Mixed Solution Research Articles

Baseband modulational instability and interacting localized mixed waves in coherently coupled optical media

We consider a coherently coupled nonlinear Schrödinger equations (model equations) that describe interacting localized waves in coherently coupled optical media. The baseband modulational instability in such regimes is investigated, leading the result that the modulational instability does not necessary imply the baseband modulational instability. By means of a set of linear transformations, the model equations are converted into two independent scalar nonlinear Schrödinger equations. Based on the generalized perturbation (n,N−n)–fold Darboux transformation, we report and discuss analytical mixed localized wave solutions of these scalar equations. A first-order rogue wave solution of the scalar nonlinear Schrödinger equations is also presented. We then show that linear superpositions of different found analytical mixed localized wave solutions of the derived scalar equations results into several kinds of coherent nonlinear mixed structures such as, coexisting brigth/dark soliton-breather, rogue wave-breather-soliton, interacting rogue waves, bright/dark breathers, and bright/dark solitons.

Development of an HPLC device with water/acetonitrile with NaCl mixed solution that induces a phase-separation multiphase flow as the eluent in the separation column.

We developed a novel HPLC device where the phase-separation multiphase flow worked as the eluent in the separation column by using a water/acetonitrile/ethyl acetate triple mixed solution as a dual-phase-separation solution. Dual-phase-separation solutions form a phase-separation multiphase flow in a microscopic space. The new separation mechanism in the HPLC is called phase-separation mode. In this study, we used water and acetonitrile with NaCl mixed solution as a dual-phase-separation solution instead of the triple mixed solution. Octadecylsilyl (ODS)-modified particle- and porous silica particle-packed separation columns were united with the HPLC device for phase-separation mode caused by phase-separation multiphase flow. NA (1-naphthol) and NDS (2,6-naphthalenedisulfonic acid) were analyzed by the device as model sample. Using the water and acetonitrile with NaCl mixed solution at the solvent volume ratio of 5:5, NA and NDS were not separated on either column at 25°C. On the other hand, they were separated with the order NDS and NA on the ODS column and separated with the order NA and NDS on the silica column in phase-separation mode at 0°C. We discuss the separation mechanism of phase-separation mode using the water and acetonitrile with NaCl mixed solution at 0°C.

Improved Bi(III) absorption and selectivity in cubic TiP2O7 with three-dimensional ion channels

TiP2O7 with enhanced adsorption capacity and selectivity removal ability has emerged as a promising adsorbent for the treatment of heavy metal ions. Herein, layered and cubic TiP2O7@C (LTO and CTO) were prepared by a solvothermal method combined with calcination at 700 and 800 °C, respectively. Compared to the large and non-uniform particles of LTO, the prepared CTO exhibits a honeycomb-like interconnected porous structure composed of uniformly sized ∼25 nm particles and provides a higher concentration of P–OH and Ti–O bonds. Benefiting from the advantages of the physicochemical structure, the adsorption capacity of CTO for Bi(III) was about 1.9 times higher than that of LTO, with a value as high as 54.5 mg g−1. Furthermore, the removal efficiency of Bi(III) from a mixed solution containing eleven ions at a concentration of 10 mg L−1 was as high as 97.5 %, demonstrating its exceptional selective adsorption capacity for Bi(III). The Bi(III) adsorption process is controlled by surface hydroxyl functional groups and follows a quasi-secondary kinetic model. This work may shed light on the synthesis of TiP2O7 and its application in water purification.

