Magnetic Carbon Nanocomposite Research Articles

Valorization and Upcycling of Acid Mine Drainage and Plastic Waste via the Preparation of Magnetic Sorbents for Adsorption of Emerging Contaminants.

Plastic waste poses a serious environmental risk, but it can be recycled to produce a variety of nanomaterials for water treatment. In this study, poly(ethylene terephthalate) (PET) waste and acid mine drainage were used in the preparation of magnetic mesoporous carbon (MMC) nanocomposites for the adsorptive removal of pharmaceuticals and personal care products (PPCPs) from water samples. The latter were then characterized using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET), and ζ potential. The results of Brunauer-Emmett-Teller isotherms revealed high specific surface areas of 404, 664, and 936 m2/g with corresponding pore sizes 2.51, 2.28, and 2.26 nm for MMC, MMAC-25%, and MMAC-50% adsorbents, respectively. Under optimized conditions, the equilibrium studies were best described by the Langmuir and Freundlich models and kinetics by the pseudo-second-order model. The maximum adsorption capacity for monolayer adsorption from the Langmuir model was 112, 102, and 106 mg/g for acetaminophen, caffeine, and carbamazepine, respectively. The composites could be reused for up to six cycles without losing their adsorption efficiency. Furthermore, prepared adsorbents were used to remove acetaminophen, caffeine, and carbamazepine from wastewater samples, and up to a 95% removal efficiency was attained.

The effect of carbon coating on the arsenite sorption by magnetic carbon nanocomposites

AbstractArsenic pollution has emerged through anthropogenic activities and natural mineral leaching processes. This study aims to advance the use of magnetic carbon nanocomposites (MCNs) in the sorption of arsenic, studying the influence of feedstock and the presence of carbon coating on magnetic nanoparticles. Previous works have shown that post-pyrolysis treatment improves the stability of MCNs by reducing iron leaching due to the formation of a carbon coating that encapsulates the iron oxide nanoparticles. However, this carbon coating could influence the adsorption properties of MCNs. This investigation deals with arsenic adsorption by four MCNs prepared by co-precipitation of magnetite (Fe3O4) nanoparticle into four carbonaceous matrixes, followed by a post-pyrolysis treatment. The pristine carbonaceous matrixes used in the present work were commercial activated carbon (CAC), charcoal (CC), hydrochar from the orange residue (HCOR), and biochar from sunflower husk (BCSFH). Pristine carbonaceous materials and MCNs without post-pyrolyzed were also used as arsenic sorbents in water solutions. Additionally, kinetic studies were carried out to explore the sorption properties of different MCNs and pristine materials, concerning the removal efficiencies (expressed as a percentage) and adsorption capacities, determining the equilibrium time. The results demonstrated that the presence of magnetite increases the adsorption of arsenic, being higher in the case of materials obtained by direct co-precipitation than in materials subjected to a post-pyrolysis process. The presence of a carbon layerprotecting the magnetite slightly decreases the adsorption of arsenic.

Synthesis of green nanosorbent from bovine serum albumin and curcumin for magnetic solid phase extraction of pesticides from food samples

For the first time, a magnetic carbon nanocomposite was synthesized using one-step hydrothermal procedure, employing bovine serum albumin, curcumin, and ferric ammonium citrate. Additionally, the application of this novel composite as an adsorbent for magnetic dispersive solid phase extraction of fungicides and pesticides from water and food samples is a unique aspect of this study. Under optimum conditions (salt concentration: 5.0% w/v, pH: 7.0, desorption solvent: ethanol, sorbent amount: 20 mg, extraction time: 20 min, desorption time: 3 min, stirring rate: 500 rpm, sample volume: 30 mL, extraction temperature: room temperature, and desorption solvent volume: 150 μL) linearity (2.5 to 1400 ng mL−1), coefficients of determination (R2 ≥ 0.997), limits of detection (0.75 to 1.5 ng mL−1), and limits of quantification (2.5 to 5.0 ng mL−1) were achieved. The method validation results showed extraction recovery ranging from 71.2% to 93.4%, and preconcentration factors ranging from 142.5 to 186.1.

