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At least 919 records · Page 51
All sourcesNASA NTRSDOE OSTI
DOE OSTI2019

Fine Calcium Carbonate Production by CO2 Mineralization of Industrial Waste Brines

Calcium carbonate production via CO2 mineralization offers an attractive route for carbon capture and utilization. The process sequesters CO2 in a stable form of fine precipitated calcium carbonate, a high-value product with unit price in the range of $230-$280/t and a global market projected to reach 99 M tons in 2020. However, two critical barriers hinders CO2 mineralization—(i) the need for costly processes such as electrolysis or addition of alkali hydroxides to maintain alkalinity during mineralization, and (ii) the geographic location mismatch between Ca-rich solutions (or brines) CO2 generation sources (e.g. power plants) which often renders efficient integration of feedstocks impractical. To simultaneously address these challenges, a new process is developed to integrate CO2 mineralization-based carbonate production into the zero liquid discharge water (ZLD) treatment systems at coal-fired power plants. In this process, Ca-rich streams, such as produced water from oil and gas extraction or carbon storage operations, serves as the Ca-source. An H+/Na+ ion-exchange cycle is designed to provision alkalinity during mineralization and regenerate the ion-exchange reagent in solutions with high salinity. Ca-depleted streams are then treated within a centralized ZLD system. The process beneficially utilizes reject streams that are available at substantial quantities in the vicinity of coal power plants within several U.S regions. In addition, the process utilizes post-desulfurization flue gas from coal-fired power plants as is. The CO2 conversion reactions are performed in alkaline streams at ambient pressure, thereby minimizing the energy burden. By beneficiation of industrial waste streams with low energy input, this process offers significant technical advantages in energy and CO2 footprint over the current paradigm of precipitated calcium carbonate production. Overall, the new process provides a unique route to integrate CO2 emissions control and wastewater treatment for coal power plants, while producing high-value product to offset the economic burden associated with waste management.

Simonetti, Dante↗
DOE OSTI2019

Fine Calcium Carbonate Production by CO 2 Mineralization of Industrial Waste Brines

Calcium carbonate production via CO 2 mineralization offers an attractive route for carbon capture and utilization. The process sequesters CO 2 in a stable form of fine precipitated calcium carbonate, a high-value product with unit price in the range of $230-$280/t and a global market projected to reach 99 M tons in 2020. However, two critical barriers hinders CO 2 mineralization—(i) the need for costly processes such as electrolysis or addition of alkali hydroxides to maintain alkalinity during mineralization, and (ii) the geographic location mismatch between Ca-rich solutions (or brines) CO 2 generation sources (e.g. power plants) which often renders efficient integration of feedstocks impractical. To simultaneously address these challenges, a new process is developed to integrate CO 2 mineralization-based carbonate production into the zero liquid discharge water (ZLD) treatment systems at coal-fired power plants. In this process, Ca-rich streams, such as produced water from oil and gas extraction or carbon storage operations, serves as the Ca-source. An H + /Na + ion-exchange cycle is designed to provision alkalinity during mineralization and regenerate the ion-exchange reagent in solutions with high salinity. Ca-depleted streams are then treated within a centralized ZLD system. The process beneficially utilizes reject streams that are available at substantial quantities in the vicinity of coal power plants within several U.S regions. In addition, the process utilizes post-desulfurization flue gas from coal-fired power plants as is. The CO 2 conversion reactions are performed in alkaline streams at ambient pressure, thereby minimizing the energy burden. By beneficiation of industrial waste streams with low energy input, this process offers significant technical advantages in energy and CO 2 footprint over the current paradigm of precipitated calcium carbonate production. Overall, the new process provides a unique route to integrate CO 2 emissions control and wastewater treatment for coal power plants, while producing high-value product to offset the economic burden associated with waste management

Simonetti, Dante↗
DOE OSTI2019

Fine Calcium Carbonate Production by CO 2 Mineralization of Industrial Waste Brines

