Synthesis and environmental degradation of polyesters based on poly (ε-caprolactone)

Poly (-caprolactone) (PCL), poly (-valerolactone) (PVL), poly (-caprolactone-co--valerolactone) [P(CL-co-VL)], and poly (-caprolactone-co-ethylene oxide-co--caprolactone) (PCL-PEO-PCL) were synthesized by ring-opening and diol-initiated polymerization of -caprolactone and -valerolactone. The degradation of the samples by chemical hydrolysis and in a soil burial test was evaluated. It was found that PCL, PVL, and P(CL-co-VL) degrade mainly enzymatically. The rate of degradation depends on their molecular weight, chemical structure, composition, and morphology. PCL-PEO-PCL block copolymers exhibit a repelling effect to the microorganisms in the soil, which depends on the molecular weight and relative amount of PEO block in the copolymer.     

Bulk carbon, oxygen, and hydrogen stable isotope composition of recent resins from amber-producing Hymenaea

Resins of Hymenaea, an angiosperm tree genus known to be a copious resin producer and a major source of amber since the Oligo-Miocene, were collected from a wide range of tropical environments from Latin America and Africa, and analyzed for their carbon, hydrogen, and oxygen stable isotope composition. The average value for ¹³C in the resins was found to be –27.0±1.3, which is very similar to the values reported for resins in other studies. ¹⁸ values for the Hymenaea resins averaged +11.2±1.6, or about 20 more depleted than normal plant cellulose. D values of the resins ranged from –196 to –319, with an average of –243±30. Rough estimates suggest a fractionation of –200 to –210 between the resins and the environmental water. This value is similar to the –200 value observed for the fractionation between other plant lipids and environmental water. The present study suggests that the stable isotope composition of fossil resins (amber) has the potential to provide information on ancient environmental waters.     

Prenatal diagnosis of mucopolysaccharidosis by two-dimensional electrophoresis of amniotic fluid glycosaminoglycans

Amniotic fluid from 72 pregnancies at risk for mucopolysaccharidosis have been analysed for glycosaminoglycans (GAG) by means of two-dimensional electrophoresis. Definite results were obtained in all cases and required only 3 days to report. Of the 66 cases for which GAG analysis was accompanied by enzyme assays on cultured amniotic fluid cells, there was agreement of results in 65. In the one case of disagreement the result of GAG analysis proved to be correct. Fourteen pregnancies were predicted to be affected and the predictions were confirmed by studies on fetal tissues and/or cultured cells, or in one case the birth of an affected infant. Of the 58 pregnancies predicted to be unaffected, 48 have so far gone to term and produced healthy infants. There have been no false negative predictions. The analytical method is simple, rapid, and, in this study, has been found completely reliable for prenatal diagnosis.     

Full-scale evaluation of mercury control with sorbent injection and COHPAC at Alabama Power E.C. Gaston

The overall objective of this project was to determine the cost and impacts of Hg control using sorbent injection into a Compact Hybrid Particulate Collector (COHPAC) at Alabama Power's Gaston Unit 3. This test is part of a program funded by the U.S. Department of Energy's National Energy Technology Laboratory (NETL) to obtain the necessary information to assess the costs of controlling Hg from coal-fired utility plants that do not have scrubbers for SO2 control. The economics will be developed based on various levels of Hg control. Gaston Unit 3 was chosen for testing because COHPAC represents a cost-effective retrofit option for utilities with existing electrostatic precipitators (ESPs). COHPAC is an EPRI-patented concept that places a high air-to-cloth ratio baghouse downstream of an existing ESP to improve overall particulate collection efficiency. Activated carbons were injected upstream of COHPAC and downstream of the ESP to obtain performance and operational data. Results were very encouraging, with up to 90% removal of Hg for short operating periods using powdered activated carbon (PAC). During the long-term tests, an average Hg removal efficiency of 78% was measured. The PAC injection rate for the long-term tests was chosen to maintain COHPAC cleaning frequency at less than 1.5 pulses/bag/hr.     