Magnetically Sensitive Carbon-Based Nanocomposites for the Removal of Dyes and Heavy Metals from Wastewater: A Review

The methods of wastewater treatment from heavy metal ions and dyes are analyzed, and the key advantages of powdered magnetically sensitive carbon nanocomposites as adsorbents are shown. Methods for selecting and preparing raw materials and activators for the synthesis of such nanocomposites are considered, and methods for synthesizing nanocomposites are analyzed. The properties, modeling of adsorption kinetics and isotherms, and efficiency of magnetic carbon nanocomposites for wastewater treatment from dyes and heavy metals are described.

Manipulating cellulose-based dual-network coordination for enhanced electromagnetic wave absorption in magnetic porous carbon nanocomposites

A novel dual-network coordination strategy was utilized to prepare carbon based magnetic porous EMW absorption nanocomposites with controllable magnetic particles deposition on carbon matrices. Due to the conversion of carboxymethyl cellulose (CMC) into Prussian blue (PB) through coordination with Fe3+, the deposition of Fe3+ gradually tends to aggregate. Consequently, significant changes occur in the polycrystalline structure of magnetic Fe3O4 particles in the pyrolysis products, including alterations in grain size, orientation, and the overall size of polycrystalline particle. Finally, the obtained Fe3O4 decorated porous carbon nanocomposites showed ultrawide effective absorption band of 6.7 GHz owing to the advantageous impedance matching and the synergistic dielectric and magnetic loss effects. Overall, this study offers valuable insights into the design and comprehension of magnetic porous nanocomposites for efficient EMW absorption through the regulation of polycrystalline structure by controllable coordination deposition.

The Use of Magnetic Porous Carbon Nanocomposites for the Elimination of Organic Pollutants from Wastewater

One of the most significant challenges the world is currently facing is wastewater treatment. A substantial volume of effluents from diverse sources releases numerous pollutants into the water. Among these contaminants, organic pollutants are particularly concerning due to the associated risk of being released into the environment, garnering significant attention. Rapid advancements in agriculture and industry on a global scale generate vast volumes of hazardous organic compounds, which eventually find their way into natural systems. Recently, the release of industrial wastewater has been increasing, due to the progress of numerous businesses. This poses a danger to humans and the environment, leading to environmental contamination. The application of carbon nanocomposites in applied nanotechnology has recently expanded due to their large surface area, substantial pore volume, low preparation cost, and environmental resilience. Expanding the use of nanomaterials in water treatment is essential, as magnetic carbon nanocomposites consistently demonstrate an efficient elimination of pollutants from water solutions. In the current study, we have highlighted the application of magnetic porous carbon nanocomposites in removing organic pollutants from wastewater.

Modification of magnetic active carbon nanocomposite with SiO2 and Zincon for efficient removal of Pb(II) and 201Pb(II); multivariate optimization and adsorption characterization

This research focuses on the development of a novel surface-modified green magnetic carbon-based nanocomposite as a new adsorbent for the efficient removal of Pb(II) and 201Pb(II) from water sources. The nanocomposite was synthesized using pomegranate peel extract modification, some renewable and sustainable raw material rich in polyphenols and biologically active constituents. Then it was modified by SiO2 and Zincon for enhancement of its selectivity and performance. The prepared nanocomposite was characterized using various analytical techniques, including Fourier-transform infrared spectrophotometry (FTIR), field emission scanning electron microscopy (FESEM) coupled with energy-dispersive spectroscopy (EDS), vibrating sample magnetometer (VSM), Brunauer-Emmett-Teller (BET), and X-ray diffraction (XRD) analyses. To optimize the adsorption process, a multivariate optimization methodology based on the Box-Behnken design was employed. The optimal conditions were found to be: pH 5.4, adsorbent mass 4.0 mg, initial concentration of lead ion 54.0 mg.L-1. Adsorption isotherms and kinetic modeling studies were conducted to understand the adsorption behavior of the nanocomposite. The maximum capacity uptake was 513.5 mg.g−1. The results indicated that the surface-modified green magnetic carbon-based nanocomposite exhibited a high adsorption capacity and rapid adsorption kinetics for both Pb(II) and 201Pb(II). The pseudo-second-order kinetic model provided the best fit to the experimental data, suggesting chemisorption as the predominant adsorption mechanism. Thermodynamic analysis revealed that the adsorption process was spontaneous and exothermic, indicating the favorable nature of the adsorption.

