Magnetic Properties Research Articles

Synthesis and characterization of activated carbon-supported magnetic nanocomposite (MNPs-OLAC) obtained from okra leaves as a nanocarrier for targeted delivery of morin hydrate

IntroductionThe method of encapsulating the drug molecule in a carrier, such as a magnetic nanoparticle, is a promising development that has the potential to deliver the medicine to the site where it is intended to be administered. Morin is a pentahydroxyflavone obtained from the leaves, stems, and fruits of various plantsmainly from the Moraceae family exhibiting diverse pharmacological activities such as anti-inflammatory, anti-oxidant, and free radical scavenging and helps treat diseases such as diabetes, myocardial infarction and cancer.MethodsIn this study, we conducted the synthesis of a nanocomposite with magnetic properties by coating biocompatible activated carbon obtained from okra plant leaves with magnetic nanoparticles.ResultsCharacterization of the synthesized activated carbon-coated magnetic nanocomposite was confirmed by Fourier transform infrared, scanning electron microscopy, dynamic light scattering, and zeta potential. The cytotoxic effects of the drug-loaded magnetic nanocomposite were examined in HT-29 (Colorectal), MCF-7 (breast), U373 (brain), T98-G (Glioblastoma) cancer cell lines, and human umbilical vein endothelial cells healthy cell line.DiscussionWe studied the loading and release behavior of morin hydrate in the activated carbon-coated magnetic nanocomposite. Activated carbon-coated magnetic nanocomposite carriers can show promising results for the delivery of Morin hydrate drugs to the targeted site.

Significance of mixed convection and heat transfer flow past a vertical Riga plate in the presence of alumina nanoparticles: Analysis of streamlines for oblique stagnation point

AbstractThe aim of the current study to inspect the magnetic flow properties and heat transport features near an oblique stagnation point of a nanofluid with mixed convection through a vertical Riga plate are examined. The Riga plate is a familiar actuator made out of permanently fixed electrodes and magnets that moved away from the plate due to an exponential decline in the Lorentz force. Nanofluid is taken into consideration due to its peculiar properties, such as remarkable thermal conductivity is the significance of the study. These properties are important in heat exchangers, electronics, advanced nanotechnology, and material sciences. Using usual similarity transformations, the group of leading partial differential equations is distorted into a group of nonlinear ordinary differential equations. Then, a very proficient procedure namely bvp4c is utilized to discover the solution. For particular values of the different influential fluid parameters, the characteristics of the dimensionless temperature and velocity along with drag force and heat transfer are investigated graphically. In addition, the symmetrical results were initiated for both cases of the slip and without slip parameters. It is demonstrated that for greater influence of the volume fraction of nanoparticles, the normal and tangential velocity profile drops down for the instances of aiding and opposing flows due to fluctuations in the presence of slip factor, and absence of slip factor. In contrast, the temperature profile intensifies in both the cases of slip parameters and without the slip parameter owing to the phenomenon of assisting flow and opposing flow subject to superior impressions of the nanoparticle volume fractions. It is also observed that depending on the equilibrium between buoyancy effects, obliqueness, velocity slip parameters, and straining motion, the location of the point of zero shear stress (friction factor on the surface of the wall) is displaced to the right or the left of the origin.

Strain-modulated antiferromagnetic Chern insulator in NiOsCl$_6$ monolayer

Abstract Recently, Chern insulators in an antiferromagnetic (AFM) phase have been suggested theoretically and predicted in a few materials. However, the experimental observation of two-dimensional AFM quantum anomalous Hall effect is still a challenge to date. In this work, we propose that an AFM Chern insulator can be realized in a two-dimensional monolayer of NiOsCl$_6$ modulated by a compressive strain. Strain modulation is accessible experimentally and used widely in predicting and tuning topological nontrivial phases. With first-principles calculations, we have investigated the structural, magnetic and electronic properties of NiOsCl$_6$. Its stability has been confirmed through molecular dynamical simulations, elasticity constant and phonon spectrum. It has a collinear AFM order, with opposite magnetic moments of 1.3 $\mu_B$ on each Ni/Os atom, respectively, and the Néel temperature is estimated to be 93 $K$. In the absence of strain, it functions as an AFM insulator with a direct gap with spin-orbital coupling included. Compressive strain will induce a transition from a normal insulator to a Chern insulator characterized by a Chern number $C = 1$, with a band gap of about 30 meV. This transition is accompanied by a structural distortion. Remarkably, the Chern insulator phase persists within the 3$\%$-10$\%$ compressive strain range, offering an alternative platform for the utilization of AFM materials in spintronic devices.

