Pure PP Research Articles

Supercritical N2 induced sandwich type lightweight and strong PP/CF foams with excellent electromagnetic shielding properties

The tremendous advances in communication technology and the explosion of electronic products led to an intensification of electromagnetic pollution, yet the efficient development of lightweight, high-strength fiber composite foams with excellent electromagnetic shielding properties was still a great challenge. Herein, this study, inspired by the sandwich structure, proposes a green foaming method with supercritical N2 to prepare a multilayered structure of carbon fiber reinforced polypropylene (PP/CF) foams, with a dense cellular structure in the core layer and a solid layer in the surface layer. The incorporation of CF improves the crystallization and rheological behavior of PP/CF, which guarantees a fine, dense and uniform cellular structure. This inner fine cellular structure and the solid layer on the surface contribute to the excellent mechanical properties. PP/30 %CF foam with a 1 mm mold opening distance displays an enhancement of 189.9 % in tensile strength and 196.3 % in flexural strength compared to pure PP. This also indicates more lightweight, high-strength and high-rigidity microcellular parts was obtained with less raw materials. Moreover, the formation of CF conductive network and internal foam structure contribute to excellent electromagnetic interference (EMI) shielding performance. The PP/CF composite foams maintain a level of EMI shielding performance greater than 30 dB despite the higher mold opening distance. Specifically, the PP/30 %CF foams at opening distance of 5 mm was enhanced to 58.3 dB·cm3/g with an improvement of 76.7 %. This implies that lightweight microcellular parts with both excellent strength and EMI shielding properties can be prepared, which enables PP/CF foams to possess a wide range of applications in various fields.

Tuning the circularly polarized luminescence in homoleptic and heteroleptic chiral CrIII complexes.

A series of highly emissive inert and chiral CrIII complexes displaying positive and negative circularly polarized luminescence (CPL) within the near-infrared (NIR) region at room temperature have been prepared and characterized to decipher the effect of ligand substitution on the photophysical properties, more specifically on the chiroptical properties. The helical homoleptic [Cr(dqp-R)2]3+ (dqp = 2,6-di(quinolin-8-yl)pyridine; R = Ph, ≡-Ph, DMA, ≡-DMA (DMA = N,N-dimethylaniline)) and heteroleptic [Cr(dqp)(L)]3+ (L = 4-methoxy-2,6-di(quinolin-8-yl)pyridine (dqp-OMe) or L = N 2,N 6-dimethyl-N 2,N 6-di(pyridin-2-yl)pyridine-2,6-diamine (ddpd)) molecular rubies were synthesized as racemic mixtures and then resolved and isolated into their respective pure PP and MM enantiomeric forms by chiral stationary phase HPLC. The corresponding enantiomers show two opposite polarized emission bands within the 700-780nm range corresponding to the characteristic metal-centered Cr(2E'→4A2) and Cr(2T1 '→4A2) transitions with large g lum ranging from 0.14 to 0.20 for the former transition. In summary, this study reports the rational use of different ligands on CrIII and their effect on the chiroptical properties of the complexes.

Morphological, Thermal, and Mechanical Assessment of Polypropylene and Ammonium Phosphate Composites Enhanced with Lignosulfonate and Zirconium.

Polypropylene and ammonium phosphate (AP) composites were synthesized at a 25 wt% concentration. The changes in the morphological, thermal, and physical behavior of the composites were analyzed with the addition of lignosulfonate (LG) and zirconium phosphate (ZrP). Additionally, metallic zirconium was deposited onto lignosulfonate using the magnetron sputtering technique to develop polypropylene and zirconium-modified lignosulfonate (LGMod) composites. Thus, composites of PP/25AP, PP/25AP/8LG/5ZrP, and PP/25AP/8LGMod were synthesized. The synthesis involved mixing the materials in a Hake mixer, followed by compression molding. The composites were characterized by field emission scanning electron microscopy (SEM-EDS), a thermogravimetric analysis (TGA) with combustion parameters, a vertical burn test (UL-94), a thermal camera, and mechanical properties. All composites achieved a V2 rating according to UL-94 standards. The PP/25AP extinguishes flames more quickly compared to other materials, approximately 99.2% faster than PP and showed the lowest temperature variation and mass loss after burning. The PP/25AP/8LG/5ZrP composite exhibited a 7% higher rigidity and 84.5% better flame retardancy compared to pure PP. Additionally, substituting ZrP with LGMod led to a lower environmental impact and improved thermal properties, despite some mechanical disadvantages.