Nanocomposites Based on Multi-Walled Carbon Nanotubes, Magnetite Nanoparticles, and Core–Shell Molecularly Imprinted Polymers in Piezoelectric Sensors for the Determination of Macrolide Antibiotics

A piezoelectric sensor with a recognition layer based on magnetic carbon nanocomposites, including multi-walled carbon nanotubes, magnetic Fe3O4 nanoparticles, and polymer nanospheres with molecular imprints of erythromycin and azithromycin, obtained by the “core–shell” method, is developed. Silicon dioxide particles are used as cores, on the surface of which a shell molecularly imprinted with macrolides is synthesized by free radical polymerization or the sol–gel method. SiO2 particles are obtained by the Stober method by varying the ratio of reagents during the synthesis. The size of the cores and nanoparticles of molecularly imprinted polymers (MIP) is determined by atomic force microscopy, and the density and uniformity of the layer on the surface of magnetic carbon nanocomposites (MCNC) are determined by the piezoelectric quartz crystal microbalance method. The optimal ratio of the reagents (template : functional monomer : cross-monomer) is established by a spectrophotometric method during the synthesis of “core–shell” nanostructures by free radical polymerization. A thin shell of SiO2 with imprints of an antibiotic based on organosilicon compounds used in the synthesis of the core is formed by the sol–gel method on the surface of the silicon dioxide core. The sensor recognition layer is formed under the action of an external magnetic field. The dependence of the analytical signal of the sensor based on MIP@SiO2/MCNC on concentration is linear in the range 5–160 µg/mL for azithromycin and 10–160 µg/mL for erythromycin, and with a recognition layer based on SiO2@SiO2/MCNC, in the concentration range 20–400 µg/mL for erythromycin.

Determination of aristolochic acid using a piezoelectric immunosensor based on magnetic carbon nanocomposites

A technique for the determination of aristolochic acid (AA) in food products using a piezoelectric immunosensor is presented. Magnetic carbon nanocomposites (MCNC) were used as the recognition layer of the sensor, on the surface of which protein conjugates of AA were immobilized. Abstract-Methods for the synthesis of Fe3O4 magnetic nuclei and their attachment to the surface of multi-walled carbon nanotubes (CNTs) have been studied. Using IR spectrometry, it was found that the formation of the recognition layer of the sensor occurs due to the formation of covalent bonds between the amino groups of AA conjugates and carboxyl groups of CNTs. The concentrations of protein conjugates based on ovalbumin (OVA) and bovine serum albumin (BSA) (0.3 and 0.2 mg/ml) and the degree of antibody dilution (0.25) were determined, which provide optimal characteristics of the piezoelectric immunosensor. The metrological characteristics of the method for determining AA have been established. The range of determined concentrations of AA and the limit of detection when using a piezoelectric immunosensor with a recognition layer based on MUNA/AA-OVA and MUNA/AA-BSA are (ng/ml): 50 – 400 and 10; 100 – 300 and 50, respectively. The sensor has been tested in the determination of AA in samples of Chinese herbal tea and dietary supplements for weight loss. No acid was found in tea, and in dietary supplements, the acid content is 3.2 μg/g.

Magnetic Carbon Nanocomposites: Preparation from Cellulose via Chemical Activation with FeCl3 and Characterization

Magnetic Carbon Nanocomposites: Preparation from Cellulose via Chemical Activation with FeCl3 and Characterization

Magnetic Carbon Nanocomposites: Preparation from Cellulose via Chemical Activation with FeCl3 and Characterization

We have studied the preparation of magnetic graphitic carbon composites, which combine the adsorption properties of activated carbon with magnetic properties and properties intrinsic to graphite. The preparation method is efficient; it comprises modifying flax shive cellulose with citric acid to enhance the chelating ability of the flax shive cellulose matrix, impregnating the modified cellulose with iron chloride, and pyrolysis in an inert atmosphere to control the composition, morphology, specific surface, and porosity of hybrid carbon materials. The scenario of cellulose matrix pyrolysis was suggested using thermogravimetry. X-ray structural analysis was used to characterize the graphitic composites. The citric acid modification of cellulose helps to prepare a high-graphite (74%) carbon composite where the graphitization level of the graphite structure approaches the graphitization level of commercially available graphite at 700°С. Low-temperature N2 adsorption–desorption and ζ-potential measurements helped to suggest the adsorption mechanism for environmentally hazardous dyes. The greatest equilibrium adsorption of Methylene Blue (MB) and Methyl Orange (MO) dyes was 127.4 and 23.7 mg/g, respectively. The prepared composites can be used as adsorbents and fillers in polymer composite materials.

