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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 73 records · Page 4
All sourcesNASA NTRSDOE OSTI
DOE OSTI2019

EXPERIMENTAL STUDY OF THE EFFECT OF START OF INJECTION AND BLEND RATIO ON SINGLE FUEL REFORMATE RCCI

A new concept of single-fuel RCCI has been proposed through the catalytic partial oxidation reformation of diesel fuel. The reformed fuel mixture is then used as the low reactivity fuel and diesel itself is used as the high reactivity fuel. In this paper, two selected reformates mixture from the reformation of diesel were selected for further analysis. Each reformate fuel mixture contained a significant fraction of inert gases (89% and 81%). The effects of the difference in the molar concentrations of the reformate mixtures were studied by experimenting with diesel as the direct injected fuel in RCCI over a varying start of injection timings and different blend ratios (i.e., the fraction of low and high reactivities fuels). The reformate mixture with the lower inert gas concentration had earlier combustion phasing and shorter combustion duration at any given diesel start of injection timing. The higher reactivity separation between reformate mixture and diesel, compared with gasoline and diesel, causes the combustion phasing of reformate-diesel RCCI to be more sensitive to the start of injection timing. The maximum combustion efficiency was found at a CA50 before TDC, whereas the maximum thermal efficiency occurs at a CA50 after TDC. The range of energy-based blend ratios in which reformate-diesel RCCI is possible is between 25% and 45%, limited by ringing intensity (RI) at the low limit of blend ratios, and COV of IMEP and combustion efficiency at the high limit. Intake boosting becomes necessary due to the oxygen deficiency caused by the low energy density of the reformate mixtures as it displaces intake air.

Hariharan, Deivanayagam↗
DOE OSTI2012

Chemical Analysis of Complex Organic Mixtures Using Reactive Nanospray Desorption Electrospray Ionization Mass Spectrometry

Reactive nanospray desorption electrospray ionization (nano-DESI) combined with high-resolution mass spectrometry was utilized for the analysis of secondary organic aerosol produced through ozonolysis of limonene (LSOA). Previous studies showed that LSOA constituents are multifunctional compounds containing aldehyde and ketone groups. In this study, we used the selectivity of the Girard T (GT) reagent towards carbonyl compounds to examine the utility of reactive nano-DESI for the analysis of complex organic mixtures. In these experiments, 1-100 {micro}M GT solution was used as a working solvent for reactive nano-DESI analysis. Abundant products of a single addition of GT to LSOA constituents were observed at GT concentrations in excess of 10 {micro}M. We found that LSOA compounds with 18-20 carbon atoms (dimers) and 27-30 carbon atoms (trimers) react with GT through a simple addition reaction resulting in formation of the carbinolamine derivative. In contrast, reactions of GT with monomeric species result in formation of both the carbinolamine and the hydrazone derivatives. In addition, several monomers did not react with GT on the timescale of our experiment. These molecules were characterized by relatively high values of the double bond equivalent (DBE) and low oxygen content. Furthermore, because addition of a charged GT tag to a neutral molecule eliminates the discrimination against the low proton affinity compounds in the ionization process, reactive nano-DESI analysis enables quantification of individual compounds in the complex mixture. For example, we were able to estimate for the first time the amounts of dimers and trimers in the LSOA mixture. Specifically, we found that the most abundant LSOA dimer was detected at ca. 0.5 pg level and the total amount of dimers and trimers in the analyzed sample was just around 11 pg. Our results indicate that reactive nano-DESI is a valuable approach for examining the presence of specific functional groups and quantification of compounds possessing these groups in complex mixtures.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
DOE OSTI2019

Phase, morphology, elemental composition, and formation mechanisms of biogenic and abiogenic Fe-Cu-sulfide nanoparticles: A comparative study on their occurrences under anoxic conditions

In this paper, we report on a systematic study on the physicochemical attributes of synthetic Fe-Cu-sulfide nanoparticles (NPs) precipitated under conditions similar to the anoxic, low temperature aqueous, sedimentary, soil and subsurface environments where these NPs have been repeatedly identified. Characterizing the basic attributes of these NPs is the first step in understanding their behaviors in various processes including in the bio-availability of essential and toxic metals, environmental remediation and resource recovery. All experiments are performed in the presence and absence of the sulfate-reducer Desulfovibrio vulgaris to elucidate biological controls on NP formation. First, the single-metal endmember NPs are determined by precipitation in solution containing either aqueous Fe(II) or Cu(II). Limited differences are observed between biogenic and abiogenic precipitates aged for up to one month; the Fe-only experiments resulted in 4-10 nm mackinawite (FeS) NPs that aggregate to form nanosheets up to ~1,000 nm in size, while the Cu-only experiments resulted in mixtures of covellite (CuS) NPs comprised of <10 nm fine nanocrystals, 20-40 x 6-9 nm nanorods and ~30 nm nanoplates. The crystal sizes of biogenic mackinawite and covellite are respectively larger and smaller than their abiogenic counterparts, indicating a mineral-specific response to biological presence. Structural defects are observable in the fine nanocrystals and nanorods of covellite in both biogenic and abiogenic experiments, indicative of intrinsic NP instability and formation mechanism via particle attachment. In contrast, covellite nanoplates are defect-free, indicating high stability and potentially rapid recrystallization following particle attachment. Next, mixed-metal sulfide NPs are precipitated at variable initial aqueous Fe-to-Cu ratios (2:1, 1:1 and 1:5). With increasing ratio of Fe-to-Cu, Fe-rich covellite, nukundamite (Cu 5.5 FeS 6.5 ), chalcopyrite (CuFeS 2 ), and Cu-rich mackinawite are formed. The Fe-rich covellite NPs are larger (100-200 nm) than covellite precipitated in the absence of Fe, indicating a role for Fe in promoting crystal growth. Chalcopyrite and nukundamite are formed through incorporation of Fe into precursor covellite NPs while retaining the original crystal morphology, as confirmed by doping a covellite suspension with aqueous Fe(II), resulting in the formation of chalcopyrite and nukundamite within days. Additionally, in the biological systems we observe the recrystallization of mackinawite to greigite (Fe 3 S 4 ) after six months of incubation in the absence of Cu, and the selective formation of chalcopyrite and nukundamite at lower initial Fe-to-Cu ratios compared to abiotic systems. These observations are consistent with NP precipitation that are influenced by the distinct (sub)micro-environments around bacterial cells compared to the bulk solution. Lastly, comparative TEM analyses indicate that the synthetic NPs are morphologically similar to NPs identified in natural environments, opening ways to studying behaviors of natural NPs using experimental approaches.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Fundamental Studies on Poly(2-oxazoline) Side Chain Isomers Using Tandem Mass Spectrometry and Ion Mobility-Mass Spectrometry

When polymer mixtures become increasingly complex, the conventional analysis techniques become insufficient for complete characterization. Mass spectrometric techniques can satisfy this increasing demand for detailed sample characterization. Even though isobaric polymers are indistinguishable using simple mass spectrometry (MS) analyses, more advanced techniques such as tandem MS (MS/MS) or ion mobility (IM) can be used. Here, we report proof of concept for characterizing isomeric polymers, namely poly(2-n-propyl-2-oxazoline) (Pn-PrOx) and poly(2-isopropyl-2-oxazoline) (Pi-PrOx), using MS/MS and IM-MS. Pi-PrOx ions lose in intensity at higher accelerating voltages than Pn-PrOx ions during collision-induced dissociation (CID) MS/MS experiments. A Pn/i-PrOx mixture could also be titrated using survival yield calculations of either precursor ions or cation ejection species. IM-MS yielded shape differences in the degree of polymerization (DP) regions showing the structural rearrangements. Combined MS techniques are thus able to identify and deconvolute the molar mass distributions of the two isomers in a mixture. Finally, the MS/MS and IM-MS behaviors are compared for interpretation. .

