Microencapsulation of Flavors in Carnauba Wax

The subject of this study is the development of flavor wax formulations aimed for food and feed products. The melt dispersion technique was applied for the encapsulation of ethyl vanillin in wax microcapsules. The surface morphology of microparticles was investigated using scanning electron microscope (SEM), while the loading content was determined by HPLC measurements. This study shows that the decomposition process under heating proceeds in several steps: vanilla evaporation occurs at around 200 °C, while matrix degradation starts at 250 °C and progresses with maxima at around 360, 440 and 520 °C. The results indicate that carnauba wax is an attractive material for use as a matrix for encapsulation of flavours in order to improve their functionality and stability in products

Open-framework aluminophosphates: synthesis, characterization and transition metal modifications

This review is a brief summary of open-framework aluminophosphates and their transition metal-substituted modifictions. The materials exhibit structural and compositional diversity, as well as a wide range of pore openings, which are crystallographically ordered and can be tuned by an appropriate choice of synthesis conditions. The diameters of the apertures, cages and channels fall in the range of 0.4 to about 1.5 nm, which recommends aluminophosphates for a novel area of application nanocatalysis. Isomorphous substitution of the framework elements by transition metal ions which possess redox ability creates active sites inside the aluminophosphate lattice and opens routes towards shape selective bi-functional catalysis. In order to obtain an insight into the location of the transition metal ions, different characterization techniques have to be used

A study of the removal of copper ions from aqueous solution using Clinoptilolite from Serbia

Toxic metal contamination of waste waters can be mitigated by metal adsorption to clay and zeolitic minerals, but in developing countries such environmental remediation can be cost prohibitive if these minerals are not readily available. Because of its abundance, low cost, and excellent selectivity for several toxic metal ions, clinoptilolite from the Zlatokop deposit in Serbia was investigated for its ability to remove copper ions from aqueous solutions and serve as an effective local resource for this purpose. The sorption capacity of the clinoptilolite at 298 K varied from 8.3 mg Cu g (for C = 100 mg Cu dm ) to 16.8 mg Cu g (for C = 400 mg Cu dm ). The sorption data were best described by the Freundlich isotherm and the sorption kinetics followed the pseudo-second-order model. Intra-particle diffusion of Cu was present but it is not the rate-limiting step. The sorption of Cu on the clinoptilolite occurred spontaneously, the free energy change decreasing with temperature. The sorption was endothermic and was accompanied by an increase in entropy. Dehydration of the Cu-loaded clinoptilolite at 540°C led to the formation of nanocrystalline Cu(I) oxide particles with an average size of ~2 nm, suggesting possible novel applications for the Cu-loaded clinoptilolite

Hydrothermal synthesis and structure of a new layered zincophosphate intercalated with 3-Methylaminopropylamine cations

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 Å 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

Synergistic anti-biofouling effect of Ag-exchanged zeolite and D-Tyrosine on PVC composite against the clinical isolate of Acinetobacter baumannii

Due to their susceptibility to bacterial biofilm formation, commercial tubes for medical use are one of the main sources of hospital infections with Acinetobacter baumannii. The anti-biofouling activity of novel composites against the clinical isolate of the multi-drug resistant A. baumannii is reported here. The composites were prepared by addition of micronised silver-exchanged natural zeolite (Ag-NZ) into poly(vinyl chloride) (PVC), followed by coating of the composites with D-Tyrosine (D-Tyr). The Ag-NZ composites (containing 1-15 wt% of Ag-NZ) coated with D-Tyr (Ag-NZ-Tyr) showed a bactericidal effect (100% or a 6.9 log CFU reduction) towards immobilised bacterial cells. The uncoated Ag-NZ composites showed a reduction of up to 70% (4.4 log CFU) of immobilised bacteria in comparison with the original PVC. Rheological testing of the composites revealed that the addition of Ag-NZ slightly affected processability and formability of the PVC and increased the elasticity of the polymer matrix