Search Results (14)

Microplastics (MP) in landfill leachate represent an analytical challenge due to matrix complexity and the need for methods that remove interferents without degrading polymers. This study evaluated the efficiency of four digestion methods (30% H₂O₂, Fenton, 10% NaOH, and 20% HCl) and three density separation solutions (CaCl₂, NaI, and ZnCl₂) for MP quantification in leachate from the Zinacantepec Sanitary Landfill, Mexico. Samples were spiked with seven polymer types (polyethylene terephthalate (PET), high-density polyethylene (HDPE), polyvinyl chloride (PVC), low-density polyethylene (LDPE), polypropylene (PP), polystyrene (PS), and polyamide (PA)). Results analyzed by ANOVA (p < 0.05) showed that Fenton reagent was the most efficient digestion method, achieving 99% MP recovery, whereas alkaline and acid digestions caused degradation of PET, PS, and PA. Regarding density separation, ZnCl₂ (1.7 g/cm³) achieved recovery exceeding 99% for all polymers. The proposed protocol enables effective isolation and identification of degraded microplastics, contributing to advance the understanding of degradation processes and transformation pathways of MP in complex environmental matrices. The combination of Fenton digestion and ZnCl₂ separation showed the highest overall performance, with an efficiency greater than 96%, supporting its use as a reliable protocol for MP quantification in leachate and contributing to methodological standardization in this field. Full article

High-voltage cable joints are critical components where electric stress concentration often leads to insulation failure. This study evaluated three materials to find optimal configurations for controlling stress in 33 kV applications: PVC tape, stress-grading mastic, and semiconductive rubber tape, with initial relative permittivities of 2.96, 2.66, and 5.07, respectively. Dielectric measurements using a Schering Bridge at voltages of up to 3700 V determined material properties and breakdown characteristics. Semiconductive rubber withstood the highest voltage of 3700 V, while mastic failed at 1350 V. Finite element simulations showed that baseline configurations without proper insulation had a peak stress of 4.3 kV/mm. Simulations of individual materials identified non-linear resistive compounds, such as ZnO-based materials and carbon-black-filled polymers, as the most effective for stress control at conductor interfaces. A three-layer graded design, arranging materials by decreasing permittivity from the conductor outward, reduced the peak stress by 33% to 2.9 kV/mm. These results demonstrate that strategic permittivity grading combined with appropriate material selection ensures uniform field distribution and improved reliability in HV cable joints. Full article

This study aims to investigate the influence of various metal compounds (ZnO, ZnCl₂, Zn(OH)₂, MgO, MgCl₂, and Mg(OH)₂) on the structural and electrochemical properties of chars derived from the pyrolysis of polyvinyl chloride (PVC). Raw PVC samples mixed with different metal compounds were firstly pyrolyzed at 500 °C in a fixed-bed reactor. The produced chars were further pyrolyzed at 800 °C. The objective was to evaluate the impact of these metal compounds on the char structure through comparative analysis. The pyrolytic chars were characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Raman spectroscopy, and Brunauer–Emmett–Teller (BET) analysis. Zinc-based additives notably increased carbon yield to 32–34 wt.%, attributed to ZnCl₂-induced cross-linking. Specifically, ZnO facilitated porous architectures and aromatic structures with six or more rings. Mg-based compounds induce the formation of a highly stacked carbon structure primarily composed of crosslinked cyclic alkenes, rather than large polyaromatic domains. Upon further thermal treatment, these aliphatic-rich stacked structures can be progressively transformed into aromatic frameworks through dehydrogenation reactions at elevated temperatures. A high-surface-area porous carbon material (PVC/ZnO-800, SSA = 609.382 m² g⁻¹) was synthesized, demonstrating a specific capacitance of 306 F g⁻¹ at 1 A g⁻¹ current density. Full article

Water pollution is a major global issue, and antibiotic drugs released into aquatic environments by the pharmaceutical industry, such as ciprofloxacin, have negative consequences on both human health and the ecosystem. In this study, the performance of PVA as a polymer ligand for ciprofloxacin (CPFX) removal is evaluated through polymer-enhanced ultrafiltration using a novel composite PVC-ZnO membrane. The initial concentration of the ciprofloxacin solution, pH, ionic strength, ideal polymer concentration, duration, and maximum retention capacity were among the factors that were examined. In order to remove ciprofloxacin from water, PVA is utilized as a polymeric binding agent in a complex manufacturing process. In this instance, the PVC-ZnO membrane with 1.0 weight percent ZnO had a 96.77% ciprofloxacin clearance rate. PVA polymer has a high clearance rate of 99.98% in 1wt% of ZnO in this composite membrane when added to the ciprofloxacin solution. Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), ultraviolet spectroscopy, and X-ray diffraction (XRD) were used to analyze the production and features of composite PVC-ZnO membranes. It is anticipated that this study’s discussion will be crucial to the development of higher-quality membrane technologies that remove pharmaceutical active chemicals from wastewater in an environmentally responsible manner without endangering the ecosystem. This investigation showed that composite PVC-ZnO membranes were effective materials for efficient removal of ciprofloxacin (CPFX). Full article