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2019

Laboratory measurements of geometrical effects in the x-ray emission of optically thick lines for ICF diagnostics

Understanding the effects of radiative transfer in High Energy Density Physics experiments is critical for the characterization of the thermodynamic properties of highly ionized matter, in particular in Inertial Confinement Fusion (ICF). In this paper, we report on non-Local Thermodynamic Equilibrium experiments on cylindrical targets carried out at the Omega Laser Facility at the Laboratory for Laser Energetics, Rochester NY, which aim to characterize these effects. In these experiments, a 50/50 mixture of iron and vanadium, with a thickness of 2000 Å and a diameter of 250 μm, is contained within a beryllium tamper, with a thickness of 10 μm and a diameter of 1000 μm. Each side of the beryllium tamper is then irradiated using 18 of the 60 Omega beams with an intensity of roughly 3 × 10 14 W cm -2 per side, over a duration of 3 ns. Spectroscopic measurements show that a plasma temperature on the order of 2 keV was produced. Imaging data show that the plasma remains cylindrical, with geometrical aspect ratios (quotient between the height and the radius of the cylinder) from 0.4 to 2.0. The temperatures in this experiment were kept sufficiently low (~1–2 keV) so that the optically thin Li-like satellite emission could be used for temperature diagnosis. This allowed for the characterization of optical-depth-dependent geometric effects in the vanadium line emission. Lastly, simulations present good agreement with the data, which allows this study to benchmark these effects in order to take them into account to deduce temperature and density in future ICF experiments, such as those performed at the National Ignition Facility.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗
DOE OSTI2017

Experimental study of the application of rotating fluidized beds to particle separation

Rotating fluidized beds provide a unique opportunity to exploit fluidization under higher particle forces. The centripetal force in a rotating fluid bed is typically on the order of 10 times the force of gravity. Since the force keeping the particles in the unit is larger, the drag force can also be larger, allowing for higher gas and slip velocities. This operating regime provides intensified gas-solids contact through higher mass transfer, heat transfer, gas throughput, and bubble suppression. One application for using a rotating fluidized bed is in Chemical Looping Combustion (CLC). When solid fuels are used, oxygen carrier and ash are mixed in the process. In order to maintain high carbon capture efficiencies and recyclability of the oxygen carrier, the ash needs to be separated from the oxygen carrier. This separation can be done aerodynamically since the oxygen carrier is larger and heavier than the ash. It is theorized that rotating fluidized beds could improve both the gas-solid and solid-solid separation process efficiency and throughput as compared to conventional fluidized beds. A 43 cm diameter, 2.5 cm long vortex chamber has been designed and constructed to investigate the application to particle separation. A series of experiments have been performed to investigate the separation of different binary mixtures of solids. These experiments demonstrate the use of a rotating fluidized bed for high-G intensified particle separation that can be combined with high-G intensified gas-solids contact and gas-solids separation.¼

01 COAL, LIGNITE, AND PEAT↗
DOE OSTI2021

Reburning of Animal Waste Based Biomass with Coal for NO x Reduction, Part I: Feedlot Biomass (FB) and Coal:FB Blends

Cattle biomass (CB or manure from cattle) is proposed as reburn fuel under slightly fuel-rich conditions. The CB includes wastes from cattle feedlots (cattle grown in feedlots to slaughter weights of 450–640 kg) termed as Feedlot Biomass (FB) and cattle wastes from dairy farms termed as Dairy Biomass (DB). NOx emissions from coal-fired power plants can be reduced by using pure CB and Coal:CB mixtures as reburn fuels (10~30% by heat) injected after the primary combustion region. Experiments with Coal:CB mixtures as reburn fuels were performed using the 30 kW burner facility. Part I deals with results from experiments using pure FB and Coal:FB blends as reburn fuels while Part II presents results on extent of NOx reduction using pure DB and Coal:DB blends as reburn fuels (RF). In the current work, results on NOx emission are presented with FB and Coal:FB blends as RF. The parametric studies include: equivalence ratio in reburn zone (ERRBZ), vitiated air, angle of reburn nozzles, presence and absence of heat exchangers (HEXs), and baseline NOx concentration. The optimum operating conditions for FB reburning were found to be conditions with vitiation at ERRBZ = 1.1 with 45° upward counter-current injection in the presence of HEXs. NOx emissions were reduced by as much as 96%.

09 BIOMASS FUELS↗
DOE OSTI2012

Alkaline solution/binder ratio as a determining factor in the alkaline activation of aluminosilicates

This study investigates the effect of the alkaline solution/binder (S/B) ratio on the composition and nanostructure of the reaction products generated in the alkaline activation of aluminosilicates. The experiments used two mixtures of fly ash and dehydroxylated white clay and for each of these, varying proportions of the solution components. The alkali activator was an 8 M NaOH solution (with and without sodium silicate) used at three S/B ratios: 0.50, 0.75 and 1.25. The {sup 29}Si, {sup 27}Al MAS NMR and XRD characterisation of the reaction products reveal that for ratios nearest the value delivering suitable paste workability, the reaction-product composition and structure depend primarily on the nature and composition of the starting materials and the alkaline activator used. However, when an excess alkaline activator is present in the system, the reaction products tend to exhibit SiO{sub 2}/Al{sub 2}O{sub 3} ratios of approximately 1, irrespective of the composition of the starting binder or the alkaline activator.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Adsorption kinetics, thermodynamics, and isotherm studies for functionalized lanthanide-chelating resins

Conventional ion exchange resins are widely utilized to remove metals from aqueous solutions, but their limited selectivity precludes dilute ion extraction. This research investigated the adsorption performance of ligand-functionalized resins towards rare earth elements (REE). Functionalized resin particles were synthesized by grafting different ligands (diethylenetriaminepentaacetic dianhydride (DTPADA), phosphonoacetic acid (PAA), or N,N-bis(phosphonomethyl)glycine (BPG)) onto pre-aminated polymeric adsorbents (diameter-0.6 mm). Lanthanide uptake trends were evaluated for the functionalized resins using batch adsorption experiments with a mixture of three REEs (Nd, Gd, and Ho at 0.1–1000 mg/L each). Resin physical-chemical properties were determined by measuring their surface area, ligand concentrations, and acidity constants. The aminated supports contained 4.0 mmol/g primary amines, and ligand densities for the functionalized resins were 0.33 mmol/g (PAA), 0.22 mmol/g (BPG), and 0.42 mmol/g (DTPADA). Kinetic studies revealed that the functionalized resins followed pseudo-second order binding kinetics with rates limited by intraparticle diffusion. Capacity estimates for total REE adsorption based on Langmuir q Max were 0.12 mg/g (amine; ≈ 0.77 µmol/g), 5.0 mg/g (PAA; ≈ 32.16 µmol/g), 3.0 mg/g (BPG; ≈ 19.30 µmol/g), and 2.9 mg/g (DTPADA; ≈ 18.65 µmol/g). Lastly, attaching ligands to the aminated resins greatly improved their REE binding strength and adsorption efficiency.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2023

Development of a Structure for Lossless Ion Manipulations (SLIM) High Charge Capacity Array of Traps

Enhancing the sensitivity of low abundance ions in a complex mixture without sacrificing experiment throughput is highly desirable. This work demonstrates a way to greatly improve the sensitivity of ion mobility (IM) selected ions by accumulating them in an array of high-capacity ion traps located inside a novel structures for lossless ion manipulations ion mobility spectrometer (SLIM-IMS) module. The array of ion traps used in this work consisted of seven independently controllable traps. Each trap was 386 mm long and possessed a charge capacity of ~4.5×10 8 charges, with a linear range extending to ~2.5×10 8 charges. Each ion trap could be used to extract a peak (or ions over a mobility range) from an ion mobility separation based on arrival time. Ions could be stored without losses for long times (>100 s) and then released all at once or one trap at a time. It was possible to accumulate large ion populations by extracting and storing ions over repeated IM separations. We report enrichment of up to seven individual ion distributions could be performed using the seven independently controllable ion traps. Additionally, the ion trapping process effectively compressed ion populations into narrow peaks, which provides a greatly improved basis for subsequent ion manipulations. The array of high charge-capacity ion traps provides a flexible addition to SLIM and a powerful tool for IMS-MS applications requiring high sensitivity.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2014