Calcium carbonate production via CO 2 mineralization offers an attractive route for carbon capture and utilization. The process sequesters CO 2 in a stable form of fine precipitated calcium carbonate, a high-value product with unit price in the range of $230-$280/t and a global market projected to reach 99 M tons in 2020. However, two critical barriers hinders CO 2 mineralization—(i) the need for costly processes such as electrolysis or addition of alkali hydroxides to maintain alkalinity during mineralization, and (ii) the geographic location mismatch between Ca-rich solutions (or brines) CO 2 generation sources (e.g. power plants) which often renders efficient integration of feedstocks impractical. To simultaneously address these challenges, a new process is developed to integrate CO 2 mineralization-based carbonate production into the zero liquid discharge water (ZLD) treatment systems at coal-fired power plants. In this process, Ca-rich streams, such as produced water from oil and gas extraction or carbon storage operations, serves as the Ca-source. An H + /Na + ion-exchange cycle is designed to provision alkalinity during mineralization and regenerate the ion-exchange reagent in solutions with high salinity. Ca-depleted streams are then treated within a centralized ZLD system. The process beneficially utilizes reject streams that are available at substantial quantities in the vicinity of coal power plants within several U.S regions. In addition, the process utilizes post-desulfurization flue gas from coal-fired power plants as is. The CO 2 conversion reactions are performed in alkaline streams at ambient pressure, thereby minimizing the energy burden. By beneficiation of industrial waste streams with low energy input, this process offers significant technical advantages in energy and CO 2 footprint over the current paradigm of precipitated calcium carbonate production. Overall, the new process provides a unique route to integrate CO 2 emissions control and wastewater treatment for coal power plants, while producing high-value product to offset the economic burden associated with waste management.

Simonetti, Dante↗
DOE OSTI2019

Fine Calcium Carbonate Production by CO 2 Mineralization of Industrial Waste Brines

Calcium carbonate production via CO 2 mineralization offers an attractive route for carbon capture and utilization. The process sequesters CO 2 in a stable form of fine precipitated calcium carbonate, a high-value product with unit price in the range of $230-$280/t and a global market projected to reach 99 M tons in 2020. However, two critical barriers hinders CO 2 mineralization—(i) the need for costly processes such as electrolysis or addition of alkali hydroxides to maintain alkalinity during mineralization, and (ii) the geographic location mismatch between Ca-rich solutions (or brines) CO 2 generation sources (e.g. power plants) which often renders efficient integration of feedstocks impractical. To simultaneously address these challenges, a new process is developed to integrate CO 2 mineralization-based carbonate production into the zero liquid discharge water (ZLD) treatment systems at coal-fired power plants. In this process, Ca-rich streams, such as produced water from oil and gas extraction or carbon storage operations, serves as the Ca-source. An H + /Na + ion-exchange cycle is designed to provision alkalinity during mineralization and regenerate the ion-exchange reagent in solutions with high salinity. Ca-depleted streams are then treated within a centralized ZLD system. The process beneficially utilizes reject streams that are available at substantial quantities in the vicinity of coal power plants within several U.S regions. In addition, the process utilizes post-desulfurization flue gas from coal-fired power plants as is. The CO 2 conversion reactions are performed in alkaline streams at ambient pressure, thereby minimizing the energy burden. By beneficiation of industrial waste streams with low energy input, this process offers significant technical advantages in energy and CO 2 footprint over the current paradigm of precipitated calcium carbonate production. Overall, the new process provides a unique route to integrate CO 2 emissions control and wastewater treatment for coal power plants, while producing high-value product to offset the economic burden associated with waste management.

Simonetti, Dante↗
DOE OSTI2019

Fine Calcium Carbonate Production by CO 2 Mineralization of Industrial Waste Brines

Calcium carbonate production via CO 2 mineralization offers an attractive route for carbon capture and utilization. The process sequesters CO 2 in a stable form of fine precipitated calcium carbonate, a high-value product with unit price in the range of $230-$280/t and a global market projected to reach 99 M tons in 2020. However, two critical barriers hinders CO 2 mineralization—(i) the need for costly processes such as electrolysis or addition of alkali hydroxides to maintain alkalinity during mineralization, and (ii) the geographic location mismatch between Ca-rich solutions (or brines) CO 2 generation sources (e.g. power plants) which often renders efficient integration of feedstocks impractical. To simultaneously address these challenges, a new process is developed to integrate CO 2 mineralization-based carbonate production into the zero liquid discharge water (ZLD) treatment systems at coal-fired power plants. In this process, Ca-rich streams, such as produced water from oil and gas extraction or carbon storage operations, serves as the Ca-source. An H + /Na + ion-exchange cycle is designed to provision alkalinity during mineralization and regenerate the ion-exchange reagent in solutions with high salinity. Ca-depleted streams are then treated within a centralized ZLD system. The process beneficially utilizes reject streams that are available at substantial quantities in the vicinity of coal power plants within several U.S regions. In addition, the process utilizes post-desulfurization flue gas from coal-fired power plants as is. The CO 2 conversion reactions are performed in alkaline streams at ambient pressure, thereby minimizing the energy burden. By beneficiation of industrial waste streams with low energy input, this process offers significant technical advantages in energy and CO 2 footprint over the current paradigm of precipitated calcium carbonate production. Overall, the new process provides a unique route to integrate CO 2 emissions control and wastewater treatment for coal power plants, while producing high-value product to offset the economic burden associated with waste management.

Simonetti, Dante↗
DOE OSTI2020

Ground-based observations of cloud and drizzle liquid water path in stratocumulus clouds

Abstract. The partition of cloud and drizzle water path in precipitating clouds plays a key role in determining the cloud lifetime and its evolution. A technique to quantify cloud and drizzle water path by combining measurements from a three-channel microwave radiometer (23.8, 30, and 90 GHz) with those from a vertically pointing Doppler cloud radar and a ceilometer is presented. The technique is showcased using 1 d of observations to derive precipitable water vapor, liquid water path, cloud water path, drizzle water path below the cloud base, and drizzle water path above the cloud base in precipitating stratocumulus clouds. The resulting cloud and drizzle water path within the cloud are in good qualitative agreement with the information extracted from the radar Doppler spectra. The technique is then applied to 10 d each of precipitating closed and open cellular marine stratocumuli. In the closed-cell systems only ~20 % of the available drizzle in the cloud falls below the cloud base, compared to ~40 % in the open-cell systems. In closed-cell systems precipitation is associated with radiative cooling at the cloud top <-100W m -2 and a liquid water path >200 g m -2 . However, drizzle in the cloud begins to exist at weak radiative cooling and liquid water path >~150 g m-2. Our results collectively demonstrate that neglecting scattering effects for frequencies at and above 90 GHz leads to overestimation of the total liquid water path of about 10 %–15 %, while their inclusion paves the path for retrieving drizzle properties within the cloud.

Cadeddu, Maria P.↗
DOE OSTI2024

Improved Characterization of Soil Organic Matter by Integrating FT-ICR MS, Liquid Chromatography Tandem Mass Spectrometry, and Molecular Networking: A Case Study of Root Litter Decay under Drought Conditions

Understanding of how soil organic matter (SOM) chemistry is altered in a changing climate has advanced considerably; however, most SOM components remain unidentified, impeding the ability to characterize a major fraction of organic matter and predict what types of molecules, and from which sources, will persist in soil. Here we present a novel approach to better characterize SOM extracts by integrating information from three types of analyses, and we deploy this method to characterize decaying root-detritus soil microcosms subjected to either drought or normal conditions. To observe broad differences in composition, we employed direct infusion Fourier-transform ion cyclotron resonance mass spectrometry (DI-FT-ICR MS). We complemented this with liquid chromatography tandem mass spectrometry (LC-MS/MS) to identify components by library matching. Since libraries contain only a small fraction of SOM components, we also used fragment spectral cosine similarity scores to relate unknowns and library matches through molecular networks. This integrated approach allowed us to corroborate DI-FT-ICR MS molecular formulas using library matches, which included fungal metabolites and related polyphenolic compounds. We also inferred structures of unknowns from molecular networks and improved LC-MS/MS annotation rates from ~5 to 35% by considering DI-FT-ICR MS molecular formula assignments. Under drought conditions, we found greater relative amounts of lignin-like vs condensed aromatic polyphenol formulas and lower average nominal oxidation state of carbon, suggesting reduced decomposition of SOM and/or microbes under stress. Our integrated approach provides a framework for enhanced annotation of SOM components that is more comprehensive than performing individual data analyses in parallel.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2019

Fluctuating phases and fluctuating relaxation times in glass forming liquids

The presence of fluctuating local relaxation times, τ r → ( t ) has been used for some time as a conceptual tool to describe dynamical heterogeneities in glass-forming systems. However, until now no general method is known to extract the full space and time dependent τ$^→_r$(t) from experimental or numerical data. Here we report on a new method for determining a local phase field, Φ r → ( t ) ≡ ∫ t d t ' τ r → ( t ' ) from snapshots { r → ( t i ) } i = 1 … M of the positions of the particles in a system, and we apply it to extract Φ r → ( t ) and τ r → ( t ) from numerical simulations. By studying how this phase field depends on the number of snapshots, we find that it is a well defined quantity. By studying fluctuations of the phase field, we find that they describe heterogeneities well at long distance scales.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2016

Transmission X-ray scattering as a probe for complex liquid-surface structures

The need for functional materials calls for increasing complexity in self-assembly systems. As a result, the ability to probe both local structure and heterogeneities, such as phase-coexistence and domain morphologies, has become increasingly important to controlling self-assembly processes, including those at liquid surfaces. The traditional X-ray scattering methods for liquid surfaces, such as specular reflectivity and grazing-incidence diffraction, are not well suited to spatially resolving lateral heterogeneities due to large illuminated footprint. A possible alternative approach is to use scanning transmission X-ray scattering to simultaneously probe local intermolecular structures and heterogeneous domain morphologies on liquid surfaces. To test the feasibility of this approach, transmission small- and wide-angle X-ray scattering (TSAXS/TWAXS) studies of Langmuir films formed on water meniscus against a vertically immersed hydrophilic Si substrate were recently carried out. First-order diffraction rings were observed in TSAXS patterns from a monolayer of hexagonally packed gold nanoparticles and in TWAXS patterns from a monolayer of fluorinated fatty acids, both as a Langmuir monolayer on water meniscus and as a Langmuir–Blodgett monolayer on the substrate. The patterns taken at multiple spots have been analyzed to extract the shape of the meniscus surface and the ordered-monolayer coverage as a function of spot position. These results, together with continual improvement in the brightness and spot size of X-ray beams available at synchrotron facilities, support the possibility of using scanning-probe TSAXS/TWAXS to characterize heterogeneous structures at liquid surfaces.

Fukuto, Masafumi↗
DOE OSTI2023

Anti-fungal bioactive terpenoids in the bioenergy crop switchgrass (Panicum virgatum) may contribute to ecotype-specific microbiome composition

Abstract Plant derived bioactive small molecules have attracted attention of scientists across fundamental and applied scientific disciplines. We seek to understand the influence of these phytochemicals on rhizosphere and root-associated fungi. We hypothesize that – consistent with accumulating evidence that switchgrass genotype impacts microbiome assembly – differential terpenoid accumulation contributes to switchgrass ecotype-specific microbiome composition. An initial in vitro Petri plate-based disc diffusion screen of 18 switchgrass root derived fungal isolates revealed differential responses to upland- and lowland-isolated metabolites. To identify specific fungal growth-modulating metabolites, we tested fractions from root extracts on three ecologically important fungal isolates – Linnemania elongata, Trichoderma sp. and Fusarium sp. Saponins and diterpenoids were identified as the most prominent antifungal metabolites. Finally, analysis of liquid chromatography-purified terpenoids revealed fungal inhibition structure – activity relationships (SAR). Saponin antifungal activity was primarily determined by the number of sugar moieties – saponins glycosylated at a single core position were inhibitory whereas saponins glycosylated at two core positions were inactive. Saponin core hydroxylation and acetylation were also associated with reduced activity. Diterpenoid activity required the presence of an intact furan ring for strong fungal growth inhibition. These results inform future breeding and biotechnology strategies for crop protection with reduced pesticide application.

09 BIOMASS FUELS↗
DOE OSTI2018

Sesame-style decomposition of KS-DFT molecular dynamics for direct interrogation of nuclear models

A common paradigm used in the construction of equations of state is to decompose the thermodynamics into a superposition of three terms: a static-lattice cold curve, a contribution from the thermal motion of the nuclei, and a contribution from the thermal excitation of the electrons. While statistical mechanical models for crystals provide tractable framework for the nuclear contribution in the solid phase, much less is understood about the nuclear contribution above the % melt temperature $(C^{(nuc)}_ν≈3R)$ and how it should transition to the high-temperature limit $(C^{(nuc)}_ν\sim\frac{3}{2}R)$. Here, we describe an algorithm for extracting both the thermal nuclear and thermal electronic contributions from quantum molecular dynamics (QMD) simulations. We then use the VASP QMD package to probe thermal nuclear behavior of liquid aluminum at normal density to compare the results to semi-empirical models – the Johnson generic model, the Chisolm high-temperature liquid model, and the CRIS model. The thermal electronic energy is also calculated from the VASP results and compared to the Kohn-Sham calculations from QE-DFT simulations, Green’s function average atom calculations, and the Thomas-Fermi atomic model.

74 ATOMIC AND MOLECULAR PHYSICS↗
DOE OSTI2021

MetFish: a Metabolomics Pipeline for Studying Microbial Communities in Chemically Extreme Environments

Metabolites have essential roles in microbial communities, including as mediators of nutrient and energy exchange, cell-to-cell communication, and antibiosis. However, detecting and quantifying metabolites and other chemicals in samples having extremes in salt or mineral content using liquid chromatography-mass spectrometry (LC-MS)-based methods remains a significant challenge. Here, we report a facile method based on in situ chemical derivatization followed by extraction for analysis of metabolites and other chemicals in hypersaline samples, enabling for the first time direct LC-MS-based exometabolomics analysis in sample matrices containing up to 2 M total dissolved salts. The method, MetFish, is applicable to molecules containing amine, carboxylic acid, carbonyl, or hydroxyl functional groups, and it can be integrated into either targeted or untargeted analysis pipelines. In targeted analyses, MetFish provided limits of quantification as low as 1 nM, broad linear dynamic ranges (up to 5 to 6 orders of magnitude) with excellent linearity, and low median interday reproducibility (e.g., 2.6%). MetFish was successfully applied in targeted and untargeted exometabolomics analyses of microbial consortia, quantifying amino acid dynamics in the exometabolome during community succession; in situ in a native prairie soil, whose exometabolome was isolated using a hypersaline extraction; and in input and produced fluids from a hydraulically fractured well, identifying dramatic changes in the exometabolome over time in the well.

59 BASIC BIOLOGICAL SCIENCES↗
DOE OSTI2020

Data for Variability in Structural Carbohydrates, Lipid Composition, and Cellulosic Sugar Production from Industrial Hemp Varieties

The aim of this study was to determine carbohydrate recovery from hemp for ethanol production and quantify biodiesel from TAG (triacylglycerol) present in hemp. The structural composition of five different hemp varieties (Seward County-SC, York County-YC, Loup County-LC, 19 m96136-19 m, and CBD Hemp-CBD) were analyzed. Concentration of glucan and xylan ranged between 32.63 to 44.52% and 10.62 to 15.48% respectively. The biomass was then pretreated with Liquid hot water followed by disk milling and then hydrolyzed enzymatically to yield monomeric sugars. High glucose (63-85%) and xylose (73-88%) recovery was achieved. Lipids were extracted from hemp using hexane and isopropanol and then transesterified to produce biodiesel. Approximately, 50% of total fatty acids in SC, LC, and CBD hemp were linoleic acid. Palmitic acid was present between 32 to 50% in varieties YC and 19 m. Highest TAG concentration at 25% of total lipids was observed in CBD hemp. The analysis on lipid composition and high sugar recovery demonstrates hemp as a potential bioenergy crop for ethanol and biodiesel coproduction.

Biomass Analytics↗
NASA NTRS1977

Thermal alteration experiments on organic matter from recent marine sediments in relation to petroleum genesis

Three fractions of organic matter: lipid (benzene:methanol-extractable), humic acid (alkali-extractable) and kerogen (residue) were extracted from a young marine sediment (Tanner Basin, offshore southern California) and heated for different times (5-116 hr) and temperatures (150-410 C). The volatile (gases) and liquid products, as well as residual material, were then analyzed. On a weight basis, the lipid fraction produced 58% of the total identified n-alkanes, the kerogen fraction 41%, and the humic acid less than 1%. The volatiles produced by heating the lipid and humic acid fractions were largely CO2 and water, whereas those produced from heated kerogen also included methane, hydrogen gas and small amounts of C2-C4 hydrocarbons. A mechanism for hydrocarbon production due to the thermal alteration of organic constituents of marine sediment is discussed.

