Showing 89 results for Composite
Zainab J. Shanan, Huda M.j. Ali, H.f. Al-Taay,
Volume 19, Issue 3 (9-2022)
Abstract
The objectives of this work is to synthesize TiO2/MgO nanocomposites using a pulse laser deposition technique. At a vacuum pressure of 2.5 10-2 mBar, TiO2/MgO nanocomposites were synthesized on substrates with a laser power of 600 mJ and a wavelength of 1064 nm. This search utilizes various pulses (500, 600, and 700) at a 6-Hertz repetition rate. X-ray diffraction was utilized to investigate crystallography of the phases in the samples, as well as average crystallite size (XRD). An increase in the average crystal size was observed with an increase in the number of shots (from 35.15 to 38.08) nm at (500 to 700) shots respectively. The impact of the number of laser shots on the surface characteristics of TiO2/MgO nanocomposites was also evaluated using atomic force microscopy (AFM) and field emission scanning electron microscopy (FE-SEM). Finally, optical characteristics were evaluated using UV-Vis spectroscopy. Increasing the number of shots increased the absorbance and thus reduced the energy gap.
Sreedevi Gogula, Sandhya Cole, Venkata Rao Kanakala, Gogula Jaya Ram Pavan Kumar, B Tirumala Rao,
Volume 19, Issue 4 (12-2022)
Abstract
The present study used a hydrothermal technique to synthesize undoped and Mn2+ doped CdS/Zn3(PO4)2 semiconducting nanocomposite materials. Powder X-ray diffraction, scanning electron microscopy, UV-Vis diffuse reflectance spectrometer, Fourier transform-Infrared Spectroscopy-FT-IR, and photoluminescence techniques were employed to study structural, optical, and luminescence properties of produced nanocomposites. The hexagonal structure of CdS and the monoclinic structure of Zn3(PO4)2 are both reflected in the powder X-ray diffraction spectra. When Mn2+ ions are present in the host lattice, a lattice distortion occurs, causing a phase change from the phase of γ-Zn3(PO4)2 to the β-phase of Zn3(PO4)2, without affecting the hexagonal phase of CdS. The average crystallite size of produced nanocomposites was 22-25 nm, and also calculated the lattice strain and dislocation density to better understand internal deformation of the samples. The FT-IR spectra were used to investigate the molecular vibrations and functional groups in the samples. The surface morphology of the nanocomposites is hexagonal spheres on rectangular shaped nano-flakes, and the interatomic distance between the hexagonal spheres is decreased as the doping concentration increases, forming a rod-like structure on the flakes. EDAX results confirm the presence of various relevant elements in the prepared samples. The quantum confinement of produced samples reduces as the Mn2+ doping concentration in the host lattice increases. The photoluminescence results demonstrate shallow trapped states due to the transition: d-d (4T1 → 6A1) of the tetrahedrally coordinated Mn2+ states and the impact of Mn2+ ions exhibiting several peaks in the UV-Visible region (365-634 nm) generating RGB (Red, Green, Blue) luminescence. Color coordinates and CCT values were calculated using the CIE diagram, and color correlated temperatures in the range of 2513–7307 K were discovered, which might be used in solid state lighting applications.
Girsha Cahya Maharani, Anne Zulfia Syahrial,
Volume 20, Issue 1 (3-2023)
Abstract
Materials that are applied to combat vehicles require an innovation as the development of the military world advances. The material innovation in this research is a lightweight hybrid laminated Al7075 composites. The main materials used in this research are aluminum 7075 plate, kevlar 29, silicon carbide (SiC) nano powder, and epoxy resin. SiC nano powder is mixed with polyethylene glycol-400 (PEG-400), then ethanol is added so that it becomes a shear thickening fluid (STF) solution which is used to impregnate kevlar. Laminate composites were prepared using the hand lay-up method with epoxy resin as an additive between layers of kevlar and aluminum 7075 plates. The thickness of laminates is various due to the number of kevlar used different of each laminated that is 8, 16, and 24 layers. The results of this study show that the composite with impregnated kevlar has higher ballistic and impact resistance values than the composite with non-impregnated kevlar, which has good potential as a base material for combat vehicles such as tanks. This is also supported by the Fourier Transfer Infrared Spectrometry (FTIR) results to determine the level of absorbance of the functional groups identified in impregnated kevlar and Scanning Electron Microscopy (SEM) results of the distribution of nano SiC filler that infiltrated to the empty space in the kevlar fiber.
