Zinc oxide can be called a multifunctional material thanks to its unique physical and chemical properties. The first part of this paper presents the most important methods of preparation of ZnO divided into metallurgical and chemical methods. The mechanochemical process, controlled precipitation, sol-gel method, solvothermal and hydrothermal method, method using emulsion and microemulsion enviroment and other methods of obtaining zinc oxide were classified as chemical methods. In the next part of this review, the modification methods of ZnO were characterized. The modification with organic (carboxylic acid, silanes) and inroganic (metal oxides) compounds, and polymer matrices were mainly described. Finally, we present possible applications in various branches of industry: rubber, pharmaceutical, cosmetics, textile, electronic and electrotechnology, photocatalysis were introduced. This review provides useful information for specialist dealings with zinc oxide.

Zinc oxide was obtained by precipitation in an emulsion system with zinc acetate used as a precursor of ZnO and potassium hydroxide or sodium hydroxide as a precipitating agent. The cyclohexane, as an organic phase, and a nonionic surfactant mixture were also used for preparation of the emulsion. By applying modifications of the ZnO precipitation process, such as changing the precipitating agent, composition of substrates, and the rate of substrate dosing, some interesting structures of ZnO particles were obtained. The morphology of the modified samples was analysed based on SEM (scanning electron microscope) and TEM (transmission electron microscope) images. Moreover the samples were characterised by determination of their dispersive properties using the noninvasive back scattering method (NIBS), adsorption parameters (BET), and crystalline structure (XRD). Thermogravimetric analysis (TG) as well as infrared spectrophotometry (FT‐IR) was also applied. For selected samples their electrical properties (dielectric permittivity and electric conductivity) were also measured. The zinc oxide obtained consisted of particles in the shapes of solids, ellipsoids, rods, and flakes, with size ranging from 164 to 2670 nm and showed well‐developed surface area with values as high as 20 m²/g.

Innovative materials were made via the combination of chitin and lignin, and the immobilization of lipase from Aspergillus niger. Analysis by techniques including FTIR, XPS and ¹³C CP MAS NMR confirmed the effective immobilization of the enzyme on the surface of the composite support. The electrokinetic properties of the resulting systems were also determined. Results obtained from elemental analysis and by the Bradford method enabled the determination of optimum parameters for the immobilization process. Based on the hydrolysis reaction of para-nitrophenyl palmitate, a determination was made of the catalytic activity, thermal and pH stability, and reusability. The systems with immobilized enzymes were found to have a hydrolytic activity of 5.72 mU, and increased thermal and pH stability compared with the native lipase. The products were also shown to retain approximately 80% of their initial catalytic activity, even after 20 reaction cycles. The immobilization process, using a cheap, non-toxic matrix of natural origin, leads to systems with potential applications in wastewater remediation processes and in biosensors.

The immobilization of Amano Lipase A from Aspergillus niger by adsorption onto Stöber silica matrix obtained by sol-gel method was studied. The effectiveness of the enzyme immobilization and thus the usefulness of the method was demonstrated by a number of physicochemical analysis techniques including Fourier Transform Infrared Spectroscopy (FT-IR), elemental analysis (EA), thermogravimetric analysis (TG), porous structure of the support and the products after immobilization from the enzyme solution with various concentration at different times. The analysis of the process’ kinetics allowed the determination of the sorption parameters of the support and optimization of the process. The optimum initial concentration of the enzyme solution was found to be 5 mg mL-1, while the optimum time of the immobilization was 120 minutes. These values of the variable parameters of the process were obtained by as ensuring the immobilization of the largest possible amount of the biocatalyst at