Microwave Hydrothermal Method Research Articles

Construction of novel dual wave-absorbing ZnFe2O4/CNTs nanoparticles with more hotspots for enhanced microwave-induced catalytic activity：Performance and mechanism

In this study, novel dual wave-absorbing ZnFe2O4/CNTs nanoparticles were successfully fabricated using a microwave hydrothermal method and applied for enhanced microwave-induced catalytic degradation of bisphenol A (BPA) in aqueous solution. The effects of various process parameters, including Fe3+ concentration (mass ratio of ZnFe2O4 to CNTs), MW irradiation time, MW power, initial BPA concentration, and catalyst dose on the degradation process were thoroughly assessed. The results indicate that ZnFe2O4/CNTs nanoparticles effectively utilize MW energy to generate more hot spots and exhibit superior MW catalytic activity at a 1.0:10.0 mass ratio (ZnFe2O4:CNTs), due to the synergistic effect between ZnFe2O4 nanoparticles and CNTs under MW irradiation. Additionally, hydroxyl radicals (·OH) play a major role in the degradation process, while superoxide radicals (·O2−) and holes (h+) play relatively minor roles. Potential intermediates and degradation pathways in the ZnFe2O4/CNTs/MW system have also been identified. Thus, the integrated ZnFe2O4/CNTs/MW technology shows great promise for treating environmental endocrine disruptors (EEDs) in water and wastewater.

Preparation of C@CuNi/TiO2 with a local surface plasmon resonance for photocatalytic degradation of organic dyes and antibiotics under visible light irradiation

A composite photocatalyst with carbon-coated CuNi nanoparticles-loaded TiO2 nanotubes (C@CuNi/TiO2) was synthesized via a microwave hydrothermal alkali stripping method combined with subsequent in-situ carbothermal reduction. The structure, morphology, and surface chemical composition were investigated using X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The findings demonstrate that the microwave hydrothermal alkali peeling enables the formation of a three-dimensional C@CuNi/TiO2 composite structure. The results of transient photocurrent response (i-t) and electrochemical impedance spectroscopy under visible light demonstrate that C@CuNi/TiO2 exhibits a reduced rate of electron-hole recombination and lower surface resistance compared to C@TiO2, C@Cu/TiO2, and C@Ni/TiO2. After a two-hour exposure to visible light, the composite photocatalyst C@CuNi/TiO2, featuring a molar ratio of 2 % CuNi nanoparticles to TiO2 nanotubes, exhibited remarkable degradation activity towards organic dyes (Rhodamine B (RhB), Methylene Blue (MB), Methyl Orange (MO)), as well as antibiotics (tetracycline (TC) and levofloxacin (LVFX)). After 5 cycles of photocatalytic reaction, the photodegradation activity of RhB remained above 79 %. It is indicated that CuNi nanoparticles effectively trap and enrich photoelectrons through the photoexcitation of TiO2 nanotubes. Additionally, the local surface plasmonic resonance (LSPR) effect of CuNi nanoparticles reduces the recombination rate of photogenerated electron/hole and the electron transport resistance in the composite photocatalyst, thereby enhancing its overall photocatalytic activity.

Defect Engineering in CuS1- x Nanoflowers Enables Low-Overpotential and Long-Cycle-Life of Lithium-Oxygen Batteries.

The defect engineering is essential for the development of efficient cathode catalysts for lithium-oxygen batteries. Herein, CuS1 -x nanoflowers are fabricated by microwave hydrothermal method. Through theoretical and experimental analysis, the S vacancies are observed, which result in augmented charge around Cu, improved adsorption of LiO2, and reduced overpotential. On the one hand, the generated electronic defects cause the Fermi level to shift toward the conduction band, which enhances the electronic conductivity and ion transfer. On the other hand, the increased S vacancies provide a large number of Cu active sites, which increase the charge transfer from Cu to LiO2, which improves the stability of the intermediate adsorption. Interactively, CuS1- x catalyst obtains a capacity of 23,227 mAh g-1 and a cycle life of 225 at 500mA g-1. This work will be helpful for obtaining an efficient cathode catalyst by providing a deep understanding of vacancy modulation in advanced catalysts.

