Filtering Enhanced Traffic Management System (ETMS) Altitude Data

Enhanced Traffic Management System (ETMS) stores all the information gathered by the Federal Aviation Administration (FAA) from aircraft flying in the US airspace. The data stored from each flight includes the 4D trajectory (latitude, longitude, altitude and timestamp), radar data and flight plan information. Unfortunately, there is a data quality problem in the vertical channel and the altitude component of the trajectories contains some isolated samples in which a wrong value was stored. Overall, the data is generally accurate and it was found that only 0.3% of the altitude values were incorrect, however the impact of these erroneous data in some analyses could be important, motivating the development of a filtering procedure. The approach developed for filtering ETMS altitude data includes some specific algorithms for problems found in this particular dataset, and a novel filter to correct isolated bad samples (named Despeckle filter). As a result, all altitude errors were eliminated in 99.7% of the flights affected by noise, while preserving the original values of the samples without bad data. The algorithm presented in this paper attains better results than standard filters such as the median filter, and it could be applied to any signal affected by noise in the form of spikes

Benzothiadiazoles And Dipyrrolyl Quinoxalines With Extended Conjugated Chromophores-fluorophores And Anion Sensors

Stable fluorescent chromophores find use in a growing number of practical applications, including their utility as laser dyes,1 emitters in light-emitting diodes,2 photoconductors,3 optical data storage,4 and optical switches.5 Stable fluorophores with high quantum yields are widely used in fluorescent sensors6 and labels.7 These became very popular lately, owing to their potential for high sensitivity at low concentration coupled with decreased cost of the required equipment.8 Recently, we have described a new class of fluorescent anion sensors bearing extended conjugated chromophores9 with incorporated 2,3-di(1H-2-pyrrolyl)quinoxaline, (DPQ), as the anion recognition element.10 Literature shows that DPQ binds anions via hydrogen bonding between pyrrole NH and anions, the hydrogen bonding nature of the DPQ−anion complex was demonstrated by 1H NMR.10a In this paper, we provide a full account of our efforts including synthesis and photophysical properties of DPQ-based fluorescent anion sensors with extended conjugated chromophores S1−S6 (Figure 1), including their benzothiadiazole precursors F1−F6, which appears to be an interesting set of highly stable fluorescent chromophores

Fluorescence Sensor Array For Metal Ion Detection Based On Various Coordination Chemistries: General Performance And Potential Application

A sensor array containing 9 cross-reactive sensing fluorescent elements with different affinity and selectivity to 10 metal cations (Ca2+, Mg2+, Cd2+, Hg2+, Co2+, Zn2+, Cu2+, Ni2+, Al3+, Ga3+) is described. The discriminatory capacity of the array was tested at different ranges of pH and at different cation concentrations using linear discriminant analysis (LDA). Qualitative identification of cations can be determined with over 96% of accuracy in a concentration range covering 3 orders of a magnitude (5-5000 mu M). Quantitative analysis can be achieved with over 90% accuracy in the concentration range between 10 and 5000 mu M. The array performance was also tested in identification of nine different mineral water brands utilizing their various electrolyte compositions and their Ca2+, Mg2+, and Zn2+ levels. LDA cross-validation routine shows 100% correct classification for all trials. Preliminary results suggest that similar arrays could be used in testing of the consistency of the purification and manufacturing process of purified and mineral waters

Simple Molecule-based Fluorescent Sensors For Vapor Detection Of Tnt

1,4-Diarylpentiptycenes (1a-e) were synthesized from 1,4-dichloro- or 1,4-difluoro-2,5-diarylbenzene derivatives by double base-promoted dehydrohalogenation to give corresponding arynes, which in the presence of anthracene undergo cycloaddition providing 1,4-diarylpentiptycenes in moderate overall yields. The resulting 1,4-diarylpentiptycenes show fluorescence modulated by the 1,4-aryl residues. The fluorescence is quenched in the presence of vapors of nitroaromatic compounds suggesting potential application in sensing of explosives

Lithium and magnetic fields in giants. HD 232862 : a magnetic and lithium-rich giant star

We report the detection of an unusually high lithium content in HD 232862, a field giant classified as a G8II star, and hosting a magnetic field. With the spectropolarimeters ESPaDOnS at CFHT and NARVAL at TBL, we have collected high resolution and high signal-to-noise spectra of three giants : HD 232862, KU Peg and HD 21018. From spectral synthesis we have inferred stellar parameters and measured lithium abundances that we have compared to predictions from evolutionary models. We have also analysed Stokes V signatures, looking for a magnetic field on these giants. HD 232862, presents a very high abundance of lithium (ALi = 2.45 +/- 0.25 dex), far in excess of the theoretically value expected at this spectral type and for this luminosity class (i.e, G8II). The evolutionary stage of HD 232862 has been precised, and it suggests a mass in the lower part of the [1.0 Msun ; 3.5 Msun ] mass interval, likely 1.5 to 2.0 solar mass, at the bottom of the Red Giant Branch. Besides, a time variable Stokes V signature has been detected in the data of HD 232862 and KU Peg, pointing to the presence of a magnetic field at the surface of these two rapidly rotating active stars.Comment: 11 pages, 9 figures ; accepted by Astronomy and Astrophysic

