Effect Of Polyvinylpyrrolidone Research Articles

Constructing Porous Energetic Spherulites via Solvation-Growth Coupling for Enhanced Combustion.

The fabrication of materials with hierarchical structures has garnered great interest, owing to the potential for significantly enhancing their functions. Herein, a strategy of coupling molecular solvation and crystal growth is presented to fabricate porous spherulites of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (CL-20), an important energetic material. With the addition of polyvinylpyrrolidone in the antisolvent crystallization, the metastable solvate of CL-20 is formed and grows spherulitically, and spontaneously desolvates to obtain the porous spherulite when filtration, in which the characteristic peak of the nitro group of CL-20 shifts detected by the in situ micro-confocal Raman spectroscopy. The effect of polyvinylpyrrolidone is thought to induce the solvation of CL-20, confirmed by density functional theory calculations, meanwhile acting on the (020) face of CL-20 to trigger spherulitic growth, demonstrated through infrared spectroscopy and Rietveld refinement of powder X-ray diffraction. Moreover, compared to common CL-20 crystals, porous spherulites exhibit enhanced combustion with increases of 6.24% in peak pressure, 40.21% in pressurization rate, and 9.63% in pressure duration effect, indicating the capability of hierarchical structures to boost the energy release of energetic crystals. This work demonstrates a new route via solvation-growth coupling to construct hierarchical structures for organic crystals and provides insight into the structure-property relations for material design.

Effect of polyvinylpyrrolidone and lithium chloride composite desiccant-coated heat exchangers on dehumidification studies

Cooling systems are necessities that remain energy intensive, particularly in tropical regions with elevated humidities and temperatures. Conventional vapor-compression air-conditioners are often inefficient because the sensible and latent heat loads are intrinsically coupled. To realize more energy-efficient cooling, solid desiccant-coated devices can be introduced to mitigate the latent heat load. Among such devices, desiccant-coated heat exchangers (DCHEs) are attractive for enabling nearly isothermal dehumidification. Hence, desiccants with high sorption capacity and rapid kinetics are essential. Solid polymeric desiccants are well-positioned to meet these requirements but comprehensive studies on the dehumidification performance of solid polymeric desiccant-coated heat exchangers are currently lacking. In this study, we investigated the potential of polyvinylpyrrolidone (PVP) and lithium chloride (LiCl) composites as desiccant materials at both material and system levels in terms of gravimetric water uptake. Specifically, LiCl is a hygroscopic salt bound by the moisture-sorbing PVP matrix. This work also demonstrates how the Elovich model accurately predicted the PVP-LiCl composite’s sorption kinetics. The results show that the optimum PVP-LiCl composite ratio is 66.7 wt%, with an equilibrium sorption capacity of 280 % at 75 % RH and 25 °C, compared to 29 % for silica gel under the same condition. With much superior sorption kinetics and capacity, the PVP-LiCl-coated prototype heat exchanger demonstrated a moisture removal capacity eight times higher than a silica gel-coated one under dynamic flow towards energy savings in air-conditioning systems.

Grain growth of ZnO nanocrystals synthesized in polyol medium with polyvinylpyrrolidone additives

In this work, we have investigated the influence of annealing temperature on the grain growth of zinc oxide nanocrystals synthesized in ethylene glycol and isothermally calcined at Ta: 300 °C, 500 °C, 700 °C for 60 min at the ambient atmosphere. The effect of polyvinylpyrrolidone (PVP) addition and annealing temperature on ZnO nanocrystal's phase composition, structural (scattering domain size of nanocrystallites L, unit lattice parameters a, c, and unit volume Vunit, theoretical density ρx) parameters, morphological (size, shape, specific surface area SSA) features, chemical composition, and grain growth kinetics were determined. It was found that Ta caused the increase in L of single-phase ZnO nanocrystals from 18 nm to 40 nm (with adding PVP) and to 45 nm (without adding PVP). Despite the surfactant composition, submicron grain sizes (D = 120–150 nm) were observed at Ta = 700 °C. The activation energy of grain growth was Q = 121.4 kJ/mol (without adding PVP) and Q = 126.4 kJ/mol (with adding PVP), while grain growth exponent was n = 1.9 (without adding PVP) and n = 2.0 (with adding PVP). ZnO nanocrystals annealed at 700 °C are forthcoming in the design of the active layers of solar cells, and at (300–500) °C are suitable for thermoelectric converters.

Stability and conductivity of water-based colloidal silver nanoparticles conductive inks for sustainable printed electronics

BackgroundDeveloping conductive inks for printed electronics has gained increasing interest in recent years as a low-cost and environmentally friendly alternative to traditional organic metal-based inks. This study aims to investigate the influence of silver nitrate (AgNO3) concentration at different temperatures and the effect of polyvinylpyrrolidone (PVP) surfactant concentration on the properties of the colloidal silver nanoparticles (AgNPs) conductive inks. MethodsIn this study, water-based AgNPs were prepared using a chemical reduction method. The effect of AgNO3 concentration, the reaction temperature, and the amount of PVP as a stabilizing agent on the size, shape, and purity of the synthesized AgNPs was investigated. The stability, thermal characteristics, and functional groups of the water-based AgNPs were also evaluated. The printed AgNPs patterns were examined for morphological and electrical properties. Significant findingsResults indicated that the concentration of AgNO3 and reaction temperature influence the size of AgNPs particles and their clustering. A high concentration of AgNO3 results in a higher yield of AgNPs and subsequently increases the electrical conductivity to 2.69×10° S/m. Adding PVP improves the stability of AgNPs for up to 45 days. Therefore, the development of water-based colloidal AgNPs conductive ink in this study can be used in inkjet printing to fabricate environmentally friendly printed electronics.

The effect of polyvinylpyrrolidone (PVP) on the growth of (1 1 0) crystal facet of BiOCl for enhanced photodegradation of RhB under LED

The effect of polyvinylpyrrolidone (PVP) on the growth of (1 1 0) crystal facet of BiOCl for enhanced photodegradation of RhB under LED

Hydroxypropyl Methylcellulose Bioadhesive Hydrogels for Topical Application and Sustained Drug Release: The Effect of Polyvinylpyrrolidone on the Physicomechanical Properties of Hydrogel.

Hydrogels are homogeneous three-dimensional polymeric networks capable of holding large amounts of water and are widely used in topical formulations. Herein, the physicomechanical, rheological, bioadhesive, and drug-release properties of hydrogels containing hydroxypropyl methylcellulose (HPMC) and polyvinylpyrrolidone (PVP) were examined, and the intermolecular interactions between the polymers were explored. A three-level factorial design was used to form HPMC-PVP binary hydrogels. The physicomechanical properties of the binary hydrogels alongside the homopolymeric HPMC hydrogels were characterized using a texture analyzer. Rheological properties of the gels were studied using a cone and plate rheometer. The bioadhesiveness of selected binary hydrogels was tested on porcine skin. Hydrophilic benzophenone-4 was loaded into both homopolymeric and binary gels, and drug-release profiles were investigated over 24 h at 33 °C. Fourier transform infrared spectroscopy (FTIR) was used to understand the inter-molecular drug-gel interactions. Factorial design analysis supported the dominant role of the HPMC in determining the gel properties, rather than the PVP, with the effect of both polymer concentrations being non-linear. The addition of PVP to the HPMC gels improved adhesiveness without significantly affecting other properties such as hardness, shear-thinning feature, and viscosity, thereby improving bioadhesiveness for sustained skin retention without negatively impacting cosmetic acceptability or ease of use. The release of benzophenone-4 in the HPMC hydrogels followed zero-order kinetics, with benzophenone-4 release being significantly retarded by the presence of PVP, likely due to intermolecular interactions between the drug and the PVP polymer, as confirmed by the FTIR. The HPMC-PVP binary hydrogels demonstrate strong bioadhesiveness resulting from the addition of PVP with desirable shear-thinning properties that allow the formulation to have extended skin-retention times. The developed HPMC-PVP binary hydrogel is a promising sustained-release platform for topical drug delivery.

