Application of in situ vitrification in the soil subsurface: Engineering-scale testing

Engineering-scale testing to evaluate the initiation and propagation of the in situ vitrification (ISV) process in the soil subsurface has been completed. Application of ISV in the soil subsurface both increases the applicable treatment depth (beyond a demonstrated 5 m) and allows treatment of local contamination, such as liquid seepage trenches (found on many US Department of Energy sites) that were designed to remove contamination at the bottom of the trench. The following observations and conclusions resulted from the test data: the ISV process can be initiated in the soil subsurface and propagated in both vertical directions, with the downward direction providing greater ease of operation; energy efficiency to process a kilogram of soil was 20% better than for an ISV melt initiated at the soil surface, increased efficiency was attributed to insulation from the soil overburden; the feasibility of initiating the process with a planar starter path was confirmed, thus increasing the number of options for initiating the process in the field; soil subsidence was pronounced and requires attention before field demonstration of subsurface ISV. Further field work at pilot-scale is recommended for this new ISV application. The key step will be the placement of starter material at depth to initiate the process

Integration of pneumatic fracturing and in situ vitrification in the soil subsurface

Pacific Northwest Laboratory is evaluating ways to increase the applicability of the in situ vitrification (ISV) process at hazardous and radioactive waste sites. One innovation is the placement of a conductive material that will facilitate initiating the ISV process at a target depth. A series of laboratory tests performed at the New Jersey Institute of Technology (NJIT) assessed the feasibility of pneumatic fracturing (PF) in the highly permeable soils of the Hanford Site. The NJIT tests included an analysis of Hanford soils, a series of PF injection tests, and a parametric analysis to determine how soil properties affect the PF process. Results suggest that the PF process can be applied to Hanford soils and that dry medium (e.g., conductive material such as graphite flake) can be injected into the fracture. This paper describes the laboratory testing performed at NJIT, its results, and the application of those results to plans for a field demonstration at Hanford

Feed process studies: Research-Scale Melter

In support of a two-phase approach to privatizing the processing of hazardous and radioactive waste at Hanford, research-scale melter (RSM) experiments were conducted to determine feed processing characteristics of two potential privatization Phase 1 high-level waste glass formulations and to determine if increased Ag, Te, and noble metal amounts would have bad effects. Effects of feed compositions and process conditions were examined for processing rate, cold cap behavior, off-gas, and glass properties. The 2 glass formulations used were: NOM-2 with adjusted waste loading (all components except silica and soda) of 25 wt%, and NOM-3 (max waste loaded glass) with adjusted waste loading of 30 wt%. The 25 wt% figure is the minimum required in the privatization Request for Proposal. RSM operated for 19 days (5 runs). 1010 kg feed was processed, producing 362 kg glass. Parts of runs 2 and 3 were run at 10 to 30 degrees above the nominal temperature 1150 C, with the most significant processing rate increase in run 3. Processing observations led to the choice of NOM-3 for noble metal testing in runs 4 and 5. During noble metal testing, processing rates fell 50% from baseline. Destructive analysis showed that a layer of noble metals and noble metal oxides settled on the floor of the melter, leading to current ``channeling`` which allowed the top section to cool, reducing production rates

ALG-2 and peflin regulate COPII targeting and secretion in response to calcium signaling

ER-to-Golgi transport is the first step in the constitutive secretory pathway, which, unlike regulated secretion, is believed to proceed nonstop independent of Ca2+ flux. However, here we demonstrate that penta-EF hand (PEF) proteins ALG-2 and peflin constitute a hetero-bifunctional COPII regulator that responds to Ca2+ signaling by adopting one of several distinct activity states. Functionally, these states can adjust the rate of ER export of COPII-sorted cargos up or down by ∼50%. We found that at steady-state Ca2+, ALG-2/peflin hetero-complexes bind to ER exit sites (ERES) through the ALG-2 subunit to confer a low, buffered secretion rate, while peflin-lacking ALG-2 complexes markedly stimulate secretion. Upon Ca2+ signaling, ALG-2 complexes lacking peflin can either increase or decrease the secretion rate depending on signaling intensity and duration—phenomena that could contribute to cellular growth and intercellular communication following secretory increases or protection from excitotoxicity and infection following decreases. In epithelial normal rat kidney (NRK) cells, the Ca2+-mobilizing agonist ATP causes ALG-2 to depress ER export, while in neuroendocrine PC12 cells, Ca2+ mobilization by ATP results in ALG-2-dependent enhancement of secretion. Furthermore, distinct Ca2+ signaling patterns in NRK cells produce opposing ALG-2-dependent effects on secretion. Mechanistically, ALG-2-dependent depression of secretion involves decreased levels of the COPII outer shell and increased peflin targeting to ERES, while ALG-2-dependent enhancement of secretion involves increased COPII outer shell and decreased peflin at ERES. These data provide insights into how PEF protein dynamics affect secretion of important physiological cargoes such as collagen I and significantly impact ER stress

Origin of pancreatic ductal adenocarcinoma from atypical flat lesions: A comparative study in transgenic mice and human tissues.

Pancreatic ductal adenocarcinoma (PDAC) and its precursor lesions, pancreatic intraepithelial neoplasia, (PanIN), display a ductal phenotype. However, there is evidence in genetically defined mouse models for PDAC harbouring a mutated kras under the control of a pancreas-specific promoter that ductal cancer might arise in the centroacinar-acinar region, possibly through a process of acinar-ductal metaplasia (ADM). In order to further elucidate this model of PDAC development, an extensive expression analysis and molecular characterization of the putative and already established (PanIN) precursor lesions was performed in the Kras(G12D/+) ;Ptf1a-Cre(ex1/+) mouse model and in human tissues, focusing on lineage markers, developmental pathways, cell cycle regulators, apomucins and stromal activation markers. The results of this study show that areas of ADM are very frequent in the murine and human pancreas and represent regions of increased proliferation of cells with precursor potential. Moreover, atypical flat lesions originating in areas of ADM are the most probable precursors of PDAC in the Kras(G12D/+) ;Ptf1a-cre(ex1/+) mice and similar lesions were also found in the pancreas of three patients with a strong family history of PDAC. In conclusion, PDAC development in Kras(G12D/+) ;Ptf1a-Cre(ex1/+) mice starts from ADM and a similar process might also take place in patients with a strong family history of PDAC