Wettability of nano-epoxies to UHMWPE fibers.

Ultra high molecular weight polyethylene (UHMWPE) fibers have a unique combination of outstanding mechanical, physical, and chemical properties. However, as reinforcements for manufacturing high performance composite materials, UHMWPE fibers have poor wettability with most polymers. As a result, the interfacial bonding strength between the fibers and polymer matrices is very low. Recently, developing so-called nano-matrices containing reactive graphitic nanofibers (r-GNFs) has been proposed to promote the wetting of such matrices to certain types of fiber reinforcements. In this work, the wettability of UHMWPE fibers with different epoxy matrices including a nano-epoxy, and a pure epoxy was investigated. Systematic experimental work was conducted to determine the viscosity of the epoxies, the contact angle between the epoxies and the fibers. Also obtained are the surface energy of the fibers and the epoxies. The experimental results show that the wettability of the UHMWPE fibers with the nano-epoxy is much better than that of the UHMWPE fibers with the pure epoxy.

Development and characterization of edible peanut protein films.

In this work, novel edible films were developed from peanut protein with sorbitol as a plasticizer. The peanut protein was extracted from peanut flour. Two groups of films were prepared. One group contained 10% in weight of natural oil/fat of the peanuts, while the other group contained no oil/fat. Six types of films with 37.5%, 44.5%, and 50% sorbitol content by weight, with and without fat, were chosen for mechanical properties characterization and microscopic observations. It was found that with the increase of sorbitol content, higher tensile strength and higher Young's modulus were achieved for the films without fat. However, films with fat exhibited maximum strength and modulus at 44.5% sorbitol content. Relationships between the mechanical properties and the microscopic features of these films were established. It was found that the higher the content of the sorbitol, the more evident the crystalline structure. Grant numbers: NCC9-51.

Aurin tricarboxylic acid, the anti-AIDS compound, prevents the binding of interferon-alpha to its receptor.

Binding of HIV to its receptor, the CD4 molecule of lymphocytes, can be prevented by chemical agents. These agents could be considered as potential anti-AIDS drugs. We have shown that aurin tricarboxylic acid (ATA, 3 microM) specifically blocks the binding of gp120, the HIV coat protein, to the CD4 molecule. We have also found that ATA prevents the binding of interferon-alpha to its receptor in a dose-dependent manner (12-50 microM range). Membrane potential shift, associated with binding of interferon-alpha to its receptor, was also blocked by ATA in a dose-dependent fashion. Our results indicate that potential anti-AIDS drugs should be screened for such undesired side effects.