17,530 research outputs found
Simulation of the CryoSat-2 satellite radar altimeter sea ice thickness retrieval uncertainty
Oxygen minimum zone expansion in the eastern tropical North Pacific during deglaciation
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/95396/1/grl21420.pd
Selected new developments in computational chemistry.
Molecular dynamics is a general technique for simulating the time-dependent properties of molecules and their environments. Quantum mechanics, as applied to molecules or clusters of molecules, provides a prescription for predicting properties exactly (in principle). It is reasonable to expect that both will have a profound effect on our understanding of environmental chemistry in the future. In this review, we consider several recent advances and applications in computational chemistry
Synthesis and analysis of jet fuel from shale oil and coal syncrudes
Thirty-two jet fuel samples of varying properties were produced from shale oil and coal syncrudes, and analyzed to assess their suitability for use. TOSCO II shale oil and H-COAL and COED syncrudes were used as starting materials. The processes used were among those commonly in use in petroleum processing-distillation, hydrogenation and catalytic hydrocracking. The processing conditions required to meet two levels of specifications regarding aromatic, hydrogen, sulfur and nitrogen contents at two yield levels were determined and found to be more demanding than normally required in petroleum processing. Analysis of the samples produced indicated that if the more stringent specifications of 13.5% hydrogen (min.) and 0.02% nitrogen (max.) were met, products similar in properties to conventional jet fuels were obtained. In general, shale oil was easier to process (catalyst deactivation was seen when processing coal syncrudes), consumed less hydrogen and yielded superior products. Based on these considerations, shale oil appears to be preferred to coal as a petroleum substitute for jet fuel production
Cruise Report GS12A - Scientific cruise to the Sleipner area in the North Sea ; R/V G.O. Sars Expedition No. 2012108/CGB2012, June 22th - 30th 2012, Bergen, Norway - Bergen, Norway
Full characterization of compounds obtained from fractional distillation and upgrading of a HTL biocrude
Integration of hydrothermal liquefaction and carbon capture and storage for the production of advanced liquid biofuels with negative CO2 emissions
The technical and economic feasibility to deliver sustainable liquid biocrude
through hydrothermal liquefaction (HTL) while enabling negative carbon dioxide
emissions is evaluated in this paper, looking into the potential of the process
in the context of negative emission technologies (NETs) for climate change
mitigation. In the HTL process, a gas phase consisting mainly of carbon dioxide
is obtained as a side product driving a potential for the implementation of
carbon capture and storage in the process (BECCS) that has not been explored
yet in the existing literature and is undertaken in this study. To this end,
the process is divided in a standard HTL base and a carbon capture add-on,
having forestry residues as feedstock. The Selexol technology is adapted in a
novel scheme to simultaneously separate the CO2 from the HTL gas and recover
the excess hydrogen for biocrude upgrading. The cost evaluation indicates that
the additional cost of the carbon capture can be compensated by revenues from
the excess process heat and the European carbon allowance market. The impact in
the MFSP of the HTL base case ranges from -7% to 3%, with -15% in the most
favorable scenario, with a GHG emissions reduction potential of 102-113%
compared to the fossil baseline. These results show that the implementation of
CCS in the HTL process is a promising alternative from technical, economic and
environmental perspective in future scenarios in which advanced liquid biofuels
and NETs are expected to play a role in the decarbonization of the energy
system
Volume-energy correlations in the slow degrees of freedom of computer-simulated phospholipid membranes
Constant-pressure molecular-dynamics simulations of phospholipid membranes in
the fluid phase reveal strong correlations between equilibrium fluctuations of
volume and energy on the nanosecond time-scale. The existence of strong
volume-energy correlations was previously deduced indirectly by Heimburg from
experiments focusing on the phase transition between the fluid and the ordered
gel phases. The correlations, which are reported here for three different
membranes (DMPC, DMPS-Na, and DMPSH), have volume-energy correlation
coefficients ranging from 0.81 to 0.89. The DMPC membrane was studied at two
temperatures showing that the correlation coefficient increases as the phase
transition is approached
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