Owing to their unique properties, use of microemulsion-based synthetic techniques for the generation of shape-controlled nanocatalyst is an area of great current interest. Nanocatalysts of any specific shape, morphology, surface area, size, geometry, homogeneity and composition are widely being prepared using the soft techniques of microemulsion. Easy handling, inexpensive equipment and mild reaction conditions make microemulsion an attractive reaction medium. Herein, a nanosized precursor reactant can be incorporated, leading to the formulation of a highly monodispersed metal nanoagglomerate with controlled size, shape and composition. Several factors such as presence of electrolyte, molar ratio of water to surfactant, nature and concentration of surfactant and solvent, size of water droplets and concentration of reducing agents influence the size of the nanoparticles. The reverse micelle method can be used for the fabrication of several nanosized catalysts with a diverse variety of suitable materials including silica, alumina, metals (e.g. Au, Pd, Rh, Pt), metal oxides, etc. The morphology, size distribution and shape of the nanocatalysts make them useable for a wide range of applications, for example, fuel cells, electrocatalysis, photocatalysis, environmental protection, etc. The recovery of nanoparticles from the reaction mixture is a challenge for the researchers. This chapter discusses the preparation of nanoparticles using microemulsion techniques, widely being used for the synthesis of nanocatalysts from a wide range of materials.

Metal nanoparticles (NPs) have received significant attention in last decade because of their unique properties. In this work, two different metal NPs have been prepared and their catalytic activities are compared with conventional catalyst. In first case, Ag NPs were synthesized by chemical reduction method in ethanolic medium. Synthesized Ag NPs were characterized by scanning electron microscope (SEM) images which indicated an average particle size of Ag around 250 nm. The catalytic activity of Ag NPs was investigated for the oxidative mineralization of methylene blue dye. Comparative studies suggested that Ag NPs possess enhanced catalytic activity compared to bulk Ag. In second approach, supported Ni NPs were fabricated using Al2O3as supporting surface; that is, Ni NPs get adsorbed on Al2O3through in situ reduction reaction. Oxidative degradation of methylene blue indicated that catalytic activity of supported Ni/Al2O3is about five times higher than simple Ni as catalyst.