Showing 484 results for in
Adeel Hassan,
Volume 20, Issue 4 (12-2023)
Abstract
Friction stir additive manufacturing (FSAM) is a variant of sheet lamination additive manufacturing used to produce large, near-net-shaped 3D parts. Unlike traditional friction stir lap welding, FSAM introduces a new plate to one that is already joined, with the effective area limited to the nugget zone. The present study focuses on exploring the microstructure and microhardness around the nugget zone in a five-plate AA 7075-T651 laminate synthesized at 1000 rpm and 35 mm/min. Microhardness increased vertically in the weldment NZ, reaching 143 HV in the top layer with 2.0 μm fine equiaxed grains. The grains on the advancing and retreating sides were coarser compared to the nugget zone. A W-shaped microhardness profile appeared across layer interfaces. These findings contribute significantly to advancing the FSAM technique, particularly in manufacturing multi-layered, multi-pass laminates.
Leila Taghi-Akbari, Mohammad Reza Naimi-Jamal, Shervin Ahmadi,
Volume 20, Issue 4 (12-2023)
Abstract
Two-dimensional molybdenum disulfide (MoS2) is used as a promising flame retardant and smoke suppressant nano additive in polymer composites due to its high thermal stability and layered structure. In this study, thermoplastic polyurethane (TPU) was melt-blended with MoS2 (1wt. %) and a halogen-free intumescent flame retardant (IFR) system. The IFR system consisted of ammonium polyphosphate (APP), Melamine polyphosphate (MPP), and pentaerythritol (PER), with a total amount of 25 wt. %. The TPU/IFR/MoS2 composite exhibited outstanding flame-retardant properties, achieving a UL-94 V-0 rating and a limiting oxygen index (LOI) value of 34%. Reaction-to-fire performance of the TPU/IFR/MoS2 composite was evaluated by cone calorimeter test (CCT). The CCT results indicated high flame-retardant efficiency and considerable smoke suppression performance, along with a significant decrease in the peak heat release rate (PHRR: 65.9%), peak smoke production rate (PSPR: 65.6%), and peak CO production (PCOP: 60.7%) compared to the neat TPU. The significant improvement in fire performance of TPU composite was mainly attributed to the effects of the physical barrier of MoS2 and catalytic carbonization of the IFR system. These resulted in forming an intumescent compact carbonized layer during the combustion, effectively restricting dripping. The continuous structure of the residual char was revealed by FESEM. Thermogravimetric analysis (TGA) indicated improved thermal behavior of the TPU composite in high temperatures. This work provides an effective method to improve the reaction to fire of TPU composites by incorporating traditional IFRs and MoS2, resulting in enhanced fire safety.
Sara Ahmadi, Reza Momeni,
Volume 20, Issue 4 (12-2023)
Abstract
The polymer modified cementitious tile adhesives are very significant in construction sector. In order to considerably improve the bond qualities of the tile adhesive in polymer modified mortars, the proportions of constituent ingredients should be carefully selected. Consequently, to design high performance tile adhesives, interactions between all the components, such as the adhesion mechanisms between the polymers film and the substrate and the effect of various additives should be recognized. The effect of vinyl acetate ethylene (EVA), high alumina cement (HAC), and additives such as calcium formate and polycarboxylate on the adhesion qualities of ceramic tile adhesive was explored in this study. The findings indicated that these ingredients had an impact on the mortars' adhesive properties, and it is necessary to find their optimal amounts in order to achieve the maximum adherence. The results showed that the tensile strength of mortar was increased with increasing the polymer amounts. A microstructural analysis revealed that the polymer was distributed homogenously throughout the mortar. The optimum amount of the used high alumina cement was determined 3 wt.%. Additionally, increasing the amount of accelerator and super plasticizer increased the tensile strength of ceramic tile adhesive by approximately 20-30%.