In lithium–polymer batteries, the electrolyte is an essential component that plays a crucial role in ion transport and has a substantial impact on the battery’s overall performance, stability, and efficiency. This article presents a detailed study on developing nanostructured composite polymer electrolytes (NCPEs), prepared using the solvent casting technique. The materials selected for this investigation include poly(vinyl chloride) (PVC) as the host polymer, lithium bromide (LiBr) as the salt, and silica (SiO₂) as the nanofiller. The addition of nano-SiO₂ dramatically enhanced the ionic conductivity of the electrolytes, with the highest value of 6.2 × 10⁻⁵ Scm⁻¹ observed for the sample containing 7.5 wt% nano-SiO₂. This improvement is attributed to an increased amorphicity resulting from the interactions between the polymer, salt, and filler components. A structural analysis of the prepared NCPEs using X-ray diffraction revealed the presence of both crystalline and amorphous phases, further validating the enhanced ionic transport. Additionally, the thermal stability of the NCPEs was found to be excellent, withstanding temperatures up to 334 °C, thereby reinforcing their potential application in lithium–polymer batteries. This work explores the electrochemical performance of a fabricated lithium-ion-conducting primary electrochemical cell (Zn + ZnSO₄·7H₂O|PVC: LiBr: SiO₂|PbO₂ + V₂O₅), which demonstrated an open circuit voltage of 2.15 V. The discharge characteristics of the fabricated cell were thoroughly studied, showcasing the promising potential of these NCPEs. With the support of superior morphological and electrical properties, as-prepared electrolytes offer an effective pathway for future advancements in lithium–polymer battery technology, making them a highly viable candidate for enhanced energy storage solutions. Full article

Antioxidant films were prepared using poly(vinyl chloride) (PVC) incorporated with 0.5% or 1.0% zinc oxide (ZnO)-flavonoid (quercetin or morin) nanoparticles (NPZnO-Q% or NPZnO-M%) via the casting method. NP incorporation within the polymer matrix influenced the structural, morphological, optical, and thermal properties of the PVC-based films, as well as their antioxidant activity as assessed using the DPPH radical scavenging method. Our results indicated that increasing ZnO-flavonoid NP concentration increased films thickness, while reducing ultraviolet light (UV) transmittance but conserving transparency. The presence of NPZnO-Q% or NPZnO-M% improved the surface uniformity and thermal stability of the active films. In terms of antioxidant activity, there was an enhancement in the DPPH radical scavenging capacity (PVC/ZnO-Q1.0% > PVC/ZnO-Q0.5% > PVC/ZnO-M0.5% > PVC/ZnO-M1.0% > PVC), suggesting that the packaging can help protect food from oxidative processes. Therefore, these antioxidant films represent an innovative strategy for using as active food packaging material, especially intended for aiding in quality preservation and extending the shelf life of fatty foods. Full article

Polyvinyl chloride (PVC) is the most widely used general flame-retardant plastic worldwide; however, the large number of plasticizers added during processing significantly reduces its flame-retardant property. To prepare a new type of PVC material with highly efficient flame retardancy and smoke suppression, antimony trioxide (Sb₂O₃), talc powder, hydromagnesite, and zinc borate were added in different proportions to PVC to explore the flame-retardant properties, thermal weight, smoke density (Ds), and mechanical properties of the composite materials. Results showed that the limiting oxygen index value of each group was higher than 27% after adding talc powder, magnesite, and zinc borate to replace part of the Sb₂O₃. This value was within the refractory-grade level and indicated a good flame retardancy performance. The replacement effect was in line with the experimental expectation. The lowest Ds peak value was 656.4 when the flame retardants were added with 10 wt% Sb₂O₃, 50 wt% hydromagnesite, 20 wt% talc, and 20 wt% Zn₃BO₆. Compared with pure Sb₂O₃ as a flame retardant, the Ds peak value decreased by 46.7%. The thermogravimetric decomposition temperature of the composites in each group was generally higher than that of the group with pure Sb₂O₃ as a flame retardant, increasing by 45.3 °C. The thermal stability of the composites was improved, and the elongation at the break and tensile strength were 234.9% and 25.8 MPa, respectively, indicating good mechanical properties. The results showed that using compound flame retardants to replace most of the Sb₂O₃ is an effective technique for obtaining good flame retardancy and mechanical properties of PVC. This study, not only reduced the manufacturing cost of flame-retardant PVC, but also effectively reduced its smoke density and the time to reach the highest smoke density, which provided a research reference for the application and promotion of flame-retardant PVC. Full article