Generalized and Scalable Synthesis of Manganese Dioxide-Based Tubular Micromotors for Heavy Metal Ion Removal.

Synthetic nano- and micromachines hold immense promise in biomedicine and environmental science. Currently, bubble-driven tubular micro/nanomotors have garnered increasing attention owing to their exceptional high-speed self-propulsions. However, complex and low-yield preparation methods have hindered their widespread applications. Herein, we present a generalized, scalable, and low-cost electrospinning-based strategy to fabricate MnO2-based composite tubular micromotors (MnO2-TMs) for efficient heavy metal ion removal. The inherent flexibility of precursor nanofibers derived from diverse matrix materials enables the creation of MnO2-TMs with a wide range of morphologies. In response to morphology changes, the MnO2-TMs, based on a bubble-propelled mechanism, exhibit multimodal motion patterns, including linear, circular, and spiral to stochastic swinging. To elucidate the underlying morphology-to-motion relationship, we conducted systematic simulations of fluid dynamics around the MnO2-TMs. Furthermore, by incorporation of Fe3O4 nanoparticles, the capabilities of MnO2-TMs can be expanded to include magnetic manipulation for directional navigation and efficient retrieval. Benefiting from these attributes, MnO2-TMs excel in removing heavy metal ions from water. The developed MnO2-MnWO4@Fe3O4 TMs exhibit prominent adsorption capacities of 586.5 mg g-1 for Cu2+ and 156.4 mg g-1 for Pb2+. Notably, the magnetic property facilitates rapid separation and retrieval of the micromotors, and the absorbed ions can be simply recovered by pH adjustment. This work establishes a general framework for developing MnO2-based tubular micro/nanomotors to address environmental challenges.

Chemical Design of Spin Frustration to Realize Topological Spin Glasses.

Patterning spins to generate collective behavior is at the core of condensed matter physics. Physicists develop techniques, including the fabrication of magnetic nanostructures and precision layering of materials specifically to engender frustrated lattices. As chemists, we can access such exotic materials through targeted chemical synthesis and create new lattice types by chemical design. Here, we introduce a new approach to induce magnetic frustration on a modified honeycomb lattice through a competition of alternating antiferromagnetic (AFM) and ferromagnetic (FM) nearest-neighbor interactions. By subtly modulating these two types of interactions through facile synthetic modifications, we created two systems: (1) a topological spin glass and (2) a frustrated spin-canted magnet with low-temperature exchange bias. To design this unconventional magnetic lattice, we used a metal-organic framework (MOF) platform, Ni3(pymca)3X3 (NipymcaX where pymca = pyrimidine-2-carboxylato and X = Cl, Br). We isolated two MOFs, NipymcaCl and NipymcaBr, featuring canted Ni2+-based moments. Despite this similarity, differences in the single-ion anisotropies of the Ni2+ spins result in distinct magnetic properties for each material. NipymcaCl is a topological spin glass, while NipymcaBr is a rare frustrated magnet with low-temperature exchange bias. Density functional theory calculations and Monte Carlo simulations on the NipymcaX lattice support the presence of magnetic frustration as a result of alternating AFM and FM interactions. Our calculations enabled us to determine the ground-state spin configuration and the distribution of spin-spin correlations relative to paradigmatic kagomé and triangular lattices. This modified honeycomb lattice is similar to the electronic Kekulé-O phase in graphene and provides a highly tunable platform to realize unconventional spin physics.

