Electrostatic Processes Research Articles

Boosting Cu ion capture in high-salinity environments with amino-functionalized millispheres.

High salinity in wastewater often hampers the performance of traditional adsorbents by disrupting electrostatic interactions and ion exchange processes, limiting their efficiency. This study addresses these challenges by investigating the salt-promoted adsorption of Cu ions onto amino-functionalized chloromethylated polystyrene (EDA@CMPS) millispheres. The adsorbent was synthesized by grafting ethylenediamine (EDA) onto CMPS, which significantly improved Cu adsorption, achieving nearly three times the capacity in saline solutions (1.65 mmol g-1) compared to non-saline solutions (0.66 mmol g-1). Mechanistic analysis showed that the presence of salts, such as NaCl, promoted the protonation of amino groups on EDA@CMPS, increasing their positive charge and enhancing their affinity for Cu ions. The solution's ionic strength further amplified this protonation, reducing electrostatic repulsion between the adsorbent and the Cu ions, thus improving binding efficiency. Additionally, the increased ionic strength altered Cu speciation, favoring the formation of Cu(NH3)42+ complexes, which were more easily adsorbed. These synergistic effects resulted in faster adsorption kinetics, higher capacity, and improved Cu ion removal, particularly in saline environments. Overall, these findings bridge the gap between material design and functional performance in high-salinity wastewater, offering a promising strategy for efficient heavy metal removal and environmental remediation.

Cooperative Molecular Interaction-Based Highly Efficient Capturing of Ultrashort- and Short-Chain Emerging Per- and Polyfluoroalkyl Substances Using Multifunctional Nanoadsorbents.

The short-chain (C4 to C7) and ultrashort-chain (C3 to C2) per- and polyfluoroalkyl substances (PFAS) are bioaccumulative, carcinogenic to humans, and harder to remove using current technologies, which are often detected in drinking and environmental water samples. Herein, we report the development of nonafluorobutanesulfonyl (NFBS) and polyethylene-imine (PEI)-conjugated Fe3O4 magnetic nanoparticle-based magnetic nanoadsorbents and demonstrated that the novel adsorbent has the capability for highly efficient removal of six different short- and ultrashort-chain PFAS from drinking and environmental water samples. Reported experimental data indicates that by capitalizing the cooperative hydrophobic, fluorophilic, and electrostatic interaction processes, NFBS-PEI-conjugated magnetic nanoadsorbents can remove ∼100% short-chain perfluorobutanesulfonic acid within 30 min from the water sample with a maximum absorption capacity q m of ∼234 mg g-1. Furthermore, to show how cooperative interactions are necessary for effective capturing of ultrashort and short PFAS, a comparative study has been performed using PEI-attached magnetic nanoadsorbents without NFBS and acid-functionalized magnetic nanoadsorbents without PEI and NFBS. Reported data show that the ultrashort-chain perfluoropropanesulfonic acid capture efficiency is the highest for the NFBS-PEI-attached nanoadsorbent (q m ∼ 187 mg g-1) in comparison to the PEI-attached nanoadsorbent (q m ∼ 119 mg g-1) or carboxylic acid-attached nanoadsorbent (q m ∼ 52 mg g-1). In addition, the role of cooperative molecular interactions in highly efficient removal of ultrashort-chain PFAS has been analyzed in detail. Moreover, reported data demonstrate that nanoadsorbents can be used for effective removal of short-chain PFAS (<92%) and ultrashort-chain PFAS (<70%) simultaneously from reservoir, lake, tape, and river water samples within 30 min, which shows the potential of nanoadsorbents for real-life PFAS remediation.

Efficient removal of Zn(II) ions from aqueous media using a facilely synthesized nanocomposite based on chitosan Schiff base