Sodium chloride assisted synthesis of porous magnetic carbon nanocomposites containing cobalt nanoparticles for high-performance electromagnetic wave-absorption

High-performance electromagnetic wave-absorbing materials have attracted much attention owing to their wide application in military stealth, camouflage, and electromagnetic protection. Carbon materials have more advantages in achieving the performance goals of thin, light, wide, and strong absorption. The combination of ferromagnetic components is commonly used to further improve the absorption ability of carbon materials. Herein, porous Co/C nanocomposites attached with different Co content were prepared through the sodium chloride assisted carbonization process of glucose precursor containing cobalt salts. Dipole polarizations and dielectric relaxation in the carbon matrix, as well as interfacial polarizations at the heterogeneous interfaces collectively contributed to the total dielectric loss. Meanwhile, the existence of Co nanoparticles effectively improved the magnetic properties and increased magnetic loss. In addition, the impedance matching performance was also improved. As a result, the prepared Co/C nanocomposites achieved an absorption bandwidth of nearly 6 GHz, covering almost the whole Ku band from 12.1 to 18.0 GHz. And the minimum reflection loss exceeded −60 dB. This work provided a simpler and more effective approach to prepare high-performance absorbing materials.

METHODS FOR TREATING WASTEWATER FROM ORGANIC POLLUTANTS

Water pollution by organic and inorganic compounds, heavy metals, dyes, radioactive and pharmaceutical compounds has a significant impact on its use. Globalization, structural changes, economic development around the world-all this contributes to the release of pollutants that cause water pollution. That is why wastewater treatment and recovery, removing pollutants from wastewater and wastewater, is one of the most important issues. This literature review examines the problems of water pollution, its sources and types of pollutants found in water, and also discusses purification methods, including methods of water purification from pollutants, in particular phenol, in the presence of nanocomposite catalysts. Recently, more and more attention has been paid to applied nanotechnology using magnetic and carbon nanocomposites due to the advantages of production cost, high surface area, pore volume and environmental sustainability. The literature review focuses on magnetic nanocomposite catalysts based on alternating and rare earth metals with advantages such as low cost of preparation for water disinfection, high surface area, pore volume and environmental resistance. Magnetic carbon nanocomposites usually demonstrate excellent adsorption characteristics of pollutants from aqueous solutions, therefore, the expansion of the use of nanotechnology in water purification is of great importance.

Removal of Metal Ions via Adsorption Using Carbon Magnetic Nanocomposites: Optimization through Response Surface Methodology, Kinetic and Thermodynamic Studies

The toxicity of metal ions on ecosystems has led to increasing amounts of research on their removal from wastewater. This paper presents the efficient application of a carbon magnetic nanocomposite as an adsorbent for the elimination of metal ions (copper, lead and zinc) from aqueous solutions. A Box–Behnken factorial design combined with the response surface methodology was conducted to investigate the effect and interactions of three variables on the pollutant removal process. Highly significant (p < 0.001) polynomial models were developed for each metal ion: the correlation coefficient was 0.99 for Cu(II) and Pb(II), and 0.96 for Zn(II) ion removal. The experimental data were in agreement and close to the theoretical results, which supports the applicability of the method. Working at the natural pH of the solutions, with a quantity of carbon magnetic nanocomposite of 1 g/L and a metal ions’ concentration of 10 mg/L, for 240 min, removal efficiencies greater than 75% were obtained. The kinetic study indicated that a combination of kinetic models pseudo-second order and intraparticle diffusion were applied appropriately for copper, lead and zinc ion adsorption on carbon magnetic nanocomposite. The maximum adsorption capacities determined from the Langmuir isotherm model were 81.36, 83.54 and 57.11 mg/g for copper, lead and zinc ions. The average removal efficiency for five adsorption–desorption cycles was 82.21% for Cu(II), 84.50% for Pb(II) and 72.68% for Zn(II). The high adsorption capacities of metal ions, in a short time, as well as the easy separation of the nanocomposite from the solution, support the applicability of the magnetic carbon nanocomposite for wastewater treatment.