Effects of annealing and cold rolling on microstructural features, magnetic properties, tensile behavior and electrical resistance of FeCoNi(MnAl)x high entropy alloys

In this study, the microstructure, magnetic properties, and tensile behavior of high entropy alloys of FeCoNi(MnAl)x (x = 0–0.6, in molar ratios) were investigated after casting, cold rolling and annealing. X-ray diffractometry (XRD), field emission scanning electron microscope (FE-SEM), vibrating sample magnetometer (VSM), and also tensile tests were used to evaluate phase formation, microstructure, magnetic behavior and tensile properties of the samples, respectively. The results showed that as the indices of x value increase to 0.6, crystallographic structures transform from FCC to FCC + BCC. This in turn decreased the magnetic saturation of FeCoNi(MnAl)0.6 from 151 to 36 emu/g. Increasing x to 0.6, also raised the values of Hc from 3 to 16 Oe. This behavior was also observed in annealed and cold rolled alloys. Annealing treatment also released the residual stresses and resulted in reduction of Hc values. However, the highest values of Hc was observed in cold rolled samples which ranged from 5 to 25 Oe. The tensile strength of cold rolled and annealed alloys for x values of 0, 0.2, and 0.4, were 510, 635, and 910 Mpa, respectively. Furthermore, the electrical resistance augmented monotonously with an increasing value of x. It is therefore concluded that cold rolled and annealed high entropy alloys of FeCoNi(AlMn)x can present a variety combinations of tensile, magnetic, and electrical behavior when compared to other soft magnetic materials.

Magnetite Survivability and Non‐Stoichiometric Magnetite Formation in Presence of Oxyhalogen Brines on Mars

AbstractThe mixed Fe(II)/Fe(III) mineral magnetite [Fe3O4] of various stoichiometric and non‐stoichiometric compositions have been reported in Martian soils and rocks by several rover missions. Magnetite is an important paleomagnetic indicator mineral and can serve as a ‘biogeobattery’ as a consequence of its magnetic properties and the mixed valence state of iron in its structure. Here, we assess the extent of oxidative weathering of magnetite in presence of chlorate and bromate containing solutions that are likely important oxidants on Mars. Oxyhalogen species, chlorate and bromate, produced non‐stoichiometric magnetite [Fe(II)/Fe(III) < 0.5] in Mars‐relevant, near‐neutral pH fluids; no other ferric minerals were produced. The same results were observed in highly acidic fluids with or without oxyhalogens. Owing to its resistance to extensive oxidation, magnetite can serve as an important archive of geochemical, paleomagnetic, and astrobiological information in samples that will be returned by the Mars Sample Return mission.

Synthesis of metallic nanoparticles using biometabolites: mechanisms and applications.

Bio-metabolites have played a crucial role in the recent green synthesis of nanoparticles, resulting in more versatile, safer, and effective nanoparticles. Various primary and secondary metabolites, such as proteins, carbohydrates, lipids, nucleic acids, enzymes, vitamins, organic acids, alkaloids, flavonoids, and terpenes, have demonstrated strong metal reduction and stabilization properties that can be utilized to synthesize nanomaterials and influence their characters. While physical and chemical methods were previously used to synthesize these nanomaterials, their drawbacks, including high energy consumption, elevated cost, lower yield, and the use of toxic chemicals, have led to a shift towards eco-friendly, rapid, and efficient alternatives. Biomolecules act as reducing agents through deprotonation, nucleophilic reactions, transesterification reactions, ligand binding, and chelation mechanisms, which help sequester metal ions into stable metal nanoparticles (NPs). Engineered NPs have potential applications in various fields due to their optical, electronic, and magnetic properties, offering improved performance compared to bulkier counterparts. NPs can be used in medicine, food and agriculture, chemical catalysts, energy harvesting, electronics, etc. This review provides an overview of the role of primary and secondary metabolites in creating effective nanostructures and their potential applications.