Ahmed Hafedh Mohammed Mohammed, Khairul Anuar Bin Shariff, Mohamad Hafizi Abu Bakar,
Volume 20, Issue 4 (12-2023)
Abstract
The coated β-tricalcium phosphate (β-TCP) with dicalcium phosphate dihydrate (DCPD) has attracted much attention in the biomaterials field due to the increase in its osteoconductivity. Besides, the porous bioceramic scaffolds with controlled pore sizes are significant in stimulating bone-like cell activity. In this study, the effect of the setting-time process and acidic-calcium phosphate (CaP) concentrations on the fabrication and properties of porous DCPD/ β-TCP scaffolds were studied. Subsequently, the specimens were examined using X-ray diffraction (XRD), scanning electron microscopy (SEM), compression strength and Fourier transforms infrared (FTIR). The study results revealed that the porous DCPD/ β-TCP scaffolds with macro- and micropore sizes were successfully obtained after the 300-600 µm of porous β-TCP granules were exposed to an acidic-CaP solution. Furthermore, the setting-time process and acidic-CaP concentrations increased the DCPD interlocking between granules, and the mechanical strengths of scaffolds increased up to 0.5 MPa. Meanwhile, the porosity levels were changed based on the formation of DCPD crystals. This study was expected to provide novel insights to researchers in the field of bioceramics through its investigation on the creation of porous DCPD/ β-TCP scaffolds.
Seyed Mohammad Mirghasemi, Ehsan Mohammad Sahrifi, Gholam Hossein Borhani, Mirtaher Seyed Beigi,
Volume 21, Issue 0 (3-2024)
Abstract
In this study, the hot deformation and dynamic recrystallization behavior of low carbon steel containing 21 ppm boron was investigated. After homogenizing the samples at 1250 ℃ for 1-hour, hot compression tests were conducted at temperatures ranging from 850 ℃ to 1150 ℃ and strain rates from 0.01 to 10 s⁻¹, resulting in strain-stress flow curves. Following corrections, calculations and modeling were performed based on Arrhenius equations. Among them, the hyperbolic sine relationship provided the most accurate estimate and was selected as the valid model for the applied strain range. According to this model, the deformation activation energy (Q), was determined to be 293.37 KJ/mol. Additionally, critical and peak stress and strain values were obtained for each temperature and strain rate, and power relationships were established to describe their variation with respect to the Zener-Hollomon parameter (Z). Recrystallization fractions were derived by comparing the hypothetical recovery curves with the material flow curves, and the results were successfully modeled using the Kolmogorov-Johnson-Mehl-Avrami (KJMA) equation. The Avrami exponent was measured at approximately 2, indicating that nucleation predominantly occurred at grain boundaries. Microstructural analysis revealed that at higher Z values, recrystallization occurred along with a fraction of elongated grains, while lower Z values resulted in a greater fraction of equiaxed dynamic recrystallization (DRX) grains. The average grain sizes after compression tests at 950 ℃, 1050 ℃, and 1150 ℃ were measured as 21.9 µm, 30.4 µm, and 33.6 µm respectively at a strain rate of 0.1 s⁻¹, and 17.7 µm, 28.7 µm, and 31.3 µm at 1 s⁻¹. The overall microstructure displayed a more uniform grain size distribution with increasing deformation temperature.
Tanaji Patil, S M Nikam, R S Kamble, Rahul Patil, Mansing Takale, Satish Gangawane,
Volume 21, Issue 1 (3-2024)
Abstract
The trimanganese tetraoxide (Mn3O4) nanostructured thin films doped with 2 mol % of nickel (Ni) and molybdenum (Mo) ions were deposited by a simple electrophoretic deposition technique. The structural, optical, and morphological studies of these doped thin films were compared with pure Mn3O4 thin films. X-ray diffraction (XRD) confirmed the tetragonal Hausmannite spinel structure. The Fourier transform infrared spectroscopy (FTIR) provided information about the molecular composition of the thin films and the presence of specific chemical bonds. The optical study and band gap energy values of all thin films were evaluated by the UV visible spectroscopy technique. The scanning electron microscopy (SEM) illustrated the morphological modifications of the Mn3O4 thin films due to doping of the nickel and molybdenum ions. The Brunauer Emmett Teller (BET) method has confirmed the mesoporous nanostructure and nanopores of the thin films. The supercapacitive performance of the thin films was studied by cyclic voltammetry (CV), and galvanostatic charge discharge (GCD) techniques using the three-electrode arrangement. An aqueous 1M Na2SO4 electrolyte was used for the electrochemical study. The 2 mol % Ni doped Mn3O4 thin film has shown maximum specific capacitance than pure and Mo doped Mn3O4 thin films. Hence, this study proved the validity of the strategy - metal ion doping of Mn3O4 thin films to develop it as a potential candidate for electrode material in the futuristic energy storage and transportation devices.