Behzad Rahimzadeh, Maisam Jalaly, Mehrdad Roshan,
Volume 20, Issue 1 (3-2023)
Abstract
Considering the widespread use of aluminum composites in various industries and the emergence of nanomaterials such as graphene and boron nitrite (BN) with their unique properties, aluminum-based nanocomposite reinforced by the graphene-BN hybrid was fabricated at different percentages. For this purpose, the graphene-BN hybrid was prepared and subjected to wet milling along with the aluminum powder. The mechanical properties of the final nanocomposite which was consolidated using the spark plasma sintering (SPS) method were examined. Aluminum-based composite specimens containing 1 wt.% graphene–0 wt.% BN (AGB1), 0.95 wt.% graphene–0.05 wt.% BN (AGB2), 0.90 wt.% graphene–0.1 wt.% BN (AGB3), and 0.85 wt.% graphene–0.15 wt.% BN (AGB4) were fabricated and compared with non-reinforced aluminum (AGB0). The hardness values of 48.1, 51.1, 56.2, 54.1, and 43.6 Hv were obtained for AGB0, AGB1, AGB2, AGB3, and AGB4, respectively. Additionally, tensile strengths of these specimens were 67.2, 102.1, 129.5, 123.7, and 114.7 MPa, respectively. According to the results of the hardness and tensile tests, it was revealed that the AGB2 specimen had the highest tensile strength (93% higher than AGB0 and 27% higher than AGB1) and hardness (17% higher than AGB0 and 10% higher than AGB1).
Ayça Tanrıverdi, Saniye Tekerek,
Volume 20, Issue 3 (9-2023)
Abstract
In this study, zinc chloride (ZnCl) was used as a precursor chemical to form boron reinforced zinc oxide (ZnO:B) particles. The supercapacitor performance of the reduced graphene oxide/boron reinforced zinc oxide (RGO/ZnO:B) composite electrodes produced by hydrothermal methods, and the impact of different boron doping ratios on the capacitance, were both examined. The characterization of the RGO/ZnO:B composites containing 5%, 10%, 15% and 20% boron by weight were performed using X-Ray diffraction (XRD) and scanning electron microscopy (SEM). The capacitance measurements of the electrodes produced were conducted in a 6 M KOH aqueous solution with a typical three electrode setup using Iviumstat potentiostat/galvanostatic cyclic voltammetry. The specific capacitance value of the 20% reinforced RGO/ZnO:B composite electrode was 155.88 F/g, while that of the RGO/ZnO composite electrode was 36.37 F/g. According to this result, the capacitance increased four-fold with a 20% boron doping concentration. Moreover, a longer cycle performance was observed for the RGO/ZnO:B electrodes with higher boron doping concentrations.
Saeedeh Mansoury, Maisam Jalaly, Mohammad Khalesi Hamedani,
Volume 20, Issue 4 (12-2023)
Abstract
In this study, an epoxy-based nanocomposite reinforced with copper oxide-graphene oxide hybrid was investigated. Initially, the hybrid powder of CuO–GO with a weight ratio of 9:1 was prepared. The hybrid filler with different weight percentages ranging from 0.1–0.5 was used to reinforce the epoxy resin. The prepared samples were analyzed using XRD, FTIR, FESEM, TEM, and tensile testing. According to the XRD results and SEM images, the hybrid powder was successfully prepared, and the mechanical testing results showed an improvement in tensile strength in the composite samples. The best composite sample in terms of tensile strength was the one containing 0.3 wt% of hybrid reinforcement, which exhibited a 73% increase in strength compared to the neat resin sample.