High performance flexible phase change hydrogel applied to thermal management of new cigarette device

To address the thermal management challenges of new heat-not-burn (HNB) cigarette devices, this study aims to enhance overall energy conversion efficiency while maintaining unchanged battery capacity. The goal is to minimize heat dissipation and reduce the temperature of the device's housing that contacts the user. In this research, CaCl2·6H2O (CCH) was selected as the phase change material (PCM), and a polyacrylamide (PAM) phase change hydrogel encapsulating CCH was prepared via in-situ polymerization. Additionally, konjac glucomannan (KGM) was incorporated into the three-dimensional network structure of PAM through hydrogen bonding to promote the formation of a porous gel structure. CNTs-CuO composites, featuring in-situ generated CuO nanoparticles on carbon nanotubes (CNTs), were synthesized using a microwave hydrothermal method and employed to enhance the thermal conductivity of the phase change hydrogel.This study demonstrates that the three-dimensional porous network structure of the hydrogel not only provides effective encapsulation protection for CCH and maintains high latent heat (144.9 J/g), but also imparts excellent flexibility and stability to the composites. The incorporation of CNTs-CuO composites introduces efficient heat transfer channels, significantly increasing the thermal conductivity of the hydrogels by approximately 37 % (0.687 W·m−1·K−1). Moreover, the hydrogel composites exhibit exceptional temperature regulation properties.The innovative design and preparation of these hydrated salt-based flexible hydrogel composites offer a novel approach in the fields of thermal management and energy storage. This material demonstrates practical applications not only in HNB devices but also in various thermal management systems, such as wearable electronics, battery thermal management, and electronic device cooling. Furthermore, its application in energy storage systems, including thermal energy storage units and smart textiles, underscores its broad applicability and significance.

Monacolin-K loaded MIL-100(Fe) metal–organic framework induces ferroptosis on metastatic triple-negative breast cancer

Breast cancer is the most common disease among women worldwide. Triple-negative breast cancer (TNBC) is the most aggressive and has the worst prognosis. MIL-100(Fe) is a promising metal–organic framework (MOF). MIL-100(Fe) was loaded with monacolin K (MK) to form MK@MIL-100(Fe). MK was a natural compound with anticancer properties. The surface of MK@MIL-100(Fe) was coated with iron oxide (Fe3O4), and the microwave hydrothermal method was used to form the material MK@MIL-100(Fe)/Fe3O4 with metal–organic properties, which effectively increases the accumulation of reactive oxygen species and lipids in cancer cells. In the mouse model of metastatic TNBC formed by tail vein injection of 4 T1 cells, MK@MIL-100(Fe)/Fe3O4 inhibited the occurrence of metastatic TNBC without hair shedding, and no side effects were found. In cell and mouse experiments, expressions of ferroptosis-related proteins, glutathione peroxidase (GPX4), and 3-hydroxy-3-methyl-glutaryl-coA reductase (HMGCR) were reduced. Apoptotic regulatory factors were increased, as BH3 interacting-domain death agonist (BID), apoptosis-inducing factor (AIF), endonuclease G (Endo-G), bcl2-associated X protein (BAX) and caspase-3 (Casp3). Therefore, we demonstrated that the MOF has been functionalized to enhance its biocompatibility and iron targeting ability, and MK@MIL-100(Fe)/Fe3O4 served as a nanomedicine to inhibit TNBC through ferroptosis and apoptosis.

Fast and green synthesis of battery-type nickel-cobalt phosphate (NxCyP) binder-free electrode for supercapattery

