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Today, one of the major concerns of environmental health is the purification of colored wastewater due to its high contamination. The present study focused on the synthesis and comprehensive characterization of environmentally friendly electrospinning membranes based on Chitosan cross linked with SBA-15 as a novel adsorbent for dye removal. Unlike most micro structured adsorbents, CTS-SBA-15 nanofibers with their special properties such as density, porosity, high surface-to-volume ratio, small and layered structures, etc. have a very high adsorption capacity to remove macromolecular pollution and microorganisms. Adsorbents were synthesized and functionalized, then produced by electrospinning instrument in the form of nanofibers sheets. In this study, FT-IR, XRD, FE-SEM, TEM, and tensile tests were employed to characterize the functional groups, surface morphology and pore diameter distribution of nanofibers. The influence of different analytical parameters was investigated to obtain the optimum conditions for the adsorption process. The optimum conditions for adsorption process obtained as following type of adsorbent CTS-SBA-15-NH2, pH 2, adsorbent dosage 0.05 g, initial concentration 60 and 40 mg/l and contact time 40 min, which followed from the Langmuir and Freundlich isotherms. So, it was found that CTS-SBA-15 can act as inexpensive and efficient adsorbent for the dye removal from the contaminated water.The addition of biomaterials such as Calcium Hydroxyapatite (cHAp) and incorporation of porosity into poly-ether-ether-ketone (PEEK) are effective ways to improve bone-implant interfaces and osseointegration of PEEK composite. Hence, the morphological effects of nanocomposite on surfaces biocompatibility of a newly fabricated composite of PEEK polymer and cHAp for a bone implant, using additive manufacturing (AM) were investigated. Fused deposition modeling (FDM) method and a surface treatment strategy were employed to create a microporous scaffold. PEEK osteointegration was slow and, therefore, it was accelerated by surface coatings with the incorporation of bioactive cHAp, with enhanced mechanical and biological behaviors for bone implants. Characterization of the new PEEK/cHAp composite was done by X-ray diffraction (XRD), differential scanning calorimetry (DSC), mechanical tests of traction and flexion, thermal dynamic mechanical analysis (DMA). Also, the PEEK/cHAp induced the formation of apatite after immersion in the simulated body fluid of DMEM for differentdays to check its biological bioactivity for an implant. In-vivo results depicted that the osseointegration and the biological activity around the PEEK/cHAp composite were higher than that of PEEK. The increase in the mechanical performance of cHAp-coated PEEK can be attributed to the increase in the degree of crystallinity and accumulation of residual polymer.TPS/MA/PLA is a blend of thermoplastic starch (TPS) and polylactic acid (PLA) compatibilized by maleic anhydride (MA) that can be a substitute for petro-based plastics in certain applications. WRW4 At the end of its life, this material must be properly disposed in treatment systems such as composting or anaerobic digestion. The biodegradability of TPS/MA/PLA, PLA, TPS and the non-compatible mixture (TPS/PLA) was evaluated in a slurry thermophilic anaerobic digestion system (STAD) according to ISO 13975-2012 standard. The anaerobic inoculum was prepared from cow manure and the organic fraction of municipal solid waste. After 31 days of incubation, the pure PLA exhibited a 12-day lag phase and 40.41% of biodegradability. TPS, TPS/PLA and TPS/MA/PLA did not exhibit lag phase and reached 92.11%, 65.48% and 64.82% of biodegradation respectively. The slow degradation rate of PLA is attributed to its high glass transition temperature and crystallinity. In TPS/MA/PLA and TPS/PLA, about 50% of PLA and 13% to 10% of the TPS remains undegraded and MA did not affect the biodegradation of TPS/MA/PLA compared to TPS/PLA. Results suggest that, in very short retention times STAD systems, PLA based materials could not exhibit enough biodegradability.The NP flame retardant ammonium salt of hydroxyethyl hexahydrotristriazine-triphosphoric acid (AHTTPA) was prepared by a one-pot synthesis method under formaldehyde-free and solvent-free conditions. The AHTTPA was finished on the biomolecule of cotton by using the dip-roll-bake method. Nuclear magnetic resonance (NMR 1H, 13C, and 31P) demonstrated that AHTTPA was successfully synthesized. The flame retardancy of AHTTPA-treated cotton was studied by limiting oxygen index (LOI), vertical flaming test (VFT), scanning electron microscopy (SEM), and cone calorimetry (CC). The results from these tests indicate that AHTTPA-treated cotton exhibited favorable flame retardancy and durability (the LOI value of 40%-treated cotton after 50 laundering cycles (LCs) was 29.8%), the flame was immediately extinguished after removal from the treated cotton, no smoldering or continued burning, the burned part formed a complete carbon frame and generally maintained its original morphology, the peak heat release rate (PHRR) and total heat release (THR) of AHTTPA-treated cotton fabric were significantly lower than pure cotton. Thermogravimetric analysis (TGA) results showed that AHTTPA improved the thermal stability of cotton. The breaking strength and softness of AHTTPA-treated cotton was also retained.The present research work was designed to develop dorzolamide-loaded chitosan-coated polycaprolactone nanoparticles (DRZ-CS-PCL-NPs) for improved ocular delivery. The nanoparticles were prepared by single-step emulsification technique and optimized using the three-factor three-level Box-Behnken design. The optimized DRZ-CS-PCL-NPs prepared with the composition of polycaprolactone (60 mg), chitosan (0.6%) and polyvinyl alcohol (1.5%). The particle size, polydispersity index, zeta potential and encapsulation efficiency of optimized DRZ-CS-PCL-NPs were found to be 192.38 ± 6.42 nm, 0.18 ± 0.04, +5.21 ± 1.24 mV, and 72.48 ± 5.62%, respectively. The dependent and independent response variables showed excellent correlation and signifying the rationality of the optimized DRZ-CS-PCL-NPs. The DRZ release from CS-PCL-NPs showed biphasic behaviour with initial burst release for 2 h after that sustained-release up to 12 h of study. The corneal flux experiment showed many fold enhancement in permeation across goat cornea.
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