Enhancing Insight into Photochemical Weathering of Flax and Miscanthus: Exploring Diverse Chemical Compositions and Composite Materials.

The accelerated weathering of flax and miscanthus fibers possessing distinct chemical compositions was investigated. The chosen fibers included raw, extractive-free (EF) and delignified samples (x3), alone and used as fillers in a stabilized polypropylene blue matrix (PP). Modifications in both color and the chemical composition of the fibers throughout the weathering process under ultraviolet (UV) light were meticulously tracked and analyzed by spectrophotometry and attenuated total reflectance with Fourier-transform infrared spectroscopy (ATR-FTIR). The inherent nature and composition of the selected fibers led to varied color-change tendencies. Raw and EF flax fibers exhibited lightening effects, while raw and EF miscanthus fibers demonstrated darkening effects. Extractives exhibited negligible influence on the color alteration of both flax and miscanthus fibers. This disparity between the fibers correlates with their respective lignin content and type, and the significant formation of carbonyl (C=O) groups in miscanthus. Better stability was noted for delignified flax fibers. A comparative study was achieved by weathering the PP matrix containing these various fibers. Contrary to the weathering observations on individual fibers, it was noted that composites containing raw and EF flax fibers exhibited significant color degradation. The other fiber-containing formulations showed enhanced color stability when compared to the pure PP matrix. The study highlights that the UV stability of composites depends on their thermal history. As confirmed by thermogravimetric analysis (TGA), fiber degradation during extrusion may affect UV stability, a factor that is not apparent when fibers alone are subjected to UV aging.

Electrical properties enhancement of dually grafting modification for polypropylene cable insulation

AbstractPolypropylene (PP) is believed to be a rather promising cable insulating material for high‐capacity electric power system with low carbon emission due to its decent thermo‐resistance and recyclable nature. In this paper, a new dually chemical grafting modification strategy by methyl acrylate (MA) and acrylic acid (AA) is put forward to tailor the charge transportation behavior in PP, thus further enhancing the electrical properties. Experimental results indicate that the dually grafted PP with 2.3 weight percent (wt%) MA and 1.9 wt% AA shows enhanced volume resistivity and electrical breakdown strength than pure PP, and the space charge injection is significantly suppressed. This work further adopts thermally stimulated depolarization current (TSDC) test and computational analysis based on density functional theory (DFT) to reveal the mechanism of enhancement. The analysis shows that grafted chemical groups can introduce quantities of deep traps and electrostatic potential wells which are strongly correlated with the carbonyl group and would hinder the charge transportation thus improving the electrical insulating performances of PP. This work would provide a new route of PP‐based dually grafting modification for the development of high‐voltage cable insulation.

A Comparative Study of Airbag Covers for Automotive Safety Using Coconut Shell Fiber/PP Composite Materials

