Characterization and tribological behaviour of Indian clam seashell-derived hydroxyapatite coating applied on titanium alloy by plasma spray technique.

Various hydroxyapatite (HA) powders synthesized at different temperatures are deposited on titanium alloy by using an atmospheric plasma spray process. These different HA powders were synthesized from Indian clam seashells through the hydrothermal technique at varying temperatures from 700 to 1000 °C for a 2 h time duration in our previous study. The synthesized HA powders are spray-dried to obtain agglomerated powders suitable for spraying during the coating application. Crystallite size, Ca/P ratio, and crystallinity of agglomerated HA powders and their respective coatings are estimated by standard methods. The microstructure and phases of the feedstock and coating materials are investigated by using a field-emission scanning electron microscope (FESEM) and X-ray diffractometer (XRD), respectively. Further, the HA coatings are characterized in terms of surface roughness, microhardness, porosity, adhesion strength, and wear resistance through the stylus profilometer, Vickers micro-hardness tester, image analysis technique, scratch tester, and ball-on-disc tribometer, respectively. The average surface roughness (Ra) and porosity of the coating are decreased with an increase in the synthesis temperature. The minimum Ra and porosity obtained for the 1000 °C coating sample suggest a high degree of melting of such powder particles. However, the highest adhesion strength noticed in the case of the 900 °C coating sample is due to the high compatibility of such coating material with Ti-alloy substrate in terms of thermal properties. The 900 °C coating sample has also shown the highest microhardness and wear-resistance properties due to its maximum crystallinity among all the HA coatings.

Synthesis, column packing and liquid chromatography of molecularly imprinted polymers for the acid black 1, acid black 210, and acid Brown 703 dyes.

Molecularly imprinted polymers have been synthesized for the acid black 1, acid black 210, and acid brown 703 dyes using methacrylic acid, ethylene glycol, and azobisisobutyronitrile as the monomer, cross-linker, and initiator, respectively, in the ratio of 1 : 10 : 44 (template:monomer:cross-linker). The MIPs were used for the selective removal of their corresponding dyes. The selective nature of the MIPs towards their respective dyes was confirmed by a homemade liquid chromatography system. The resultant polymer materials were packed in a stainless steel column and checked for the separation of mixtures of dyes in liquid chromatography. The dyes complementary in structure to the imprinted cavities in the MIPs had long retention times, showing the highly selective nature of the MIPs. The pH, quantity of the MIPs, time, and concentration of the dyes were optimized for the highly efficient removal of the newly synthesized MIP adsorbents in batch adsorption studies. First-order, second-order, and intra-particle diffusion models were applied to all the three MIP-based adsorbents for their kinetic investigations towards the dyes. All the three MIPs selectively absorbed their target template molecule in the presence of four other template dyes having closely related structures with % RSD < 4% for the three batch experiments. The synthesized MIPs were characterized by FTIR, SEM imaging and liquid chromatography. FTIR results strongly confirmed the presence of hydrogen bonding interactions (600-900) between the template and the individual monomers present in the unwashed MIPs. Liquid chromatography revealed the highly selective nature of the MIPs towards their template molecules. The synthesized polymeric substances possess excellent thermal, chemical, and mechanical stability and can be reused several hundred times. The MIPs were applied in the removal of dyes from spiked water samples (river water, tap water and distilled water) where the % removal of the dyes by their corresponding MIPs was greater than 90%.