THE EFFECT OF ASPHALT COMPOSITION ON THE FORMATION OF ASPHALTENES AND THEIR CONTRIBUTION TO ASPHALT VISCOSITY

Interactions among asphalt components have significant effects on the performance of asphalt binder. To understand those interactions, four asphalts, SHRP AAA-I, AAD-I, AAF-I, and AAG-I, were fractionated into three generic fractions according to Corbett's procedure and reblended into asphaltenes/aromatics/saturates ternary mixtures in various ratios. Mixtures were oxidatively aged with atmospheric air at temperatures of 87.7, 93.3, and 98.8°C for 5 to 33 days. The changes in chemical composition and physical properties were monitored using fourier transform infrared spectroscopy (FT-IR) and dynamic mechanical rheometry

The formation of asphaltenes is a major factor in the hardening of asphalt with aging. The data collected in this study indicate that the saturate content in the maltene phase has a profound impact on the contribution that asphaltenes have on the viscosity of aged asphalt. The data also suggest that the aromatics fraction is solely responsible for the formation of asphaltenes as an asphalt oxidizes.     

Pole assignment in linear time-invariant multivariable systems with constant disturbances

Necessary and sufficient conditions are derived for a minimal order realizable, linear, time invariant differential feedback control system to exist for a linear time-invariant system with constant unknown disturbances, such that the eigenvalues of the closed-loop system take on pre-assigned values in the left hand part of the complex plane and such that the outputs of the system tend to zero as t → ∞. Some numerical examples are included to illustrate the result.     

Analysis of polyacrylamide gels for trace metals using diffusive gradients in thin films and laser ablation inductively coupled plasma mass spectrometry

A simple method for the analysis of polyacrylamide diffusive gradients in thin film (DGT) gels by laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS), employing a novel use of (115)In internal standardization, has been developed. This method allows the determination of Co, Ni, Cu, Zn, Cd, and Pb concentrations (at the DGT filter face) or fluxes in sediments at a spatial resolution of 100 microm. Single-layered gels, using an optimized laser defocus of 4000 microm at 400 mJ power, showed high precision (generally approximately 10%) and a linear response during solution deployment. Of the elements Sc, In, Ba, La, Ce, and Tb, Ba most closely tracked variations in laser energy and showed the highest analytical precision but could not be used as an internal standard due to its elevated presence in natural sediments. Therefore, internal standardization, necessary to normalize data collected on different days, was carried out using (115)In contained within a second layer of backing gel and dried along with the analyte layer as a dual-gel disk. This multilayered gel standard required a laser defocus setting of 1000 microm and a laser power of approximately 800 mJ. Analytical precision for a 64-spot ablation grid at 100-microm spacing was approximately 10%. Verification of this method was carried out on DGT sediment probes deployed in Priest Pot (English Lake District). Results obtained by conventional slicing techniques and aqueous elution agreed with laser ablation results when the different sampling areas were considered. The elution results varied by a factor of <2, whereas the laser ablation technique showed a variability of approximately 4, indicating localized elevated concentrations of Co. This higher resolution LA-ICPMS method could ultimately lead to an improved understanding of the geochemical processes responsible for metal uptake and release in sediments.     

Plasma LH progesterone concentrations in the turkey hen during the ovulatory cycle

Progesterone and luteinizing hormone (LH) were measuured in the plasma of Large White turkey hens at frequent intervals during the ovulatory cycle and during the periods when ovulations did not occur. The hormones were quantitated at the beginning and the end of the reproductive season to follow the change in patterns and concentrations of these hormones. Radioimmunoassay procedures were used to assay both hormones. Both progesterone and LH reached a peak amount at about 8 to 2 hours before ovulation. At no time did the progesterone peak precede that of LH. On the other hand, the peak of progesterone was observed to last somewhat longer than the LH peak. Progesterone and LH concentrations demonstrated no peak during the non-ovulatory periods. The patterns of both hormones at the end of the reproductive season was about the same as at the beginning of the season, but with lower concentrations.