Electrical and thermal conductivities in dense plasmas

Expressions for the electrical and thermal conductivities in dense plasmas are derived combining the Chester-Thellung-Kubo-Greenwood approach and the Kramers approximation. The infrared divergence is removed assuming a Drude-like behaviour. An analytical expression is obtained for the Lorenz number that interpolates between the cold solid-state and the hot plasma phases. An expression for the electrical resistivity is proposed using the Ziman-Evans formula, from which the thermal conductivity can be deduced using the analytical expression for the Lorenz number. The present method can be used to estimate electrical and thermal conductivities of mixtures. Comparisons with experiment and quantum molecular dynamics simulations are done.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗
DOE OSTI2015

Hydrogen plasma dynamics in the spherical theta pinch plasma target for heavy ion stripping

Due to the superior ability of dense and highly ionised plasmas to ionise penetrating heavy ion beams to degrees beyond those reachable by common gas strippers, many experiments have been performed to find suitable plasma generators for this application. In the field of gas discharges, mainly z-pinch devices have been investigated so far, which are known to be limited by the nonlinear focusing effects of the plasma columns sustaining current and by electrode erosion. The spherical theta pinch has therefore been proposed as a substitution for the z-pinch, promising progress by inductive rather than capacitive coupling and displacement of the outer magnetic field by the dense, diamagnetic discharge plasma. As yet mainly experiments with argon/hydrogen mixture gas have been performed, which is not suitable for the application as a plasma stripper, this paper describes the first detailed analysis of the plasma parameters and dynamics of a hydrogen plasma created by the spherical theta pinch. These include the time integrated and time resolved electron density, the dynamics of the plasma in the discharge vessel, the comparison with the argon dominated plasma, and an outlook to reachable characteristics with similar devices.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗
DOE OSTI2016

A versatile dual-species Zeeman slower for caesium and ytterbium

We describe the design, construction, and operation of a versatile dual-species Zeeman slower for both Cs and Yb, which is easily adaptable for use with other alkali metals and alkaline earths. With the aid of analytic models and numerical simulation of decelerator action, we highlight several real-world problems affecting the performance of a slower and discuss effective solutions. To capture Yb into a magneto-optical trap (MOT), we use the broad {sup 1}S{sub 0} to {sup 1}P{sub 1} transition at 399 nm for the slower and the narrow {sup 1}S{sub 0} to {sup 3}P{sub 1} intercombination line at 556 nm for the MOT. The Cs MOT and slower both use the D2 line (6{sup 2}S{sub 1/2} to 6{sup 2}P{sub 3/2}) at 852 nm. The slower can be switched between loading Yb or Cs in under 0.1 s. We demonstrate that within a few seconds the Zeeman slower loads more than 10{sup 9} Yb atoms and 10{sup 8} Cs atoms into their respective MOTs. These are ideal starting numbers for further experiments on ultracold mixtures and molecules.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2017

Catalytic Depolymerization and Upgrading of Lignin for Vanillin Production: Cooperative Research and Development Final Report, CRADA Number CRD-14-545

Examine catalytic conversion of lignin using multifunctional catalysts that are able to depolymerize and oxidize lignin to a vanillin-rich stream. Examine separation processes for isolation of vanillin from product mixtures. Conduct preliminary experiments to determine if deconstructed lignin streams can be metabolized by Pseudomonas putida.

09 BIOMASS FUELS↗
DOE OSTI2021

Thermal Property Characterization of Molten Salt Reactor–Relevant Salts

The thermochemical and thermophysical properties of molten salt systems are necessary input for the design, licensing, and deployment of molten salt reactor concepts. The thermochemical and thermophysical property measurement capabilities being used and developed at Oak Ridge National Laboratory (ORNL) include liquid density, volumetric thermal expansion, viscosity, vapor pressure, phase behavior, and heat capacity and thermal conductivity measurement capabilities. Properties of eutectic LiF-NaF-KF (FLiNaK) and NaCl-KCl are being measured to validate the measurement techniques to be used to provide data to reactor developers and to better quantify the uncertainty of measurements. This report summarizes the status of thermal conductivity, viscosity, specific heat capacity, and density. A method for property estimation using Redlich Kister expansion is also described. This technique will be used to help validate measured properties and to guide future experiments by targeting mixtures or components for which data are uncertain or lacking.