Fast and Sensitive Determination of Iodide Based on Ternary Chalcogenides Nanoparticles

A fluorescent probe based on ternary AgFeS2 quantum dots has been prepared for the design of ternary chalcogenides. The nanoparticles are synthesized with oleylamine as a stabilizer at a low temperature (particle size in the range of 2 to 3 nm) and they exhibit an intense blue emission in aqueous media. As for their internal structure, each nanoparticle’s relative stoichiometric ratio (AgFe1.01S1.91) is very close to the theoretical value of 1:1:2. Their magnetic properties have been studied with a vibrating sample magnetometer and they have ferromagnetism between 4 K and 298 K (applied magnetic field ranging between −10,000 and 10,000 Oe). In the presence of iodide ions, the emission at 458 nm derived from AgFeS2 QDs has been observed to give rise to fluorescence quenching. The detection system is based on a static quenching process and morphological change between iodide ions and AgFeS2, which has a good linear range from 0 to 37.5 μmol/L, with a limit of detection of 0.99 μM. The nanoprobe responds within 30 s for the efficient detection of iodide. Such functional quantum dots will provide a powerful indicator in environmental and bio-sensing applications.

Investigation of electrical, dielectric, magnetic and electrochemical characteristics of a BaFe12O19/Co0.5Zn0.5Fe2O4 nanocomposite

BaFe12O19 (barium ferrite, i.e., BaF) nanoparticles, Co0.5Zn0.5Fe2O4 (cobalt zinc ferrite, i.e, CZF) nanoparticles and their nanocomposite were synthesized for the investigation of electrical, magnetic, dielectric, and electrochemical properties. The X-ray diffraction (XRD) pattern revealed the formation of hexagonal structure for BaF nanoparticles and cubic structure for CZF nanoparticles with crystallite size of 32.44 nm and 31.30 nm, respectively. Whereas, for nanocomposite, the crystallite size obtained is 34.21 nm were shifting of peaks revealed the formation of nanocomposite. The Fourier transform Infrared (FTIR) spectra revealed the presence of metal-oxygen vibrational peaks for all the samples. The dielectric data revealed the increase in dielectric constant of nanocomposite as compared to pristine CZF whereas, loss reduced for nanocomposite significantly. Single semicircle in Nyquist plot for all the samples revealed the contribution of grain resistance in impedance. The hysteresis loop showed the increase in specific saturation magnetization from 16.963 emu/g to 21.305 emu/g for nanocomposite when compared with pristine BaF. Whereas specific remnant magnetization increased to 10.305 emu/g for nanocomposites. The electrochemical properties presented by Cyclic voltammetry showed the presence of cathodic and anodic peaks which revealed the presence of redox reaction in all samples. The specific capacitance calculated for all samples at different scan rate revealed that a nanocomposite showed highest Cs value 16.43 F/g at 25 mV, whereas it increased to 27.01 F/g, 35.93 F/g and 38.87 F/g with the increase in scan rate to 50 mV, 75 mV and 100 mV, respectively.

Crystallite Size Effects on Electrical Properties of Nickel Chromite (NiCr2O4) Spinel Ceramics: A Study of Structural, Magnetic, and Dielectric Transitions

The effect of sintering temperature on the structural, magnetic, and dielectric properties of NiCr2O4 ceramics was investigated. A powder X-ray analysis indicates that the prepared nanocrystallites effectively inhibit the cooperative Jahn–Teller distortion, thereby stabilizing the high-temperature cubic phase structure with space group Fd-3m. Multiple transitions are confirmed by temperature-dependent magnetization M(T) data. Moreover, the magnetization value decreases and the Curie temperature increases with a decrease in the crystallite size. The low-temperature-dependent real permittivity (ε′-T) for a NiCr2O4 crystallite size of 78 nm exhibits a broad maximum at 40 K that is independent of frequency. This establishes a correlation between electric ordering and the underlying magnetic structure. The temperature dependency of the dielectric constant at fixed frequencies for both NiCr2O4 crystallite sizes rises with temperature for a certain range of frequencies. A significant improvement is evident: the dielectric constant (ε’) at room temperature reaches approximately 5738 for the sample with 28 nm crystallites, while the 78 nm crystallite sample shows a noticeable drop to ε’~174. The frequency-dependent conductivity curves for both types of NiCr2O4 nanocrystallites have different conductivity values. The lower-crystallite-size sample demonstrates higher conductivity values than the 78 nm crystallite size one. This observation is attributed to the decrease in crystallite size, which increases the number of grain boundaries and, consequently, scatters a higher number of charge carriers.