Active packaging has played a significant role in consumers’ health and green environment over the years. Synthetic polymers, such as poly(ethylene terephthalate) (PET), polyethylene (PE), polypropylene (PP), polystyrene, poly(vinyl chloride) (PVC), polycarbonate (PC), poly(lactic acid) (PLA), etc., and naturally derived ones, such as cellulose, starch, chitosan, etc., are extensively used as packaging materials due to their broad range of desired properties (transparence, processability, gas barrier properties, mechanical strength, etc.). In recent years, the food packaging field has been challenged to deliver food products free from microbes that cause health hazards. However, most of the used polymers lack such properties. Owing to this, active agents such as antimicrobial agents and antioxidants have been broadly used as potential additives in food packaging substrates, to increase the shelf life, the quality and the safety of food products. Both synthetic active agents, such as Ag, Cu, ZnO, TiO₂, nanoclays, and natural active agents, such as essential oils, catechin, curcumin, tannin, gallic acid, etc., exhibit a broad spectrum of antimicrobial and antioxidant effects, while restricting the growth of harmful microbes. Various bulk processing techniques have been developed over the years to produce appropriate food packaging products and to add active agents on polymer matrices or on their surface. Among these techniques, extrusion molding is the most used method for mass production of food packaging with incorporated active agents into polymer substrates, while injection molding, thermoforming, blow molding, electrospinning, etc., are used to a lower extent. This review intends to study the antimicrobial and antioxidant effects of various active agents incorporated into polymeric substrates and their bulk processing technologies involved in the field of food packaging. Full article

The new research presents highly conductive polymeric membranes with a large surface area to volume ratio of metal oxide nanoparticles that were used to determine atropine sulfate (AT) in commercial dosage forms. In sensing and biosensing applications, the nanomaterials zinc oxide (ZnONPs) and magnesium oxide (MgONPs) were employed as boosting potential electroactive materials. The electroactive atropine phosphotungstate (AT-PT) was created by combining atropine sulfate and phosphotungstic acid (PTA) and mixing it with polymeric polyvinyl chloride (PVC) with the plasticizer o-nitrophenyl octyl ether (o-NPOE). The modified sensors AT-PT-ZnONPs or AT-PT-MgONPs showed excellent selectivity and sensitivity for the measurements of atropine with a linear concentration range of 6.0 × 10⁻⁸ − 1.0 × 10⁻³ and 8.0 × 10⁻⁸ − 1.0 × 10⁻³ mol L⁻¹ with regression equations of E_(mV) = (56 ± 0.5) log [AT] − 294 and E_(mV) = (54 ± 0.5) log [AT] − 422 for AT-PT-NPs or AT-PT-MgONPs sensors, respectively. The AT-PT coated wire sensor, on the other hand, showed a Nernstian response at 4.0 × 10⁻⁶ − 1.0 × 10⁻³ mol L⁻¹ and a regression equation E_(mV) = (52.1 ± 0.2) log [AT] + 198. The methodology-recommended guidelines were used to validate the suggested modified potentiometric systems against various criteria. Full article

Using introduction of MoO₄²⁻ and Fe³⁺, Cu²⁺, or Zn²⁺ into amphiphilic polymers (DN) via an ion-exchange reaction, different transition metal complexes, as retardants and smoke suppressants, including (DN)Mo, Fe(DN)Mo, Cu(DN)Mo, and Zn(DN)Mo were synthesized. Combined with the results of X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR), it could be determined that ionic bonding of these ions with DN occurred. Subsequently, the influence of flame-retardant, smoke-suppression, and mechanical properties of (DN)Mo, Fe(DN)Mo, Cu(DN)Mo, and Zn(DN)Mo on polyvinyl Chloride (PVC) were tested. It was demonstrated that transition metal complexes of three metal elements, Fe(DN)Mo, Cu(DN)Mo, and Zn(DN)Mo, showed better flame retardancy, smoke suppression, and thermal stability as confirmed by microcalorimetry, limiting oxygen index (LOI), smoke density, and thermogravimetric analysis (TGA) tests, in which Cu(DN)Mo worked best due to the Lewis acid mechanism and reductive coupling mechanism. Scanning electron microscopy (SEM) showed that the addition of (DN)Mo, Fe(DN)Mo, Cu(DN)Mo, and Zn(DN)Mo promoted the formation of a dense carbon layer on the PVC surface during combustion, which could protect the interior PVC. The addition of these transition metal complexes hardly impaired the mechanical properties of PVC. Full article