Pravin Jadhav, R.s.n Sahai, Deepankar Biswas, Asit Samui,
Volume 20, Issue 4 (12-2023)
Abstract
The present work deals with the effect of Multi-walled Carbon Nanotube (MWCNT) and functionalized (carboxyl and amine) MWCNT on the mechanical properties of the PAEK (Poly Aryl Ether Ketone) polymer composite. The MWCNT and functionalized (carboxyl and amine) MWCNT concentration varied as 0.25, 0.5 and 0.75 weight percentages. Compositeswere prepared by using a melt compounding method using a twin-screw extruder and all testing samples were prepared using an injection molding machine as per American Society for Testing and Materials (ASTM) standards. Samples were tested for tensile strength, impact strength, flexural strength, heat deflection temperature, hardness, and density. There is an increase in the tensile strength, impact strength, flexural strength, and heat deflection temperature, with percentage increase in filler loading up to 0.5 %, followed by decrease in it with higher filler loading. The increase is maximum for amine functionalized MWCNT.
Muhammad Shahzad Sadiq, Muhammad Imran, Abdur Rafai, Muhammad Rizwan,
Volume 21, Issue 2 (6-2024)
Abstract
With increasing energy demand and depletion of fossil fuel resources, it is pertinent to explore the renewable and eco-friendly energy resource to meet global energy demand. Recently, perovskite solar cells (PSCs) have emerged as plausible candidates in the field of photovoltaics and considered as potential contender of silicon solar cells in the photovoltaic market owing to their superior optoelectronic properties, low-cost and high absorption coefficients. Despite intensive research, PSCs still suffer from efficiency, stability, and reproducibility issues. To address the concern, the charge transport material (CTM) particularly the electron transport materials (ETM) can play significant role in the development of efficient and stable perovskite devices. In the proposed research, we synthesized GO-Ag-TiO2 ternary nanocomposite by facile hydrothermal approach as a potential electron transport layer (ETL) in a regular planar configuration-based PSC. The as synthesized sample was examined for morphological, structural, and optical properties using XRD, and UV-Vis spectroscopic techniques. XRD analysis confirmed the high crystallinity of prepared sample with no peak of impurity. The optimized GO-Ag-TiO2 ETL exhibited superior PCE of 8.72% with Jsc of 14.98 mA.cm-2 ,Voc of 0.99 V, and a fill factor of 58.83%. Furthermore, the efficiency enhancement in comparison with reference device is observed which confirms the potential role of doped materials in enhancing photovoltaic performance by facilitating efficient charge transport and reduced recombination. Our research suggests a facile route to synthesize a low-cost ETM beneficial for the commercialization of future perovskite devices.
Alireza Zibanejad-Rad, Ali Alizadeh, Seyyed Mehdi Abbasi,
Volume 21, Issue 2 (6-2024)
Abstract
Pressureless sintering was employed at 1400 °C to synthesize Ti matrix composites (TMCs) reinforced with in-situ TiB and TiC reinforcements using TiB2 and B4C initial reinforcements. The microstructure and wear behavior of the synthesized composites were evaluated and compared and the results showed that B4C caused the formation of TiB-TiC in-situ hybrid reinforcements in the Ti matrix. Also, TiB was in the form of blades/needles and whiskers, and TiC was almost equiaxed. Moreover, the volume fraction of the in-situ formed reinforcement using B4C was much higher than that formed using TiB2. In addition, although the hardness of the B4C-synthesized composites was higher, the composite synthesized using 3 wt.% TiB2 exhibited the highest hardness (425 HV). The wear test results showed that the sample synthesized using 3 wt.% TiB2 showed the lowest wear rate at 50 N, mainly because of its higher hardness. The dominant wear mechanism in the samples synthesized using 3 wt.% B4C was abrasive and delamination at 50 N and 100 N, respectively while in the samples synthesized 3 wt.% TiB2, a combination of delamination and adhesive wear and adhesive wear was ruling, respectively.