Study on the effects of strain and electrostatic doping on the magnetic anisotropy of GaN/VTe2van der Waals heterostructure.

Using a first-principles approach, this study delves into the effects of strain and electrostatic doping on the electronic and magnetic properties of the GaN/VTe2van der Waals heterostructure. The results reveal that when the GaN/VTe2van der Waals heterostructure is doped with 0.1h/0.2hof electrostatic charge, its magnetization direction undergoes a remarkable reversal, shifting from out-of-plane orientation to in-plane direction. Therefore, we conduct a thorough investigation into the influence of electron orbitals on magnetic anisotropy energy. In addition, as the strain changes from -1% to 1%, the 100% spin polarization region of the GaN/VTe2vdW heterostructure becomes smaller. It is worth noting that at a doping concentration of 0.1h, the GaN/VTe2vdW heterostructure has a Curie temperature of 30 K above room temperature. This comprehensive study provides valuable insights and provides a reference for analyzing the electronic and magnetic properties of low-dimensional systems.

Enhancement of magnetic properties of bismuth-substituted Mn-Mg-Cu-Zn ferrite prepared by sol-gel route

Enhancement of magnetic properties of bismuth-substituted Mn-Mg-Cu-Zn ferrite prepared by sol-gel route

Effect of Pouring Techniques and Funnel Structures on Crucible Metallurgy: Physical and Numerical Simulations

In the planar flow casting process of amorphous strips, the flow behavior of molten metal and the inclusion content in the crucible are crucial to the morphology and magnetic properties of the material. This study conducts a comparative analysis of the effects of non-immersed and immersed funnels, as well as various funnel structures, on the fluid flow and inclusion removal efficiency in the crucible by integrating numerical and physical models. The findings reveal that for the same pouring flow rate, the diameter of the liquid column in non-immersed pouring conditions is smaller than that of the funnel outlet, leading to a faster injection flow velocity. As a result, the melt in the crucible is subjected to severe impacts, accompanied by an increased possibility of slag entrapment. Conversely, immersed pouring substantially reduces the velocity of the molten metal at the funnel outlet, thereby extending the residence time in the crucible and diminishing the volume of the dead zone. Additionally, the molten metal backflows due to the negative pressure formed in the inner chamber of the funnel. The design of a trumpet-shaped funnel increases the effective volume while reducing the height of the backflow fluid, consequently reducing the velocity of the molten metal at the funnel outlet and prolonging the residence time. Compared to the conventional pouring process with the non-immersed funnel, the outlet velocity is reduced from 1.1 m/s to 0.12 m/s by adopting the immersed funnel with an inverted trapezoidal trumpet structure. This reduction results in a stable flow state, a 9.69% reduction in the dead zone volume fraction, and a 22.96% increase in average inclusion removal efficiency. These improvements demonstrate that a crucible funnel with a well-designed structure and the implementation of an immersion process can significantly improve the metallurgical effects in the planar flow casting process.

Simple and Effective Identification of Local 6π- and Global [4n + 2] Aromaticity of Macrocyclic Conjugated Hydrocarbons by 1H/13C Chemical Shifts and the Corresponding Ring Current Effect.

Structures, 1H/13C chemical shifts, and the ring current effects (spatial magnetic properties: through-space NMR shieldings [TSNMRSs]) of various π-conjugated macrocyclic hydrocarbons and the corresponding charged analogues have been calculated at the B3LYP/6-311G(d,p) theory level using the GIAO perturbation method and employing the nucleus-independent chemical shift (NICS) characterization. The spatial magnetic properties (TSNMRS) are visualized as iso-chemical shielding surfaces (ICSSs) of various size and direction and together with especially the δ(1H)/ppm chemical shifts employed to unequivocally qualify and quantify local 6π-aromaticity of individual benzenoid building blocks and the global ([4n + 2], n > 1) aromaticity of the macrocyclic ring.