An optimisation study for leaching synthetic scheelite in H2SO4 and H2O2 solution

ABSTRACT Tungsten production primarily relies on scheelite, a secondary resource due to its complex ore composition and lower grade compared to high-grade wolframite. Synthetic scheelite gains significance for its low impurity content and accessibility in ongoing laboratory-based investigations. Recent advancements offer a feasible environment-friendly leaching method using a mixed solution of H2SO4 and H2O2 under normal pressure and moderate temperatures. However, comprehensive research on this novel method is lacking, emphasising the need for collaborative exploration and operational optimisation. The present work is to provide insights and improvements in reagent usage to promote economic and environmental sustainability. A detailed investigation into the thermal decomposition process was also conducted without compromising leaching efficiency. The findings suggest the potential for eco-friendly lixivium recycling with reduced levels of chemicals, decreasing operational costs. Notably, optimising the thermal decomposition duration to 6 hours at an L/S (mL/g) ratio of 10 enhances H2WO4 crystallization. Furthermore, experiments without H2SO4 supplementation highlight the system's optimisation potential. Finally, the leaching process was optimised by decreasing H2SO4 concentration to 1 mol/L from 3 mol/L, increasing the temperature to 60°C, and extending the leaching duration to 120 minutes. This leads to a cost-effective synthetic scheelite leaching process with environmental benefits.

Component Effects in Binary Droplet Impact Behaviors on the Heated Plate: Comparison Study of Ethanol/Propanol and Ethanol/Water Droplets and Observation of Novel Bubble Shrinkage Phenomenon

This work aims to investigate the effect of liquid physical properties on the behavior of binary droplets impact on the heated smooth aluminum alloy plate with a high-speed imaging system. Two groups of mixed solutions with similar boiling point differences are selected as the working liquid, in which the low-boiling-point components are both ethanol and the high-boiling point components are propanol and water, respectively. Compared to the ethanol/propanol binary droplets, the experimental results show that the ethanol/water binary droplets have diverse impact phenomena and significantly broad transition boiling regimes, as well as the reduced droplet residence time and increased Leidenfrost temperature point. With the decreasing ethanol content in ethanol/water binary droplets, these effects become more prominent. For secondary atomization, the ethanol/water binary droplet undergoes parent droplet breakup into fragment droplets with larger diameters (Ds > 0.3 mm). Both binary droplets produce satellite droplets with small diameters (Ds < 0.3 mm) by puffing and ejection. In terms of the ethanol/propanol binary droplet impact, the probability of puffing is higher and the satellite droplet diameters are small. In the ethanol/water binary droplet impact, the probability of ejection is higher and the satellite droplet diameter distribution is wider. When an ethanol/water binary droplet of 25 vol.% ethanol content impacts the heated wall at Ts = 120 °C, a novel large bubble shrinkage phenomenon occurs at the late stage of droplet evaporation. This phenomenon is proposed to be relevant to the increasing surface tension and saturation temperature with decreasing ethanol content, as well as the decreasing ambient temperature above the top surface of the bubble.

System optimization study of hybrid K-edge/XRF densitometer for uranium–plutonium solution measurement

In this paper, a comprehensive hybrid K-edge/XRF densitometer (HKED) device model is constructed using MCNP simulation. After the modeling process, a systematic simulation study is conducted to analyze the physical parameters and material selection of KED and XRF. The simulation results reveal that the optimal parameters for the X-ray tube are an X-ray source voltage of 160 kV and a 1 mm Fe filter. The sample should be placed in a vial with an inner diameter of 1.4 cm and an outer diameter of 2 cm. For the KED technique, the determined main parameters are a 1.9 cm Fe filter rod and an inner diameter of 0.08 cm for the collimator. For the XRF technique, the determined main parameters are a 0.01 cm Gd filter and an inner diameter of 0.3 cm for the collimator, with a detector angle of 150°. After selecting appropriate parameters, the average calibration factor Δμ of the KED technique was found to be 3.301 cm2 g−1, with a relative standard deviation (RSD) of 3.36%. Additionally, the comparison between the simulated and calculated values of uranium concentration revealed a minimum measurement error of 0.4%. The minimum detection concentration of KED for uranium solutions is approximately 1 g/L. For plutonium solutions ranging from 0.5 to 20 g/L, linear fitting of the Ka1 net peak area and plutonium concentration showed a coefficient of determination (R2) of 0.999. The detection limit of XRF for plutonium measurement was 2.33✕10−4 g/L. The linear fitting coefficients (R2) of uranium concentration versus K-edge transmission rate and plutonium concentration versus Ka1 net peak area for the hybrid technique in measuring uranium-plutonium mixed solutions are determined as 0.999 and 0.996, respectively, demonstrating the response relationship of the HKED device to uranium and plutonium under different concentrations.