Wed Abed, Haider Abdulelah, Sanaa Q.badr,
Volume 21, Issue 2 (6-2024)
Abstract
Satish Ahire, Ashwini Bachhav, Bapu Jagdale, Thansing Pawar, Prashant Koli, Dnyaneshwar Sanap, Arun Patil,
Volume 21, Issue 2 (6-2024)
Abstract
Hybrid photocatalysts, comprising both inorganic and organic polymeric components, are the most promising photocatalysts for the degradation of organic contaminants. The nanocomposite, Titania-Polyaniline (TiO2-PANI) was synthesized using the chemical oxidative polymerization method. Various characterization techniques were employed to assess the properties of the catalysts. The ultraviolet diffuse reflectance spectroscopy (UV-DRS) analysis revealed that the TiO2 absorbs only UV light while the TiO2-PANI nanocomposite absorbs light from both UV and visible regions. The X-ray diffraction (XRD) results confirmed the presence of TiO2 (anatase) in both TiO2 nanoparticles and TiO2-PANI (Titania-Polyaniline) nanocomposite. The phases of the catalysts were verified through Raman, TEM, and SAED techniques where all results are in good agreement with each other. The average crystallite size of TiO2 nanoparticle and TiO2-PANI nanocomposite were 13.87 and 10.76 nm. The thermal stability of the catalysts was assessed by the Thermal gravimetric analysis (TGA) technique. The order of the thermal stability is TiO2 > TiO2-PANI > PANI. The crystal lattice characteristics were confirmed using Transmission electron microscopy (TEM). The surface area measurements were confirmed from the Brunauer-Emmett-Teller (BET) study and were employed for the evaluation of the photocatalytic efficiency of both, TiO2 nanoparticles and TiO2-PANI nanocomposite catalysts. The energy dispersive spectroscopy (EDS) study was employed for elemental detection of the fabricated materials. While Raman spectroscopy was employed for the chemical structure and the phase characteristics of the materials. The standard conditions for the degradation of the CF dye were 8 g/L of catalyst dosage, 20 mg/L of dye concentration, and a pH of 7. The TiO2-PANI nanocomposite exhibited superior efficiency as compared to pure TiO2 nanoparticles, achieving almost 100 % degradation in just 40 minutes.
Ahabboud Malika, Gouitaa Najwa, Ahjyaje Fatimazahra, Lamcharfi Taj-Dine, Abdi Farid, Haddad Mustapha,
Volume 21, Issue 4 (12-2024)
Abstract
This paper reports the preparation and characterization of (1-x) PbZr0.52Ti0.48O3 -xBiFeO3 (1-x)PZTxBFO) (x= 0.00, 0.15, 0.30, 0.45, 0.60 and 1.00) multiferroic ceramics which were prepared by a sol-gel method for PZT and hydrothermal reaction process for BFO. The perovskite structure of the composite system was confirmed by X-ray diffraction and Raman spectroscopy, while the composite microstructure w:as char:acterized by scanning electron microscopy. XRD results and Rietveld analysis for the (1-x)PZT-xBFO composites confirm the coexistence of these three phases; rhombohedral (R3m) and tetragonal phases (P4mm) for pure PZT and only the rhombohedral phase (R3c) for pure BFO. Raman spectroscopy of the (1-x)PZT-xBFO composites shows two clear bands around 150 and 180 cm-1. When the BFO content increases, the intensities of Raman modes are decreased. The SEM results suggested a formation of agglomerate and form into large complex clusters as BFO increased and a higher grain size was obtained for the BFO sample compared with the other composites. The EDS spectra of our pellets show that all the characteristic lines of the chemical elements Pb, Zr, Ti, and O and Bi, Fe, and O are present for the PZT and BFO materials respectively. The temperature-dependent dielectric constant shows different behavior dependent on BFO content. Indeed, the dielectric properties are found to be improved with an increase in dopant concentration of BFO in PZT, and novel dielectric behavior, resonance, and antiresonance, were obtained.
