Viscosity index. I. Evaluation of selected copolymers incorporating n-octadecyl acrylate as viscosity index improvers

Compositionally and structurally varied copolymers all containing n-octadecyl acrylate were prepared and evaluated as viscosity index improvers in a common base oil under conditions of low shear. Systems evaluated over a range of copolymer and blend composition were: copolymers of n-octadecyl acrylate with, respectively, methyl methacrylate, 2-ethylhexyl acrylate, and n-dodecyl acrylate; and homopolymers of poly(n-octadecyl acrylate), prepared with a wide range of molecular weights. Properties were compared with those of blends of commercial methacrylate copolymers (acryloids) which had been freed of their entraining liquid. Mixtures of base oil with copolymers of n-octadecyl acrylate and methyl methacrylate, compared at fixed SAE viscosities, were the most efficient of all blends studied. They had the smallest rate of change of viscosity with temperature (as measured by their ASTM slopes), particularly in the composition region of incipient polymer precipitation at room temperature. Efficiency of certain of these composition was somewhat greater than that of the acryloids. A parameter that related concentration and weight-average molecular weight was used to correlate all of the data for ASTM slope and viscosity. Empirical relations developed by using this parameter enabled rheological data to be estimated that agree within 6% of experimental values for the case of thermodynamically good base oil solvents. These data demonstrated the relatively small contributions of copolymer structure to viscosity index improvement.     

Characteristics of Bi-metallic Interfaces Formed During Direct Energy Deposition Additive Manufacturing Processing

Metallurgical and Materials Transactions B - Various additive manufacturing processes are being evaluated to reduce the time and cost for fabrication of low volume, complex, and multifunctional...     

Aging effects of nanoscale ceria in ceria–platinum composite electrodes for direct alcohol electro-oxidation

Nanocrystalline Pt/CeO₂ composite electrodes were fabricated to study the electrochemical oxidation of methanol and ethanol. The performance of the electrodes was tested as the ceria solutions aged over time. It was observed that the performance oscillated with time, suggesting that the catalytic behavior towards alcohol oxidation was greatly dependent on the aging of the particles. These results point to a great dependence of the catalytic effect on the redox state of the ceria particles.     

Speciation and distribution of alkali,alkali earth metals and major ash forming elements during gasification of fuel cane bagasse

Gasification of fuel cane bagasse, the waste residue from fuel cane, a hybrid of wild and commercial clones of sugar cane, was carried out in a novel 50 kWe air-blown autothermal downdraft gasifier. The speciation and distribution of alkali, alkali earth metals and major ash forming elements during gasification were investigated to evaluate the extent of volatilisation of these elements into the syngas and to determine the likely impact on syngas fuelled solid oxide fuel cell systems. Also assessed was the potential for defluidisation of the fuel bed due to agglomerate and deposit formation. Chemical fractionation studies showed that 30% of the potassium was captured by aluminosilicates and was retained in the ash, thereby reducing the alkali loading in the syngas and that more than 50% of the alkali earth metals were released to the syngas. In contrast, although the major ash forming elements were transformed from acid insoluble to acid soluble forms during gasification they remained hard bound in the ash and less than 30% of each one was released into the gas phase. The composition of clinkers and agglomerates produced during gasification was investigated by SEM-EDX and XRD which confirmed the presence of the eutectic systems KAlSi₂O₆–SiO₂, KAlSi₂O₆–CaMgSi₂O₆–SiO₂ and CaMgSi₂O₆–NaAlSi₃O₈. A preliminary model of the distribution behaviour during gasification of the ash forming elements has been developed.