In this study, we compared the physical properties of coconut fiber/polypropylene (PP) composite materials with coconut fiber as a reinforcing agent, produced through a hybrid injection molding process and a layered hot-pressing process. Through comparative experiments, the mechanical properties of both the hybrid injection-molded and layered hot-pressed materials were validated. The results indicated that, when using a coconut fiber content of 5%, the layered hot-pressed composite material exhibited optimal comprehensive performance. Specifically, its tensile strength reached 25.12 MPa, showing a 37.6% increase over that of pure PP materials of the same brand and batch. Its tensile modulus was 1.17 GPa, representing an 11.4% decrease. Additionally, its bending strength was 35.94 MPa, marking a 49.8% increase, and its bending modulus was 2.69 GPa, which is nearly double that of pure PP materials. Furthermore, through Creo modeling and an ANSYS simulation analysis, it was verified that this material could be applied to airbag covers in the field of automotive safety. This study confirmed that layered hot-pressed coconut fiber/PP composite materials exhibit superior mechanical properties to traditional materials and injection-molded composite materials, making them more suitable for airbag covers.

The thermal conductivity of 3D network reinforced polypropylene matrix composites was constructed by the pickering‐like emulsion method

AbstractPolypropylene (PP) has the advantages of corrosion resistance, easy processing, and low dielectric loss, but its low thermal conductivity limits the application of its composites in fields such as electronic packaging. To solve this problem, in this work, composite microspheres with the segregated structure were prepared by coating boron nitride nanosheets (BNNSs) on the PP surface by Pickering‐like emulsion method, and BNNSs@PP composites with three‐dimensional thermal conductivity network were obtained after molding. Due to the high thermal conductivity of BNNSs and the formation of perfect thermal conduction pathways, the thermal conductivity of the composites reached 1.71 W m−1 K−1 when the content of BNNSs was 10.1 wt%, which was a 713% increase in thermal conductivity for that of pure PP. At the same time, the mechanical properties of the composites were ensured. This method provides a simple and effective technique to improve the thermal conductivity of PP‐based thermally conductive composites, which has a wide application potential in electronic packaging.

Deformation mechanism of thermoplastic vulcanizate (TPV) from a view of micromechanical scale

Thermoplastic vulcanizates (TPVs) combine recyclability with strength but lack elasticity compared to elastomers. A Region Growing-Monte Carlo model accurately captured TPV's mesoscopic structure, showing just a 3.28 % deviation from experiments. Pure PP and PP network body models quantify PP matrix plastic deformation during stretching. TPV's rebound performance is influenced by the PP network and EPDM. During 30 % stretching, the equatorial PP matrix region exceeds 70 % strain and enters plastic flow, while other areas remain less strained. At particle intersections, the strain rate drops below 8 %. In recovery, the equatorial region opposes the process mechanically, a vital aspect of TPV's rebound mechanism. Non-equatorial PP matrix regions act as bonding points, with permanent deformation reflected in TPV's macroscopic behavior. This work provides key insights into enhancing TPV resilience from a micromechanical perspective.

Oil-Loaded Mesoporous Silica to Enhance the Lubrication of Polypropylene Resin Composite Materials

Polymer self-lubricating materials have advantages such as low friction coefficient, good wear resistance, and high work efficiency, giving them wide application potential in friction and wear. This work fabricated polymer-based self-lubricating materials by incorporating oil-loaded mesoporous silica nanoparticles (MSNs + YR1800) in the polypropylene resin (PP). The effects of different content of MSNs + YR1800 on the tribological and mechanical properties of the obtained self-lubricating composite materials were studied. The results indicate that the content of MSNs + YR1800 in composite materials significantly impacts their tribological properties. When the content of MSNs + YR1800 was 10 wt%, the coefficient of friction reduced to 0.09,which was 84.5% lower than for PP and 78.6% lower than for composite materials containing 5 wt% mesoporous silica nanoparticle (MSNs). Compared with pure PP, the wear rate decreases from 4.93 × 10−11 m3∙Nm−1 to 4.43 × 10−13 m3∙Nm−1, which is reduced by two orders of magnitude. The excellent tribological properties of composite materials are attributed to the high specific surface area, large pore volume, strong adsorption capacity, and high oil loading capacity of mesoporous silica nanoparticle as nanofillers. The MSNs + YR1800 release lubricants to form a lubricating oil film during the friction process under load conditions, preventing direct contact between the friction pair and the surface of the composite material. Compared with polymer-silica hybrid oil-loaded microcapsules, MSNs + YR1800 can effectively reduce lubricant leakage, prolong operation life, improve lubrication efficiency, and ensure the continuous and stable existence of lubricating oil films.