Binder-free electrodes are increasingly important in energy storage technologies owing to the direct growth of active material on conducting substrates without binders, providing a shorter conduction channel for rapid electron transport. Various methods have been employed to synthesize binder-free electrodes, but most approaches often prove time-consuming, and some require elevated synthesis temperatures. Herein, a rapid and eco-friendly microwave-hydrothermal method was introduced to fabricate the battery-type nickel–cobalt phosphate (NxCyP) binder-free electrodes for supercapattery. The use of microwave accelerates heating and reduces the activation energy of the reaction, resulting in shorter synthesis time and lower reaction temperature. The NxCyP electrodes were fabricated at different parameters, such as temperature (90–200 °C), time (5–20 min), and Ni:Co precursor ratios (4:0, 3:1, 2:2, 1:3, 0:4). The optimization study was carried out via Design Expert v13 software, and the optimized parameter was the temperature of 123.5 °C, duration of 10.5 min, and Ni:Co of 2:2, namely N2C2P binder-free electrode. The N2C2P electrode exhibited larger flake- and flower-like morphologies, providing more space for electrolyte ion diffusion and a larger surface area for faradaic reactions. Consequently, it demonstrated outstanding electrochemical performance by displaying a high specific capacity (1699.7C/g at 3 mV/s), superior capacity retention, and the lowest resistances than other NxCyP electrodes. As a result, the N2C2P//AC supercapattery was created by merging it with an activated carbon (AC) electrode, showing a superior energy density (213.0 Wh/kg) and high electrochemical stability with 92.9 % retention after 3000 cycles at 10 A/g.

Improved Structural and Electrochemical Properties of Mg-Doped Nickel Cobaltite Nanoparticles Synthesized Using Low-Temperature Microwave Hydrothermal Method

The specific capacitance of materials influences the energy storage capacity. A series of MgxNi1-xCo2O4 (x = 0.0 - 0.1) nanoparticles using the low-temperature microwave-hydrothermal (M-H) method at 160 0C temperature, and sintered at 600 °C. The samples were then characterized using X-ray diffraction (XRD), Field Emission Scanning electron microscopy (FE-SEM), Fourier transform infrared (FTIR), and X-ray photoelectron spectroscopy (XPS). It is observed from X-ray diffraction that all the samples are cubic spinel in nature with space group Fd-3m, and the lattice parameter varies between 8.097 (x = 0.0) and 8.083 (x = 0.10). The nanoparticles have a hexagonal nanoflake-like shape morphology with an average particle size of 180 nm to 350 nm. The tetrahedral and octahedral absorption bands were observed at 561 cm-1 and 654 cm-1, respectively. The valence states of Ni2+/Ni3+, Co2+/Co3+, and Mg2+ were confirmed by X-ray photoelectron spectroscopy. The electrochemical studies using CV and GCD were performed on all the samples. High values of specific capacitance of 332 F g−1, energy densityof 9.05 Wh kg-1, and power density of 224.84 W kg-1 were observed for the sample x = 0.08. Therefore, Mg0.08Ni0.92Co2O4 sintered at 600 °C shows good impedance and electrochemical properties, which are helpful for supercapacitor applications. Figure 1

Two-Dimensional High-Entropy Selenides for Boosting Visible-Light-Driven Photocatalytic Performance.

High-entropy materials (HEMs) have garnered extensive attention owing to their diverse and captivating physicochemical properties. Yet, fine-tuning morphological properties of HEMs remains a formidable challenge, constraining their potential applications. To address this, we present a rapid, low-energy consumption diethylenetriamine (DETA)-assisted microwave hydrothermal method for synthesizing a series of two-dimensional high-entropy selenides (HESes). Subsequently, the obtained HESes are harnessed for photocatalytic water splitting. Noteworthy is the optimized HESes, Cd0.9Zn1.2Mn0.4Cu1.8Cr1.2Se4.5, showcasing an output rate of hydrogen of 16.08 mmol h-1 g-1 and a quantum efficiency of ca. 30% under 420 nm monochromatic LED irradiation. It is revealed that the photocatalytic performance of these HESes stems not only from the enlarged specific surface area and enhanced photogenerated charge carrier utilization efficiency but also from the promoted formation of the Cd-Hads bond, influenced by multiple principal elements on the Cd. These findings provide a guide for the design of HEMs tailored for various applications.