Samrat Mane,
Volume 21, Issue 1 (3-2024)
Abstract
In this research work, Cadmium Sulphide thin film deposited on to glass substrate in a non-aqueous medium at 80 °C. The various physical preparative parameters and the deposition conditions, such as the deposition time and temperature, concentrations of the chemical species, pH, speed of mechanical stirring, etc., were optimized to yield good quality films. The as-prepared sample is tightly adherent to the substrate's support, less smooth, diffusely reflecting and was analyzed for composition. The synthesized film is characterized using X- ray diffraction (XRD), electrical and optical properties. It appears that the composites are rich in Cd. The grown CdS thin film had an orange-red color. A band gap of CdS thin film is 2.41 eV. The average crystallite size of the CdS film was 21.50 nm. The resistivity of the CdS thin film is about 5.212 x 105 W cm.
Amit Bandekar, Pravin Tirmali, Paresh Gaikar, Shriniwas Kulkarni, Nana Pradhan,
Volume 21, Issue 1 (3-2024)
Abstract
The Mn-Zn ferrite with a composition of Mn0.25Mg0.08Cu0.25Zn0.42Fe2O4 has been synthesized in this study using the chemical sol-gel technique at a pH of 7. The sample was prepared and subsequently annealed at a temperature of 700°C. The nanocrystalline ferrite samples were subjected to characterization using X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), Thermogravimetry (TG), and Differential thermal analysis (DTA). The findings of these observations are delineated and deliberated. The sample's phase composition was verified using X-ray diffraction examination. The crystalline size was determined using Scherrer's formula and was observed to be within the range of 20-75 nm. Two notable stretching bands were seen in the FTIR spectra within the range of 400-650 cm-1. The spinel structure of the produced nanoparticles was confirmed by these two bands. The magnetic characteristics of the powder were examined using a Vibrating Sample Magnetometer (VSM). The presence of M-H hysteresis loops suggests that the produced nanoparticles have superparamagnetic properties, as evidenced by their low coercive force, remanent magnetization, and saturation magnetization values.
Sandesh Jirage, Kishor Gaikwad, Prakash Chavan, Sadashiv Kamble,
Volume 21, Issue 1 (3-2024)
Abstract
The Cu2ZnSnS4 (CZTS) thin film is newly emerging semiconductor material in thin film solar cell industry. The CZTS composed of economical, common earth abundant elements. It has advantageous properties like high absorption coefficient and best band gap. Here we have applied low cost chemical bath deposition technique for synthesis of CZTS at low temperature, acidic medium and it’s characterization. The films were characterized by different techaniques like X-Ray diffraction, Raman, SEM, Optical absorbance, electrical conductivity and PEC study. The X-Ray diffraction, Raman scattering techniques utilized for structural study. The XRD revels kasterite phase and nanocrystalline nature of CZTS thin films. These results and its purity confirmed further by advanced Raman spectroscopy with 335 cm-1 major peak. The crystallite size which was found to be 50.19 nm. The optical absorbance study carried by use of UV-Visible spectroscopy analyses its band gap near about 1.5 eV and its direct type of absorption. The electrical conductivity technique gives p-type of conductivity. The scanning electron microscopy (SEM) study finds it’s rock like unique morphology. The EDS technique confirms its elemental composition and it’s fair stoichiometry. The analysis of PEC data revealed power conversion efficiency-PCE to 0.90%.
The Cu2ZnSnS4 (CZTS) thin film is newly emerging semiconductor material in thin film solar cell industry. The CZTS composed of economical, common earth abundant elements. It has advantageous properties like high absorption coefficient and best band gap. Here we have applied low cost chemical bath deposition technique for synthesis of CZTS at low temperature, acidic medium and it’s characterization. The films were characterized by different techaniques like X-Ray diffraction, Raman, SEM, Optical absorbance, electrical conductivity and PEC study. The X-Ray diffraction, Raman scattering techniques utilized for structural study. The XRD revels kasterite phase and nanocrystalline nature of CZTS thin films. These results and its purity confirmed further by advanced Raman spectroscopy with 335 cm-1 major peak. The crystallite size which was found to be 50.19 nm. The optical absorbance study carried by use of UV-Visible spectroscopy analyses its band gap near about 1.5 eV and its direct type of absorption. The electrical conductivity technique gives p-type of conductivity. The scanning electron microscopy (SEM) study finds it’s rock like unique morphology. The EDS technique confirms its elemental composition and it’s fair stoichiometry. The analysis of PEC data revealed power conversion efficiency-PCE to 0.90%.