An investigation into the effect of polyvinylpyrrolidone on the size and distribution of nickel catalyst particles for controlling CNTs’ morphology and growth mechanisms in fabricated hybrid CF-CNT nanocomposite

An investigation into the effect of polyvinylpyrrolidone on the size and distribution of nickel catalyst particles for controlling CNTs’ morphology and growth mechanisms in fabricated hybrid CF-CNT nanocomposite

Characterisation and modelling the mechanics of cellulose nanofibril added polyethersulfone ultrafiltration membranes

The performance of the membranes can be improved by adding the appropriate amount of nanomaterials to the polymeric membranes that can be used for water/wastewater treatment. In this study, the effects of polyvinylpyrrolidone (PVP), the impact of different amounts (0.5% and 1% wt.) of cellulose nanofibril (CNF), and the combined effects of PVP-CNF on the properties/performance of the polyethersulfone-based (PES-based) membrane are investigated. All PES-based ultrafiltration (UF) membranes are manufactured employing the phase inversion method and characterised via Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and the relevant techniques to determine the properties, including porosity, mean pore size, contact angle, water content, and pure water flux tests. Furthermore, the thermal properties of the prepared membranes are investigated using thermal gravimetric analysis (TGA) and differential thermal analysis (DTA) techniques. Experimental and numerical methods are applied for the mechanical characterisation of prepared membranes. For the experimental process, tensile tests under dry and wet conditions are conducted. The finite element (FE) method and Mori-Tanaka mean-field homogenisation are used as numerical methods to provide more detailed knowledge of membrane mechanics.

Effects of polyvinylpyrrolidone as a dispersant agent of reduced graphene oxide on the properties of carbon fiber-reinforced polymer composites

The electrical and mechanical properties of carbon fiber-reinforced polymer (CFRP) composites have a close dependence on the use of modifiers like polyvinylpyrrolidone (PVP), as well as on the processing techniques to disperse functional charges such as graphene-related materials into the epoxy base. In the present work, reduced graphene oxide (RGO), prepared by a natural antioxidant agent, astaxanthin, was used as a filler material in the epoxy matrix of the carbon fiber composites. The astaxanthin reduction leads to an increase in the sp2 ordering in RGO; some residual epoxy and C-O groups that enhance the interaction with the epoxy matrix remain after reduction. The effects of RGO and PVP-modified RGO (PVP-RGO) fillers with different contents (0.05, 0.1, and 0.15% wt.) on the electrical conductivity, bending properties, and dynamic mechanical properties of CFRP were investigated. The incorporation of 0.15 wt.% RGO with and without PVP-modification, leads to through-the-thickness (Z-direction testing) conductivity values 7.4 and 9.6 times higher than those of the neat composite, respectively. The conductivity tests indicate that the RGO/epoxy composite behaves as a continuous conductor due to the formation of agglomerates of RGO within the matrix, while at the added contents of the PVP-RGO filler, the composite is below the percolation threshold, then conducting by electron tunneling, due to a better dispersion of the PVP-RGO filler within the epoxy matrix. The dynamic mechanical analysis shows that the glass transition temperature is indicative of the interactions among the filler, the epoxy matrix, and the carbon fiber, that is, the PVP-RGO filler increases the chain mobility due to its higher dispersion in the matrix. While Tg of the neat epoxy/CFRP composite is 92.5°C, a minimum Tg of 88.5°C was achieved with a 0.10 % wt. PVP-RGO filler contents, and a maximum Tg of 94.5°C with a 0.15 % wt. of RGO filler amount. For constant filler content (0.15 wt.%), CFRP composite containing RGO and PVP-modified RGO exhibited 9.73% and 13.87% increase in flexural strength values, respectively, compared to the neat composite. The bending test revealed that PVP modification to RGO is beneficial to improve flexural strength of CFRP composites.

Polyvinylpyrrolidone assisted-preparation of AgBr with enhanced visible light responsive photocatalytic activity

• AgBr was prepared by a hydrothermal method with PVP. • Separation of photoactivated carriers has been largely promoted. • The level of •O 2 - was greatly boosted. • PVP-AgBr possess superior photocatalytic activity. In this paper, AgBr photocatalyst was prepared by a precipitation method using silver nitrate and potassium bromide as raw materials. The effects of polyvinylpyrrolidone (PVP) on the preparation and photocatalytic property of AgBr were investigated. The samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), surface photovoltage (SPS), ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS) and specific surface area (BET). Using rhodamine B as a model pollutant, photocatalytic performance of the photocatalyst prepared was tested under visible light irradiation. The results indicate that AgBr prepared by adding of PVP has superior photocatalytic activity. Under visible light irradiation, the destruction rate constant of rhodamine B (RhB) on PVP-AgBr is 4.79 times of that on the reference AgBr.