Light-Controlled Magnetic Properties: An Energy-Efficient Opto-Mechanical Control over Magnetic Films by Liquid Crystalline Networks.

Magnetostrictive materials are essential components in sensors, actuators, and energy-storage devices due to their ability to convert mechanical stress into changes in magnetic properties and vice-versa. However, their operation typically requires physical contact to apply stress or relies on magnetic field sources to control magnetic properties. This poses significant limitations to devices miniaturization and their integration into contactless technologies. This work reports on an approach that overcomes these limitations by using light to transfer mechanical stress to a magnetostrictive device, thereby achieving non-contact and reversible opto-mechanical control of its magnetic and electrical properties. The proposed solution combines a magnetostrictive Fe70Ga30 thin film with a photo-responsive Liquid Crystalline Network (LCN). Magnetic properties are modulated by changing the light wavelength and illumination time. Remarkably, the stable shape change of the LCN induced by ultraviolet (UV) light leads to the retention of magnetic properties even after the light is switched off, resulting in a magnetic memory effect with an energy consumption advantage over the use of conventional magnetic field applicators. The memory effect is erased by visible light, which releases the mechanical stress in the photoresponsive layer. Therefore, this new composite material creates a fully reconfigurable magnetic system controlled by light.

Theoretical Study of the Co‐doping Effects at Sr and Fe Sites on the Magnetic and Optical Properties of SrFe12O19

For the first time, the magnetic and optical (bandgap) properties of co‐doped Mg/Dy, Al/Dy, and Mn/Nd (SFO) at Sr and Fe sites are investigated using a microscopic model and the Green's function theory. It is shown that the co‐doping at both Sr and Fe sites can change the behavior of the magnetization which decreases by transition metal or nonmagnetic ion doping at the Fe site (with doping ions larger than the host Fe ions), but by additive co‐doping at the Sr site with rare‐earth ion (which ionic radius is smaller than that of Sr) the magnetization increases with increasing the co‐doping concentration. The bandgap energy decreases in the co‐doped SFO. The mechanism of this co‐doping effect is explained on microscopic level. It is due to the changes of the spin‐exchange interaction constants at the doped sites caused by the appearance of different strain by the doping with two ions. The theoretical results are compared with the existing experimental data and are in good qualitative agreement.

Peristaltic propulsion of Ree-Eyring nanofluids: investigations on the role of magnetic field and variable thermophysical properties

Peristaltic propulsion of Ree-Eyring nanofluids: investigations on the role of magnetic field and variable thermophysical properties

Porous Metal Phosphonate Frameworks: Construction and Physical Properties.