Ferroelectricity‐Induced Surface Ferromagnetism in Core–Shell Magnetoelectric Nanoparticles

Magnetoelectric nanoparticles (NPs) present an important class of nanomaterials with a wide interest in piezocatalytic and biomedical applications. Herein, the results of magnetoelectric and magnetization measurements performed on core–shell NPs having magnetic core (MnFe2O4, MFO) and ferroelectric shell (Ba0.85Ca0.15Ti0.5Zr0.5O3, BCZT) synthesized by the microwave hydrothermal method are reported. Magnetic results are compared with the measurements on reference MFO NPs prepared under identical conditions. Detailed SQUID magnetometer measurements of the magnetization hysteresis loops M(H) down to 2 K reveal the existence of a clear exchange bias effect in pure MFO NPs attributed to the coexistence of ferromagnetic and antiferromagnetic short‐range interactions. When the magnetic core is covered by the thin ferroelectric BCZT shell, it is observed that 1) the shell suppresses the apparent bias effect and 2) induces an “extra” ferromagnetic magnetization at T < 20 K. The results indicate that this “extra” ferromagnetism has a 2D character and it is most likely related to the interface interactions between the MFO core and BCZT shell. Ferroelectric properties and strong magnetoelectric effect in core–shell NPs are revealed via piezoresponse force microscopy under magnetic field. The mechanisms of the observed effects are discussed.

Synthesis, characterization, and temperature-dependent luminescence of Tb3+-activated and self-activated Sr10(PO4)6Cl2 phosphors

In this work, a series of new nanosized phosphors based on strontium chlorapatite (Sr10(PO4)6Cl2, abbreviated as SrClAp) with varying terbium concentration were synthesized using a modified microwave-hydrothermal method. This study meticulously investigated the impact of Tb3+ concentration and annealing temperature on factors such as crystal purity, particle morphology, photoluminescence, chromatic properties, and the mechanism of thermal quenching.The synthesized phosphors underwent characterization using X-Ray Diffraction (XRD) and scanning electron microscopy (SEM) to verify their crystal structure purity and examine their morphology. Upon near-ultraviolet (NUV) excitation at the 378 nm line, the obtained nanosized powders emitted green light arising from the characteristic 5D4→7FJ (J = 6, 5, 4, 3) transitions of Tb3+ ions. Notably, a broad host-related emission was discernible at 80 K, with its intensity diminishing as the temperature increased. The mechanism governing this host-related emission and the process of its thermal quenching have been proposed. Moreover, a comprehensive exploration of the influence of ambient temperature on the emission of Tb3+-doped SrClAp was undertaken.

Innovative synthesis of high-strength α-hemihydrate gypsum: Effects and mechanisms of TA modification under microwave hydrothermal conditions

Titanium gypsum (TG), a byproduct of the titanium dioxide industry, is recognized as a significant contributor to environmental pollution due to high water content, poor crystallinity and other characteristics that make it difficult to be reused/recycled effectively. This study evaluated the feasibility to recycle TG to produce α-hemihydrate gypsum via microwave hydrothermal method, wherein tricarballylic acid (TA) was employed as modifier to modulate the crystallization of α-HH. The impact of TA dosage on the characteristics of α-HH crystals is comprehensively assessed through a series of microscale analyses. The findings reveal a notable reduction in the Length/Diameter ratio (L/D ratio) of α-HH crystals, diminishing from 17.79 to 0.96, in response to the incremental introduction of TA, ranging from 0 % to 0.13 %. An optimum TA dosage of 0.1 % is found to yield a commendable compressive strength of 37.4 MPa. Additionally, this study validates the interaction between TA and α-HH crystals. Based on the experimental results, it is further postulated that microwave heating is conducive to expediting the rate of Ca2+ and SO42− ion accumulation at the (002) surface, thus altering the degree of solution supersaturation and consequently accelerating the growth kinetics of α-HH crystals. This study offers valuable insights into the utilisation of this methodology in various industrial and scientific applications.