In this work, polymeric fibers of polystyrene (PS) with incorporated ZnO nanoparticles have been deposited onto an aluminum alloy substrate (6061T6) by using the electrospinning technique. In order to optimize the deposition process, the applied voltage and flow rate have been evaluated in order to obtain micrometric electrospun fibers with a high average roughness and superhydrophobic behavior. Thermogravimetric analysis (TGA) has also been employed in order to corroborate the amount of ZnO incorporated into the electrospun fibers, whereas differential scanning calorimetry (DSC) has been performed in order to determine the glass transition temperature (T_g) of the polymeric electrospun fibers. In addition, a specific thermal treatment (T_g + 20 °C) of the synthesized electrospun fibers has been evaluated in the resultant corrosion resistance. A comparative study with previously reported results corresponding to polyvinyl chloride (PVC) fibers is carried out along this paper to show the changes in behavior due to the different compositions and fiber diameters. The coating has produced an important reduction of the corrosion current of the aluminum substrate in two orders of magnitude, showing also an important enhancement against pitting corrosion resistance. Finally, this deposition technique can be used as an innovative way for the design of both superhydrophobic and anticorrosive surfaces in one unique step over metallic substrates with arbitrary geometry. Full article

A new di-mannitol adipate ester-based zinc metal alkoxide (DMAE-Zn) was synthesized as a bi-functional poly(vinyl chloride) (PVC) thermal stabilizer for the first time. The materials were characterized with Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA). Characterization results confirmed the formation of Zn–O bonds in DMAE-Zn, and confirmed that DMAE-Zn had a high decomposition temperature and a low melting point. The thermal stability of DMAE-Zn on PVC also was tested by a conductivity test, a thermal aging test, and a UV-visible spectroscopy (UV-VIS) test. PVC stabilized by DMAE-Zn had a good initial color and excellent long-term stability. UV-VIS also showed that the conjugated structure in PVC stabilized by DMAE-Zn was almost all of the triene, suggesting that the addition of DMAE-Zn would suppress the formation of conjugated structures above tetraene. The dynamic processing performance of PVC samples tested by torque rheometer indicated that, having a good compatibility with PVC chains in the amorphous regions, DMAE-Zn contributed a good plasticizing effect to PVC. DMAE-Zn thus effectively demonstrates bi-functional roles, e.g., thermal stabilizers and plasticizers to PVC. Furthermore, FT-IR, a HCl absorption capacity test, and a complex ZnCl₂ test were also used to verify the thermal stability mechanism of DMAE-Zn for PVC. Full article

This paper reports the use of the electrospinning technique for the synthesis of nanocomposite micro/nanofibers by combining a polymeric precursor with hydrophobic behavior like polyvinyl chloride (PVC) with nanoparticles of a corrosion inhibitor like ZnO. These electrospun fibers were deposited on substrates of the aluminum alloy 6061T6 until forming a coating around 100 μm. The effect of varying the different electrospinning deposition parameters (mostly applied voltage and flow-rate) was exhaustively analyzed in order to optimize the coating properties. Several microscopy and analysis techniques have been employed, including optical microscopy (OM), field emission scanning electron microscopy (FE-SEM), atomic force microscopy (AFM), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). Water contact angle (WCA) measurements have been carried out in order to corroborate the coating hydrophobicity. Finally, their corrosion behavior has been evaluated by electrochemical tests (Tafel curves and pitting potential measurements), showing a relevant improvement in the resultant corrosion resistance of the coated aluminum alloys. Full article

A simple approach to decorate multi-walled carbon nanotube (MWCNT)–reduced graphene oxide (RGO) hybrid nanoparticles with zinc oxide (ZnO) nanorods is developed to improve the electrical and mechanical properties of poly(vinyl chloride) (PVC)/MWCNT–RGO composites. The ZnO nanorods act as “joint” in three-dimensional (3D) MWCNT–RGO networks and the hybrid particles strongly interact with PVC chains via p-π stacking, hydrogen bonds, and electrostatic interactions, which we confirmed by scanning electron microscopy (SEM) and Raman analysis. By introducing the ZnO nanorods, the RGO–ZnO–MWCNT hybrid particles increased 160% in capacitance compared with MWCNT–RGO hybrids. Moreover, the addition of RGO–ZnO–MWCNT to PVC resulted in the mechanical properties of PVC being enhanced by 30.8% for tensile strength and 60.9% for Young’s modulus at the loadings of 2.0 weight percent (wt.%) and 1.0 wt.%, respectively. Meanwhile, the electrical conductivity of PVC increased by 11 orders of magnitude, from 1 × 10⁻¹⁵ S/m to 1 × 10⁻⁴ S/m for MWCNT–ZnO–RGO loading at 5.0 wt.%. Full article