Mohammad Derakhshani, Saeed Rastegari, Ali Ghaffarinejad,
Volume 21, Issue 2 (6-2024)
Abstract
In this research, a nickel-tungsten coating as a catalyst for hydrogen evolution reaction (HER) with different current densities was synthesized and the resulting electrocatalytic properties and morphology were assessed. Linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS), and chronoamperometry in 1 M NaOH were used to evaluate the electrocatalytic activity for HER. By increasing the current density of electrodeposition up to 500 mA/cm2, a columnar morphology was observed. The cyclic voltammetry test (CV) revealed that when the plating current density increases, Cdl has increased from 248 to 1310 µF/cm2 and the active surface area increases 5 times. The results showed that by modifying the coating morphology, the current density of the hydrogen evolution increased up to two times.
Seyed Farzad Dehghaniyan, Shahriar Sharafi,
Volume 21, Issue 2 (6-2024)
Abstract
Mechanical alloying was employed to synthesize a nanostructured alloy with the chemical formula of (Fe80Ni20)1-xCrx (x= 0, 4). The microstructural and magnetic properties of the samples were investigated using scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), and a vibrating sample magnetometer (VSM). Additionally, theoretical calculations were performed using density functional theory (DFT) under the generalized gradient approximation (GGA). Simulations have demonstrated that an appropriate quantity of chromium (Cr) can dissolve within the BCC-Fe (Ni) structure, resulting in a favorable enhancement of the magnetic moment of the lattice. The XRD results indicated that after 96 hours of milling, Fe (Ni) and Fe (Ni, Cr) with a body-centered cubic (BCC) structure were formed. With increasing milling time, the grain size decreased while the microstrain increased. The saturation magnetization (Ms) of Fe80Ni20 composition increased up to 32 hours of milling, but further milling (up to 96 h) resulted in a decrease in the saturation magnetization However, for the (Fe80Ni20)96Cr4 powders, milling up to 64 h caused a reduction in Ms. The coercivity (Hc) trend was different and increased with longer milling times (up to 96 h) for both compositions.
Rakhesh V, Sreedev P, Ananthakrishnan A,
Volume 21, Issue 2 (6-2024)
Abstract
Organic and Perovskite solar cells have attracted a lot of attention recently since they can be used with flexible substrates and have lower manufacturing costs. The configuration and materials employed in their construction, including the Electron Transport Layer (ETL), active layer, electrode contact, and hole transport layer greatly influence the stability and performance of these solar cells. This research focuses on the simulation of solar cells, specifically utilizing zinc oxide (ZnO) as the electron transport layer. A 0.1 molar ZnO thin film was prepared from Zinc acetate salt and was deposited on a glass substrate using the cost effective Successive Ionic Layer Adsorption and Reaction (SILAR) method. In-depth investigations were carried out on several factors, including structural, surface, optical and numerical analysis. The obtained parameters were utilized in the General-Purpose Photovoltaic Device Model (GPVDM) software to perform numerical simulations of the organic solar cell and Perovskite solar cell. Both Organic solar cells and Perovskite solar cells were designed numerically and through careful observations, electrical parameters like Open circuit Voltage (Voc), Short circuit current (Jsc), Fill Factor (FF), and Power Conversion Efficiency (PCE) were identified. The studies indicate the promising performance of simulated solar cells with SILAR-synthesized ZnO thin film as the ETL.
Padmanaban Ramasamy,
Volume 21, Issue 2 (6-2024)
Abstract
The present investigation delves into the friction stir welding of AA5052 and AZ31B alloys, examining the effects of three distinct parameter configurations. A face-centered central composite design, structured to incorporate full replications for comprehensive and reliable analysis, was employed. A pivotal element of this study is implementing an advanced deep neural network (DNN) model. Characterized by its varied activation functions, structural parameters, and training algorithms, this DNN model was adeptly configured to precisely predict the tensile strength and microhardness of the welded joints. This comprehensive examination also included a quantitative assessment of the parameter effects on joint microstructure and mechanical properties. Flawless welds with exemplary surface characteristics were attained through a meticulously optimized set of parameters: a tool rotation speed set at 825 rpm, a tool traverse speed of 15 mm/min, and a shoulder diameter of 18 mm. During the welding process, the formation of intermetallic compounds, specifically Al12Mg17 and Al3Mg2, was observed. An exceptionally refined grain size of 2.23 µm was observed in the stir zone, contributing to the joint's enhanced tensile strength, measured at 180 MPa. The hardness of the specimen fabricated at the high rotational speed is more elevated due to the brittle intermetallic compounds. The better mechanical properties are related to the reduction and distribution of intermetallic compounds formed in the interface zone.
