scholarly journals A Cross-laboratory Comparison Study of Titan Haze Analogs: Surface Energy

2022 ◽  
Vol 3 (1) ◽  
pp. 2
Author(s):  
Jialin Li ◽  
Xinting Yu ◽  
Ella Sciamma-O’Brien ◽  
Chao He ◽  
Joshua A. Sebree ◽  
...  

Abstract In Titan’s nitrogen-methane atmosphere, photochemistry leads to the production of complex organic particles, forming Titan’s thick haze layers. Laboratory-produced aerosol analogs, or “tholins,” are produced in a number of laboratories; however, most previous studies have investigated analogs produced by only one laboratory rather than a systematic, comparative analysis. In this study, we performed a comparative study of an important material property, the surface energy, of seven tholin samples produced in three independent laboratories under a broad range of experimental conditions, and we explored their commonalities and differences. All seven tholin samples are found to have high surface energies and are therefore highly cohesive. Thus, if the surface sediments on Titan are similar to tholins, future missions such as Dragonfly will likely encounter sticky sediments. We also identified a commonality between all the tholin samples: a high dispersive (nonpolar) surface energy component of at least 30 mJ m−2. This common property could be shared by the actual haze particles on Titan as well. Given that the most abundant species interacting with the haze on Titan (methane, ethane, and nitrogen) are nonpolar in nature, the dispersive surface energy component of the haze particles could be a determinant factor in condensate−haze and haze−lake liquid interactions on Titan. With this common trait of tholin samples, we confirmed the findings of a previous study by Yu et al. that haze particles are likely good cloud condensation nuclei for methane and ethane clouds and would likely be completely wetted by the hydrocarbon lakes on Titan.

Author(s):  
Monisha Baby ◽  
Vijayalakshmi K. Periya ◽  
Bhuvaneshwari Soundiraraju ◽  
Nisha Balachandran ◽  
Suchithra Cheriyan ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 444
Author(s):  
María Taeño ◽  
David Maestre ◽  
Julio Ramírez-Castellanos ◽  
Shaohui Li ◽  
Pooi See Lee ◽  
...  

Achieving nanostructures with high surface area is one of the most challenging tasks as this metric usually plays a key role in technological applications, such as energy storage, gas sensing or photocatalysis, fields in which NiO is gaining increasing attention recently. Furthermore, the advent of modern NiO-based devices can take advantage of a deeper knowledge of the doping process in NiO, and the fabrication of p-n heterojunctions. By controlling experimental conditions such as dopant concentration, reaction time, temperature or pH, NiO morphology and doping mechanisms can be modulated. In this work, undoped and Sn doped nanoparticles and NiO/SnO2 nanostructures with high surface areas were obtained as a result of Sn incorporation. We demonstrate that Sn incorporation leads to the formation of nanosticks morphology, not previously observed for undoped NiO, promoting p-n heterostructures. Consequently, a surface area value around 340 m2/g was obtained for NiO nanoparticles with 4.7 at.% of Sn, which is nearly nine times higher than that of undoped NiO. The presence of Sn with different oxidation states and variable Ni3+/Ni2+ ratio as a function of the Sn content were also verified by XPS, suggesting a combination of two charge compensation mechanisms (electronic and ionic) for the substitution of Ni2+ by Sn4+. These results make Sn doped NiO nanostructures a potential candidate for a high number of technological applications, in which implementations can be achieved in the form of NiO–SnO2 p-n heterostructures.


1982 ◽  
Vol 36 (5) ◽  
pp. 576-581 ◽  
Author(s):  
Tuan Vo-Dinh

This paper discusses the figures of merit associated with the synchronous luminescence (SL) technique in multicomponent analysis of complex samples. Spectral interferences and experimental factors that influence the choice of experimental conditions are investigated. The efficacy of SL is demonstrated in the direct determination of anthracene and 2-methylanthracene in a raw coal liquid. The application of the second-derivative technique to the SL measurement of organic samples is shown. Special emphasis is directed toward the applicability of the SL technique as a practical and cost-effective screening procedure in the routine analysis of complex organic samples.


2013 ◽  
Vol 102 (7) ◽  
pp. 2282-2296 ◽  
Author(s):  
Xi Han ◽  
Laila Jallo ◽  
Daniel To ◽  
Chinmay Ghoroi ◽  
Rajesh Davé

Joule ◽  
2018 ◽  
Vol 2 (8) ◽  
pp. 1511-1521 ◽  
Author(s):  
Nien-Chu Lai ◽  
Guangtao Cong ◽  
Zhuojian Liang ◽  
Yi-Chun Lu

Biochar ◽  
2020 ◽  
Author(s):  
Marlene C. Ndoun ◽  
Herschel A. Elliott ◽  
Heather E. Preisendanz ◽  
Clinton F. Williams ◽  
Allan Knopf ◽  
...  

Abstract Biochars produced from cotton gin waste (CG) and guayule bagasse (GB) were characterized and explored as potential adsorbents for the removal of pharmaceuticals (sulfapyridine-SPY, docusate-DCT and erythromycin-ETM) from aqueous solution. An increase in biochar pyrolysis temperature from 350 οC to 700 οC led to an increase in pH, specific surface area, and surface hydrophobicity. The electronegative surface of all tested biochars indicated that non-Coulombic mechanisms were involved in adsorption of the anionic or uncharged pharmaceuticals under experimental conditions. The adsorption capacities of Sulfapyridine (SPY), Docusate (DCT) and Erythromycin (ETM) on biochar were influenced by the contact time and solution pH, as well as biochar specific surface area and functional groups. Adsorption of these pharmaceutical compounds was dominated by a complex interplay of three mechanisms: hydrophobic partitioning, hydrogen bonding and π–π electron donor–acceptor (EDA) interactions. Despite weaker π–π EDA interactions, reduced hydrophobicity of SPY− and increased electrostatic repulsion between anionic SPY− and the electronegative CG biochar surface at higher pH, the adsorption of SPY unexpectedly increased from 40% to 70% with an increase in pH from 7 to 10. Under alkaline conditions, adsorption was dominated by the formation of strong negative charge-assisted H-bonding between the sulfonamide moiety of SPY and surface carboxylic groups. There seemed to be no appreciable and consistent differences in the extent of DCT and ETM adsorption as the pH changed. Results suggest the CG and GB biochars could act as effective adsorbents for the removal of pharmaceuticals from reclaimed water prior to irrigation. High surface area biochars with physico-chemical properties (e.g., presence of functional groups, high cation and anion exchange capacities) conducive to strong interactions with polar-nonpolar functionality of pharmaceuticals could be used to achieve significant contaminant removal from water. Graphic Abstract


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