Green Fabrication of Superhydrophilic/Underwater Superoleophobic Composite Membrane for High-Efficiency Oil/Water Separation in Harsh Environments.

Due to the high oil spill incidence and industrial wastewater discharge including oil and emulsified oil, designing and synthesizing oil-water separation materials which can maintain stability under harsh environmental conditions with high separation efficiencies remains a great challenge. The present work developed an easy, green, cost-effective, and easily scaled-up approach for fabricating cellulose-based membranes. First, we coated polydopamine (PDA) onto fibers of filter membrane (FM). Then, the PDA-FM membrane was immersed into the mixed solution of poly(vinyl alcohol)/poly(acrylic acid) (PVA/PAA) and further thermally cross-linked at 150 °C to create a superhydrophilic/underwater superoleophobic membrane (PVA/PAA@PDA-FM) to separate oil/water mixtures. The simple thermally cross-linking process promotes multiple covalent chemical bonds generation between cellulose filter membrane, PAA, PDA, and PVA, endowing membranes with excellent stability and resistance to acidity, alkalinity, and salinity. The PVA/PAA@PDA-FM membrane not only demonstrates great separation performance (>99.8%) and great flux (>1000 L m-2 h-1) in oil-water immiscible mixtures but also maintains high separation efficiency under conditions of high acidity, alkalinity, and salinity. Additionally, the PVA/PAA@PDA-FM membrane exhibits excellent separation capacity in oil-water emulsions, which can maintain the >99.6% separation efficiency even after 40 cycles in harsh environments, showing outstanding reusability. Thus, due to the multiple cross-linked networks in the membrane, the excellent performance makes the PVA/PAA@PDA-FM membrane a good application prospect in water purification and oily wastewater treatment.

Mixed series solution for vibration and stability of porous bi-directional functionally graded beams

Mixed series solution for vibration and stability of porous bi-directional functionally graded beams

Solvent Regulation Induced Cathode Aggregation-Induced Electrochemiluminescence of Tetraphenylethylene Nanoaggregates for Ultrasensitive Zearalenone Analysis.

Zearalenone (ZEN) is an extremely hazardous chemical widely existing in cereals, and its high-sensitivity detection possesses significant significance to human health. Here, the cathodic aggregation-induced electrochemiluminescence (AIECL) performance of tetraphenylethylene nanoaggregates (TPE NAs) was modulated by solvent regulation, based on which an electrochemiluminescence (ECL) aptasensor was constructed for sensitive detection of ZEN. The aggregation state and AIECL of TPE NAs were directly and simply controlled by adjusting the type of organic solvent and the fraction of water, which solved the current shortcomings of low strength and weak stability of the cathode ECL signal for TPE. Impressively, in a tetrahydrofuran-water mixed solution (volume ratio, 6:4), the relative ECL efficiency of TPE NAs reached 16.03%, which was 9.2 times that in pure water conditions, and the maximum ECL spectral wavelength was obviously red-shifted to 617 nm. In addition, "H"-shape DNA structure-mediated dual-catalyzed hairpin self-assembly (H-D-CHA) with higher efficiency by the synergistic effect between the two CHA reactions was utilized to construct a sensitive ECL aptasensor for ZEN analysis with a low detection limit of 0.362 fg/mL. In conclusion, solvent regulation was a simple and efficient method for improving the performance of AIECL materials, and the proposed ECL aptasensor had great potential for ZEN monitoring in food safety.