The development of nanomaterials incorporating organic components holds significant importance in addressing the efficient removal of metal ions through adsorption. Hence, in this study, a novel MnFe2O4/chitosan/Schiff base nanocomposite was successfully synthesized by crosslinking MnFe2O4 nanoparticles with functionalized chitosan using a novel Schiff base. The Schiff base was created through the condensation reaction between 2-aminophenol and terephthalaldehyde. Comprehensive characterization of the synthesized nanocomposite was performed through FT-IR, XRD, SEM, and VSM analyses, revealing a less crystalline arrangement compared to pure chitosan, a rough and non-uniform surface morphology, and a reduced magnetization value of 30 emu/g. Furthermore, the synthesized MnFe2O4/chitosan/Schiff base nanocomposite was working as an adsorbent for the effective disposal of Zn(II) ions from aqueous solutions. The synthesized nanocomposite exhibited a maximum sorption capacity of 289.86 mg/g for Zn(II) ions. Additionally, the results indicated that the removal of Zn(II) ions by the synthesized nanocomposite was a spontaneous, chemical, and endothermic process, aligning well with the Langmuir isotherm as well as the pseudo-second-order model. Furthermore, at pH 7.5, with a contact duration of 100 min and a temperature of 328 K, the fabricated nanocomposite reached its maximum sorption capacity for Zn(II) ions. The results of this study demonstrate the effectiveness of the newly synthesized MnFe2O4/chitosan/Schiff base nanocomposite in removing Zn(II) ions from aqueous media. The novel synthesis approach and the high adsorption capacity of 289.86 mg/g underscore the potential of this composite for practical applications in industrial wastewater treatment. The dual removal mechanism involving electrostatic attraction and complexation processes further enhances its utility, making it a valuable contribution to the field of environmental remediation.

Effect of Specific Surface Area and Hydrophobicity of Electrospun Nanofibers on the Sustained Release Performance of Diclofenac Sodium.

Nanofibers produced by electrospinning are suitable options for slow-release materials. Diclofenac sodium (DS) is a nonsteroidal anti-inflammatory medication with a brief half-life that can serve as an effective sustained-release agent. This paper presents a novel method for producing DS-sustained release nanofibers by electrostatic spinning processes. During the preparation, the slow-release capabilities of biodegradable materials poly(lactic acid) (PLA) and polycaprolactone (PCL) are investigated. A composite drug-carrying scaffold is prepared to enhance the sustained-release performance. The sustained release ability is affected by the specific surface area of the nanofibers and the hydrophobicity of the polymer. The findings indicate that the composite nanofiber with a PLA/PCL ratio of 1:1 demonstrates the most effective sustained-release performance. The release rate is mostly influenced by the hydrophobicity of the polymer at this point. Sustained-release kinetic simulations were performed and revealed that the release of nanofibers follows a first-order release paradigm. This work presents a straightforward approach for creating a sustained-release formulation of DS.

Modified Ordered Mesoporous Carbons for Cr(VI) Removal from Wastewater.

The pristine CMK-3 carbon was ozonized and then chemically modified by the Zr and Fe compounds. The synthesized carbonaceous materials were characterized with physicochemical methods. The obtained carbons had a high specific surface area (ca. 800 m2 g-1) and an acidic surface. The Cr(VI) adsorption properties of the oxidized and Zr/Fe-modified carbon were studied. The highest static adsorption capacity towards Cr(VI) ions was evaluated for Zr/Fe-modified carbon (50.1 mg g-1) at pHeq = 5.8 after 240 min. The Elovich and Freundlich theoretical models were well fitted to the Cr(VI) adsorption kinetic and isotherm data on the Zr/Fe-modified CMK-3-type carbon. The leading Cr(VI) adsorption mechanism acting on the Zr/Fe-modified carbon was probably based on the redox reactions between Cr(VI) and the carbonaceous surface. Electrostatic attraction and surface complexation processes could also occur during Cr(VI) adsorption in the studied system. The effect of the competitive anions on the concentration level, such as in the galvanic wastewater for Cr(VI) adsorption onto chemically modified carbon, was negligible. The HCl and HNO3 media were insufficient for the Zr/Fe-modified carbon regeneration after Cr(VI) adsorption. The Zr/Fe-modified carbon was successfully applied for the efficient (>90%) Cr(VI) removal from the model galvanic wastewater.

Electrodynamic interaction between tumor treating fields and microtubule electrophysiological activities.