Vapor–Liquid Equilibria of Quaternary Systems of Interest for the Supercritical Antisolvent Process

In the Supercritical Antisolvent process (SAS), the thermodynamic behavior of complex multicomponent systems can influence the particles’ morphology. However, due to the limited thermodynamic data for multicomponent systems, the effect of solutes is often neglected, and the system is considered as pseudo-binary. It has been demonstrated that the presence of a solute can significantly influence the thermodynamic behavior of the system. In particular, when the SAS process is adopted for the production of drug/polymer coprecipitated microparticles, the effect of both the drug and the polymer in the solvent/CO2 mixture should be considered. In this work, the effect of polyvinylpyrrolidone (PVP), used as the carrier, and of the liposoluble vitamins menadione (MEN) and α-tocopherol (TOC), as model drugs, was investigated as a deviation from the fundamental thermodynamic behavior of the DMSO/CO2 binary system. Vapor–liquid equilibria (VLE) were evaluated at 313 K, with a PVP concentration in the organic solution equal to 20 mg/mL. The effect of the presence of PVP, MEN, and TOC on DMSO/CO2 VLE at 313 K was studied; furthermore, the effect of PVP/MEN and PVP/TOC, at a polymer/drug ratio of 5/1 and 3/1, was determined. Moreover, SAS precipitation experiments were performed at the same polymer/drug ratios using a pressure of 90 bar. Thermodynamic studies revealed significant changes in phase behavior for DMSO/CO2/PVP/TOC and DMSO/CO2/PVP/MEN systems compared to the binary DMSO/CO2 system. From the analysis of the effect of the presence of a single compound on the binary system VLE, it was noted that PVP slightly affected the thermodynamic behavior of the system. In contrast, these effects were more evident for the DMSO/CO2/TOC and DMSO/CO2/MEN systems. SAS precipitation experiments produced PVP/MEN and PVP/TOC microparticles, and the obtained morphology was justified considering the quaternary systems VLE.

Fabrication, characterization, and performance of poly (aryl ether nitrile) flat sheet ultrafiltration membranes with polyvinyl pyrrolidone as additives

Abstract Poly(aryl ether nitrile) (PEN) was used to fabricate ultrafiltration membrane via immersion precipitation phase inversion method. The effects of polyvinyl pyrrolidone (PVP) of different molecular weights and concentrations on the structure and performance of PEN membranes were investigated. The membranes were observed by scanning electron microscope, atomic force microscope, equilibrium water content (EWC), porosity (ε), and so on. The membranes were subjected to ultrafiltration characterizations such as pure water flux (PWF), compaction factor (CF), hydraulic permeability (P m), and bovine serum albumin (BSA) rejection rate. The hydrophilicity was characterized by infrared spectroscopy and contact angle tests. Results showed that molecular weight of PVP had significant effect on PEN membrane formation, which the membrane prepared by PVP-k30 exhibited excellent comprehensive performance. Meanwhile, the concentration of PVP-k30 could effectively control the select-permeability of PEN membrane. With PVP-k30 concentration increased from 7 to 13 wt%, the prepared PEN membranes got higher EWC, ε, CF, and P m. The PWF increased from 146.5 to 249.1 L m−2 h−1 bar−1, while the overall rejection of BSA remained above 90%. Further increasing the addition amount to 16 wt%, the membrane performance began to decline. Finally, the addition of PVP-k30 could effectively improve the hydrophilicity of prepared PEN membrane surface.

Nanoemulsions Containing Megestrol Acetate: Development, Characterization, and Stability Evaluation.

Many active pharmaceutical ingredients (API) are poorly soluble in water and their low oral bioavailability is a major hindrance to their potential use. Megestrol acetate (MGA) is insoluble in water and its oral absorption is limited and considerably affected by food. Nanoemulsions (NEs) can be used as effective oral drug delivery systems where the hydrophobic API is loaded into the oil phase. In this study, MGA-loaded NEs were prepared based on the spontaneous emulsification technique. The effects of different excipients such as ethanol, Tween 80, Lipoid E80, and medium-chain triglyceride (MCT) on the NEs characterization were investigated. The experimental results indicated that optimum MGA-loaded NEs (F20) were nanometer-sized droplets (166.9 ± 3.0 nm) with negative zeta potential (-12.2 ± 1.1 mV). The effect of polyvinylpyrrolidone (PVP) on characteristic properties of F20 was also evaluated. On the selected NEs, in vitro dissolution tests and stability studies in various mediums and storage conditions were performed. The encapsulation efficiency of NEs were > 99%. The overall droplet size of F20 and PVP-2 (PVP-coated NEs) remained relatively stable as the pH changed from 1.2 to 6.8. It was determined that F20 and PVP-2 remained stable at 4°C until 12 weeks and had higher cytotoxicity on MCF-7 cells. To conclude, droplet size, surface charge, and stability are important properties for NEs to have sufficient effectiveness. In this study, alternative oral NEs of low-solubility drug MGA were developed considering the above features.