Precipitation of swine and cattle manure phosphorous using limestone dust

The effectiveness of SPS and PULPRO, fine limestone dusts, in precipitating swine and dairy manure phosphorous (P) was determined in the laboratory. Both manures were sieved before being treated with limestone, to reproduce the treatment of mechanically separated manure and to observe the precipitation effect of limestone without that of the large manure solid particles. P precipitation was optimized by varying precipitation conditions (propeller blade speeds, mixing time and limestone levels) and limestone particle size. P precipitation was optimized using a propeller blade mixing speed of 0.3 m s(-1) for at least 5 minutes, using 3% limestone (dry limestone mass over wet manure mass). In terms of particle size, PULPRO 20 (limestone with a particle size of 0.02 mm) produced the most P precipitation and the smallest volume and mass of sludge, as compared to PULPRO 10, PULPRO 3 and SPS (limestone with a particle size of 0.01, 0.003 and 0.3 to 0.003 mm, respectively). For both 9.5% TS (total solids) dairy and 8.8% TS swine manure, mechanical separation followed by limestone precipitation concentrated 90% of manure TS and TP in a sludge volume representing 45% of the initial raw manure mass.     

Biodegradability of wheat gluten based bioplastics

A large variety of wheat gluten based bioplastics, which were plasticized with glycerol, were subjected to biodegradation. The materials covered the total range available for the biochemical control parameter Fi, which expresses the percentage of aggregated proteins. This quantity can be related to the density of covalent crosslinks in the wheat gluten network, which are induced by technological treatments. The biodegradability tests were performed in liquid medium (modified Sturm test) and in farmland soil. All gluten materials were fully degraded after 36 days in aerobic fermentation and within 50 days in farmland soil. No significant differences were observed between the samples. The mineralization half-life time of 3.8 days in the modified Sturm test situated gluten materials among fast degrading polymers. The tests of microbial inhibition experiments revealed no toxic effects of the modified gluten or of its metabolites. Thus, the protein bulk of wheat gluten materials is non-toxic and fully biodegradable, whatever the technological process applied.     

Sorption and transport of iodine species in sediments from the Savannah River and Hanford Sites

Iodine is an important element in studies of environmental protection and human health, global-scale hydrologic processes and nuclear nonproliferation. Biogeochemical cycling of iodine is complex, because iodine occurs in multiple oxidation states and as inorganic and organic species that may be hydrophilic, atmophilic, and biophilic. In this study, we applied new analytical techniques to study the sorption and transport behavior of iodine species (iodide, iodate, and 4-iodoaniline) in sediments collected at the Savannah River and Hanford Sites, where anthropogenic (129)I from prior nuclear fuel processing activities poses an environmental risk. We conducted integrated column and batch experiments to investigate the interconversion, sorption and transport of iodine species, and the sediments we examined exhibit a wide range in organic matter, clay mineralogy, soil pH, and texture. The results of our experiments illustrate complex behavior with various processes occurring, including iodate reduction, irreversible retention or mass loss of iodide, and rate-limited and nonlinear sorption. There was an appreciable iodate reduction to iodide, presumably mediated by the structural Fe(II) in some clay minerals; therefore, careful attention must be given to potential interconversion among species when interpreting the biogeochemical behavior of iodine in the environment. The different iodine species exhibited dramatically different sorption and transport behavior in three sediment samples, possessing different physico-chemical properties, collected from different depths at the Savannah River Site. Our study yielded additional insight into processes and mechanisms affecting the geochemical cycling of iodine in the environment, and provided quantitative estimates of key parameters (e.g., extent and rate of sorption) for risk assessment at these sites.     

Uranium distribution and cycling in Scots pine (Pinus sylvestris L.) growing on a revegetated U-mining heap

We determined the uranium distribution in soil and its allocation in compartments of 35-year-old Scots pine developed on a revegetated U-mining heap. The processes controlling the dynamics of U recycling were identified and further quantified in terms of annual fluxes. As pine developed, an acid humus layer emerged leading to weathering of the alkaline mining debris but this had little effect on U mobility in the soil profile. Increased U mobility mainly involved a translocation of U to metal-humus chelates in surface layers. The root compartment accounted for 99.3% of the U budget in tree, thus serving as an effective barrier which restricts U uptake. The current root uptake and transfer of U to upper parts of the tree amounted to about 3g ha(-1) y(-1), i.e. less than 0.03% of the current NH4-exchangeable U pool in the soil (0-30 cm). Allocation and translocation pattern made it clear that a dominant fraction of the translocated U moves passively with the ascent xylem sap, most likely as a soluble complex, and steadily accumulates in the needles. Consequently, 97% of the U annual uptake is returned to the soil through litterfall. At the studied site, the risk of U dissemination due to biomass turnover or trunk harvest was low when considered in relation to the current "exemption level" for U.