Do you want to publish a course? Click here

Integration of hydrothermal liquefaction and carbon capture and storage for the production of advanced liquid biofuels with negative CO2 emissions

59   0   0.0 ( 0 )
 Added by Eliana Lozano
 Publication date 2020
  fields Physics
and research's language is English




Ask ChatGPT about the research

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.



rate research

Read More

Global temperature is a fundamental climate metric highly correlated with sea level, which implies that keeping shorelines near their present location requires keeping global temperature within or close to its preindustrial Holocene range. However, global temperature excluding short-term variability now exceeds +1degC relative to the 1880-1920 mean and annual 2016 global temperature was almost +1.3degC. We show that global temperature has risen well out of the Holocene range and Earth is now as warm as during the prior interglacial, when sea level reached 6-9 meters higher than today. Further, Earth is out of energy balance with present atmospheric composition, implying more warming is in the pipeline, and we show that the growth rate of greenhouse gas climate forcing has accelerated markedly in the past decade. The rapidity of ice sheet and sea level response to global temperature is difficult to predict but is dependent on the magnitude of warming. Targets for limiting global warming should aim to avoid leaving global temperature at Eemian or higher levels for centuries. Such targets require negative emissions, extraction of CO2 from the air. If phasedown of fossil fuel emissions begins soon, improved agricultural and forestry practices may provide much of the extraction, and the magnitude and duration of global temperature excursion above the natural range of the current interglacial could be limited and irreversible impacts minimized. In contrast, continued high emissions place a burden on young people to undertake massive technological CO2 extraction to limit climate change and its consequences. Proposed methods of extraction have minimal estimated costs of 89-535 trillion dollars this century and have large risks and uncertain feasibility. Continued high emissions unarguably sentences young people to a massive, implausible cleanup, growing deleterious climate impacts or both.
The search for earth abundant, efficient and stable electrocatalysts that can enable the chemical reduction of CO2 to value-added chemicals and fuels at an industrially relevant scale, is a high priority for the development of a global network of renewable energy conversion and storage systems that can meaningfully impact greenhouse gas induced climate change. Here we introduce a straightforward, low cost, scalable and technologically relevant method to manufacture an all-carbon, electroactive, nitrogen-doped nanoporous carbon-carbon nanotube composite membrane, dubbed HNCM-CNT. The membrane is demonstrated to function as a binder-free, high-performance electrode for the electrocatalytic reduction of CO2 to formate. The Faradaic efficiency for the production of formate is 81%. Furthermore, the robust structural and electrochemical properties of the membrane endow it with excellent long-term stability.
132 - Jay Fuhrman 2020
Chinas pledge to reach carbon neutrality before 2060 is an ambitious goal and could provide the world with much-needed leadership on how to limit warming to +1.5C warming above pre-industrial levels by the end of the century. But the pathways that would achieve net zero by 2060 are still unclear, including the role of negative emissions technologies. We use the Global Change Analysis Model to simulate how negative emissions technologies, in general, and direct air capture (DAC) in particular, could contribute to Chinas meeting this target. Our results show that negative emissions could play a large role, offsetting on the order of 3 GtCO2 per year from difficult-to-mitigate sectors such as freight transportation and heavy industry. This includes up to a 1.6 GtCO2 per year contribution from DAC, constituting up to 60% of total projected negative emissions in China. But DAC, like bioenergy with carbon capture and storage and afforestation, has not yet been demonstrated at anywhere approaching the scales required to meaningfully contribute to climate mitigation. Deploying NETs at these scales will have widespread impacts on financial systems and natural resources such as water, land, and energy in China.
The method is proposed for estimation of regional CO2 and other greenhouses and pollutants production responcibility. The comparison of CO2 local emissions reduction data with world CO2 atmosphere data will permit easy to judge for overall effect in curbing not only global warming but also chemical polution.
The catalytic activities of the atomic Y-, Ru-, At-, In-, Pd-, Ag-, Pt-, and Os- ions have been investigated theoretically using the atomic Au- ion as the benchmark for the selective partial oxidation of methane to methanol without CO2 emission. Dispersion-corrected density-functional theory has been used for the investigation. From the energy barrier calculations and the thermodynamics of the reactions, we conclude that the catalytic effect of the atomic Ag-, At-, Ru-, and Os- ions is higher than that of the atomic Au- ion catalysis of CH4 conversion to methanol. By controlling the temperature around 290K (Os-), 300K (Ag-), 310K (At-), 320K (Ru-) and 325K (Au-) methane can be completely oxidized to methanol without the emission of CO2. We conclude by recommending the investigation of the catalytic activities of combinations of the above negative ions for significant enhancement of the selective partial oxidation of methane to methanol.
comments
Fetching comments Fetching comments
Sign in to be able to follow your search criteria
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا