Search Results (51)

Vanadium-bearing beryl is a vanadium-bearing variety of green beryl (distinct from emerald) that exhibits an “electro-optical” green (blue-green) color, which has led to its commercial popularity. However, the underlying coloration mechanism remains unclear. The present study adopted standard gemological tests and non-destructive spectroscopic tests, such as X-ray fluorescence, UV-visible-near infrared (UV-Vis-NIR), infrared and Raman spectroscopy, to analyze the vanadium-bearing beryl from Nigeria. The results of these tests indicated the presence of Fe as the predominant chromogenic element of vanadium-bearing beryl, followed by V, at a level exceeding that of Cr. Furthermore, the samples displayed lower levels of alkali and magnesium when compared to other beryls, accompanied by lower refractive indices and specific gravities. Spectroscopic analysis indicates that the structural channels are dominated by type I H₂O, with CO₂, HDO, and D₂O molecules also present. The inclusions observed in vanadium-bearing beryl bear a resemblance to those found in typical aquamarines, which are raindrop-shaped inclusions, and to those found in emeralds of various origins, which are irregular, jagged, gas–liquid two-phase/three-phase inclusions. The broad UV-Vis-NIR absorption bands at 427 and 610 nm are characteristic of V³⁺ (and a minor amount of Cr³⁺). Charge transfer between Fe²⁺ and Fe³⁺ may also contribute to the 610 nm band, which is superimposed on the absorption bands of V³⁺ and Cr³⁺. These factors primarily contribute to the blue-green coloration of beryl. The absorption induced by V³⁺ in the visible violet-blue region exhibits stronger intensity and a greater tendency towards the blue region compared to Cr³⁺. Consequently, the resultant vanadium-bearing beryl acquires the yellow-green hue (induced by V) overlaid with the light blue (induced by charge transfer between Fe²⁺-Fe³⁺ pairs), resulting in the so-called “electro-optical” green (blue-green) beryl. Full article

Three new amide-preformed triphenylamine-diamine monomers, namely 4,4′-bis(p-aminobenzamido)triphenylamine (4), 4,4′-bis(p-aminobenzamido)-4″-methoxytriphenylamine (MeO-4), and 4,4′-bis(p-aminobenzamido)-4″-tert-butyltriphenylamine (t-Bu-4), were synthesized and subsequently used to produce three series of electroactive aromatic poly(amide-imide)s (PAIs) via two-step polycondensation reactions with commercially available tetracarboxylic dianhydrides. Strong and flexible PAI films could be obtained by solution casting of the poly(amic acid) films followed by thermal imidization or direct solution casting from the organosoluble PAI samples. The PAIs had high glass-transition temperatures of 296–355 °C and showed no significant decomposition below 500 °C. The PAIs based on diamines MeO-4 and t-Bu-4 showed high electrochemical redox stability and strong color changes upon oxidation. For the PAIs derived from diamine 4, the TPA radical cation formed in situ during the electro-oxidative process could dimerize to a tetraphenylbenzidine structure, resulting in an additional oxidation state and color change. These PAIs exhibited increased solubility, lowered oxidation potentials, and enhanced redox stability compared to their polyimide analogs. Full article

This paper presents a comprehensive investigation into the phenomenon of gamut boundary distortion that occurs during the gamut conversion process in LED full-color display systems. This phenomenon is influenced by the electro-optical transfer function. First, a CIE-xyY colorimetric framework specifically designed for LEDs is developed and established as the foundation for gamut conversion in LED applications. Next, the principles of gamut conversion based on this model are detailed. Additionally, a set of indices, including the Laplacian operator, entropy function, and magnitude of deviation of distorted color points, is integrated to form a comprehensive descriptive methodology. This methodology enables a thorough quantification of distribution patterns and effectively illustrates the outcomes of distortion. The findings of this research are significant for improving color conversion strategies and enhancing the color performance of display devices, making meaningful contributions to related fields. Full article

Atmospheric refraction is a significant challenge to accurate distance and angle measurements in open-air environments, often limiting the precision of measurements obtained using electro-optic geodetic instruments despite their nominal accuracies. This study introduces a novel model, 3D-RM, designed to mitigate atmospheric effects on both distance and vertical angle measurements. The 3D-RM integrates in situ meteorological data from a network of automatic data-loggers, terrain information from a digital terrain model (DTM), and sensible heat flux from the fifth generation of European Centre for Medium-Range Weather Forecast reanalysis (ERA5), which is used in the application of the Turbulence Transfer Model (TTM) for estimating vertical refractivity gradients at various height levels. The model was tested with total station observations to 10 target points during two field campaigns. The results show that applying the model for distance correction leads to improvements in terms of closeness to reference values when compared to the standard method, which relies only on meteorological data collected at the station. Furthermore, the model has been additionally tested by removing the station meteorological data (3D-RM2). The results demonstrate that accurate corrections can be obtained even without the need of meteorological sensors specifically installed at the station point, which makes it more flexible. The 3D-RM is a cost-effective and relatively easy-to-implement solution, offering a promising alternative to existing methodologies, such as measuring meteorological values at both station and target points or the development of new instruments that can compensate the refractivity (such as a multiple-color electronic distance meter). Full article

The impact of cold atmospheric plasma (CAP) treatment on the enamel of twelve primary teeth (incisors, canines, and molars) collected from six children was examined in order to evaluate the possibility of using the CAP technique in dental applications. A radio-frequency dielectric barrier discharge (DBD) plasma jet operating at a voltage of 3.25 kV using a mixture of helium and oxygen as the working gas was used for the generation of plasma as part of the electro-technological method for the treatment of biological material. The plasma exposure time for the primary teeth was 5, 10, and 20 min. The properties of tooth enamel (color, contact angles, surface roughness, surface topography, elemental composition) were examined before (control) and after the plasma treatment. As shown by the results, the plasma treatment time is a key parameter that can induce desired features, such as whitening or improved wettability. However, with prolonged plasma treatment (20 min), the enamel surface may be permanently damaged. The cold-plasma-treated samples were characterized by a higher value of the brightness L* parameter and thus a lighter color, compared to the CAP-untreated teeth. It was also evidenced that the plasma treatment increased the hydrophilicity of tooth surfaces, and the contact angles effectively decreased with the time of the CAP treatment. The tooth surface also became much more heterogeneous and rough with much greater amplitudes in heights. The surface of the primary teeth after the CAP treatment lost its homogeneity, as evidenced by the SEM micrographs. The analysis of the elemental composition revealed only minor changes after the plasma process, which may suggest that the observed morphological changes in the enamel surface are mainly physical and are not a consequence of chemical reactions between the enamel and the reactive components of the cold plasma. Plasma treatment of teeth opens up new possibilities of using this method as an alternative to whitening or pre-treatment before other dental procedures. Full article

Polymers containing π-conjugated segments are a diverse group of large molecules with semiconducting and emissive properties, with strong potential for use as active layers in Organic Light-Emitting Diodes (OLEDs). Stable blue-emitting materials, which are utilized as emissive layers in solution-processed OLED devices, are essential for their commercialization. Achieving balanced charge injection is challenging due to the wide bandgap between the HOMO and LUMO energy levels. This study examines the optical and photophysical characteristics of blue-emitting polymers to contribute to the understanding of the fundamental mechanisms of color purity and its stability during the operation of OLED devices. The investigated materials are a novel synthesized lab scale polymer, namely poly[(2,7-di(p-acetoxystyryl)-9-(2-ethylhexyl)-9H-carbazole-4,4′-diphenylsulfone)-co-poly(2,6-diphenylpyrydine-4,4′-diphenylsulfone] (CzCop), as well as three commercially supplied materials, namely Poly(9,9-di-n-octylfluorenyl-2,7-diyl) (PFO), poly[9,9-bis(2′-ethylhexyl) fluorene-2,7-diyl] (PBEHF), and poly (9,9-n-dihexyl-2,7-fluorene-alt-9-phenyl-3,6-carbazole) (F6PC). The materials were compared to evaluate their properties using Spectroscopic Ellipsometry, Photoluminescence, and Atomic Force Microscopy (AFM). Additionally, the electrical characteristics of the OLED devices were investigated, as well as the stability of the electroluminescence emission spectrum during the device’s operation. Finally, the determined optical properties, combined with their photo- and electro-emission characteristics, provided significant insights into the color stability and selectivity of each material. Full article

We performed an electrochromic investigation to optimize the composition of reactive magnetron-sputtered mixed layers of zinc oxide and tin oxide (ZnO-SnO₂). Deposition experiments were conducted as a combinatorial material synthesis approach. The binary system for the samples of SnO₂-ZnO represented the full composition range. The coloration efficiency (CE) was determined for the mixed oxide films with the simultaneous measurement of layer transmittance, in a conventional three-electrode configuration, and an electric current was applied by using organic propylene carbonate electrolyte cells. The optical parameters and composition were measured and mapped by using spectroscopic ellipsometry (SE). Scanning Electron Microscopy (SEM) and Energy-Dispersive X-ray Spectroscopy (EDS) measurements were carried out to check the SE results, for (TiO₂-SnO₂). Pure metal targets were placed separately from each other, and the indium–tin-oxide (ITO)-covered glass samples and Si-probes on a glass holder were moved under the two separated targets (Zn and Sn) in a reactive argon–oxygen (Ar-O₂) gas mixture. This combinatorial process ensured that all the compositions (from 0 to 100%) were achieved in the same sputtering chamber after one sputtering preparation cycle. The CE data evaluated from the electro-optical measurements plotted against the composition displayed a characteristic maximum at around 29% ZnO. The accuracy of our combinatorial approach was 5%. Full article

The azomethine TPA-(BTZ)₃-TPA with a donor–acceptor–acceptor–acceptor–donor structure has been synthesized and characterized. Azomethine TPA-(BTZ)₃-TPA exhibited luminescence properties and a positive solvatochromic effect. Electropolymerization on terminated triphenylamine groups was used to obtain a thin layer of the polyazomethine poly-[TPA-(BTZ)₃-TPA]. Further investigation of oxidation/reduction properties of poly-[TPA-(BTZ)₃-TPA] via cyclic voltammetry showed that the polymer undergoes two reversible oxidation/reduction processes due to the presence of tetraphenylbenzidine moieties. Electrochromic properties of the polyazomethine poly-[TPA-(BTZ)₃-TPA] were investigated via spectroelectrochemistry. It was observed that the polymer in its neutral state is orange, and the color changes to green upon electro-oxidation. The stability of the polymer during multiple oxidation/reduction cycles, response times, and coloration efficiency were also investigated. Full article

This study reports, for the first time, on the assessment of a multistage sequential system composed of coagulation–flocculation with different electro-Fenton-based configurations, followed by neutralization (N), for the treatment of raw textile wastewater heavily contaminated with acid black 194 dye and other pollutants. Electrochemical peroxidation (ECP-N), electro-Fenton (EF-N) and peroxi-coagulation (PC-N) were tested at laboratory scale and compared in terms of their efficiency for the removal of organic matter and color, current efficiency and energetic parameter, operating cost and environmental sustainability using life cycle analysis conducted in large-scale virtual reactors. The three electro-Fenton-based systems complied with current environmental standards (color removal > 87%, COD < 400 mg/L, among others) requiring different electrolysis times: ECP-N (52 min) < PC-N (120 min) < EF-N (160 min); energy consumptions: ECP-N (2.27 kWh/m³) < PC-N (4.28 kWh/m³) < EF-N (33.2 kWh/m³); operational costs: ECP-N (2.63 USD/m³) < EF-N (6.65 USD/m³) < PC-N (6.98 USD/m³); among others. Electricity (for ECP-N and EF-N) and reagents (for ECP-N and PC-N) were found as main environmental hotspots. ECP-N presented the lowest carbon footprint of 10.3 kg CO₂-Eq/FU (<PC-N (26.3 kg CO₂-Eq/FU) < EF-N (38.0 kg CO₂-Eq/FU), had lower incidence in all the impact categories analyzed (ReCiPe-2016 at midpoint level) and can be considered technically, economically and environmentally sustainable for large-scale applications. Full article

Background: Tooth whitening with peroxide is linked to a number of negative consequences. This study aimed to evaluate the effect of tooth bleaching and color safety using no-ozone cold atmospheric-pressure plasma (NCP) with distilled water (DW) and to assess the microhardness and mineral composition of the treated teeth. Methods: The enamel of 90 extracted human teeth were randomly assigned to three groups (n = 30): Group 1 (no treatment), Group 2 (NCP + DW), and Group 3 (only DW). The overall color change (ΔE) was observed at 10 min, 20 min, 30 min, 1 day, 7 days, 1 month, 3 months, and 6 months after treatment and quantified. Six cadavers treated with NCP and DW for 30 min were evaluated for color change using ShadeEye NCC and the VITA Easyshade. Furthermore, the microhardness and mineral composition of the teeth were evaluated using a Vickers hardness tester and an electro micro analyzer, respectively. All statistical data were analyzed at a significance level of 5%. Results: Group 1 showed no color change. The ΔE values of Group 2 were 17.67 and 5.62 times higher than those of Group 3 after 30 min and 6 months, respectively. Methylene blue solution revealed that the concentration of hydroxyl radicals was higher in Group 2. The average ΔE value using ShadeEye NCC for cadaveric teeth was 4.0. Evaluation via VITA Easyshade showed that the brightness was increased by 5 levels. No significant differences were observed among the groups in terms of the microhardness of the enamel and dentin or the Ca, P, Na, Cl, Zn, and Mg values in the enamel and dentin. Conclusions: Tooth bleaching using NCP with DW exhibited high efficacy without inducing damage or demineralization in the dental hard tissue. Full article

A method for accurately determining the chemical composition of deposits at the bottom of pores during the electrocoloring (e-coloring) of aluminum anodic oxide (AAO) layers in tin-based solutions is developed. The aluminum samples were AC e-colored after DC sulfuric anodization. Free-standing, tin e-colored aluminum oxide film was obtained by selective dissolution of the metallic aluminum from the AAO in copper chloride solution to access the deposit directly at the bottom of the pore. This allowed us to conduct XPS analysis directly on the deposits at pore bottoms without any interference from the base material or insulating barrier layer. The results revealed the presence of a mixture of tin oxide and metal in the deposits, which were richer in oxide content. Furthermore, a cyclic voltammetry experiment mimicking real polarization conditions during AC conditions was optimized and used to gain a deeper understanding of the electrochemical reactions that occur during AC electrocoloring. The comparison of CV results in tin-free and tin-containing electrolytes indicated that the tin deposited during a cathodic cycle is oxidized in the anodic cycle. The formation of tin-based deposits radically changed the CV behavior. The XPS and cyclic voltammetry results consistently show that the deposits formed during e-coloring comprised a mixture of metallic and oxidic tin species richer in oxide content. Full article

The treatment of stabilized leachates with high refractory organic matter content, which are over 10 years old, presents a challenge. This study explored the potential of electro-coagulation (EC) and electro-oxidation (EO) treatment systems to address this issue. The objective of this study was to investigate the phytotoxicity of the proposed treatment system on seed growth and examine possible relationships between phytotoxicity results and the characterization of leachates, effluents, soil, and radicles. Phytotoxicity tests were conducted on seeds of Lactuca sativa, Cucumis sativus, and Phaseolus vulgaris, using Inductively Coupled Plasma-Optical analysis. The evolution of organic matter was monitored by fractionating the chemical oxygen demand (COD) and humic substances. The biodegradability index increased from 0.094 in raw leachate to 0.26 and 0.48 with EC and EO, respectively. Removal rates of 82%, 86%, 99%, and 81% were achieved for COD, dissolved organic carbon, color, and ammoniacal nitrogen, respectively. The biodegradable COD increased from 26% in raw leachate to 39% in the EC process and 58% in the EO process effluent. The proposed treatment system successfully broke the aromatic structures of the humic substances present in the raw leachate, thereby increasing the content of biodegradable material. Phytotoxicity tests revealed that the proposed treatment system significantly reduced the phytotoxicity of the generated effluents. Full article

Food colorants are important in food selection because they improve the gastronomic appeal of foods by improving their aesthetic appeal. However, after prolonged use, many colorants turn toxic and cause medical problems. A synthetic azo-class dye called carmoisine gives meals a red color. Therefore, the carmoisine determination in food samples is of great importance from the human health control. The current work was developed to synthesis ZnO hollow quasi-spheres (ZnO HQSs) to prepare a new electrochemical carmoisine sensor that is sensitive. Field emission-scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD) have been used to analyze the properties of prepared ZnO HQSs. A screen-printed graphite electrode (SPGE) surface was modified with ZnO HQSs to prepare the ZnO HQSs-SPGE sensor. For carmoisine detection, the ZnO HQSs-SPGE demonstrated an appropriate response and notable electrocatalytic activities. The carmoisine electro-oxidation signal was significantly stronger on the ZnO HQSs-SPGE surface compared to the bare SPGE. Cyclic voltammetry (CV), linear sweep voltammetry (LSV), chronoamperometry (CHA), and differential pulse voltammetry (DPV) have been utilized to investigate the suggested protocol. The DPV results revealed an extensive linear association between variable carmoisine concentrations and peak current that ranged from 0.08 to 190.0 µM, with a limit of detection (LOD) as narrow as 0.02 µM. The ZnO HQSs-SPGE’s ability to detect carmoisine in real samples proved the sensor’s practical application. Full article

In nature, some organisms have the ability to camouflage to adapt to environmental changes; they blend with the environment by changing their skin colors. Such a phenomenon is of great significance for the research of adaptive camouflage materials. In this study, we propose a novel design scheme for the study of angle-independent photonic materials and successfully prepare an electrically tunable multi-color display angle-independent inverse opal photonic gel (IOPG). After photopolymerization of hydroxyethyl methacrylate with ionizable monomer acrylic acid (AA) in a long-range disordered opal template and etching, the angle-independent inverse opal photonic gel is obtained, presenting a single structural color. The electrically responsive color changes can be achieved at different angles. The color of the disordered AA-IOPG changes from green to blue-green when applying +4 V bias voltage and from green to orange when applying −4 V bias voltage. The electrochromism of the disordered AA-IOPG is mainly due to the local pH change caused by water electrolysis under bias voltage, which leads to a change of the swelling ratio. The disordered AA-IOPG shows high color tunability and durability through repeated opposite bias voltage tests, indicating that it is a promising conductive photonic material. Full article

In this paper, dye-doped polymer-dispersed liquid crystalline (DDPDLC) films were prepared with high mechanical properties and low driving voltage by doping different dichroic anthraquinone dyes. The effects of various dye and doping concentrations on microscopic morphology, electro-optical characteristics, and mechanical characteristics were investigated. The optimal doping concentrations of different dyes were also explored. The results show that the addition of all dyes decreased the contrast ratio (CR) and the transmittance and mechanical properties of the polymer-dispersed liquid crystalline (PDLC) films. Similar mechanisms underlie the effects of solvent red 111 and solvent blue 104, which lower the driving voltages of the PDLC films. With the increasing concentration of the dye, the haze of the films first decreased and then increased after the content of the dye reached a certain level. For PDLC films doped with solvent green 28, the driving voltage and haze increased with the increasing content of the dye. According to different influencing factors, the dye content corresponding to the best performance of solvent red 111, solvent green 28 and solvent blue 104 is 0.8 wt%, 2.0 wt% and 0.3 wt%. Electrochromic PDLC films have been prepared based on the research results of dye content. The mechanical properties, electro-optical properties and microstructures of the films have been studied. The results show that the DDPDLC films could change color by tuning the applied voltages. The research provides a theoretical basis for obtaining PDLC films with a wider color gamut and supports the practical application of visible light camouflage technology in the military. Full article