A comparative study on in vitro behavior of calcium silicate ceramics synthesized from biowaste resources

Calcium silicate ceramics have received significant attention for biomedical applications for their excellent bioactivity and osteoconduction properties. Sol-gel process is extensively used for the fabrication of calcium silicates. In sol-gel process, calcium nitrate tetra hydrate (Ca(NO₃)₂·4H₂O) and tetraethylorthosilicate (TEOS) are used as precursors. However, these precursors are expensive. The objective of this work was to compare in vitro behavior of calcium silicate (CaSiO₃) produced using biowaste such as rice husk ash (RHA) and eggshells (coded; NCS) with CaSiO₃ prepared using TEOS and Ca(NO₃)₂·4H₂O (coded; CCS). Thermal investigation results revealed that the crystallization temperature for NCS is relatively lower (772°C) than for CCS (870°C). Bioactivity was studied in vitro using simulated body fluid (SBF) with respect to mineralization rate of hydroxyapatite. Mineralization of a greater hydroxyapatite was observed on NCS ceramics than CCS ceramics after incubation for 3, 7, 14 days in SBF solution, which was confirmed using X-ray diffractometer, Fourier transform infrared spectroscopy, scanning electron microscopy-energy dispersive spectroscopy. Degradation studies were conducted in Tris-HCl solution and the test results revealed that NCS ceramics has lower dissolution rate than CCS ceramics. The antimicrobial assay has shown that NCS samples exhibit significant zone of inhibition against Escherichia coli and Staphylococcus aureus which confirmed that the CaSiO₃ prepared from RHA and eggshell can prevent bacteria from adhering to the surface. In addition cell culture studies revealed that NCS ceramics possess good cytocompatibility with MG-63 cells and significantly promoted cell proliferation.     

Simulation Based Investigation of Triple Heterojunction TFET (THJ-TFET) for Low Power Applications

Silicon - We designed a new model tunnel field-effect transistor (TFET) based on Triple Heterojunction Tunnel Field Effect Transistor (THJ-TFET) is investigated and designed in this paper. This...     

Properties of ligno‐cellulose fiber Hildegardia

Studies on some properties such as the density, the degradation temperatures, the morphology and the spectral features of the ligno‐cellulose fiber Hildegardia were carried out in both untreated and alkali treated form. The fibers are found to have good morphology and moderate initial and final degradation temperatures. On alkali treatment, the lignin was found to be eliminated. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2216–2221, 2002     

Synthesis, Characterization and Photocatalytic Activity of Titania Loaded Cd-MCM-41

Catalysts consisting of cadmium incorporated into MCM-41 mesoporous molecular sieves (Cd-MCM-41) with Si/Cd = 80 have been synthesized by the hydrothermal method using cadmium acetate as the source of cadmium. This was then loaded with titania via the sol-gel method to explore the photoactivity in UV light. These two materials were characterized by various physicochemical techniques such as N₂ physisorption, O₂ chemisorption, diffuse reflectance UV-vis, X-ray diffraction (XRD), Raman and X-ray photoelectron spectroscopy (XPS). The pore size of the Cd-MCM-41 was higher and the BET surface area was lower than those commonly found in our siliceous MCM-41. This is due to the partial pore breakage, as recorded by pore size distribution analysis. The oxygen chemisorption results shows that the dispersion of cadmium is quite high, and decreased after loading of titania. The XRD patterns of Cd-MCM-41 and 25%TiO₂/Cd-MCM-41 are similar to those of siliceous MCM-41; however, the intensity of the d ₁₀₀ peak is decreased and the unit-cell parameter increased with titania loading. Raman spectra could not detect any peaks, whereas peaks were detected at 144, 397, 518 and 641 cm_-1 with loading of titania, these peaks being associated with the anatase phase of titania. The surface composition and binding energy of the Cd 3d_5/2 peak for Cd-MCM-41 and 25%TiO₂/Cd-MCM-41 was analyzed by XPS and showed considerable infusion of cadmium ions on to the surface upon loading of titania. The Cd/Si surface atomic ratio measured by XPS increases 10 times with loading of titania on Cd-MCM-41, indicating that the two separate surface electronic levels such as Cd-O-Si and Cd-O-Ti were found for 25%TiO₂/Cd-MCM-41. The 25%TiO₂/Cd-MCM-41 showed higher activity than 25%TiO₂/MCM-41 for photocatalytic degradation of formic acid. The activity results are compared with the pure titania based on the transformation per site of Ti.     

