The use of fast FT-IR spectroscopy as a sensitive method to estimate a change of the crosslinking kinetics of epoxy resin with polyamine adducts is described in this study. A new epoxy formulation based on the use of polyamine adducts as the hardeners was analyzed. Crosslinking reactions of the different stoichiometric mixtures of the unmodified GY250 epoxy resin with the aliphatic EH606 and the cycloaliphatic EH637 polyamine adducts were studied using mid FT-IR spectroscopic techniques. As the crosslinking proceeded, the primary amine groups in polyamine adduct are converted to secondary and the tertiary amines. The decrease in the IR band intensity of epoxy groups at about 915 cm−1, as well as at about 3,056 cm−1, was observed due to process. Mid IR spectral analysis was used to calculate the content of the epoxy groups as a function of crosslinking time and the crosslinking degree of resin. The amount of all the epoxy species was estimated from IR spectra to changes during the crosslinking kinetics of epichlorhydrin.

The natural zeolitic tuff from the Zlatokop mine (Vranjska Banja deposit) has been investigated as a starting material for obtaining a low cost adsorbent for the removal of nitrate from water media. The tuff riched with zeolite - clinoptilolite was modified by simple procedures by several oxides: iron(III), manganese(IV) and magnesium in order to make clinoptilolite surface accessible for binding the nitrate ions. The obtained oxide-modified zeolite samples were characterized by scanning electron microscopy and energy dispersive X-ray analysis (SEM/EDS), powder X-ray diffraction (PXRD), infrared spectroscopy (FTIR) and by measurement of specific surface area. The effects of the adsorbent dosage (0.5, 1.0, 1.5 and 2.0 g), temperature (25, 35 and 45 ?C) and initial nitrate concentration (C0= 100, 200 and 300 mg dm-3) on the binding efficiency were also studied. For all adsorbents the efficiency increases with temperature. The type of oxides effects the adsorption mechanism and Fe(III) oxide modified zeolite exhibits the best binding ability. For this adsorbent the adsorption kinetics was studied and found that it is best represented by the pseudo-second-order model. [Projekat Ministarstva nauke Republike Srbije, br. 172018]

1,3-Diaminopropane (DAP) was used as a structure-directing agent for the hydrothermal synthesis of an organically templated iron phosphate. During crystallization at 180 ?C, iron phosphate (FePO-DAP) with a layered structure was formed after one day. Longer crystallization yielded a mixture of FePO-DAP and leucophosphite, raising the question whether a transformation of FePO-DAP to leucophosphite occurs, or whether DAP decomposes under hydrothermal conditions resulting in leucophosphite formation. Lattice energy and free energy calculations strongly support the supposition that a decomposition of DAP occurs prior to the formation of leucophosphite.

Summary Carp production in Serbia is traditionally conducted in large area fish farms under a semiintensive farming system. Total area under fish farms in Serbia amounts

A novel layered zincophosphate (ZnPO?MPA) was prepared by hydrothermal crystallization using 3-methylaminopropylamine (MPA) as a structure-directing agent. The structure consists of macroanion [Zn2P3O8(OH)3]2- layers which are built up of 4-membered ring channels. The channels (of about 3.7 ? diameter) arise through the connection of the neighbouring rings by two oxygen bridges. The negative charge of the layers is compensated by diprotonated MPA molecules which are stacked parallel to the ring channels. ZnPO?MPA is stable up to 300 ?C. At higher temperatures MPA decomposition begins followed by a dehydration, which occurs through condensation of the framework hydroxyl groups. The activation energy of the MPA decomposition is high due to the fact that the layers and MPA cations are held together by strong hydrogen bonds.