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.
Ahad Saeidi, Sara Banijamali, Mojgan Heydari,
Volume 21, Issue 2 (6-2024)
Abstract
This study explores the fabrication, structural analysis, and cytocompatibility of cobalt-doped bioactive glass scaffolds for potential applications in bone tissue engineering. A specific glass composition modified from Hench's original formulation was melted, quenched, and ground to an average particle size of 10 μm. The resulting amorphous powder underwent controlled sintering to form green bodies and was extensively characterized using simultaneous differential thermal analysis (DTA), Raman spectroscopy, and Fourier Transform Infrared analysis (FTIR). After mixing with a resin and a dispersant, the composite was used in digital light processing (DLP) 3D printing to construct scaffolds with interconnected macropores. Thermal post-treatment of 3D printed scaffolds, including debinding (Removing the binder that used for shaping) and sintering, was optimized based on thermogravimetric analysis (TG) and the microstructure was examined using FE-SEM and XRD. In vitro bioactivity was assessed by immersion in simulated body fluid (SBF), while cytocompatibility with MC3T3 cells was evaluated through SEM following a series of ethanol dehydrations. The study validates the fabrication of bioactive glass scaffolds with recognized structural and morphological properties, establishing the effects of cobalt doping on glass behavior and its implications for tissue engineering scaffolds. Results show, Low cobalt levels modify the glass network and reduce its Tg to 529 oC, while higher concentrations enhance the structure in point of its connectivity. XRD results shows all prepared glasses are amorphous nature, and DTA suggests a concentration-dependent Tg relationship. Spectroscopy indicates potential Si-O-Co bonding and effects on SiO2 polymerization. Cobalt's nucleating role promotes crystalline phases, enhancing bioactivity seen in rapid CHA layer formation in SBF, advancing the prospects for bone tissue engineering materials.
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.
Ramin Dehghani, Seyed Mojtaba Zebarjad,
Volume 21, Issue 3 (9-2024)
Abstract
Acrylic resins are one of the most important thermoplastic resins used in various industries due to their significant properties. However, they are inherently brittle and addition plasticizers to them is very common. In this study, role of both Polyethylene Glycol (PEG) and Triacetin on the mechanical properties of acrylic resin have been investigated. To do so tensile test, bending and wear tests have been performed. To achieve the optimal mixture of plasticizers, a tensile test has been carried out, and the best percentage of the mixture has been determined. Subsequently, bending and wear tests were conducted, which showed a significant increase in the bending strength of the acrylic resin after the addition of plasticizers. Furthermore, it was found that the abrasion mechanism of the resin was significantly altered compared to its pure state.
Ghada Ben Salah,
Volume 21, Issue 3 (9-2024)
Abstract
This study reported the biological changes occurring after γ-irradiation of in vivo rat model and the osteochondral protective effect of Gelatine-Chitosan-Ginger (GEL-CH-GING). The results showed that Electron Paramagnetic Resonance (EPR) Spectroscopy of GEL-CH-GING showed two paramagnetic centres which correspond to g=2.19 and g= 2.002. The Fourier transform infrared spectroscopy (FTIR) analyses revealed an increase in peak intensity at C–H chains, as well as, C=O carbonyl groups. The X-ray diffraction (XRD) analysis showed no change of crystallinity. After gamma ray exposure, the rat groups have received an osteochondral defect and then were treated with GEL-CH-GING composite. Sixty days post-surgery, a significant reduction in thiobarbituric acid-reactive compounds (TBARs) was seen when compared to non-implanted rat group. Concerning oxidative stress status, GEL-CH-GIN significantly improved Superoxide Dismutase (SOD) 76 nmol/l, Catalase (CAT) 0.79 nmol/l, and Glutathione Peroxidase (GPx) 1.77 nmol/l activities in osteochondral tissue. Regarding the histomorphometric parameters of cartilaginous tissue (nCg.Th, µm), (cCg.Th, µm), (Cg.Th, µm), irradiated-GEL-CH-GIN group showed a significant increase as compared to irradiated group with 116, 74 and 188 µm, respectively (p<0.01). The microanalysis showed a high percentage of O and C in the regenertaed osteochondral tissue and indicated the deposition of novel collagen matrix. The biomechanical behaviour showed a significantly enhanced hardness measurement (1.73±0 .029 VH, p<0.05) when compared with that of irradiated group
Biochemical markers suggested an osteocartilage repair capacity. In fact, the levels of IL-1β, IL-6, TNF-α and VEGF in the implanted rat with GEL-CH-GING composite exhibited 51±3.48, 30.05±5.18, 65.12±4.33 and 40.42±3.32 ng/l, respectively. Our findings suggested that GEL-CH-GING composite might have promising potential applications for cartilage healing.