Tumor treating fields (TTFields) are a type of sinusoidal alternating current electric field that has proven effective in inhibiting the reproduction of dividing tumor cells. Despite their recognized impact, the precise biophysical mechanisms underlying the unique effects of TTFields remain unknown. Many of the previous studies predominantly attribute the inhibitory effects of TTFields to mitotic disruption, with intracellular microtubules identified as crucial targets. However, this conceptual framework lacks substantiation at the mesoscopic level. This study addresses the existing gap by constructing force models for tubulin and other key subcellular structures involved in microtubule electrophysiological activities under TTFields exposure. The primary objective is to explore whether the electric force or torque exerted by TTFields significantly influences the normal structure and activities of microtubules. Initially, we examine the potential effect on the dynamic stability of microtubule structures by calculating the electric field torque on the tubulin dimer orientation. Furthermore, given the importance of electrostatics in microtubule-associated activities, such as chromosome segregation and substance transport of kinesin during mitosis, we investigate the interaction between TTFields and these electrostatic processes. Our data show that the electrodynamic effects of TTFields are most likely too weak to disrupt normal microtubule electrophysiological activities significantly. Consequently, we posit that the observed cytoskeleton destruction in mitosis is more likely attributable to non-mechanical mechanisms.

The hyper-crosslinked aniline polymer@MOFs hybrid materials reinforced with active ionic sites for efficient and fast Cr(VI) removal

The adsorption of toxic metal ions by composite materials of metal–organic frameworks (MOFs) has attracted significant attention in recent years. In this work, a series of hybrid materials HPAN@M−x consisting of protonated hyper-crosslinked aniline polymer (HPAN) and MOFs were synthesized via the Friedel-Crafts reaction between aniline and dimethoxymethane in the presence of MIL-101(Cr), followed by protonation with hydrogen bromide. These hybrid materials exhibited enhanced adsorption rate and capacity for Cr(VI) ions compared to both individual MIL-101(Cr) and HPAN. The effects of the ratio of aniline to MIL-101(Cr), solution pH, adsorption temperature, impurity ions on the removal of Cr(VI) ions were systematically investigated. Notably, HPAN@M−b not only achieved an adsorption capacity up to 290.9 mg·g−1 in 7 min but also exhibited excellent cycling stability by maintaining a high Cr(VI) removal efficiency of 95.6 % after five cycles. The enhanced adsorption performance is attributed to the synergistic effect between MIL-101(Cr) and HPAN. Mechanism studies indicated that the removal for Cr(VI) ions involved a combination of ion exchange and electrostatic adsorption processes. Additionally, the desorbed Cr(VI) ions were transformed into added-value barium chromate (BaCrO4) precipitates, allowing for resource utilization of Cr(VI) ions. This study represents a significant advancement towards developing MOFs-based hybrid materials for practical treatment of chromium-containing wastewater.

Analysis of the adsorption and fixation process of ammonium nitrogen in arable soil by biochar based on molecular dynamics simulation

The ammonia nitrogen in arable land soil is susceptible to environmental and anthropogenic influences, leading to nutrient loss. This study utilized indoor soil column leaching experiments, combined with adsorption mathematical models, traditional characterization methods, and molecular dynamics simulation methods, to analyze the effects of biochar on changes in ammonium ions in different soil layers and leachate of arable land soil. The study found that applying biochar at a ratio of 10 % to arable land soil could effectively increase the ammonium ion content in the 0–10 cm soil layer by 1.57–2.36 times and reduce loss by 44.83–72.27 %. The adsorption and fixation process of biochar is controlled by electrostatic attraction and ion exchange processes. Interactions between molecules, electrostatic forces, and system internal energy also have certain effects on the process. Near the structure of C6H12O6, there are low-energy adsorption sites for ammonium ions, which can provide the energy required for electrostatic attraction. Structures such as C5H10O5, C-S-H, C-SO3, and C4H7NO4 respectively play roles in physical adsorption or chemical adsorption through displacement reactions, electron exchange, and other forms. The adsorption free energy is −394,590.84 kcal/mol, indicating stable adsorption and a process that tends to interact with the biochar surface. This study addresses issues such as the easy loss of ammonia nitrogen in arable land soil and the unclear adsorption mechanism of biochar on ammonium ions, providing a theoretical basis for the field of environmental science.