Dispersion and Lubrication of Zinc Stearate in Polypropylene/Sodium 4-[(4-chlorobenzoyl) amino] Benzoate Nucleating Agent Composite.

Zinc stearate (Znst) was physically blended with the sodium 4-[(4 chlorobenzoyl) amino] benzoate (SCAB) to obtain the SCAB-Znst composite nucleating agent. Znst was used to improve the dispersion property of SCAB and exert a lubricating effect on the PP matrix. The scanning electron microscopy and the fracture surface morphology of the PP/SCAB composite illustrated that the addition of Znst greatly reduced the aggregation phenomenon of SCAB in the PP matrix. The result of the rotary rheometer indicated that Znst exhibits internal lubrication in PP. The DSC result illustrated that the crystallization properties of PP were improved. Compared with pure PP, the Tc of the PP/SCAB composite increased by 1.44 °C (PP/Znst), 13.48 °C (PP/SCAB), and 14.96 °C (PP/SCAB-Znst), respectively. The flexural strength of pure PP, PP/SCAB, and PP/SCAB-Znst were 35.8 MPa, 38.8 MPa, and 40.6 MPa, respectively. The tensile strength of the PP/SCAB and PP/SCAB-Znst reached the values of 39.8 MPa and 42.9 MPa, respectively, compared with pure PP (34.1 MPa). The results demonstrated that Znst can promote the dispersion of SCAB in the PP matrix while exerting a lubricating effect, which enabled the enhancement of the crystalline and mechanical properties of PP.

Titanium Dioxide and Calcium Sulfate Whiskers Are Used for the Preparation of High Performance Polypropylene and Reduce White Pollution.

The anti-aging agent TiO2-polyacrylonitrile (PAN) and the mechanical strengthening agent CSW-PAN were prepared by radical polymerization using rutile nano-titanium dioxide (TiO2) and anhydrous calcium sulfate whisker (CSW) as raw materials. The structures of TiO2-PAN and CSW-PAN were characterized using Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Simultaneously, the mechanical properties, aging properties, and thermal stability of TiO2-PAN/CSW-PAN/polypropylene (PP) composites were studied, and the results showed that the surfaces of nano-titanium dioxide and calcium sulfate whiskers were successfully grafted with acrylonitrile. Owing to the introduction of new elements, such as acrylonitrile, nano-titanium dioxide and calcium sulfate whiskers have anti-aging properties. In comparison of the impact strength and tensile strength of TiO2-PAN/PP and TiO2-PAN/CSW-PAN/PP before aging, it can be proven that adding CSW-PAN can significantly enhance the mechanical properties of TiO2-PAN/CSW-PAN/PP. After 1000 h of aging, the tensile strength of the ternary composite TiO2-PAN/CSW-PAN/PP was 19.88 MPa when the addition amount of TiO2-PAN and CSW-PAN was 3%. Moreover, the impact strength of the ternary composite material TiO2-PAN/CSW-PAN/PP after 1000 h of aging is even better than that of non-aging pure PP materials, proving that the service life of improved PP products is extended, unnecessary waste and environmental pollution can be relieved, and the needs of specific engineering fields can be met.

