scholarly journals Heavy Positive Ion Groups in Titan’s Ionosphere from Cassini Plasma Spectrometer IBS Observations

2021 ◽  
Vol 2 (1) ◽  
pp. 26
Author(s):  
Richard P. Haythornthwaite ◽  
Andrew J. Coates ◽  
Geraint H. Jones ◽  
Anne Wellbrock ◽  
J. Hunter Waite ◽  
...  
2020 ◽  
Author(s):  
Richard Haythornthwaite ◽  
Andrew Coates ◽  
Geraint Jones ◽  
Anne Wellbrock ◽  
Hunter Waite

2021 ◽  
Author(s):  
Richard Haythornthwaite ◽  
Andrew Coates ◽  
Geraint Jones ◽  
Anne Wellbrock ◽  
Hunter Waite ◽  
...  

<p><strong>Introduction</strong></p><p>Titan is the largest moon of Saturn and has a thick extended atmosphere along with a large ionosphere. Titan's ionosphere contains a plethora of hydrocarbons and nitrile cations and anions as measured by the Ion Neutral Mass Spectrometer and Cassini Plasma Spectrometer (CAPS) onboard the Cassini spacecraft<sup>1</sup>.</p><p>Previous ion composition studies in Titan’s ionosphere by Cassini instruments revealed "families" of ions around particular mass values and a regular spacing of 12 to 14 u/q between mass groups<sup> 2</sup>. These are thought to be related to a carbon or nitrogen backbone that dominates the ion chemistry<sup>2</sup>. Previous studies also identified possible heavy ions such as naphthalene, anthracene derivatives and an anthracene dimer at 130, 170 and 335 u/q respectively<sup>1</sup>. </p><p> </p><p><strong>Methodology</strong></p><p>               The CAPS Ion Beam Spectrometer<sup>3</sup> is an electrostatic analyser that measures energy/charge ratios of ions. During the Titan flybys Cassini had a high velocity (~6 km/s) relative to the low ion velocities (< 230 m/s) observed in the ionosphere. The ions were also cold, having ion temperatures around 150K. The combination of these factors meant that the ions appeared as a highly-directed supersonic beam in the spacecraft frame. This means the ions appear at kinetic energies associated with the spacecraft velocity and the ion mass, therefore the measured energy spectra (eV/q) can be converted to mass spectra (u/q).</p><p> </p><p><strong>Results and Conclusions</strong></p><p>Positive ion masses between 170 and 310 u/q are examined with ion mass groups identified between 170 and 275 u/q containing between 14 and 21 heavy (carbon/nitrogen/oxygen) atoms<sup>4</sup>. These groups are the heaviest positive ion groups reported so far from the available in situ ion data at Titan.</p><p>The ion group peaks are found to be consistent with masses associated with Polycyclic Aromatic Compounds, including Polycyclic Aromatic Hydrocarbon (PAH) and nitrogen-bearing polycyclic aromatic molecular ions. The ion group peak identifications are compared with previously proposed neutral PAHs<sup>5 </sup>and are found to be at similar masses, supporting a PAH interpretation. The spacing between the ion group peaks is also investigated, finding a spacing of 12 or 13 u/q indicating the addition of C or CH. Lastly, the occurrence of several ion groups is seen to vary across the five flybys studied, possibly relating to the varying solar radiation conditions observed across the flybys.</p><p>The discovery of these groups will aid future atmospheric chemical models of Titan through identification of prominent heavy positive ions and further the understanding between the low mass ions and the high mass negative ions, as well as the process of aerosol formation in Titan's atmosphere.</p><p><strong>References</strong></p><p>1. Waite et al., The Process of Tholin Formation in Titan’s Upper Atmosphere, Sci., 2007, doi:10.1126/science.1139727</p><p>2. Crary et al., Heavy ions, temperatures and winds in Titan's ionosphere: Combined Cassini CAPS and INMS observations, P&SS, 2009, doi:10.1016/j.pss.2009.09.006.</p><p>3. Young et al., Cassini Plasma Spectrometer Investigation. Space Sci. Rev., 2004, doi:10.1007/s11214-004-1406-4</p><p>4. Haythornthwaite et al., Heavy Positive Ion Groups in Titan's Ionosphere from Cassini Plasma Spectrometer IBS Observations, eprint arXiv:2009.08749</p><p>5. López-Puertas et al., Large Abundances of Polycyclic Aromatic Hydrocarbons in Titan's Upper Atmosphere, ApJ, 2013, doi:10.1088/0004-637X/770/2/132</p>


