1H T2‐NMR monitoring of crosslinked polyolefin aging

This work examines the correlation between the ¹H‐NMR T₂ relaxation constant and the mechanical properties of aged crosslinked polyolefin cable insulation. T₂ experiments on unswollen samples could not differentiate between unaged and highly aged materials; all exhibited ¹H T₂ constants of approximately 0.5 ms. To accentuate the effects of aging, samples were swollen in various solvents. Unaged samples had T₂ values of approximately 15 ms in good solvents. With thermal aging, T₂ values decreased as the ultimate tensile elongation decreased. However, the correlation between T₂ and elongation differed for samples irradiated with high‐energy radiation and for materials aged above versus below the crystalline melting temperature. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2578–2582, 2003     

Determining the Strength of Coarse‐Grained AlON and Spinel

The strength of two coarse‐grained (grain size > 200 μm) cubic ceramics, a magnesium aluminate spinel (MgAl₂O₄) and an AlON , along with a fine‐grained (1.5 μm) MgAl₂O₄, was determined by conducting a series of four‐point and equibiaxial flexure tests on specimens of different sizes. Weibull strength size scaling revealed a linear relationship on a log–log plot between average flexure strength and effective specimen area for the fine‐grained spinel, but a nonlinear relationship for both coarse‐grained materials. Initial fractography showed that each material had a single flaw population limiting the strength over the entire specimen size range, which does not account for the nonlinear size scaling relationship in the two coarse‐grained materials. However, further fractography revealed that in both materials there was an initial flaw and a critical flaw. The former appears to be machining/polishing damage that started the fracture process while the latter was a cleaved grain in AlON or a cracked grain boundary in the HP/HIP spinel that lead to fracture of the specimen. The difference between the initial and critical flaw size coupled with a detailed analysis of the strength as a function of test specimen thickness accounted for the nonlinear strength size scaling relationship. As a result, strength values obtained using thin test specimens can lead to an erroneous strength prediction for large components made of these ceramics. The implication of these findings is that strength tests must be conducted using appropriately thick specimens to obtain a representative strength value. If appropriately thick specimens cannot be tested, then fractography must be conducted to determine the flaw size. If the flaw size is sufficiently large, compared with the specimen thickness, then the strength must be adjusted according to a stress field correction factor to obtain a more accurate strength value.     

Enhanced Coercivity of CaLaCo‐Doped SrM Hexaferrites by Microwave‐Calcination Technique

The effects of microwave calcination (MC) and conventional muffle furnace calcination (CC) on the microstructure and magnetic properties of M‐type hexagonal ferrite Ca_0.15La_0.39Sr_0.46Fe_11.7Co_0.3O₁₉ were investigated. The phase composition, microstructure, and magnetic properties of calcined materials were examined using X‐ray diffraction (XRD), scanning electron microscopy (SEM), and vibrating sample magnetometry. Experiments indicated that the MC method can achieve both pure phase, and fine and uniform grains for both calcined and sintered M‐type hexaferrites. MC treatments resulted in a magnetization at 15 kOe of 67 emu/g and an increase in coercivity by 12% over the CC technique. The improved magnetic properties resulting from microwave‐assisted calcination were attributed to the formation of a fine‐grained morphology, which yielded a narrow grain size distribution. The microwave calcinating technique was shown here to possess unique potential for fabrication of high‐performance ferrites and possibly other ceramics.