Visible-light driven photocatalyzing degradation of antibiotics and dyes enabled by 0D/1D Tb2O3/Er2O3/TiO2@C hybrids

It remains a huge challenge to design a kind of high performance, multifunctional and low cost photocatalysts driven by visible light for the remediation of pollutants from waste water. In this work, the carbon coated Tb2O3/Er2O3/TiO2 nanotubes (Tb2O3/Er2O3/TiO2@C) 0D/1D hybrid photocatalysts were synthesized by a microwave hydrothermal method. Essentially, the Er2O3 nanoparticles can absorb low-energy photons at 800–980 nm and emit high-energy photons to TiO2 through the up-conversion effect, meanwhile, the Tb2O3 act as a redox center to promote the separation of photoinduction charges since the instantaneous photoelectric density was increased by 10 times by compared to TiO2@C. As a result, the photodegradation efficiency of the optimized Tb2O3/Er2O3/TiO2@C photocatalysts is about 15.7 times higher than that of TiO2@C under visible light irradiation for decomposing rhodamine B, respectively. Moreover, the photodegradation efficiency remained above 70 % after reused for 5 times. Thus, the enhanced synergistic effect between Er2O3 and Tb2O3 promises the excellent photodegradation activity and reduce cost.It remains a huge challenge to design a kind of high performance, multifunctional and low cost photocatalysts driven by visible light for the remediation of pollutants from waste water. The carbon coated Tb2O3/Er2O3/TiO2 nanotubes (Tb2O3/Er2O3/TiO2@C) 0D/1D hybrids were synthesized by a microwave hydrothermal method. The Er2O3 nanoparticles can absorb low-energy photons at 800–980 nm and emit high-energy photons to TiO2 through the up-conversion effect, meanwhile, the Tb2O3 act as a redox center to promote the separation of photoinduction charges since the instantaneous photoelectric density was increased by 10 times by compared to TiO2@C. As a result, the photodegradation efficiency of the optimized Tb2O3/Er2O3/TiO2@C photocatalysts is about 15.7 times higher than that of TiO2@C under visible light irradiation for decomposing rhodamine B. Moreover, the photodegradation efficiency remained above 70 % after reused for 5 times. Thus, the enhanced synergistic effect between Er2O3 and Tb2O3 promises the excellent photodegradation activity and reduce cost.

Microwave-hydrothermal synthesis of calcium borate whiskers: Influencing factors and formation mechanism

The synthesis of whiskers is an important means of high-value utilization of calcium resources. Calcium borate (Ca2B2O5·H2O) whiskers were synthesized by microwave hydrothermal method using CaCl2, Na2B4O7·10H2O and NaOH as raw materials at 140 °C for 2 h. A series of characterizations were conducted on the obtained calcium borate whiskers, including phase identification (XRD and FT-IR), crystal morphology (SEM), crystal structure (TEM and SAED), and thermal stability (TG). Through batch experiments under the control of influencing factors, the effects on product phase and morphology were systematically studied, such as raw material concentration (Ca2+ concentration and the molar ratio of boron/calcium), reaction temperature, holding time and pH value. For the prepared calcium borate whiskers, SAED demonstrated that the whiskers have a single crystal structure, characterized by a sarciniform shape with diameter ranging from 1.2 to 3.1 μm and a length of 50 to 120 μm. And thermal analysis revealed that the calcium borate whiskers remained stable without losing crystalline water at a synthesis temperature of 140 °C, while releasing crystalline water at a temperature range of 383.6 °C to 430.9 °C. The optimal conditions for Microwave-Hydrothermal synthesis were identified based on experimental phenomena, and the solution-liquid–solid (SLS) process of whisker formation was proposed and analyzed. The possible chemical reactions and growth mechanisms of calcium borate whiskers under microwave hydrothermal synthesis were briefly proposed by adjusting the reaction conditions and observing the process of morphological changes.

Effect of CdS on microstructure and performance of ZnO composite photocatalyst

AbstractIn this study, Nd‒Dy‒ZnO and CdS‒Nd‒Dy‒ZnO photocatalysts were prepared by microwave hydrothermal method to improve the photocatalytic performance of ZnO. The microstructure and performance of samples were characterized by X‐ray diffraction, scanning electron microscopy, ultraviolet (UV)‒visible, and X‐ray photoelectron spectroscopy, and evaluated with the methylene blue. The results showed that CdS attached to the ZnO crystal surface in the form of flocculent particles, and the combination with CdS promoted the growth of ZnO crystals, while an excess of CdS was found to be detrimental to the crystallization of ZnO. When nCdS/nZnO = 0.30 mol%, composite materials achieved the optimal photocatalytic performance, which made the degradation rate of methylene blue reach 93.42% under UV irradiation for 4 h. CdS‒Nd‒Dy‒ZnO composite photocatalytic material can generate active oxygen groups such as hydroxyl and superoxide radicals simultaneously, which greatly enhances the photocatalytic efficiency of the composite material.