Dewi Qurrota A'yuni, Hadiantono Hadiantono, Velny Velny, Agus Subagio, Moh. Djaeni, Nandang Mufti,
Volume 21, Issue 3 (9-2024)
Abstract
Rice husk carbon by-product from the industrial combustion is a promising source to produce a vast amount of activated carbon adsorbent. This research prepared rice husk-activated carbon adsorbent by varying the concentration of potassium hydroxide solution (5, 10, 15, 20 % w/v) and activation time (2, 4, 6, 8 hours). Fourier-transform infrared spectral characterization (FTIR) indicated a significant effect before and after activation, especially the presence of hydroxyl groups. Based on the iodine adsorption, the specific surface area of the produced-activated carbon was approximately 615 m2/g. Experimental results showed that increasing potassium hydroxide concentration and activation time increases the water vapor adsorption capacity of the activated carbon. Compared with the rice husk carbon, the KOH-activated carbon enhanced the water vapor adsorption capacity to 931%. In the adsorption observation, changing the temperature from 15 to 27 ℃ caused a higher water vapor uptake onto the activated carbon. Two adsorption kinetics (pseudo-first- and pseudo-second-order models) were used to evaluate the adsorption mechanism. This research found that rice husk-activated carbon performed a higher water vapor adsorption capacity than other adsorbents (silica gel, zeolite, and commercially activated carbon).
Muddukrishnaiah Kotakonda, Sajisha V.s, Aiswarya G, Safeela Nasrin Pakkiyan, Najamol A Alungal, Mayoora Kiliyankandi K, Divya Thekke Kareth, Naheeda Ashraf Verali Parambil, Saranya Sasi Mohan, Renjini Anil Sheeba, Sarika Puthiya Veettil, Dhanish Joseph, Nishad Kakkattummal, Afsal Bin Haleem Mp, Safeera Mayyeri, Thasneem Chemban Koyilott, Nasiya Nalakath, Samuel Thavamani B, Famila Rani J, Aruna Periyasamy, Chellappa V Rajesh, Rameswari Shanmugam, Marimuthu Poornima, Tina Raju, Roshni E R, Sirajudheen Mukriyan Kallungal, Lekshmi Ms Panicker, Saranya K G, Shilpa V P,
Volume 21, Issue 3 (9-2024)
Abstract
Biogenic synthesis of papain-conjugated copper metallic Nanoparticles and their antibacterial and antifungal activities Papain metallic conjugated nanoparticles (Papain-CuNPs) were synthesised using Papain and CuSO4.5H2O. Papain-CuNPs were characterized using UV-visible spectroscopy, FT-IR, HR-TEM, XRD, FE-SEM, zeta potential, and a zeta sizer. The antibacterial activity of papain-CuNPs against human infectious microorganisms (Citrobacter spp, Pseudomonas aeruginosa and Candida albicans) was investigated. The mechanism of action of papain-CuNPs was evaluated using FE-SEM and HRTM. UV spectroscopy confirmed the plasma resonance (SPR) at 679 nm, which indicated the formation of papain-CuNPs. The FT-IR spectrum absorbance peaks at 3927, 3865, 3842, 3363, 2978, and 2900 cm-1 indicate the presence of O-H and N-H of the secondary amine, and peaks at 1643 and 1572 cm-1 represent C=O functional groups in Papain-CuNPs. EDAX analysis confirmed the presence of copper in the papain-CuNPs. The zeta potential (-42.6 mV) and zeta size (99.66 d. nm) confirmed the stability and size of the nanoparticles. XRD confirmed the crystalline nature of the papain-CuNPs. FE-SEM and HRTM showed an oval structure, and the nano particles' 16.71244–34.84793 nm. The synthesized papain-NPs showed significant antibacterial activity against clinical P. aeruginosa (15 mm). MIC 125 µg/ml) showed bactericidal activity against P. aeruginosa and the mechanism of action of Papain-NPs was confirmed using an electron microscope by observing cell damage and cell shrinking. Papain-CuNPs have significant antibacterial activity and are thus used in the treatment of P. aeruginosa infections