Collection of nanoparticles by electrostatic precipitation operating over a wide range of electric fields

ABSTRACT In the electrostatic precipitation of microparticles, it is common to evaluate the voltages between the corona onset voltage and the breakdown point. However, the charging of particles in the nanoscale size range mainly occurs by diffusion, suggesting the possibility of its occurrence, even at low values. This paper investigates the implications of a wide range of electric fields applied in the collection of nanoparticles (6.15–241.4 nm). Two electrostatic precipitators (P.I. and P.II.), both with plates 10 cm high and 30 cm long, but with different plate spacings (4 and 6.5 cm), were tested using three air velocities (1.9, 2.9, and 3.9 cm/s) and 36 electric fields (0.0 − 5.0 kV/cm). Under the highest electric fields, both precipitators showed efficiencies above 99.9%. Furthermore, nanoparticles were collected before the corona onset voltage, with efficiencies of around 28% (P.I.) and 35% (P.II.). Even though no current was detected by the high voltage source, charges on the particles were measured in electric fields lower than 3.0 kV/cm. The higher the applied voltage, the higher the residual charge of the particles at the precipitator outlet. It is expected that the findings of this work should contribute to the technological development of electrostatic processes for air treatment.

Evaluation of a modern point discharge sensor as an atmospheric electricity instrument

Point discharge sensors have been used for a long period of time, but are still not fully understood. The data collected by one of these sensors has been investigated along with electric field data in an attempt to parameterise the sensor. It was found that the sensor was best described by an equation with terms dependent on the atmospheric electric field and the first derivative of this electric field, with respect to time. This behaviour implies that both electrostatic and electrodynamic processes are important to the operation of the sensor. The inclusion of the electrodynamic term means that although this sensor is able to detect electrical disturbances, it is more difficult to recover the precise nature of the electric field using this sensor.

Exploring the Use of Terrestrial Robots for Atmospheric Electricity Measurement

Measuring the electric field is a central goal in electrostatics research, such as the study of electrostatics in atmospheric processes. It serves as a key indicator for various atmospheric phenomena, including the presence of lightning, dust or charged clouds. Traditionally, electric field measurements have been conducted from static platforms, with limited mobile measurements from airborne platforms such as balloons or, more recently, Unmanned Aerial Vehicles (UAVs). Here, we explore the potential of terrestrial robots to measure the electric field with some level of autonomy, such as during supervised navigation between user-defined waypoints. We mount a field mill on a four-wheeled rover and use a Global Navigation Satellite System (GNSS) to track the position of its measurements during an outdoor survey. The robot has a depth camera for 3D terrain mapping to contextualise local field measurements. We present plans for future research, including the use of semi-autonomous identification and exploration of electrostatic ‘hotspots’; and deployment of multiple robots (e.g., six) in a ‘sparse swarm’ configuration. We consider opportunities to employ such a robot system in environmental science or space research, for instance on Mars or the moon, where an understanding of electrostatic processes could be significant for future space missions.

Electrostatic catalysis of a click reaction in a microfluidic cell

Electric fields have been highlighted as a smart reagent in nature’s enzymatic machinery, as they can directly trigger or accelerate chemical processes with stereo- and regio-specificity. In enzymatic catalysis, controlled mass transport of chemical species is also key in facilitating the availability of reactants in the active reaction site. However, recent progress in developing a clean catalysis that profits from oriented electric fields is limited to theoretical and experimental studies at the single molecule level, where both the control over mass transport and scalability cannot be tested. Here, we quantify the electrostatic catalysis of a prototypical Huisgen cycloaddition in a large-area electrode surface and directly compare its performance to the conventional Cu(I) catalysis. Our custom-built microfluidic cell enhances reagent transport towards the electrified reactive interface. This continuous-flow microfluidic electrostatic reactor is an example of an electric-field driven platform where clean large-scale electrostatic catalytic processes can be efficiently implemented and regulated.

Efficiency, mechanism and application prospect of ammonium adsorption and desorption over a sodium-acetate-modified synthetic zeolite.

Adsorption is an effective approach for remediating ammonium pollution, and zeolite has exceptional efficacy for the adsorption of ammonium. The investigation of ammonium adsorption using coal-fly-ash-based zeolite has gained remarkable attention in contemporary research. In this work, a sodium-acetate-modified synthetic zeolite (MSZ) was used to absorb ammonium in simulated wastewater. The MSZ had an adsorption capacity for ammonium of 27.46 mg g-1, and the adsorption process followed the Langmuir isotherm model and pseudo-second-order kinetics model. The adsorption and desorption of ammonium were controlled by ion exchange, pore diffusion, and electrostatic attraction processes. Ion exchange was responsible for 77.90% of the adsorption process and 80.16% of the desorption process. The MSZ was capable of continuously removing large amounts of ammonium from wastewater through fixed bed adsorption. After 5 regeneration cycles, MSZ still maintained 75% adsorption characteristics for ammonium. Using MSZ adsorbed with ammonium as a soil amendment increased the germination rate of mung beans by 10%. Furthermore, it also increased the stem length, root length, and fresh weight by 20-30%. These findings suggest that MSZ provides a promising application prospect to mitigate ammonium pollution and recycle ammonium resources.

