The U.S. Department of Energy (DOE) promotes the production of a range of liquid fuels and fuel blendstocks from lignocellulosic biomass feedstocks by funding fundamental and applied research that advances the state of technology in biomass collection, conversion, and sustainability. As part of its involvement in this program, the National Renewable Energy Laboratory (NREL) investigates the conceptual production economics of these fuels.Between 1999 and 2012, NREL conducted a campaign to quantify the economic implications associated with measured conversion performance for the biochemical production of cellulosic ethanol, with a formal program between 2007-2012 to set cost goals and to benchmark annual performance toward achieving these goals, namely the pilot-scale demonstration by 2012 of biochemical ethanol production at a price competitive with petroleum gasoline based on modeled assumptions for an "n th " plant biorefinery. This goal was successfully achieved through NREL's 2012 pilot plant demonstration runs, representing the culmination of NREL research focused specifically on cellulosic ethanol, and a benchmark for industry to leverage as it commercializes the technology. This important milestone also represented a transition toward a new Program focus on infrastructure-compatible hydrocarbon biofuel pathways, and the establishment of new research directions and cost goals across a number of potential conversion technologies.This report describes in detail one potential conversion process to hydrocarbon products by way of biological conversion of lignocellulosic-derived sugars. The pathway model leverages expertise established over time in core conversion and process integration research at NREL, while adding in new technology areas primarily for hydrocarbon production and associated processing logistics. The overarching process design converts biomass to a hydrocarbon intermediate, represented here as a free fatty acid, using dilute-acid pretreatment, enzymatic saccharification, and bioconversion. Ancillary areas-feed handling, hydrolysate conditioning, product recovery and upgrading (hydrotreating) to a final blendstock material, wastewater treatment, lignin combustion, and utilities-are also included in the design. Detailed material and energy balances and capital and operating costs for this baseline process are also documented.This benchmark case study techno-economic model provides a production cost for a cellulosic renewable diesel blendstock (RDB) that can be used as a baseline to assess its competitiveness and market potential. It can also be used to quantify the economic impact of individual conversion performance targets and prioritize these in terms of their potential to reduce cost. The analysis presented here also includes consideration of the life-cycle implications of the baseline process model, by tracking sustainability metrics for the modeled biorefinery, including greenhouse gas (GHG) emissions, fossil energy demand, and consumptive water use.Building on prior design reports for bioch...

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SUMMARY Crosslinking of IgE-bound FcεRI triggers mast cell degranulation. Previous FRAP and phosphorescent anisotropy studies suggested that FcεRI must immobilize to signal. Here, single quantum dot (QD) tracking and hyperspectral microscopy methods are used to redefine relationships between receptor mobility and signaling. QD-IgE-FcεRI aggregates of at least three receptors remain highly mobile over extended times at low concentrations of antigen that induce Syk kinase activation and near-maximal secretion. Multivalent antigen, presented as DNP-QD, also remains mobile at low doses that support secretion. FcεRI immobilization is marked at intermediate and high antigen concentrations, correlating with increases in cluster size and rates of receptor internalization. The kinase inhibitor PP2 blocks secretion without affecting immobilization or internalization. We propose that immobility is a feature of highly crosslinked immunoreceptor aggregates, is a trigger for receptor internalization, and is not required for tyrosine kinase activation leading to secretion.

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