Ishiwatari, R.↗
NASA NTRS1987

The indirect electrochemical refining of lunar ores

Recent work performed on an electrolytic cell is reported which addresses the implicit limitations in various approaches to refining lunar ores. The cell uses an oxygen vacancy conducting stabilized zirconia solid electrolyte to effect separation between a molten salt catholyte compartment where alkali metals are deposited, and an oxygen-evolving anode of composition La(0.89)Sr(0.1)MnO3. The cell configuration is shown and discussed along with a polarization curve and a steady-state current-voltage curve. In a practical cell, cathodically deposited liquid lithium would be continuously removed from the electrolytic cell and used as a valuable reducing agent for ore refining under lunar conditions. Oxygen would be indirectly electrochemically extracted from lunar ores for breathing purposes.

Semkow, Krystyna W.↗
NASA NTRS1993

Evaporation Of Clusters Of Drops In A Jet

Report presents theoretical study of evaporation of clusters of liquid drops injected with gas jet flowing into hot ambient gas. One in series of studies of various aspects of behavior of sprays. Simplified mathematical models used to extract qualitative information on trends in interactions.

Bellan, Josette↗
NASA NTRS1998

Purification and Crystal Growth of Lead Iodide by Physical Vapor Transport Method

Lead iodide (PbI2) is a layered compound semiconductor being developed as room temperature x- and gamma-ray detector. Compared to the more studied material, mercuric iodide, PbI2 has a higher melting temperature and no phase transition until liquid phase which are indications of better mechanical properties. In this study, the source material was purified by the zone-refining process, and the purest section was extracted from center of the the zone-refined ingot to be grown by physical vapor transport (PVT) method. The zone-refined material and as-grown crystals were characterized by optical microscopy and differential scanning calorimetry (DSC) to reveal the surface morphology, purity and stoichiometry. The results shows that both materials are near-stoichiometric composition, with the purity of the as-grown crystals higher than zone-refined materials. The resistivity of the as-grown crystal (10" Omega-cm) was derived from current-voltage (I-V) measurement, and is 10 times higher than the zone-refined materials. Detail results will be presented and discussed.

Wright, G. W.↗
NASA NTRS2011

Distinct Purine Distribution in Carbonaceous Chondrites

Carbonaceous chondrite meteorites are known to contain a diverse suite of organic compounds, many of which are essential components of biochemistry. Amino acids, which are the monomers of proteins, have been extensively studied in such meteorites (e.g. Botta and Bada 2002; Pizzarello et aI., 2006). The origin of amino acids in meteorites has been firmly established as extraterrestrial based on their detection typically as racemic mixtures of amino acids, the presence of many non-protein amino acids, and non-terrestrial values for compound-specific deuterium, carbon, and nitrogen isotopic measurements. In contrast to amino acids, nucleobases in meteorites have been far less studied. Nucleobases are substituted one-ring (pyrimidine) or two-ring (purine) nitrogen heterocyclic compounds and serve as the information carriers of nucleic acids and in numerous coenzymes. All of the purines (adenine, guanine, hypoxanthine, and xanthine) and pyrimidines (uracil) previously reported in meteorites are biologically common and could be interpreted as the result of terrestrial contamination (e.g. van del' Velden and Schwartz, 1974.) Unlike other meteoritic organics, there have been no observations of stochastic molecular diversity of purines and pyrimidines in meteorites, which has been a criterion for establishing extraterrestrial origin. Maltins et al. (2008) performed compound-specific stable carbon isotope measurements for uracil and xanthine in the Murchison meteorite. They assigned a non-terrestrial origin for these nucleobases; however, the possibility that interfering indigenous molecules (e.g. carboxylic acids) contributed to the 13C-enriched isotope values for these nucleobases cannot be completely ruled out. Thus, the origin of these meteoritic nucleobases has never been established unequivocally. Here we report on our investigation of extracts of II different carbonaceous chondrites covering various petrographic types (Cl, CM, and CR) and degrees of aqueous alteration (l, 2, and 3) and one ureilite. Analysis via liquid chromatography coupled with electrospray triple-stage mass spectrometry or orbitrap mass spectrometry employed a targeted approach for analysis focused on the five canonical RNA/DNA nucleobases as well as 14 non-canonical pyrimidines and purines, which have bcen observed under plausible prebiotic reactions.

Callahan, Michael P.↗