STATISTICAL ANALYSIS OF ORGANOSULFUR EXTRACTION DATA OF OHIO 5/6 COAL USING THE PERCHLOROETHYLENE COAL CLEANING PROCESS

The perchloroethylene coal cleaning process removes both organic and pyritic forms of sulfur using perchloroethylene as the solvent medium. The effect of process variables including temperature, extraction time, solvent to coal ratio and particle size of coal has been studied by a systematic 2⁴ full factorial experimental design with a single replicate. The process was found to be strongly dependent on the type of coal. Hence, this variable was controlled by choosing one single type of coal, i.e., Ohio 5/6 (1:1 mixture of Ohio 5 and Ohio 6 coals) throughout this entire investigation. The significant effects and interactions have been quantified by F-tests. The estimates of significant effects have been obtained by Yates algorithm. Residual probability and normal probability plots have been obtained to test model adequacy. Finally, a computational model has been developed to predict the organosulfur extraction efficiency of this coal at various values of process variables. The parity plots conclude that the model has a good interpolational predictive capability.     

Policy Analysis, Peer Reviewed: Evaluation of Bioaccumulation Factors in Regulating Metals

Regulations.     

The distribution and phylogenetic significance of desmethylsterols inChenopodium andAtriplex: Coexistence of Δ7- and Δ5 -sterols

Twenty-one species in the Chenopodiaceae were analyzed for sterol composition. In ten of eleven species ofChenopodium, the major desmethylsterols were Δ⁷-sterols accompanied by lower proportions of Δ⁵-sterols. InC. fremontii this pattern was reversed. The sterol profiles of five species ofAtriplex were characterized by the coexistence of Δ⁷- and Δ⁵-sterols in ratios of 0.3∶1 to 0.4∶1. MaleAtriplex plants contained higher proportions of Δ⁵-sterols than femaleAtriplex plants. OneCeratoides and twoSalicornia species contained Δ⁵-sterols as their predominant sterols.     

Determination of the Fe2+/Fe3+ Ratio in Nuclear Waste Glasses

The Fe²⁺/Fe³⁺ ratios of 47 simulated nuclear waste glass samples with ratios varying from 0.01 (oxidized) to 1.6 (reduced) were determined by wet-chemical and Mössbauer spectral analyses. The wet-chemical method involved the spectrophotometric determination of Fe²⁺ and total iron using remote spectroscopy with fiber optic chemical sensing. Interferences from other species present in these glasses were examined and alternative analytical techniques were investigated. Results of wet-chemical and Mössbauer spectral analysis were comparable; however, the wet-chemical method is probably preferable for the analysis of highly radioactive glasses until such glasses have been shown to have satisfactory Mössbauer spectra.     

Polymer-assisted formation of hydrophobized,shape-anisotropic zinc oxide nanoparticles via an inverse emulsion technique

A one-step inverse emulsion process using amphiphilic surface-active copolymers for the synthesis of hydrophobized, shape-anisotropic inorganic nanoparticles is presented. While such structures are normally prepared sequentially by particle formation and hydrophobization, we have combined both reactions. This approach is demonstrated exemplarily with zinc oxide (ZnO) nanoparticles. A key issue is the design of amphiphilic copolymers that act as emulsifiers to enable an aggregate-free redispersion of the particles and to stabilize the inverse emulsion for the precipitation in the droplets. In a first approach, the stabilizing as well as the hydrophobizing property of the copolymers are combined with the ability to control the crystallization in one polymer (structure-directing emulsifier—SDE). In a second approach, a mixture of two polymers is applied: an amphiphilic copolymer for hydrophobizing/stabilizing the inorganic nanoparticles and a polar or double hydrophilic polymer that induces the anisotropic growth of the ZnO nanocrystals (structure-directing agents—SDA). Homopolymers and block copolymers, consisting of phosphonic acid groups or propylene oxide groups, were used as SDAs. Typically, hydrophobized shape-anisotropic particles of up to 600 nm in length and with an aspect ratio of 1:4 were obtained.     