N-doped magnetic carbon nanosheets for broad, strong, stable and thin microwave absorption properties

The novel magnetic carbon nanocomposite, in which N-doped onion-like carbon encapsulated FeNi nanoparticles are embedded into N-doped carbon nanosheets, are prepared for realizing “broad, strong, stable and thin” microwave absorption behaviors. Good impedance match between magnetic FeNi nanoparticles and dielectric carbon and the large attenuation capability accompanied with strong dielectric loss ability induced by interfacial polarization loss, defect dipole polarization loss, Debye relaxation loss, conductive loss and magnetic loss originating from natural/exchange resonance and eddy current loss ensure the good microwave absorption ability. This nanocomposite exhibits the minimal reflection loss value of –27.62 dB at 4.72 GHz and the effective absorbing bandwidth of 5.76 GHz (covering 12.24–––18 GHz) at 1.9 mm and the peak of reflection loss basically locates at −21.62 dB- −27.62 dB from 1.7 mm to 5.0 mm.

Polyaniline‐co‐polyindole functionalized magnetic porous carbon derived from MIL‐53(Fe) for separation/enrichment of nitrophenols pollutants before determination with high‐performance liquid chromatography‐ultraviolet detection

Herein, a novel polyaniline-co-polyindole functionalized magnetic porous carbon derived from MIL-53(Fe) was prepared and employed as an excellent nano-adsorbent to preconcentrate trace amounts of nitro-phenols in water and wastewater samples. Briefly, magnetic MIL-53(Fe) was synthesized by the addition of magnetite nanoparticles, terephthalic acid, and FeCl3 to the reaction medium. The magnetic MIL-53(Fe) was pyrolyzed under nitrogen protection to obtain a magnetic porous carbon nanocomposite, and finally, the nanomaterial was functionalized with polyaniline-co-polyindole via oxidation polymerization. The obtained nano-adsorbent was characterized via X-ray diffraction, Fourier-transform infrared spectroscopy, vibrating sample magnetometry, and transmission and scanning electron microscopies. After that, the fabricated nano-material was utilized as an excellent nano-adsorbent for the preconcentration of trace nitro-phenols (2-nitrophenol, 4-nitrophenol, and 2,4-dinitrophenol) in environmental water, and wastewater samples. The detection limits were obtained from 0.1 to 0.15μg/L after performing the optimization process. The new method was in the range of 0.4-300μg/L. The proposed method exhibited a good precision from 3.2% to 9.6% for within-day assay, and 5.2%-13.2% for between-day assay at three concentration levels (1, 50, and 250μg/L). Eventually, this method was utilized to preconcentrate/determine the target analytes in three water, and wastewater samples, satisfactory (relative standard deviations, 5.4%-9.3%; relative recovery, 88%-109%).

Super magnetic loss induced by tunable damping coefficient through Ni nanoparticles size matching in magnetic carbon

For dielectric-magnetic dual loss absorbers, magnetic loss capacity is the main contributor for improving microwave absorbing performances. Shape anisotropy induced by different morphologies and large out-of-plane anisotropy field in the material system are main common strategies to increase magnetic loss ability. We herein propose a new idea for enhancing magnetic loss capacity induced by tunable damping coefficient through Ni particle-size matching in magnetic carbon nanocomposites. As an example, for annealed magnetic carbon at 700 °C, it delivers imaginary part of permeability up to 0.462 and super magnetic loss of 0.6, resulting in minimal reflection loss of −41.91 dB at absorbing layer thickness of 3.4 mm and efficient absorbing bandwidth of 4.24 GHz at absorbing layer thickness of 2.9 mm. By applying the combination of Gilbert equation and effective medium theory, the effective permeability calculations reveals that the significant enhancement originates from the tunable damping coefficient through Ni particles size matching. The relationship model between damping coefficient and size matching has been proposed, which is well consistent with experimental data. This work is of great significance for understanding the physical process of particle size matching to strengthen electromagnetic loss ability, and provides an alternative for the design of electromagnetic absorbing materials with strong magnetic loss ability.