Insights into hydroelectric nanogenerators: numerical simulation and experimental verification

Good simulation! The simulation of the output electrical performance of hydroelectric nanogenerators is coupled with the electrostatic and dynamic electrical processes to match the experimental results.

Effect of ambient humidity on the tribo-electrostatic separation of granular plastic wastes

The separation of plastic mixtures from waste electrical and electronic equipment is an increasingly active domain of research. Several electrostatic separation processes and devices have been developed to recover plastic waste. All these processes are based on the use of the triboelectric effect to charge the plastic granules to separate them in an intense electric field. The objective of this study is to investigate the effect of ambient humidity on the efficiency of the triboelectric charging and electrostatic separation process, especially in an industrial environment where granular plastic waste may contain residual moisture due to previous processing by flotation or inappropriate storage. The experiments were carried out using a rotating-multi-cylinder tribocharger and a roll-type electrostatic separator. The samples were composed in equal proportions of either: (1) acrylonitrile butadiene styrene (ABS) and polystyrene (PS) or (2) polypropylene (PP) and polyethylene (PE), the average particle diameter of which was between 2 and 6 mm. The efficiency of the tribo-electrostatic separation was evaluated by measuring the purity and recovery of the products. The results confirm that separating (ABS + PS) and (PP + PE) mixtures is feasible. The best separation results were obtained when the materials were stored and processed at an ambient relative humidity of around 50%.

Amino-modified hemp stem for high-capacity adsorption of Cr(VI) from aqueous solution

Two novel adsorbents, triethylenetetramine-grafted hemp stems (HS-TETA) and choline chloride-grafted hemp stems (HS-CL), were prepared by using epichlorohydrin as etherifying agent. The obtained adsorbents were comprehensively characterized, and the adsorption capacity for hexavalent chromium (Cr(VI)) was evaluated under various single-factor conditions, including adsorbent dosage, contact time, solution pH, initial hexavalent chromium concentration, and temperature. HS-TETA and HS-CL exhibit excellent adsorption performance, with maximum adsorption capacities of 396.88 and 335.04 mg/g, respectively, outperforming previous relevant studies. The adsorption behavior of Cr(VI) by HS-TETA and HS-CL was investigated using adsorption kinetics, adsorption isotherms, and adsorption thermodynamics. The adsorption process follows the pseudo-second-order kinetic model and the Langmuir isotherm model, suggesting a monolayer adsorption process with chemical adsorption. Thermodynamic analysis reveals that the adsorption of Cr(VI) on two adsorbents is spontaneous and exothermic. Combined with the characterization, it can be speculated that the adsorption of Cr(VI) on two adsorbents involves electrostatic effects, reduction, and complexation processes. HS-TETA and HS-CL exhibit good recyclability. After 5 cycles, HS-TETA and HS-CL maintain over 50% and 85% of their initial adsorption capacity, respectively. The cycling performance of HS-CL containing quaternary ammonium and amine groups is significantly superior to that of HS-TETA containing only an amine group, indicating that the introduction of the quaternary ammonium group enhances the cycling performance of the adsorbent. HS-TETA and HS-CL, as cost-effective and efficient adsorbents, offer a promising solution for the treatment of Cr(VI)-contaminated wastewater and facilitate the recycling of agricultural waste.