Study on the mechanical properties of ramie fiber/polypropylene composites prepared by hot pressing after the carding machine mixing

AbstractA growing variety of composites utilize natural plant fibers with naturally occurring veins structured hierarchically in an effort to reduce dependence on petroleum‐based materials. In this article, ramie fibers were extracted by alkaline delignification. Then, ramie fibers and PP matrix, were prepared in filament form and an amino‐silane coupling agent KH550, and maleic anhydride grafted polypropylene were added to improve interfacial compatibility. Ramie fiber/polypropylene fiber‐reinforced polymer composites (FRC) were prepared by hot pressing after using a carding machine. This method preserves the structure and length of ramie fibers to a large extent, thus greatly improving the mechanical properties of the material. After optimization, the FRC prepared from plant fibers of 2 cm length and 60% content had a density of 0.95 g/cm3, showed an increase in tensile and flexural strength of 276% and 339%, respectively, compared to the pure PP matrix. The specific strength of the FRC in the work was higher than galore FRC prepared from talc, carbon fiber, other plant fibers, and so forth. The FRC has a wide range of potential applications due to its own low‐cost, lightweight, and high‐performance, and is highly feasible in replacing the current polymers in the preparation of numerous everyday items.Highlights The preparation method of FRC resulted in a more complete fiber length and structure. The mechanism to improve the interfacial compatibility of RF and PP is discussed. The effect of varying fiber length on the FRC mechanical properties was investigated.

Nonpolar sub-10 nm TiO2 nanocrystal for high energy density polypropylene nanocomposites

Film capacitors have shown great potential in high-power energy storage devices due to their high breakdown strength and low dielectric loss. However, the state-of-the-art commercial capacitor dielectric, biaxially oriented polypropylene (BOPP), exhibits limited energy storage density below 2 J cm−3 because of its low dielectric constant (approximately 2.2 at 103 Hz). In this work, we present a novel PP-based nanocomposites by incorporating nonpolar sub-10 nm sized TiO2 nanoparticles into the PP matrix for the first time. The nonpolar TiO2 nanoparticles are functionalized with Trioctylphosphine oxide (TOPO) ligands, ensuring excellent compatibility and dispersion of the TiO2 fillers in the PP matrix, resulting in a homogeneous dielectric PP nanocomposite. Moreover, the TOPO ligand, with lower LUMO energy level and higher HOMO level than that of PP matrix, serves as an energy trap to capture carriers upon their occurrence. Furthermore, the well-dispersed sub-10 nm sized TiO2 nanoparticles enlarges the interfacial area, thereby increasing the interfacial polarization and the dielectric constant. The resultant PP nanocomposites exhibit a high discharged energy density of 4.19 J cm−3 at 600 MV m−1, representing a remarkable 74.9% increase compared to that of the pure PP films. This work provides a brand-new strategy for constructing homogeneous PP nanocomposite dielectrics by incorporating nonpolar sub-10 nm sized TiO2 nanoparticles as fillers. And this approach is critical for the design of high energy density PP-based nanocomposites.

The influence and mechanism of elastomer types on electrical and mechanical properties of polypropylene insulation materials for high voltage cables

AbstractPolypropylene (PP) becomes a superior candidate material for new environmentally friendly cable main insulation with its excellent heat resistance, electrical properties, and degradability. However, in practical application, PP material is aging and vulnerable and its toughness is poor. The mechanical properties of PP material can be improved by elastomer modification, but the effects of different elastomers on the comprehensive properties of composite specimens are quite different. In this paper, the electrical and mechanical properties of different types of elastomer‐modified PP composites are compared and analyzed by combining experimental and molecular simulation (MS) methods. The experimental results show that the SEBS/PP composite material has the lowest trap energy levels among all kinds of composite materials, its space charge accumulation is 1.96 × 10−9C, and the mechanical and rheological properties improvement of the composite is the most remarkable. Meanwhile, the volume resistivity is reduced by two orders of magnitude compared with pure PP. However, the breakdown strength of all kinds of composite materials decreases by different degrees after the modification. The solubility parameters (δ) and the free volume are further investigated by the molecular simulation, which shows that the δ of SEBS is similar to that of PP, which represents the best compatibility. Moreover, the SEBS/PP composite material has the strongest inter‐molecular force and the most excellent toughness improvement for PP. This work provides a theoretical basis for elastomer selection in PP modification.