Pyrolyzed magnetic NiO/carbon-derived nanocomposite from a hierarchical nickel-based metal-organic framework with ultrahigh adsorption capacity

Herein, a simple one-pot solvothermal approach is used to create magnetic porous carbon nanocomposites which obtained from a nickel-based metal-organic framework (Ni-MOF) and examined for their ability to uptake methyl orange (MO) dye. Derived carbons with exceptional porosity and magnetic properties were created during the different pyrolysis temperatures of Ni-MOF (700, 800, and 900 °C) under a nitrogen atmosphere. The black powders were given the names CDM-700, CDM-800, and CDM-900 after they were obtained. A variety of analysis methods, including FESEM, EDS, XRD, FTIR, VSM, and N2 adsorption-desorption were used to characterize as-prepared powders. Furthermore, adsorbent dosage, contact time, pH variation, and initial dye concentration effects was investigated. The maximum adsorption capacities were 307.38, 5976.35, 4992.39, and 2636.54 mg/g for Ni-MOF, CDM-700, CDM-800, and CDM-900, respectively, which show the ultrahigh capacity of the resulted nanocomposites compared to newest materials. The results showed that not only the crystallinity turned but also the specific surface area was increased about four times after pyrolyzing. The results showed that the maximum adsorption capacity of MO dye for CDM-700 was obtained at adsorbent dosage of 0.083 g/L, contact time of 60 min, feed pH of 3, and temperature of 45 °C. The Langmuir model has the best match and suggests the adsorption process as a single layer. According to the results of reaction kinetic studies using well-known models, the pseudo-second-order model (R2 = 0.9989) displayed high agreement with the experimental data. The synthesized nanocomposite is introduced as a promising superadsorbent for eliminating dyes from contaminated water due to strong recycling performance up to the fifth cycle.

Magnetic carbon nanocomposites via the graphitization of glucose and their induction heating

Carbon nanocomposites containing iron-based nanoparticles are attractive materials for the catalyst supports used for magnetic (induction) heating catalysis. The metallic, soft-magnetic iron nanoparticles provide local heating of the support in an alternating magnetic field and ensure rapid magnetic separation of the nanocomposite particles from reaction suspensions. In this work, magnetic carbon nanocomposites were prepared by annealing the precursor particles consisting of iron-oxide nanoparticles dispersed in a carbohydrate matrix. The annealing was conducted at 600 °C and 750 °C in an Ar atmosphere. At both temperatures the carbothermal reduction of iron oxide to Fe/Fe3C was observed; however, at the lower temperature the rate of reduction and the growth of the nanoparticles were considerably slower. The Fe3C was formed in negligible amounts only after a prolonged period of annealing at 600 °C. A detailed structural analysis showed that the Fe/Fe3C nanoparticles catalyze the graphitization of the carbonaceous precursor material already at 600 °C, resulting in the formation of a graphitic shell that surrounds them. This shell is tight enough to prevent the areal oxidation of the encapsulated Fe nanoparticles; their magnetic properties remained unchanged even after 1 year of storage under ambient conditions. At the higher annealing temperature, the growth of the Fe/Fe3C nanoparticles caused bursting of the graphitic shell and thus partially exposed their surfaces to the atmosphere. All the nanocomposites exhibited ferromagnetic behavior in accordance with their compositions. The nanocomposite that was predominantly composed of a graphitic shell, encapsulated Fe nanoparticles and a negligible amount of Fe3C, showed the highest specific absorption rate (760 W/gFe at 274 kHz), even at a relatively low AC-field amplitude (88 mT).

Use of Magnetic Carbon Nanocomposites in the Formation of a Recognition Layer of a Piezoelectric Immunosensor for the Determination of Penicillin G

Conditions for the formation of a recognition layer of a piezoelectric immunosensor based on magnetic carbon nanocomposites (MCNCs) under the action of an external magnetic field are studied. The effects of the size and number of magnetic nanoparticles (MNPs) in the composite on the analytical characteristics of the gravimetric immunosensor are revealed. Scanning electron microscopy is used to determine the average sizes of Fe3O4 magnetic nanoparticles synthesized by coprecipitation. It is noted that the minimum weight and stability of the recognition layer were observed for the nanocomposite obtained at a ratio of carbon nanotubes and MNPs with an average diameter of 22 nm equal to 3 : 1. The formation of peptide bonds between the MCNCs and a penicillin G conjugate was established by IR spectrometry. It was shown that the use of magnetic carbon nanocomposites in the formation of a recognition layer makes it possible to significantly simplify the procedure for preparing a piezoelectric sensor for analysis and reduce its duration from 24 to 1.5 h. The range of the determined antibiotic concentrations is 1–450 ng/mL, the limit of detection is 0.5 ng/mL.