Study on the microwave absorbing properties of SiC@Ni powders with core@shell structure

Hybridization of dielectric and magnetic materials is considered a promising option for the preparation of electromagnetic wave absorbing materials with excellent properties. In this paper, SiC@Ni powders were prepared by a surface heat-assisted process, in which SiC was first cleaned sequentially with anhydrous ethanol and NaOH solutions, and the samples were etched into a mixed solution of HF and HCl, the SiC@Ni powders were then mixed at high speed at 120 °C under argon atmosphere. The sample were characterized by Scanning electron microscopy (SEM) and vector network analyzer (VNA). It is found that the absorption characteristics of SiC@Ni in the 2–18 GHz band are significantly enhanced due to the introduction of the ni layer which enhances the loss of the sample to solve the problem of a single absorption mechanism and high impedance of SiC. The reflection loss value of SiC@Ni in the 8.7 GHz band decreases to − 22.45 dB when the material thickness is 2.5 mm, the effective absorption frequency width is 2.5 GHz, which is a significant advantage over the initial SiC. The experimental methodology of this work is simple and easy to follow, and provides some guidance for the large-scale production of SiC-based microwave absorbing materials.

Coordination and non-coordination functional hmta directed 2-D iodoplumbate hybrids with efficient visible-light-driven photocatalytic performance

The solvothermal reaction of PbI2, KI and HI in a H2O/DMF mixed solution in the presence of the coordination functional template hexamethylenetetramine (hmta) produced a 2-D iodoplumbate hybrid [Hhmta]2[(hmta)2Pb4I10]·2DMF·H2O (1). The hmta molecule was methylated by MeOH to form a mhmta+ (mhmta+ = N-methylhexamethylenetetramine) cation in the same reaction in H2O/MeOH solution. The mhmta+ cation lost its coordination function, leading to the formation of the 2-D iodoplumbate hybrid [mhmta]4[Pb3I10]·H2O (2). In 1, the PbI5 units are interconnected via edge- and face-sharing into a 1-D chain [Pb4I10]n2n−. The [Pb4I10]n2n− chains are linked by μ-hmta bridging ligand to form a 2-D [(hmta)2Pb4I10]n2n− layer. In 2, three PbI6 octahedra are joined by face-sharing to form a trinuclear [Pb3I12] SBU. The [Pb3I12] SBUs are connected into a 2-D [Pb3I10]n4n− anionic layer by corner- sharing. Compounds 1 and 2 exhibited rapid photocurrent responses with steady current densities of 7.71 μA·cm−2 and 10.68 μA·cm−2, respectively. These compounds exhibited high catalytic activity in the photodegradation of crystal violet with degradation rates of 96.5 % over 1 and 97.8 % over 2.

Transport and separation behaviors of crosslinked GO/PVA sponge with high porosity

Separation materials (technology) with high efficiency and high precision is a goal that researchers are relentlessly pursuing. Here, crosslinked graphene oxide and polyvinyl alcohol (GO/PVA) sponges with high porosity are reported, which were constructed by crosslinking a dilute solution of GO/PVA. The structure and transport characteristics of the sponges were investigated. It was found that it took 150 days for 30 mg/L methylene blue (MB) to diffuse from the side of crosslinked GO/PVA sponge (10 mm thickness) to the other side (breakthrough) even though the porosity of sponge was up to 92.9 %, while it needed only 2 days in PVA sponge and 13 days for methyl orange (MO) in the sponge. Hence, the transport and separation behaviors of more substances were explored and it is found that not only a precise separation of more than 99 % was achieved for MB/MO (similar molecular weight) mixed solution due to the extremely wide difference of transport rate, but also a water permeability of (4.3 × 105 L·m−2·h−1·Mpa-1) was reached under 10 cm height of water column pressure (0.01 bar), which is three orders of magnitude higher than that of nanofiltration membrane. The extremely high selectivity and efficiency to MB are attributed to the structural features of the sponge, i.e., the fully dispersed GO nanosheets and their crosslinking structure with PVA. Thus, the adsorption amount, adsorption rate, and adsorption strength to MB were greatly improved due to a synergistic effect of GO and PVA, and the highly efficient, precise, and rapid separation of MB was realized. In addition, the structural characteristics of the sponges favor the slow transport of many substances, which will extend their applications to the controlled release field.