Ferda Mindivan,
Volume 21, Issue 4 (12-2024)
Abstract
Natural-reinforced hybrid composites, called "eco-materials," are becoming increasingly important for protecting the environment and eliminating waste problems. In this study, hybrid biocomposites were produced by the colloidal mixing method using seashell (SS) as natural waste, two graphene derivatives (graphene oxide (GO) and reduced graphene oxide (RGO)) as filler material, and polyvinyl chloride (PVC) as the polymer matrix. The crystallization and mechanical properties of hybrid biocomposites were examined based on their thermal properties using TGA and DSC analysis. In comparison to PVC/GO and PVC/RGO composites with identical weight percentages of GO and RGO, the PVC/GO composite exhibited superior thermal stability and crystallinity, resulting in elevated hardness values for the same composite. These results were attributed to the better interaction of GO with PVC due to the higher number of oxygen-containing functional groups in GO than in RGO. However, the PVC/RGO/SS hybrid biocomposites exhibited superior properties than PVC/GO/SS hybrid biocomposites. The greatest crystallinity values were 39.40% for PVC/RGO/SS-20 compared to PVC/RGO at 20 wt% SS content and 29.21% for PVC/GO/SS-20 compared to PVC/GO. The PVC/RGO/SS-20 hybrid biocomposite showed the greatest gain in hardness value, up 18.47% compared to the PVC/RGO composite. No significant change was observed in the melting and weight loss temperatures as the SS content increased; however, the crystallinity and glass transition temperatures in hybrid biocomposites increased as the SS content increased. All analysis results demonstrated the achievement of SS-graphene-PVC interactions, suggesting that SS waste could enhance the thermal and mechanical properties of composite production.
Maryam Hajiebrahimi, Sanaz Alamdari, Omid Mirzaee,
Volume 21, Issue 4 (12-2024)
Abstract
Dual nanocomposites based on metal sulfide nanomaterials with a narrow band gap are favorable candidates for future optoelectronic applications and ionizing ray sensors. In this study, novel silver-doped zinc sulfide/ cadmium sulfide (ZnS/CdS: Ag) nanocomposites were synthesized using the cost-effective solvothermal approach. For the first time, the radiation sensitivity of the newly developed nanocomposite was assessed using a 241Am alpha source and ion beam-induced luminescence (IBIL) measurements. The ZnS/CdS: Ag nanocomposite demonstrated significant light emission in the blue-green spectrum when measured at room temperature. When exposed to alpha irradiation, the ZnS/CdS: Ag nanocomposite film displayed exceptional sensitivity compared to pure ZnS or CdS films. The FESEM images revealed a uniform distribution of semi-spherical and rod-shaped nanoparticles, with an average particle size measuring 180 nm. The results from XRD and EDX demonstrated distinct peaks corresponding to ZnS, CdS, and associated elements within the nanocomposite. The existence of several groups within the nanocomposite was confirmed through Fourier transform infrared spectroscopy. Evaluations revealed that the optical quality of the ZnS/CdS: Ag nanocomposite showed enhancement in comparison to pure ZnS and CdS. The results suggest that the ZnS/CdS: Ag nanocomposite film holds great promise for applications in optoelectronic devices and detection technologies.
Adil Kadum Shakir, Ebrahim Ghanbari-Adivi, Aref S. Baron Baron, Morteza Soltani,
Volume 22, Issue 1 (3-2025)
Abstract
Nanomaterials have significantly transformed multiple scientific and technological fields due to their exceptional properties, which result from their quantum confinement effects and high surface-to-volume ratios. Among these materials, zinc oxide (ZnO) and titanium dioxide (TiO2) nanoparticles have attracted considerable interest because of their diverse applications.
In this study, TiO2-ZnO nanocomposites were synthesized using varying calcination times of 1, 1.5, 2, 2.5, and 3 hours. Characterization of fabricated samples through X-ray diffraction (XRD) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), and energy-dispersive X-ray spectroscopy (EDXS) confirmed the successful fabrication of the nanocomposites. In this regard, XRD analysis revealed anatase TiO2 and hexagonal wurtzite ZnO phases. Raman spectroscopy also supported these findings, identifying characteristic peaks of both TiO2 and ZnO.