1976 ◽  
Author(s):  
T. MASEK ◽  
H. COHEN
Keyword(s):  
Ion Beam ◽  

1985 ◽  
Author(s):  
R. Robson ◽  
W. Williamson ◽  
J. Hyman
Keyword(s):  

2020 ◽  
Vol 17 (1) ◽  
pp. 95-105
Author(s):  
Ramji Rathod ◽  
Faraat Ali ◽  
Amrish Chandra ◽  
Robin Kumar ◽  
Meenakshi Dahiya ◽  
...  

Background: A simple and sensitive Ultra Performance Liquid Chromatography-Mass Spectrometry method was developed and validated to measure the concentrations of Alogliptin (ALO), Linagliptin (LIN), Saxagliptin (SAX), and Sitagliptin (SIT) using Pioglitazone (PIO) as an internal standard. Methods: Chromatographic separation of six gliptins was achieved on a C-18 column (100×2.1 mm, 2.7 μm) using a mobile phase consisting of formic acid in water, 0.1%v/v: acetonitrile in gradient elution. Electrospray ionization (ESI) source was operated in the positive ion mode. Targeted MS/MS mode on a QTOF MS was used to quantify the drug utilizing the transitions of 340.1(m/z), 473.2 (m/z), 316.2 (m/z), 408.1 (m/z), and 357.1 (m/z) for ALO, LIN, SAX, SIT and PIO respectively. Results: As per ICH Q2R1 guidelines, a detailed validation of the method was carried out and the standard curves were found to be linear over the concentration ranges of 1516.0-4548.1 ng mL-1, 519.8- 1559.4 ng mL-1, 1531.4-4594.3 ng mL-1and 1519.6-4558.8 ng mL-1 for ALO, LIN, SAX and SIT respectively. Precision and accuracy results were within the acceptable limits. The mean recovery was found to be 98.8 _ 0.76 % (GEM), 102.2 _ 1.59 % (LIN), 95.3 _ 2.74 % (SAX) and 99.2 _ 1.75 % (SIT) respectively. Conclusions: The optimized validated UPLC QTOF-MS/MS method offered the advantage of shorter analytical times and higher sensitivity and selectivity. The optimized method is suitable for application in quantitative analysis of pharmaceutical dosage forms for QC laboratory.


1963 ◽  
Vol 59 ◽  
pp. 1695 ◽  
Author(s):  
D. A. Hutchinson
Keyword(s):  

Author(s):  
Rebecca A Mastrovito ◽  
Donna M Papsun ◽  
Barry K Logan

Abstract Novel illicit benzodiazepines are among the most active areas of new illicit drug manufacture and use. We describe a method for the detection and quantification of etizolam and its metabolite α-hydroxyetizolam, flubromazolam, clonazolam, diclazepam, delorazepam, bromazepam, flubromazepam, phenazepam, flualprazolam, flunitrazolam, and nitrazolam in human whole blood. After addition of internal standards, samples are buffered and extracted using a liquid–liquid extraction. Analysis is performed using positive-ion electrospray tandem mass spectrometry for detection and quantitation. Calibration ranges were established based on the method performance and differed from compound to compound. Replicates at the lowest calibration point for each compound performed within 5% of CV (Coefficient of Variation). The correlation coefficient was >0.990 for all compounds. Relative standard deviation for all compounds was ≤10% of CV and accuracy was  ±10% for both within- and between-run experiments. The maximum average intra- and inter-run imprecision were 5.7%. The maximum average intra- and inter-run imprecision was −8.7%. As part of evaluating the scope for relevancy, samples testing positive in immunoassay but confirmed to be negative in traditional benzodiazepine confirmation method were re-analyzed using this method. The presence of at least one novel benzodiazepine was identified in 70% of these samples. The appearance of these novel “designer” benzodiazepines demonstrates the challenge for toxicology testing and the need for continually updated confirmation methods.


Sign in / Sign up

Export Citation Format

Share Document