Temperature-dependent dynamics of electrokinetic conservative and reactive transport in porous media: A model-based analysis

Electrokinetic techniques employ direct current electric fields to enhance the transport of amendments in low permeability porous media and have been demonstrated effective for in situ remediation of both organic contaminants and heavy metals. The application of electric potential gradients give rise to coupled chemical, hydraulic and electric fluxes, which are at the basis of the main transport mechanisms: electromigration and electroosmosis. Previous research has highlighted the significant impacts of charge interactions and fluid composition, including temperature-dependent properties such as electrolyte conductivity and density, on these transport phenomena. However, current models of electrokinetic applications often assume isothermal conditions and overlook the production of heat resulting from Joule heating.This study provides a detailed model-based investigation, systematically exploring the effects of temperature on electrokinetic conservative and reactive transport in porous media. By incorporating temperature-dependent material properties and progressively investigating the impact of temperature on each transport mechanism, we analyze the effects of temperature variations in both 1D and 2D systems. The study reveals how temperature dynamically influences the physical, chemical and electrostatic processes controlling electrokinetic transport. A temperature increase results in a higher speed of amendments delivery by both electromigration and electroosmosis and increases the kinetics of degradation reactions. The simulations also reveal a feedback mechanism in which higher aqueous conductivity results in increased Joule heating, leading to a faster temperature rise and, subsequently, to higher electrolyte conductivity. Finally, we estimate the electric energy requirements of the system at varying temperatures and show how these changes impact the rate of contaminant removal.

An Overview of the Advances in Polymer-Based Electrode Materials in Supercapacitors

A special family of polymers known as conducting polymers (CPs) is able to carry charge via conjugated double bonds. CPs are intricate dynamic structures that capture the interest of those working in the field of intelligent materials. Electrical stimulation can cause significant changes in the electrical, mechanical, and chemical features of CPs. Nanocomposites made of CPs have been used in sensors, batteries, flexible electronics, and supercapacitors (SCs). A supercapacitor is a device used to store electrical charge through electrostatic and electrochemical processes. They have the potential to replace conventional batteries and capacitors. They have been used in the automotive, railways, military, renewable, and power industries. The development of electrical parameter models, reliability testing, and industry norms are all challenges that SCs are now dealing with. In this article, the introduction of supercapacitors (SCs), the potential of different types of CPs-based nanocomposite materials in the electrode material of SCs, current studies, future perspectives, opportunities, and challenges have been discussed.

Facile Preparation of Magnetic CuFe2O4 on Sepiolite/GO Nanocomposites for Efficient Removal of Pb(II) and Cd(II) from Aqueous Solution.

CuFe2O4 nanoparticles were synthesized and immobilized on sepiolite fibers and graphene oxide sheets, producing a CuFe2O4/sepiolite/GO (CFSG) nanocomposite via a facile single-pot method. The synthesized nanocomposite was characterized using TEM, FTIR, SEM-EDX, XRD, and TGA techniques to determine its composition, structure, and thermal stability. The adsorptive removal of Pb(II) and Cd(II) heavy metal ions from aqueous solutions was studied using the synthesized CFSG nanocomposite. Adsorption parameters such as CFSG loading, pH, contact time, and temperature were investigated. The CFGS nanocomposite showed a higher Pb(II) removal (qm = 238.1 mg/g) compared to Cd(II) (qm = 14.97 mg/g) in a Pb(II) and Cd(II) binary system. The Pb(II) and Cd(II) adsorption fitted well with the Langmuir model, followed by the pseudo-second-order model, and was found spontaneous. Adsorption thermodynamic analysis showed that the Pb(II) adsorption process was exothermic while Cd(II) adsorption was endothermic. The CuFe2O4 nanoparticles on the CFSG surface could facilitate the adsorption of heavy metal ions through electrostatic interaction and complexation processes.

Bimetallic nanocubes embedded in biomass-derived porous carbon to construct magnetic/carbon dual-mechanism layered structures for efficient microwave absorption

Biomass-derived porous carbon materials have great potential for the development of lightweight and efficient broadband microwave absorbers. In this study, we reported the successful immobilization of Co3O4/CoFe2O4 nanocubes on porous carbon derived from ginkgo biloba shells by activated carbonization and electrostatic self-assembly processes. The optimal reflection loss value of the prepared BPC@Co3O4/CoFe2O4 reaches −68.5 dB when the filling load is 10 wt%, and the effective absorption bandwidth is 6.2 GHz with a matching thickness of 2 mm. The excellent microwave absorption (MA) performance is attributed to the rational three-dimensional structural design, the modulation of magnetic/carbon components, the optimized impedance matching, and the coordinated action of multiple mechanisms. It was further demonstrated by high-frequency structural simulation that the composite can effectively dissipate microwave energy in practical applications. Therefore, the results indicate a favorable potential of the synthesis and application of semiconductor/magnetic component/biomass-derived carbon microwave absorbing materials.