Rheological Properties and Its Effect on the Lubrication Mechanism of PVP K30 and PVP 40-50 G as Artificial Synovial Fluids

The effect of polyvinylpyrrolidone (PVP) on the rheological properties of joint prostheses is still unclear, despite its good lubricity and biocompatibility. In the present work, PVP K30 and PVP 40-50 G solutions at different concentrations were analyzed for rheological and lubrication properties. The rheological properties of the samples were measured at a shear rate range of 0–1800 s−1 (advanced air bearing rheometer Bohlin Gemini 2 and Plate MCR 72/92 rheometer for PVP30 and PVP 40-50 G, respectively). It was found that both the viscosity and shear stress of the samples reduced with a shear rate increase. PVP 40-50 G/sterile water showed higher viscosity as compared to the PVP K30/sterile water sample at a lower shear rate. However, at a higher shear rate, the PVP K30 sample produced better results. Further numerical study results showed the pressure and molecular viscosity distributions. The inclusion of PVP improved the load caring capacity and hence, it is a promising lubrication additive for artificial joints.

Evaluation of inhibition effect of poly vinyl pyrrolidone on corrosion of bronze in simulated acid rain using thin layer activation technique

In the present work development of a suitable nontoxic corrosion inhibitor to control corrosion of bronze in simulated acid rain has been investigated using thin layer activation (TLA) technique. Poly vinyl pyrrolidone (PVP) has been identified as an inhibitor and the inhibition action of PVP has been evaluated at different experimental conditions. The result of the study proved that PVP showed good inhibitive characteristics to control corrosion of bronze in the test solution. Kinetic and thermodynamic parameters of the corrosion inhibition process have been determined. The adsorption of inhibitor on bronze surface obeyed Langmiur adsorption isotherm.

Preparation, characterization and dyeing wastewater treatment of a new PVDF/PMMA five-bore UF membrane with β-cyclodextrin and additive combinations.

A new type of polyvinylidene fluoride (PVDF)/polymethyl methacrylate (PMMA) hollow fiber membrane (HFM) with five bores was prepared. The effects of polyvinylpyrrolidone (PVP), β-cyclodextrine (β-CD), polyethylene glycol (PEG) and polysorbate 80 (Tween 80) and their combinations on the PVDF/PMMA five-bore HFMs were investigated. The performance and fouling characteristics of five-bore HFMs for dyeing wastewater treatment were evaluated. Results indicated that adding 5 wt.% PVP increased the porosity and water flux of the membrane but decreased the bovine serum albumin (BSA) rejection rate. Adding 5 wt.% β-CD significantly improved the tensile strength and rejection of the HFMs with no effect on the increase of water flux. The characteristic of the HFMs with different additive combinations proved that the mixture of 5 wt.% PVP and 1 wt.% β-CD gave the best membrane performance, with a pure water flux of 427.9 L/ m2·h, a contact angle of 25°, and a rejection of BSA of 89.7%. The CODcr and UV254 removal rates of dyeing wastewater treatment were 61.10% and 50.41%, respectively. No breakage or leakage points were found after 120 days of operation, showing their reliable mechanical properties. We set the operating flux to 55 L/m2·h and cross-flow rate to 10%, which can effectively control membrane fouling.

Effect of PVP Coating on LiMnBO3 Cathodes for Li-Ion Batteries.

LiMnBO3 is a potential cathode for Li-ion batteries, but it suffers from a low electrochemical activity. To improve the electrochemical performance of LiMnBO3, the effect of polyvinyl pyrrolidone (PVP) as carbon additive was studied. Monoclinic LiMnBO3/C and LiMnBO3-MnO/C materials were obtained by a solid-state method at 500 °C. The structure, morphology and electrochemical behavior of these materials are characterized and compared. The results show that carbon additives and ball-milling dispersants affect the formation of impurities in the final products, but MnO is beneficial for the performance of LiMnBO3. The sample of LiMnBO3-MnO/C delivered a high capacity of 162.1 mAh g−1 because the synergistic effect of the MnO/C composite and the suppression of the PVP coating on particle growth facilitates charge transfer and lithium–ion diffusion.