Amplification Ratio of a Recycled Plastics-Compliant Mechanism Flexure Hinge

This research focuses on the fabrication of plastic flexure hinges from diverse plastics such as ABS, PP, HDPE, and LDPE. To enhance hinge efficiency, the recycling ratios are also investigated. The amplification ratio of different recycle ratios and plastic types are measured. The results show that the input and output displacements of all PP, ABS, and HDPE hinges are linear. The presence of recycled plastics has no impact on this basis. The pure PP, ABS, and HDPE flexure hinges achieve the highest amplification ratios of 5.728, 8.249, and 5.668. The addition of recycled plastics reduces the amplification ratio. This decrease in the amplification ratio, however, is small. At a 25% recycle ratio, the PP, ABS, and HDPE flexure hinges have 12%, 13.3%, and 21.7% lower amplification ratios than the pure plastic hinges. Furthermore, the utilization of recycled plastics may lessen the need for new plastic made from raw materials. With the PP flexure hinge, a maximum input value of 157 µm could result in an output value of 886 µm. At a maximum input value of 115 µm, the ABS flexure hinge could achieve an output value of 833 µm. Finally, a maximum input value of 175 µm might result in an output value of 857 µm when using the HDPE flexure hinge. The average amplification ratio values for all recycling ratios for PP, ABS, and HDPE flexure hinges are, respectively, 5.35, 7.60, and 5.02. The ABS flexure hinge frequently outperforms the PP and HDPE flexure hinge in terms of amplification ratios. Among these plastics, HDPE flexure hinges have the lowest amplification ratio. In general, increasing the thermoplastic polyurethane (TPU) content of the LDPE/TPU blend increases the amplification ratio. The cause could be the TPU’s high compatibility with the LDPE polymer. The LDPE/TPU blend hinge offers a broader range of the amplification ratio of 2.85–10.504 than the PP, ABS, and HDPE flexure hinges. It is interesting that changing the blend percentage has a much greater impact on the amplification ratio than changing the recycling ratio. The findings broaden the range of applications for plastic flexure hinges by identifying optimal plastic types. The impact of the hinge shape on the performance of the injected plastic flexure hinge might be studied in further research.

Seismic fluid identification method based on the joint PP‐ and SH–SH‐wave stochastic inversion

AbstractPre‐stack seismic inversion is an effective method for elastic parameter inversion using seismic data, which facilitates seismic fluid identification. However, pure PP‐wave inversion has issues of strong multi‐solution and limited prediction accuracy. Therefore, we propose a seismic fluid identification approach based on the joint PP‐ and SH–SH‐wave stochastic inversion. First, the linearized SH–SH‐wave amplitude variation with offset approximation parameterized by shear modulus and density is derived. Numerical simulations demonstrate that the SH–SH‐wave amplitude variation with offset approximation has a good accuracy. Reflection coefficient contribution analysis indicates that the new formulation has better parameter sensitivity to shear modulus and density than the PP wave amplitude variation with offset approximation derived by Russell, which helps one to improve the inversion of shear modulus and density. On this basis, we construct a joint inversion equation of PP and SH–SH waves for a Russell fluid indicator, a shear modulus and density and present a novel joint stochastic inversion method based on the ensemble smoother with multiple data assimilation. Stanford VI‐E model tests reveal that the Russell fluid indicator factor, shear modulus and density obtained from the joint PP‐ and SH–SH‐wave inversion have higher identification accuracy and smaller relative errors than those from pure PP‐wave inversion. Furthermore, field data tests indicate that this method has practical applicability in seismic fluid identification.

