Stiff gelatin hydrogels can be photo-chemically synthesized from low viscous gelatin solutions using molecularly functionalized gelatin with a high degree of methacrylation

Gelatin is a very promising matrix material for in vitro cell culture and tissue engineering, e.g. due to its native RGD content. For the generation of medical soft tissue implants chemical modification of gelatin improves the mechanical properties of gelatin hydrogels and the viscous behavior of gelatin solutions for liquid handling. We present a systematic study on the influence of high degrees of methacrylation on the properties of gelatin solutions and photo-chemically crosslinked hydrogels. Changes from shear thinning to shear thickening behavior of gelatin solutions were observed depending on mass fraction and degree of methacrylation. Degrees of swelling of crosslinked hydrogels ranged from 194 to 770?% and storage moduli G′ from 368 to 5?kPa, comparable to various natural tissues including several types of cartilage. Crosslinked gels proofed to be cytocompatible according to extract testings based on DIN ISO 10933-5 and in contact with porcine chondrocytes.     

Chitosan as template for the synthesis of ceria nanoparticles

Cerium oxide (CeO₂), nanoparticles were prepared using chitosan as template, cerium nitrate as a starting material and sodium hydroxide as a precipitating agent. The resultant ceria–chitosan spheres were calcined at 350 °C. The synthesized powders were characterized by, XRD, HRTEM, UV–vis, FTIR, and TG-DTA. The average size of the nanoparticles obtained was ∼4 nm and BET specific surface area ∼105 m² g⁻¹. Blueshifts in the ultraviolet absorption spectra have been observed in cerium oxide nanocrystallites. The band-gap was found to be 4.5 eV. The blueshifts are well explained for diameters down to less than a few nanometers by the change in the electronic band structure.     

Microstraining in titania-, alumina- and silica-supported V2O5-catalysts

Commonly used catalysts in industry are compositions of highly dispersed particles. Typical systems consist of precious metals or transition metal oxides like V₂O₅ on oxide supports, especially TiO₂, Al₂O₃ and SiO₂. Support and active compound show a different chemical and material behaviour. A very important influence of the support on the active compound is the formation of microstrains due to the different thermal expansion behaviour. On the surface of a stiff linear elastic support the active compound is certainly strain hindered. In order to monitor the development of strain hindrance and further effects, in situ experiments were carried out at temperature both in an X-ray and in a neutron powder diffractometer. The width of the reflexes indicated a strong influence of the thermal expansion mismatch on peak width. The strain hindrance creates mismatch stresses high enough to overcome the yield stress of V₂O₅. The Williamson–Hall plots showed both a particle size effect as well as a stress widening but the measurements were difficult because of the materials anisotropy. The TEM work showed again very fine particles which agrees with the X-ray measurements. The support effect may be seen as thermal stress induced formation of a mosaic structure in the active compound. Moreover, the peak width correlated with the catalytic activity. The low ordered regimes in the mosaic structure are acting as further active centres for the catalytic reaction.     

Effect of release rate and ratio of (Z)-11-hexadecen-1-ol from synthetic pheromone blends on trap capture ofHeliothis subflexa (Lepidoptera: Noctuidae)

Response of maleHeliothis subflexa to pheromone-baited traps containing blends of tetradecanal, (Z)-9-tetradecanal, hexadecanal, (Z)-7-hexadecenal, (Z)-9-hexadecenal, (Z)-11-hexadecenal, hexadecan-1-ol acetate, (Z)-7-hexadecen-1-ol acetate, (Z)-9-hexadecen-1-ol acetate, (Z)-11-hexadecen-1-ol acetate, (Z)-9-hexadecen-1-ol, and (Z)-11-hexadecen-1-ol was evaluated. Analysis of trap capture data indicated that (Z)-11-hexadecen-1-ol was a critical component of the pheromone blend. It was determined from emission rate data and measurements of the ratio of pheromone components emitted from rubber septa tested that a significant increase in trap capture of maleH. subflexa occurred when the blends investigated released the alcohol in a narrow range relative to the total amount of pheromone emitted. The optimum range of release ratio of the alcohol for the capture of males in sticky traps was determined to be 0.9–3.5% of the pheromone blend. This release ratio range was reduced to 0.9–1.6% when bucket traps were used.