied ring band structure reveals localized, episodic environmental variations. Radiation and medium-temperature annealing produce H3 centers, which depict stagnation throughout the ascent of kimberlite magma and are responsible for the green fluorescence. Full article