Micropatternable Ink Composed of MAX Phase ZIF-8 for Gas Sensing Applications

This work provides a detailed introduction to the preparation methods, structural characteristics, and various performance tests of the Ti3C2/ZIF-8 composite material. Initially, the composite material is obtained through the synthesis, mixing, and subsequent processing of MXene solution and ZIF-8 nanoparticles. The coating structure and properties were comprehensively characterized using SEM, TEM, and XRD. These analyses revealed the material's layered structure, high crystallinity, and surface activity. BET analysis of Ti3C2/ZIF-8 also shows excellent gas adsorption-desorption performance, having an especially high-efficiency adsorption capacity for VOCs. TGA further demonstrates the thermal stability and chemical stability of Ti3C2/ZIF-8 and its printability was tested indicating widespread application potential in coating preparation through ultrasonic spray technology. Finally, we show methods to regulate and control coating thickness and roughness for precision manufacturing. These analyses together emphasize the application value of Ti3C2/ZIF-8 in fields such as gas-storage, gas-separation, and environmental monitoring.

Facile Fabrication of Porous Adsorbent with Multiple Amine Groups for Efficient and Selective Removal of Amaranth and Tartrazine Dyes from Water.

The development of an advanced dye adsorbent that possesses a range of beneficial characteristics, such as high adsorption capacity, swift adsorption kinetics, selective adsorption capability, and robust reusability, remains a challenge. This study introduces a facile method for fabricating an amine-rich porous adsorbent (ARPA), which is specifically engineered for the adsorptive removal of anionic dyes from aqueous solutions. Through a comprehensive assessment, we have evaluated the adsorption performance of ARPA using two benchmark dyes: amaranth (ART) and tartrazine (TTZ). Our findings indicate that the adsorption process reaches equilibrium in a remarkably short timeframe of just 20 min, and it exhibits an excellent correlation with both the Langmuir isotherm model and the pseudo-second-order kinetic model. Furthermore, ARPA has demonstrated an exceptional maximum adsorption capacity, with values of 675.68 mg g-1 for ART and 534.76 mg g-1 for TTZ. In addition to its high adsorption capacity, ARPA has also shown remarkable selectivity, as evidenced by its ability to selectively adsorb TTZ from a mixed dye solution, a feature that is highly desirable for practical applications. Beyond its impressive adsorption capabilities, ARPA can be efficiently regenerated and recycled. It maintains a high level of original removal efficiency for both ART (76.8%) and TTZ (78.9%) even after five consecutive cycles of adsorption and desorption. Considering the simplicity of its synthesis and its outstanding adsorption performance, ARPA emerges as a highly promising material for use in dye removal applications. Consequently, this paper presents a straightforward and feasible method for the production of an effective dye adsorbent for environmental remediation.

Open-Nanogap-Induced Strong Electromagnetic Enhancement in Au/AgAu Monolayer as a Stable and Uniform SERS Substrate for Ultrasensitive Detection.

Nanogap-based plasmonic metal nanocrystals have been applied in surface-enhanced Raman scattering detection, while the closed and insufficient electromagnetic fields as well as the nonreproducible Raman signal of the substrate greatly restrict the actual application. Herein, a highly uniform Au/AgAu monolayer with abundant nanogaps and huge electromagnetic enhancement is prepared, which shows ultrasensitive and reproducible SERS detection. Au/AgAu with an inner nanogap is first prepared based on Au nanotriangles, and the nanogap is opened from the three tips via a subsequent etching process. The open-gap Au/AgAu displays much higher SERS efficiency than Au and Au/AgAu with an inner nanogap on detecting crystal violet due to the open-gap induced electromagnetic enhancement and improved molecular absorption. Furthermore, the open-gap Au/AgAu monolayer is prepared via interfacial self-assembly, which shows further improved SERS due to the dense and strong hotspots in the nanocavities induced by the electromagnetic coupling between adjacent open gaps. The monolayer possesses excellent signal stability, uniformity, and reproducibility. The analytic enhancement factor and relative standard deviation reach to 2.12 × 108 and 4.65% on detecting crystal violet, respectively. Moreover, the monolayer achieves efficient detection of thiram in apple juice, biphenyl-4-thiol, 4-mercaptobenzoic, melamine, and a mixed solution of four different molecules, showing great promise in practical detection.