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗
DOE OSTI2019

Influence of Calcite on Uranium(VI) Sorption onto Montmorillonite Clay

Currently, most proposed methods for the long-term storage of nuclear waste include engineered buffer systems (EBS) in underground geologic repositories. The design of EBS typically involves a layer of geological buffer material such as bentonite. Bentonite is an ideal material for these systems, since it largely consists of the swelling smectite clay montmorillonite, which provides two types of surface sites available for the sorption of radionuclides, such as uranium(VI) (U(VI)). However, the presence of calcite, a common accessory mineral in bentonite, may potentially alter the sorption of U(VI) onto montmorillonite in multiple ways. First, calcite provides an additional surface for U(VI) sorption reactions. In addition, calcite dissolution will lead to dissolved calcium in porewater solutions, which may in turn affect U(VI) solution speciation, U(VI) ion exchange reactions, and the stacking and interlayer spacing of smectite layers. Last, a potential formation of U(VI)-Ca-carbonate co-precipitates may remove U(VI) from solution. As a first step, we characterized the sorption of U(VI) onto montmorillonite in the presence and absence of dissolved calcium at various ionic strength conditions in batch sorption envelope experiments. The presence of dissolved calcium resulted in decreased U(VI) sorption onto montmorillonite in acidic environments, but in no apparent changes in U(VI) sorption in near-neutral pH ranges. At higher pH values, there may be a possible decrease in U(VI) sorption, which needs to be further investigated. The observed trends at low pH can be explained by the preferential binding of Ca 2+ cations relative to UO 2 2+ , which resulted in a competition between the two cations for clay surface sites. This hypothesis is further supported by the results of additional sorption experiments, which were performed at various ionic strengths, but in the absence of calcium. In a next step, we will expand our experiments to include mixtures of calcite and montmorillonite as solids.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2018

Experimental investigation of subcooled flow boiling of a 50/50 ethylene glycol/water mixture in finned rectangular aluminum channels

Subcooled flow boiling heat transfer experiments were performed with a 50/50 ethylene glycol/water mixture in a finned aluminum channel. The channel represented a hybrid electric vehicle power electronic cold plate receiving a 50/50 mixture from the radiator at 105 degrees C and 2atmospheres. Experiments used a range of mixture flow rates and both top- and bottom-heating situations. Boiling curves were generated, and subcooled flow boiling heat transfer coefficients were determined including the test channel fin effects. Subcooled flow boiling heat transfer coefficients showed a 25-30% increase compared to single-phase convection.

boiling curve↗
DOE OSTI2016

ELECTRON IRRADIATION AND THERMAL PROCESSING OF MIXED-ICES OF POTENTIAL RELEVANCE TO JUPITER TROJAN ASTEROIDS

In this work we explore the chemistry that occurs during the irradiation of ice mixtures on planetary surfaces, with the goal of linking the presence of specific chemical compounds to their formation locations in the solar system and subsequent processing by later migration inward. We focus on the outer solar system and the chemical differences for ice mixtures inside and outside the stability line for H{sub 2}S. We perform a set of experiments to explore the hypothesis advanced by Wong and Brown that links the color bimodality in Jupiter's Trojans to the presence of H{sub 2}S in the surface of their precursors. Non-thermal (10 keV electron irradiation) and thermally driven chemistry of CH{sub 3}OH–NH{sub 3}–H{sub 2}O (“without H{sub 2}S”) and H{sub 2}S–CH{sub 3}OH–NH{sub 3}–H{sub 2}O (“with H{sub 2}S”) ices were examined. Mid-IR analyses of ice and mass spectrometry monitoring of the volatiles released during heating show a rich chemistry in both of the ice mixtures. The “with H{sub 2}S” mixture experiment shows a rapid consumption of H{sub 2}S molecules and production of OCS molecules after a few hours of irradiation. The heating of the irradiated “with H{sub 2}S” mixture to temperatures above 120 K leads to the appearance of new infrared bands that we provisionally assign to SO{sub 2}and CS. We show that radiolysis products are stable under the temperature and irradiation conditions of Jupiter Trojan asteroids. This makes them suitable target molecules for potential future missions as well as telescope observations with a high signal-to-noise ratio. We also suggest the consideration of sulfur chemistry in the theoretical modeling aimed at understanding the chemical composition of Trojans and KOBs.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