The Effect of PVP Molecular Weight on Dissolution Behavior and Physicochemical Characterization of Glycyrrhetinic Acid Solid Dispersions

The effect of polyvinylpyrrolidone (PVP) as glycyrrhetic acid (GA) solid dispersions carrier at different molecular weights on the dissolution behavior and physicochemical properties was investigated. PVP-GA-SDs prepared with all four molecular weight PVPs displayed good enhancement of dissolution rate and equilibrium solubility compared with pure drug and corresponding physical mixtures. The results showed that the enhancement effect of molecular weight on dissolution rate and equilibrium solubility follows PVP K 30 > PVP K 60 > PVP K 17 > PVP K 15 . In addition, the dissolution rate and solubility of the SDs with a carrier-drug ratio of 8 : 1 were better than the samples of 4 : 1. The DSC and XRD patterns showed that the crystallization of GA in SDs prepared by PVP K30 and PVP K60 was significantly inhibited, and both were transformed to amorphous. Based on FTIR and Raman detection, a hydrogen-bond between PVP and drug molecules is formed. SEM results showed that there were no significant differences in the appearance of SDs prepared with four PVPs, and no crystalline morphology of GA was seen. In conclusion, the findings of this study demonstrated that the dissolution performance of the PVP-GA-SDs prepared by the solvent method is related to the molecular weight of PVP, and the change in the molecular weight of PVP does not cause a monotonic change in dissolution of GA. The samples with PVP K30 as the carrier have the best dissolution performance.

Effect of PVP content on photocatalytic properties of CuSbS2 particles with chemical etching

In the paper, the effects of polyvinylpyrrolidone (PVP) concentration and chemical wet etching on morphologies and phase composition of CuSbS2 particles synthesized by microwave irradiation method were investigated. The phase structure, morphologies, and optical and photocatalytic properties were analyzed by using characterization techniques. The results showed that the morphology of as-prepared particles was spherical and the shape of particles etched in Na2S solution was tetragonal rod-like structure. The optical band gap of the particles with 1.5 g PVP after chemical etching was about 1.41 eV. The photocatalytic performance of CuSbS2 could be significantly improved after Na2S chemical etching. The amounts of PVP had an obvious influence on specific surface area of as-synthesized CuSbS2 particles. The CuSbS2 particles with 1.5 g PVP had the best photocatalytic performance after chemical etching treatment, and the C/C0 value reached 0.36.

Effect of polyvinylpyrrolidone on the catalytic properties of Pd/γ-Fe2O3 in phenylacetylene hydrogenation

Maghemite nanoparticles modified with polyvinylpyrrolidone were synthesized using the chemical co-precipitation method. Palladium ions have then been immobilized on the PVP/γ-Fe2O3 magnetic support. The Pd-PVP/γ-Fe2O3 catalyst obtained was characterized using X-ray diffraction, thermogravimetry coupled with differential scanning calorimetry and quadrupole mass spectrometry, scanning electron microscopy combined with energy dispersive X-ray analysis, transmission electron microscopy, nitrogen adsorption–desorption and vibrating sample magnetometry. Morphology, microstructure, particle sizes and textural properties of the Pd-PVP/γ-Fe2O3 were compared with those of the unmodified Pd/γ-Fe2O3 catalyst, synthesized using the same method. The polymer has affected the size of γ-Fe2O3 nanoparticles and their agglomeration, forming compact microstructure with decreased mesopores (4.5 nm). Palladium nanoparticles with size of 3–5 nm were found both on the surface of the PVP/γ-Fe2O3 particles (6–10 nm) and inside the pores formed by them. The Pd-PVP/γ-Fe2O3 has demonstrated improved catalytic properties in phenylacetylene hydrogenation under mild conditions of 40 °C and 0.1 MPa, compared to Pd/γ-Fe2O3 and similar catalysts prepared using polyethylene glycol and pectin. The hydrogenation rate of C–C triple bond on Pd-PVP/γ-Fe2O3 achieved 2.8 × 10–6 mol s−1 and selectivity to styrene was 92%. The catalyst showed weak ferromagnetic and soft magnetic properties (MS = 51 emu g−1, Mr = 5.4 emu g−1, and HC = 71 Oe) and, therefore, can be easily recovered with an external magnet and reused for at least 11 runs without significant degradation in the catalytic activity.