Microstructure development of Ti scaffold by laser powder bed fusion with chemical polishing and its mechanical properties, biocompatibility

AbstractTitanium (Ti) dental scaffolds are widely used in dental prosthetics due to their excellent mechanical properties and biocompatibility. However, conventional Ti scaffolds manufactured through machining often do not fit perfectly with the bone defect site. Laser powder bed fusion (LPBF) technology enables the personalised manufacturing of custom‐made Ti scaffolds. A custom‐made Ti scaffold was prepared using LPBF and its surface roughness was improved through chemical polishing. To enhance the surface roughness, a nitric acid mixed solution with a specific composition of HF: HNO3:C3H6O3 = 2:2:3 was used. The polishing mechanism was investigated by adjusting the F/Ti ratio to control the formation and dissolution of the oxide film. As a result, the surface of the Ti scaffold after polishing exhibited a smooth and flat appearance compared to the LPBF part, with a reduced surface roughness (Ra) of 1.23 ± 0.19 μm. The custom‐made Ti scaffold also demonstrated favourable mechanical properties, with a bending strength of 335.18 ± 33.62 MPa and stiffness of 2.13 ± 0.21 GPa. Furthermore, in vitro cell tests confirmed the excellent biocompatibility of the custom‐made Ti scaffold. The authors present a feasible strategy for the further clinical application of custom‐made Ti scaffolds, offering enhanced surface properties and addressing the limitations of conventional machining methods.

Towards the understanding of convective dissolution in confined porous media: thin bead pack experiments, two-dimensional direct numerical simulations and physical models

We consider the process of convective dissolution in a homogeneous and isotropic porous medium. The flow is unstable due to the presence of a solute that induces a density difference responsible for driving the flow. The mixing dynamics is thus driven by a Rayleigh–Taylor instability at the pore scale. We investigate the flow at the scale of the pores using Hele-Shaw type experiment with bead packs, two-dimensional direct numerical simulations and physical models. Experiments and simulations have been specifically designed to mimic the same flow conditions, namely matching porosities, high Schmidt numbers and linear dependency of fluid density with solute concentration. In addition, the solid obstacles of the medium are impermeable to fluid and solute. We characterise the evolution of the flow via the mixing length, which quantifies the extension of the mixing region and grows linearly in time. The flow structure, analysed via the centreline mean wavelength, is observed to grow in agreement with theoretical predictions. Finally, we analyse the dissolution dynamics of the system, quantified through the mean scalar dissipation, and three mixing regimes are observed. Initially, the evolution is controlled by diffusion, which produces solute mixing across the initial horizontal interface. Then, when the interfacial diffusive layer is sufficiently thick, it becomes unstable, forming finger-like structures and driving the system into a convection-dominated phase. Finally, when the fingers have grown sufficiently to touch the horizontal boundaries of the domain, the mixing reduces dramatically due to the absence of fresh unmixed fluid. With the aid of simple physical models, we explain the physics of the results obtained numerically and experimentally. The solute evolution presents a self-similar behaviour, and it is controlled by different length scales in each stage of the mixing process, namely the length scale of diffusion, the pore size and the domain height.

