No abstract

We report a green synthesis of CdSe quantum dots (QDs) using bio-based materials (castor oil and ricinoleic acid) as capping agents. The absorption spectra of the as-synthesized CdSe QDs showed typical features of quantum confinement. The particle sizes of QDs were determined using the absorption band edges and found to be 3.81 to 6.80 nm and 5.91 to 8.31 nm for the entire range of reaction temperatures for QD-capped with castor oil (CSTO) and ricinoleic acid (RA), respectively. The photoluminescence spectra showed narrow emission peaks. The transmission electron microscopy (TEM) images showed spherical particles with sizes comparable to those determined from the absorption spectra. Comparatively, large particles were observed for RA capped CdSe QDs than those stabilized by CSTO. X-ray diffraction patterns revealed that the synthesized CdSe quantum dots have cubic structure. The particle sizes of CdSe deduced from X-ray diffraction measurements were in excellent agreement with those deduced from absorption spectra and TEM images. The d-spacings from the HRTEM images were consistent with those reported in literature. The surface area and the agglomeration number for as-synthesized CdSe QDs of different sizes are also reported.

The stationary state distribution of radicals in compartmentalized systems initiated by oil‐soluble initiators have been calculated for various cases of single radical formation as well as a simultaneous generation of single radicals and pairs of radicals in the particles. The effect of a contribution from radicals produced by initiator dissolved in the aqueous phase has been considered. Desorption and reabsorption of radicals, aqueous phase termination, total rate of radical formation and the water‐solubility of the initiator are quantified in terms of dimensionless parameters. The calculations predict that single radicals generated in the particles are kinetically indistinguishable from radicals produced in the aqueous phase over a wide range of variation of the parameters. It is shown that if the rate of generation of single radicals constitutes only about 10 per cent of the overall rate of radical formation in the particles, the former radicals account for the major part of the rate of polymerization. The mechanisms previously proposed to account for the similar kinetic behaviour observed with water‐soluble and oil‐soluble initiators are discussed. It is concluded that the present calculations support the view that this similarity is mainly due to radicals produced by the water‐soluble fraction of the initiator. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2347–2354, 1997

A green solution-based thermolysis method for the synthesis of lead chalcogenide (PbE, E = S, Se, Te) nanocrystals in castor oil (CSTO) and its isolate ricinoleic acid (RA) is described. The blue shift observed from the optical spectra of CSTO and RA-capped PbE nanocrystals (NCs) confirmed the evidence of quantum confinement. The dimensions of PbE NCs obtained from NIR absorption spectra, transmission electron microscopy (TEM), and X-ray diffraction (XRD) studies were in good agreement. The particle sizes estimated were in the range of 20, 25, and 130 nm for castor oil-capped PbS, PbSe, and PbTe, respectively. Well-defined close to cubic-shaped particles were observed in the scanning electron microscopy (SEM) images of PbSe and PbTe nanocrystals. The high-resolution TEM and selective area electron diffraction (SAED) micrographs of the as-synthesized crystalline PbE NCs showed distinct lattice fringes with d-spacing distances corroborating with the standard values reported in literature.

Spherical Polymeric Particles (SPP) have been prepared from Tanzanian Cashew Nut Shell Liquid (CNSL) by suspension polymerization technique involving either step-growth or chaingrowth polymerization mechanisms. The sizes of the SPP, which ranged from 0.1 to 2.0 mm were strongly influenced by the amounts of stabilizers in polymerization recipes used. The particles showed variable surface areas, indicative of the presence of pores in some of the preparations and the highest surface area recorded was about 260 m 2 g-1. The particles were found to exhibit Langmuir-type adsorption isotherms with saturation capacity of about 9.0 and 44.2 mg/g for Na + and Ca 2+ , respectively. Step-growth polymerization produced SPP with relatively smaller surface areas and lower adsorption capacities of sodium and calcium ions compared to the particles produced through the chain-growth mechanism. Other particle characteristics depended strongly on the recipe employed and the surface OH functional groups apparently determine the potential applications of the SPP.