Flame-retardant PVC compound for cable applications

The low-melting ternary sulfate and modified sulfate glasses based on transition metals like copper, nickel, and vanadium reduce the smoke generation during burning of the PVC compound. With increase in concentration of these glasses, the smoke-density rating values decrease without appreciably altering the oxygen index values. Although trihydrated alumina and potash alum improve flame-retarding properties, the latter cannot be used as it considerably reduces the thermal stability of the PVC compound. Formulations to meet the flame-retardant requirements of a PVC compound suitable for cable sheathing have been developed.     

A study on the effect of new cyanate and phenoxy polymer on TGDDM/DDS/GMP formulations

An attempt was made on the modification of the tetraglycidyl‐4,4′‐diaminodiphenyl methane/diaminodiphenyl sulfone (TGDDM/DDS) system to improve properties for several industrial applications. Epoxy resins [TGDDM and 1‐glycidyloxy‐4‐methoxy phenol (GMP)] were synthesized in the laboratory. Also, a new cyanate ester and phenoxy polymer were synthesized and characterized by FTIR, ¹H‐/¹³C‐NMR, and thermal studies. GMP was added as a diluent and a new cyanate ester (DCDPT) was introduced to reduce the tight crosslinking density. Further, a new phenoxy polymer was added to improve the toughness property. A variety of neat resin casts using different compositions of the blends were made and their physical, chemical, thermal, and mechanical properties were evaluated to study the effect of GMP as a diluent, cyanate ester as a comonomer, and phenoxy polymer as a toughener. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2963–2973, 2003     

Visible‐light‐induced controlled/living radical polymerization of styrene with a phenyl seleno group at one terminal chain end: 1‐(Phenylseleno)ethyl benzene as a photoiniferter

The photopolymerization of styrene with a well‐defined molecular architecture and a low polydispersity index and with methyl and phenylseleno (? SePh) groups at α‐ and ω‐chain ends, respectively, was performed via a controlled/living radical polymerization with a new initiating system, 1‐(phenylseleno)ethyl benzene/tert‐butyl diphenyl (phenylseleno) silane, through the absorption of visible light at room temperature. A novel initiating living radical polymerization was examined. The yield and number‐average molecular weight (M_n) of the resulting polymer increased with the reaction time. Furthermore, a linear relationship was found in a plot of M_n versus the polymer yield. These results indicated that this polymerization proceeded through a living radical mechanism. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 348–355, 2004     

Recovery of deuterium from hydrogen–deuterium mixture using palladium

The applicability of palladium for the separation of hydrogen isotopes (hydrogen and deuterium) is evaluated systematically by generating isotherm data and conducting column experiments in a laboratory set-up. Effect of various parameters such as concentration of the isotopic mixture, particle size, eluent flow rate, etc. is studied experimentally. A fixed-bed chromatographic model is developed and validated using the experimental data. The model is further used to predict the performance of a multi-column configuration for large-scale separation. Chromatographic separation is thus found to be a promising technique to achieve the required purity and hence it may be clubbed with the existing systems (e.g. cryogenic distillation) to obtain enhanced performance.     

HEAT TRANSFER IN A THIN LIQUID FILM IN THE PRESENCE OF AN ELECTRIC FIELD

Heat transfer enhancement in an evaporating thin liquid film utilizing a electric field under isothermal interfacial condition is presented. A new mathematical model subjected to van der Waals attractive forces, capillary pressure, and an electric field is developed to describe the heat transfer enhancement in the evaporating thin liquid film. The effect of the electrostatic field on the curvature of the thin film, evaporative flux, pressure gradient distribution, heat flux, and heat transfer coefficient in the thin film is presented. The results show that applying an electric field can enhance heat transfer in a thin liquid film significantly. In addition, utilizing electric fields on the evaporating film will be a way to expand the extended meniscus region to attain high heat transfer coefficients and high rates of heat flux.     

Photocatalytic,magnetic, and electrochemical properties of La doped BiFeO3 nanoparticles

We successfully prepared La_1?xBi_xFeO₃ (L_xB_1?xFO, x?=?0.01–0.1) nanoparticles using a sol-gel technique, and studied their photocatalytic, magnetic, and electrochemical properties. Structural refinement studies of the prepared nanoparticles revealed a gradual structural transition from rhombohedral to orthorhombic. The average grain size was observed to decrease with increasing the concentration of La. The photocatalytic degradation of Rhodamine B (RhB) in the presence of the prepared nanoparticles was studied under visible light irradiation. The L_0.06B_0.94FO nanoparticles showed higher degradation efficiency compared to pure BiFeO₃ (BFO) nanoparticles. Magnetic studies showed that La doping improved the magnetization of BFO due to the reduction in grain size and destruction of cycloid coupling of spins. Higher specific capacitance values were obtained for La doped BFO (LBFO) nanoparticles compared to BFO nanoparticles. A maximum specific capacitance of 219?F?g^?1 was obtained at a current density of 1?A?g^?1 for LBFO nanoparticles.