Ecosystem,Location, and Climate Effects on Foliar Secondary Metabolites of Lodgepole Pine Populations from Central British Columbia

Lodgepole pines, Pinus contorta Douglas ex Louden var. latifolia Engelm. ex S. Watson, are encountering increased abiotic stress and pest activity due to recent increases in temperature and changes in precipitation throughout their range. This tree species counters these threats by producing secondary metabolites, including phenolics and terpenoids. We examined foliar levels of lignin, soluble phenolics, monoterpenoids, sesquiterpenoids, and diterpenoids in 12 stands in British Columbia, Canada. We used these data to assess associations among foliar secondary metabolite levels and ecosystem, geographic, and climatic variables. Regressions were also performed to observe which combinations of variables best explained secondary metabolite variance. Stands of P. c. latifolia in the Coastal Western Hemlock and Interior Cedar/Hemlock biogeoclimatic zones had consistently greater foliar levels of almost all measured secondary metabolites than did other stands. Lignin was present in greater amounts in Boreal White/Black Spruce ecosystem (i.e., northern) stands than in southern stands, suggesting a role for this metabolite in pine survival in the boreal forest. Attempts to develop regression models with geographic and climatic variables to explain foliar secondary metabolite levels resulted in multiple models with similar predictive capability. Since foliar secondary metabolite levels appeared to vary most between stand ecosystem types and not as much due to geographic and climatic variables, metabolic profiles appeared best matched to the stress levels within local environments. It is unknown if differences in secondary metabolite levels are the result of genetic adaptation or phenotypic plasticity, but results from this and other studies suggest that both are important. These results are interpreted in light of ongoing efforts to assist in the migration of certain populations of P. c. latifolia northward in an effort to counter predicted effects of climate change.     

Enhancing the solubility and bioavailability of isoflavone by particle size reduction using a supercritical carbon dioxide-based precipitation process

Isoflavones are a group of small molecular compounds found in many plants. Genistein is the most well studied isoflavones because of its beneficial effects in reducing menopausal symptoms, anti-oxidant and anti-cancer. The major difficulty in developing isoflavone-based healthcare products is their low water solubility. In this study, the solubility and oral bioavailability of genistein were increased by reducing its particle size using supercritical CO₂ as an antisolvent in the precipitation process. The effects of various process parameters including type of solvent, pressure of precipitation, and concentration of genistein solution on particle formation were evaluated. We found that under optimized conditions: dissolving 4 mg/mL genistein in acetone and precipitating them with supercritical CO₂ under 100 bar at 40 °C, the size of genistein particles was reduced from its original width of 10–50 μm to ∼254 nm. The reduction of genistein particle size not only increased its water solubility by 2 fold but more importantly increased its 24 h-plasma concentration by 2.6 fold after orally administrated to rats. These results proof the concept of using supercritical CO₂ as an antisolvent in the precipitation process to reduce particle size of water insoluble compounds such as genistein and to improve its oral bioavailability.     

Comparison of N-Heterocyclic Aromatics Dibenzo[c,g]Carbazole and Dibenz[a,j]Acridine : Metabolism,DNA Binding and Mutation

N-Heterocyclic aromatics, such as carbazole and acridine derivatives, are environmental carcinogenic pollutants. Examples of these compounds are 7H-dibenzo[c,g]carbazole (DBC) and dibenz[a,j]acridine (DBA). The ionization potential (IP) for DBC is lower than for DBA. DBC is metabolized in lung and liver by way of phenols or directly through radical cations. DBC-induced liver and lung tumors have mutations in the 61^st codon of ras. DBA is metabolized in skin by way of a diol-epoxide of DBA. DBA-induced skin tumors have mutations in 12^th, 13^th and 61^st codons of ras. In summary, the metabolic activation of DBC proceeds through different adduction pattern pathways than does DBA and leads to different ras mutational spectra.