The calcination time had a minimal effect on the crystal structures and also morphology of the nanocomposites, which gave rise to its negligible impact on optical properties and biological activities of the samples. Optical properties assessed by means of UV-visible and photoluminescence (PL) spectroscopy showed consistent band gap absorption and emission profiles across all samples, among which the nanocomposite calcined for 1 hour exhibited the best optical properties.
The sample prepared at 1 hour not only showed the most favorable optical properties, but also demonstrated significant antibacterial, antifungal, and cytotoxic activities, which make it suitable for various applications. In this regard, a reduction of more than 99.9% occurred in the number of Escherichia coli and Staphylococcus aureus bacteria and also Candida albicans fungus by using TiO2-ZnO nanocomposite. Besides, addition of 500 µg/ml of nanocomposite decreased the cell viability to 34.47%, which signifies its high cytotoxicity activity.
Zeinab Abbasali Karajabad, Adrine Malek Khachatourian, Mohammad Golmohammad, Ali Nemati,
Volume 22, Issue 1 (3-2025)
Abstract
Hybrid asymmetric supercapacitors using distinct cathode/anode materials offer enhanced energy density by expanding operational potential windows compared to symmetric configurations. In this work rGO/α-Fe₂O₃ and rGO/TiO₂ nanocomposites were synthesized via hydrothermal method for hybrid asymmetric supercapacitors applications. Field emission scanning electron microscope (FESEM) revealed uniform distribution of spherical α-Fe₂O₃ and TiO₂ nanoparticles on rGO sheets. The X-ray diffractometry (XRD) analysis confirmed the presence of the hematite and anatase in the rGO/α-Fe2O3 and rGO/TiO2 nanocomposites, respectively. Additionally, in the XRD spectra of both nanocomposites, a broad peak corresponding to the (002) crystalline planes of rGO was observed. Electrochemical testing showed specific capacities of 130 F/g (rGO/α-Fe₂O₃) and 253 F/g (rGO/TiO₂) at 5 mV/s in 1M KOH. The assembled hybrid asymmetric supercapacitors (rGO/α-Fe₂O₃//rGO/TiO₂) achieved a 1.6 V operational potential window. Power density and energy density of 1066 W kg-1 and 9.7 Wh kg-1 were achieved at a current density of 1 A/g, respectively.
Mohammad Derakhshani, Saeed Rastegari, Ali Ghaffarinejad,
Volume 22, Issue 1 (3-2025)
Abstract
In this research, the morphology of the Ni-W coating was modified by adding graphene oxide (GO) nanosheets in such a way that a foam-like structure with high porosity and holes in the form of intertwined tunnels was obtained. Different amounts of GO nanosheets were added to the plating bath and the resulting coating was examined. In order to estimate the electrochemically active surface area, the cyclic voltammetry (CV) test was used. Moreover, the linear polarization test (LSV) and chronoamperometry in 1 M NaOH were conducted to investigate the electrocatalytic activity for the hydrogen evolution reaction (HER). It was found that by adding 0.4 g/L GO to the electroplating bath, the electrocatalytic properties are doubled and the active surface of the electrode is significantly increased.
Ali Keramatian, Mohammad Hossein Enayati, Fatemehsadat Sayyedan, Sima Torkian,
Volume 22, Issue 2 (6-2025)
Abstract
The aim of this study was to investigate the effect of current density on the microstructure of electrodeposited Ni–WC–TiC composite coatings on 304 stainless steel and compare the corrosion resistance of the coating and substrate in a 3.5 wt.% sodium chloride solution. A Watts nickel bath was employed under direct current (DC) conditions. Microstructure, elemental composition, and phase composition analyses were conducted using scanning electron microscopy (SEM) equipped with energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD), respectively. The results revealed that the coating formed at a current density of 40 mA/cm² exhibited a denser microstructure with higher cohesion and uniformity compared to coatings produced at other current densities. The corrosion resistance of the coating and substrate was evaluated using Tafel and electrochemical impedance spectroscopy (EIS) analyses. The corrosion test results indicated that the substrate exhibited superior corrosion resistance compared to the coating. Based on the dynamic polarization test plots, the corrosion mechanism of the substrate is active-quasi passive, with a pseudo-passive layer forming on the sample which remains stable within the potential range of -0.17 to 0.17 V. Beyond this potential range, the sample becomes susceptible to pitting. In the coated sample, the corrosion behavior is similar to that of the substrate, with the exception that the pseudo-passive layer remains stable within a narrower potential range of -0.19 to 0.08 V.