ConspectusPorous metal phosphonate frameworks (PMPFs) as a subclass of metal-organic frameworks (MOFs) have promising applications in the fields of gas adsorption and separation, ion exchange and storage, catalysis, sensing, etc. Compared to the typical carboxylate-based MOFs, PMPFs exhibit higher thermal and water stability due to the strong coordination ability of the phosphonate ligands. Despite their robust frameworks, PMPFs account for less than 0.51% of the porous MOFs reported so far. This is because metal phosphonates are highly susceptible to the formation of dense layered or pillared-layered structures, and they precipitate easily and are difficult to crystallize. There is a tendency to use phosphonate ligands containing multiple phosphonate groups and large organic spacers to prevent the formation of dense structures and generate open frameworks with permanent porosity. Thus, many PMPFs are composed of chains or clusters of inorganic metal phosphonates interconnected by organic spacers. Using this feature, a wide range of metal ions and organic components can be selected, and their physical properties can be modulated. However, limited by the small number of PMPFs, there are still relatively few studies on the physical properties of PMPFs, some of which merely remain in the description of the phenomena and lack in-depth elaboration of the structure-property relationship. In this Account, we review the strategies for constructing PMPFs and their physical properties, primarily based on our own research. The construction strategies are categorized according to the number (n = 1-4) of phosphonate groups in the ligand. The physical properties include proton conduction, electrical conduction, magnetism, and photoluminescence properties. Proton conductivity of PMPFs can be enhanced by increasing the proton carrier concentration and mobility. The former can be achieved by adding acidic groups such as -POH and/or introducing acidic guests in the hydrophilic channels. The latter can be attained by introducing conjugate acid-base pairs or elevating the temperature. Semiconducting PMPFs, on the other hand, can be obtained by constructing highly conjugated networks of coordination bonds or introducing large conjugated organic linkers π-π stacked in the lattice. In the case of magnetic PMPFs, long-range magnetic ordering occurs at very low temperatures due to very weak magnetic exchange couplings propagated via O-P-O and/or O(P) units. However, lanthanide compounds may be interesting candidates for single-molecule magnets because of the strong single-ion magnetic anisotropy arising from the spin-orbit coupling and large magnetic moments of lanthanide ions. The luminescent properties of PMPFs depend on the metal ions and/or organic ligands. Emissive PMPFs containing lanthanides and/or uranyl ions are promising for sensing and photonic applications. We conclude with an outlook on the opportunities and challenges for the future development of this promising field.

Control Voltage Effect on Operational Characteristics of Vehicle Magnetorheological Damper

Considering the increasingly large-scale application of magnetic fluids in various industries, we can confidently state that in the near future magnetorheological dampers will be widely used in adaptive automotive suspensions due to their operational flexibility and simplicity of controlling damping forces by changing the magnetic fluid properties according to parameters of surrounding electromagnetic field. The antivibration efficiency during operation is achieved by regulating the hydraulic resistance of the “magnetic” shock absorber by applying voltage to the windings of its coil. In addition to the physical properties of the oil used in the “magnetic” shock absorber, the viscosity of the working magnetorheological fluid is greatly influenced by the shape of the control signal. The paper focuses on the theoretical aspects of constructing a mathematical model of ac magnetorheological damper and presents the results of a computer experiment to assess effectiveness of its use as part of the adaptive suspension a passenger vehicle. In this case, the actual parameters of the “magnetic” shock absorber, used in modeling the dynamic process, were determined experimentally on a test bench, and the adequacy of the developed mathematical model was confirmed by the results of a semi-natural experiment. Using a verified model, the magnetorheological damper characteristics were obtained and compared for various forms of control signal, including rectangular voltage pulses of various frequencies and duty cycles, sinusoidal pulses and constant voltage signals. The analysis of the antivibration efficiency was carried out on the basis of the developed “quarter” model of a semi-active car suspension with a verified submodel of a magnetorheological damper integrated into its structure. Moreover, the simulation scenarios were based on the selected strategy for controlling the voltage supplied to the windings of the “magnetic” shock absorber. As the results of theoretical and experimental studies have shown in terms of energy consumption, expansion of the working area of the damping characteristic and achieving smooth control of the damping force, the most effective is the use of a sinusoidal pulse voltage signal in the control circuit, which ensures a reduction in both the amplitude and damping time of oscillations. However, when de-signing and manufacturing a controller, creating a pulse modulator for generating sinusoidal pulses coinciding in phase and frequency with the vibrations of the car body is very difficult due to the random nature of external disturbances from the road surface. When a constant voltage is applied to the magnetorheological damper winding, the damping properties of the suspension are also improved compared to the basic design based on a traditional hydraulic shock absorber. Moreover, there is a proportional relationship between the voltage supplying the damper, the amplitude and damping time of the vibrations of the car body is observed. An increase in the control signal voltage from 1 to 2 V leads, in comparison with passive control of a magnetic shock absorber, to a decrease in the maximum amplitude of vibrations of the car body by 6.25 and 11.25 %, respectively, and a decrease in the vibration damping time by 0.72 and 1.41 s.