A competitive strategy toward 1 T/2H MoS2 to balance impedance for optimizing electromagnetic wave absorption

Interface engineering and phase engineering play crucial roles in enhancing the design and development of advanced electromagnetic wave (EMW) absorbers. However, there is a lack of focus on designing phase structures and interfaces from a microscopic perspective to adjust impedance matching and EMW absorption. This study introduced a competitive strategy involving 1 T/2H MoS2. The phase structure and composition of MoS2 were controlled using a microwave hydrothermal method. By creating a diverse phase interface within the material in the form of 1 T/2H, a balance between conduction loss and polarization loss was achieved, leading to improved EMW absorption through enhanced impedance matching. The results indicated that the incorporation of the 1 T phase boosted the electron transfer capability of MoS2, increasing conduction loss. The 1 T/2H phase interface enhanced interface polarization, thereby amplifying polarization loss. At a thickness of 2.8 mm, the absorber demonstrated a minimum reflection loss of −64.9 dB and an effective absorption bandwidth of 4.6 GHz. In far-field conditions, the maximum radar cross-section (RCS) of the 1 T/2H phase MoS2 nanoflowers was −27.5 dBm2. This study elucidates the relationship between 1 T/2H phase MoS2 content and phase interfaces with impedance matching, offering a novel approach for developing high-performance MoS2-based EMW absorbing materials.

Preparation of Pt(II/IV)Clx/BiOHC2O4/Bi2O2CO3 composite microrods with enhanced photocatalytic performance for levofloxacin degradation in water

BiOHC2O4 microrods were initially prepared via a straightforward microwave hydrothermal method. These microrods then served as templates for the growth of BiOHC2O4/Bi2O2CO3 composites via anion exchange. Pt loading onto the composite microrods was achieved through photodeposition and chemical reduction methods. The obtained samples were analyzed by XRD, SEM, TEM, XPS, FT-FIR, UV–Vis DRS, PL, N2 physical adsorption, photocurrent and Nyquist impedance measurements. The photocatalytic performance of the fabricated materials for levofloxacin degradation was evaluated under both UV–visible and visible light irradiation. The results showed the formation of Pt(II/IV)Clx species on hierarchical BiOHC2O4/Bi2O2CO3 structure following photodeposition, while metallic Pt was produced via NaBH4 reduction. Pt(II/IV)Clx/BiOHC2O4/Bi2O2CO3 composites displayed superior photocatalytic performance under both light conditions. This enhanced performance can be linked to the presence of Pt(II/IV)Clx, which significantly improves light absorption and facilitates the transfer of photoelectrons and holes (e− and h+). Pt(II/IV)Clx served as a dual-functioning agent, acting as both a photosensitizer to enable visible light activity and as an inhibitor suppressing the recombination of photogenerated carriers. Loading around 4%Pt(wt%), BiOHC/BiOC demonstrated the highest rates of TOC removal, under full light spectrum irradiation for 75 min and visible light irradiation for 300 min, respectively.

Lattice variation as a function of concentration and grain size in MgO–NiO solid solution system

The study aimed to understand how changes in crystal's size affect the lattice parameters and crystal structure of Mg1-xNixO solid solution for six X values ranging from x = 0 to x = 1. Mg1-xNixO was synthesized via two different wet-chemical techniques: the sol-gel and the microwave hydrothermal method, both followed by calcination at different temperatures of 673, 873, 1073, 1273 and 1473 K. As annealing caused grain growth, the varied temperature range allowed to examine a wide range of grain sizes. The lattice parameters and x values were determined from XRD (X-ray diffraction) peak positions and intensities respectively. The grain size was evaluated by XRD line profile analysis and supported by SEM (scanning electron microscope) observations. At the temperatures of 673 and 873 K grain size was in the nanometric range and from 1073 K and above grain size was in the micrometric range. A non-monotonic lattice variation versus grain size was found for each concentration. When grain size decreased there was a slight contraction, however for grain size in the nanometric range there was a severe lattice expansion. Both lattice parameter changes were explained by two effects acting together: contraction due to surface stress and expansion due to weakening of the ionic bonding at nanocrystalline particles. In this current research study, the lattice parameter was mapped in two dimensions: concentration and grain size. The findings of this study provided valuable insights into the lattice variation in the MgO–NiO solid solution system.