Nur Aziah Suhada Naim, Muhammad Faiq Abdullah, Sung Ting Sam, Wan Ahmad Radi Wan Ahmad Yaakub,
Volume 22, Issue 2 (6-2025)
Abstract
Despite being an effective material for food packaging, chitosan (CS) exhibited poor ductility when processed into film, which restricted its use in this industry. In this study, composite films with enhanced properties were developed by incorporating polyvinyl alcohol (PVA) into CS through a simple solution casting method. The effects of different PVA/CS weight ratios (70:30, 50:50, and 30:70 w/w) on the morphology, mechanical properties, antibacterial activity, and soil degradation of the composite films were analyzed. Compared to the pristine PVA film, increasing the CS content in the PVA/CS composite film enhanced thickness, stiffness, roughness, antibacterial efficiency, and degradation rate, while reducing tensile strength and elongation at break. Fourier transform infrared (FTIR) spectroscopy revealed the highest intermolecular interactions in the PVA/CS composite film with 70:30 w/w. Antibacterial activity tests and soil burial analysis demonstrated that the PVA:70/CS:30 composite exhibited significantly higher antibacterial activity toward Escherichia coli and Bacillus subtilis bacteria as opposed to PVA film, along with a moderate degradation rate of 76.76% following 30 days soil burial, effectively balancing biodegradability and material integrity. These findings suggest that the PVA:70/CS:30 composite is a promising alternative for sustainable and functional biodegradable packaging solutions.
Amin Rezaei Chekani, Malek Naderi, Reza Aliasgarian, Yousef Safaei-Naeini,
Volume 22, Issue 2 (6-2025)
Abstract
This paper presents the novel fabrication method of a three-dimensional orthogonally woven (3DW) C/C-SiC-ZrB2 composite and the effects of ZrB2 and SiC particles on microstructure and the ablation behavior of the C/C–SiC–ZrB2 composite are studied. C/C–SiC–ZrB2 composite was prepared by isothermal-chemical vapor infiltration (I-CVI), slurry infiltration (SI), and liquid silicon infiltration (LSI) combined process. Pyrolytic carbon (PyC) was first infused into the 3DW preform by I-CVI at 1050°C using CH4 as a precursor in order to form a C/C preform with porous media. The next step was graphitization at 2400°C for 1hr. Then ZrB2 was introduced into 3DW C/C preform with a void percentage of 48 by impregnating the mixture of ZrB2 and phenolic resin, followed by a pyrolysis step at 1050°C. A liquid Si alloy was infiltrated, at 1650 °C, into the 3DW C/C composites porous media containing the ZrB2 particles to form a SiC–ZrB2 matrix. An oxyacetylene torch flame was utilized to investigate The ablation behavior. ZrB2 particles, along with the SiC matrix situated between carbon fiber bundles, form a compact ZrO2-SiO2 layer. This layer acts as a barrier, restricting oxygen infiltration into the composite and reducing the erosion of carbon fibers. The findings were supported by FESEM imaging and further confirmed through x-ray diffraction and EDS analysis. The addition of ZrB2 to the C/C-SiC composite resulted in a lower mass and linear ablation rate; 2.20 mg/s and 1.4 µm/s respectively while those for C/C-SiC composite were 4.8 mg/s and 6.75 µm/s after ablation under an oxyacetylene flame (2500°C) for 120 s.