Soliton Solutions of Some Ocean Waves Supported by Physics Informed Neural Network Method

In this study, we aim to obtain numerical results of the modified Benjamin-Bona-Mahony equation, Ostrovsky-Benjamin-Bona-Mahony equation and Mikhailov-Novikov-Wang equation via the physics-informed neural networks (PINN) method. The equations are modeled for shallow and long water waves, as well as fundamental and phenomenonal models in ocean engineering. According to the implementation, we obtained the PINN solutions of kink, bright, multisoliton (two-soliton) and mixed dark-bright soliton solutions. According to the inference from the obtained results, we achieved good results in some cases compared to other approximate solution methods in the literature. However, it was also observed that the best possible results could not be obtained in cases where the soliton type was intricate and layered. While the results were obtained, the number of hidden layers and the number of neural networks in the layers also varied. These results are shown in tables. Since it is known that the aforementioned models are not solved by the PINN method, we anticipate that the study will lead to other studies in the field of ocean engineering.

Fabrication of Al doped α-GaOOH nanorod arrays on FTO for self-powered photoelectrochemical solar-blind UV photodetectors

Al doped α-GaOOH nanorod arrays were grown on FTO via hydrothermal processes by using gallium nitrate and aluminum nitrate mixed aqueous solutions with fixed 1:1 mole ratio as precursors. With increasing the gallium nitrate precursor concentrations, the Ga/Al atom ratios in nanorod arrays increase from 0.36 to 2.08, and the length becomes much longer from 650 nm to 1.04 μm. According to the binding energy difference between Ga 2p3/2 core level and its background in x-ray photoelectron spectroscopy, the bandgap is estimated to be around 5.3 ± 0.2 eV. Al doped α-GaOOH nanorod array/FTO photoelectrochemical photodetectors show enhanced self-powered solar-blind UV photodetection properties, with the decrease of Ga precursor concentrations. The maximum responsivity at 255 nm is 0.09 mA W−1, and the fastest response time can reach 0.05 s. The improved photoresponse speed is ascribed from much shorter transportation route, accelerated carrier recombination by recombination centers, and smaller charge transfer resistance at the α-GaOOH/electrolyte interface with decreasing the gallium nitrate precursor concentrations. The stability and responsivity should be further improved. Nevertheless, this work firstly demonstrates the realization of self-powered solar-blind UV photodetection for α-GaOOH nanorod arrays on FTO via Al doping.

Research on infrared spectroscopy detection of furfural content in transformer oil based on acetonitrile extraction

Abstract The stable operation of power transformers depends on the oil-paper insulation system, in which the aging degree of insulating paper is the key to evaluate the remaining life of the transformer. Currently, methanol extraction is widely used to detect the furfural content in oil to evaluate the aging state of insulating paper, but it ignores the influence of methanol produced during the operation of the transformer on the extraction results. To address this issue, this paper proposes a new method that can replace methanol extraction for detecting furfural in oil through simulation and experiment. Firstly, through simulation and experiment, it is proved that the strong vibration absorption peaks at 1677 cm-1 for furfural carbonyl and 2240 cm-1 for acetonitrile cyano can be used to establish a new method for extracting furfural content in oil using acetonitrile. A quantitative model between the concentration x of furfural in the furfural-acetonitrile mixed solution and the area y of the infrared absorption peak at 1677 cm-1 is established, with a goodness of fit of 0.9974. Secondly, a comparison between direct detection and acetonitrile extraction methods is conducted. The results show that direct detection is simple to operate, but the minimum detection concentration is 40mg/L, which is difficult to meet practical requirements. Acetonitrile extraction can reduce the minimum detection concentration to 0.1mg/L. At the same time, the extraction conditions are analyzed to determine the extraction ratio of 30, extraction times of 5, and extraction rate of 60%. Finally, the proposed detection method is applied to thermal aging tests on insulating paper of different types. The experimental results show that the proposed method has good repeatability and improves the detection resolution of furfural content. This paper combines infrared spectroscopy with acetonitrile extraction technology to open up a more efficient and practical new method for detecting furfural content in transformer oil.