Plant-Mediated Synthesis of Magnetite Nanoparticles with Matricaria chamomilla Aqueous Extract.

Magnetite nanoparticles (NPs) possess properties that make them suitable for a wide range of applications. In recent years, interest in the synthesis of magnetite NPs and their surface functionalization has increased significantly, especially regarding their application in biomedicine such as for controlled and targeted drug delivery. There are several conventional methods for preparing magnetite NPs, all of which mostly utilize Fe(iii) and Fe(ii) salt precursors. In this study, we present a microwave hydrothermal synthesis for the precipitation of magnetite NPs at temperatures of 200 °C for 20 min and 260 °C for 5 min, with only iron(iii) as a precursor utilizing chamomile flower extract as a stabilizing, capping, and reducing agent. Products were characterized using FTIR, PXRD, SEM, and magnetometry. Our analysis revealed significant differences in the properties of magnetite NPs prepared with this approach, and the conventional two-precursor hydrothermal microwave method (sample MagH). FTIR and PXRD analyses confirmed coated magnetite particles. The temperature and magnetic-field dependence of magnetization indicate their superparamagnetic behavior. Importantly, the results of our study show the noticeable cytotoxicity of coated magnetite NPs-toxic to carcinoma cells but harmless to healthy cells-further emphasizing the potential of these NPs for biomedical applications.

Co-Fe synergistic interaction mediated novel peroxymonosulfate activators: High-efficiently degradation and outstanding mineralization

The search for immobilization methods is the key to current research on environmentally friendly catalysts. In this study, Fe-Co bimetallic organic framework material was prepared by microwave hydrothermal method. After further carbonization, structural frame self-fixing catalyst Fe/CoC was obtained for the activation of peroxymonosulfate (PMS). Based on a stable three-dimensional structure, high specific surface area, variable polymetallic ion valence and remarkable catalytic performance, Fe/CoC achieved 99.59 % treatment efficiency and 93.38 % mineralization efficiency of norfloxacin (NOR) within 30 min. The universality was evaluated in multiple antibiotics and actual water configuration solutions. The matching redox potentials and synergistic interactions between the bimetals enhanced the activation catalytic efficiency, which was attributed to the generation of radical SO4•− and non-radical 1O2. In addition, the voltammetry characteristic curve proved the existence of direct electron transfer in the system. Finally, a relatively complete NOR degradation pathways were proposed based on the 13 intermediates. This work has enriched the development of stable catalysts for PMS activation and provided a new idea for MOFs to participate in antibiotic removal.

Radio Frequency (RF) Mediated Hyperthermia of Nickel Ferrites-A Potential Application of Cancer Therapy

We present an invitro study of the hyperthermia application of nanomaterials for the cancer treatment by Radiofrequency (RF). Nickel-ferrite nano materials are synthesized by using microwave hydrothermal method at different pH values under a lower temperature of 160°C for a short holding time of 30 minutes. RF source generator is being used that opeartes at 100 KHz and a temperature regulator monitors the temperature of the solution.The in-vivo experimemnt was conducted with the nanomaterials dispersed in the ferrofluid, and RF energy is appiled when the solution is being placed in a magnetic stirrer. The results shows that the temperature of the nanomaterials has increased beyond 40°C and went up to 45°C with the increase in frequency of the RF under the constant magnetic field of 100 Oe. As the strength of the magnetic field increases the Nanomaterials have shown rapid variation in their temperature Characteristics. The nickel-ferrites have shown linear temperature characteristics under the magnetic field of 100Oe with the RF frequency of 100 KHz. Hence the nickel-ferrites are most suitable for the Hyperthermia application of cancer treatment..The cancerous cells are destroyed by ‘Active cell destruction’ or they are swollen till the cells burst. The superconductivity property of nano particles and Radio Frequency coils used plays the major role in the treatment.