The impact of the glass microparticles features on the engineering response of isotactic polypropylene in material extrusion 3D printing

Glass in the type of powder, flakes, and beads was reinforced into a PP matrix and then used for filament production, through a thermomechanical process, in different loadings each (3.0 wt%, 6.0 wt%, 9.0 wt%,), with the aim of optimizing the concentrations. Thermogravimetric and Raman analysis were utilized for the determination of thermal stability and composition. With the assistance of material extrusion (MEX) 3D printing, specimens, suitable for tensile, flexural, impact, and microhardness tests were made and exploited for mechanical performance evaluation. Scanning electron microscopy (SEM) helped in capturing pictures for the evaluation of fractographic characteristics. Glass beads, flakes, and powder all exhibited great improvements in mechanical properties, with respect to pure PP. Still, differences exist between the glass types. Especially the PP/ Glass 3.0 wt% showed the most ameliorations. Such composites expand the capabilities of the MEX 3D printing process, employing an eco-friendly additive, such as glass.

Tribological and thermomechanical evaluation of polypropylene nanocomposites containing different dimensional structures of carbon and ceramic nanoparticles

ABSTRACT This study describes the development of PP nanocomposites using hydrothermally assembled carbon nanotubes (CNTs)/barium titanium (BT) (denoted as BTC) and graphene nanosheets (GNs)/boron nitride (BN) (denoted as BNG) nanoparticles. The PP nanocomposites were fabricated via the development of a masterbatch using polypropylene maleic anhydride (PPMA), followed by diluting with pure PP via melt compounding. The wear resistance and thermomechanical properties of the nanocomposites exhibited a substantial improvement, where about 96.8% increase in wear resistance and low coefficient of friction were recorded. While about 230% increase in glass transition temperature was measured with the nanocomposites relative to the pure PP. The developed nanocomposites have potential applications in automobile and other machine components where high wear resistance and thermal-mechanical properties are required.

Chitosan and TiO2 functionalized polypropylene nonwoven fabrics with visible light induced photocatalytic antibacterial performances

Chitosan/TiO2 functionalized polypropylene (CS/TiO2/PP) nonwoven fabrics were fabricated through crosslinking of chitosan with glutaraldehyde followed by loading of TiO2 nanoparticles. The functionalized CS/TiO2/PP has super hydrophilicity and excellent visible light induced photocatalytic antibacterial properties owing to the synergistic effects of CS and TiO2. The photocatalytic degradation performance was determined by assessing the degradation of methyl blue under simulated visible light irradiation and its recyclability was also evaluated. In addition, SEM images demonstrated that TiO2 nanoparticles were distributed evenly on the surface of the 2 g/L CS/TiO2/PP. Meanwhile, the polypropylene surface showed a significant increase in hydrophilicity after being treated with chitosan and TiO2. The photocatalytic degradation results revealed that CS/TiO2/PP had higher photocatalytic properties than those of pure PP under visible light, and the degradation rate of methylene blue reached 96.4 % after 90 min of light exposure. Compared to pure PP, the antibacterial properties of CS/TiO2/PP significantly increased, and the bacterial reduction percentages were increased to 98.7 % and 96.3 %, against E. coli and S. aureus, respectively. The functionalized CS/TiO2/PP composites exhibited promising potential in environmentally friendly antibacterial materials.

Influence of electric field on the thermal properties of PP+NC nanocomposites for environmental chemistry application

Using Differential Thermal Analysis (DTA) method the thermal-physical properties of nanocomposites PP+NC for environmental and environmental chemistry applications were studied and the thermal-destruction processes after aging in an electric field were determined. The influence of various external factors (strong electric field, electric discharge, temperature, radiation, etc.) on polymers and composites based on polymers penetrates into the deep layers of the matrix and leads to the destruction and reconstruction of the structure. Changes in the ratio of crystalline and amorphous phase occur due to the formation of an interlayer crystalline phase in the matrix. In this regard, the thermal properties of pure PP and PP+2.0% NC nanocomposites were investigated using the derivatographic method to study the influence of the electric field on the aging process, melting temperature, and crystallization rate and depolymerization process.