A Preliminary Study of Thermosets from Epoxy Resins Made Using Low-Toxicity Furan-Based Diols.

Glycidyl ethers are prepared from a series of furan-based diols and cured with a diamine to form thermosets. The furan diols demonstrate lower toxicity than bisphenol-A in a prior study. The diglycidyl ethers show improved thermal stability compared to the parent diols. Cured thermosets are prepared at elevated temperature using isophorone diamine (IPDA). Glass transition temperatures are in the range of 30-54 °C and depend on the structure of the furan diol. Coatings are prepared on steel substrates and show very high hardness, good adhesion, and a range of flexibility. Properties compare favorably with a control based on a bisphenol-A epoxy resin. The study demonstrates that epoxy resins based on furan diols, which have been shown to have lower toxicity than bisphenol-A, can form thermosets having properties comparable to a standard epoxy resin system; and thus, are viable as replacements for bisphenol-A epoxy resins.

Effect of surface modification of polymer beads on the mechanical properties of acrylic bone cement.

The effect of surface modification of polymer filler on the static mechanical properties of acrylic bone cement was studied. The surface of polymer beads was modified with carboxylic and amino groups by photochemical reaction with azide compounds. Monomer modifiers (maleic anhydride, methacrylic acid and p-aminostyrene) are attached to the functionalized surface of polymer beads. Functional allyl groups, which are capable of the graft polymerisation reaction, are attached to the surface via photochemical reaction with N-(2-nitro-4-azidophenyl)-N-(-propen) amine. This approach to bone cement provides the additional covalent bonds between the polymer beads and the inter-bead matrix. The static mechanical properties of bone cements containing modified polymer beads were investigated and compared with the static mechanical properties of unmodified cements. The absolute values of compressive strength for the modified and unmodified cements were found to be similar. An increase in flexural strength for the modified cements (dry and after water storage) was observed. The structure of the surface functional groups affects the methyl methacrylate grafting resulting in a higher value of flexural strength for the maleic anhydride- and p-aminostyrene-modified cements. The scanning electron microscopy examination of the fracture surface of the cement samples showed an improvement of the adhesion between the beads and the matrix after modification.

Graft polymerization from a silica surface initiated by adsorbed peroxide macroinitiators. I. Adsorption and structure of the adsorbed layer of peroxide macroinitiators on a silica surface.

The adsorption features of two peroxide macroinitiators (PMIs) with various functionalities from their semi-dilute solutions on the silica surface were thoroughly investigated in the present work. These investigations include the study of the adsorption kinetics of PMI in diverse solvents and a detailed examination of the adsorbed layer structure with the aid of ellipsometry, scanning force microscopy (SFM), and contact angle measurements. Rearrangements of PMI macromolecules at the solid surface are supposed to be the main reason for the appearance of extremes on the kinetic curves and, besides, have a more pronounceable effect on adsorption rate than their diffusion rate to the surface even at the initial stage of the process. Both island-like and densely packed structures of absorbed layers were revealed by combining contact angle measurements and SFM. Surprisingly, even in the case when saturation of the adsorbed layer is reached, PMI does not completely occupy the substrate surface which is at least particularly reachable for the wetting liquids. PMIs adsorbed at the solid surface are intended for the formation of tethered polymer "brushes" via the initiation of "grafting from" polymerization.