Synthesis, Structure, Anion Binding, And Sensing By Calix[4] Pyrrole Isomers

The synthesis, structure, and anion binding properties of chromogenic octamethylcalix[4] pyrroles (OMCPs) and their N-confused octamethylcalix[4] pyrrole isomers (NC-OMCPs) containing an inverted pyrrole ring connected via alpha\u27- and beta-positions are described. X-ray diffraction analyses proved the structures of two synthesized isomeric pairs of OMCPs and NC-OMCPs. The addition of anions to solutions of chromogenic OMCPs and NC-OMCPs resulted in different colors suggesting different anion-binding behaviors. The chromogenic NC-OMCPs showed significantly stronger anion-induced color changes compared to the corresponding chromogenic OMCP, and the absorption spectroscopy titrations indicated that chromogenic OMCPs and NC-OMCPs also possess different anion binding selectivity. Detailed NMR studies revealed that this rather unusual feature stems from a different anion-binding mode in OMCPs and NC-OMCPs, one where the beta-pyrrole C-H of the inverted pyrrole moiety participates in the hydrogen-bonded anion-NC-OMCP complex. Preliminary colorimetric microassays using synthesized chromogenic calixpyrroles embedded in partially hydrophilic polyurethane matrices allow for observation of analyte-specific changes in color when the anions are administered in the form of their aqueous solutions and in the presence of weakly competing anions

Supramolecular Chemistry Approach To The Design Of A High-resolution Sensor Array For Multianion Detection In Water

Reliable sensing of structurally similar anions in water is a difficult problem, and analytical tests and sensor devices for reliable sensing of multiple anions are very rare. This study describes a method for fabrication of simple colorimetric array-based assays for aqueous anion solutions, including complex analytes encountered in real-life applications. On the fundamental level, this method shows how the discriminatory capacity of sensor arrays utilizing pattern recognition operating in multianalyte environments may be dramatically improved by employing two key features. The synergy between the sensor and hydrogel host resembles the cooperative effects of an apoenzyme and cofactor: the host hydrogel helps extract the target anions from the bulk analyte while stripping the solvate molecules off the anions. In addition, the supramolecular studies of the affinity and selectivity of the potential sensors for target analytes allow for constructing an array predesigned for a particular analyte. To illustrate both aspects, an eight-sensor array utilizing colorimetric sensor materials showing selectivity for fluoride and pyrophosphate while displaying significant cross-reactivity for other anions such as carboxylates, phosphate, or chloride was used to differentiate between 10 anions. The quantitative analyses were also performed to show that the eight-sensor array was found to operate across 4 orders of magnitude concentrations (0.20-360 ppm; 10 mu M to 20 mM). The applicability of this approach was demonstrated by analyzing several toothpaste brands. The toothpastes are complex analytes comprising both known and unknown anions in various concentrations. The fluoride-selective yet cross-reactive array is shown to utilize the fluoride content as the main differentiating factor while using the remaining anionic components for further differentiation between toothpaste brands

Rational Design Of A Minimal Size Sensor Array For Metal Ion Detection

The focus of this study was to demonstrate that, in the luminescent sensors, the signal transduction may possibly be the most important part in the sensing process. Rational design of fluorescent sensor arrays for cations utilizing extended conjugated chromophores attached to 8-hydroxyquinoline is reported. All of the optical sensors utilized in the arrays comprise the same 8-hydroxyquinoline (8-HQ) receptor and various conjugated chromophores to yield a different response to various metal cations. This is because the conjugated chromophores attached to the receptor are partially quenched in their resting state, and upon the cation coordination by the 8-HQ, the resulting metalloquinolinolate complex displays a change in fluorescence. A delicate balance of conjugation, fluorescence enhancement, energy transfer, and a heavy metal quenching effect results in a fingerprint-like pattern of responses for each sensor-cation complex. Principal component analysis (PCA) and linear discriminant analysis (LDA) are used to demonstrate the contribution of individual sensors within the array, information that may be used to design sensor arrays with the smallest number of sensor elements. This approach allows discriminating between 10 cations by as few as two or even one sensor element. Examples of arrays comprising various numbers of sensor elements and their utility in qualitative identification of Ca2+, Mg2+, Cd2+, Hg2+, Co2+, Zn2+, CU2+, Ni2+, Al3+, and Ga3+ ions are presented. A two-member array was found to identify 11 analytes with 100% accuracy. Also the best two of the sensors were tested alone and both were found to be able to discriminate among the samples with 99% and 96% accuracy, respectively. To illustrate the utility of this approach to a real-world application, identification of enhanced soft drinks based on their Ca2+, Mg2+, and Zn2+ cation content was performed. The same approach to reducing array elements was used to construct three- and two-member arrays capable of identifying these complex analytes with 100% accuracy

Design and Development of a Laboratory-Scale Ice Adhesion Testing Device

When an aircraft traverses through clouds containing supercooled water droplets, in-flight icing can occur that negatively affects vehicle performance by increasing weight and drag leading to loss of lift. Super-cooled water droplets present in clouds that impact vehicle surfaces can lead to inflight icing any time during the year.1 Most events occur at temperatures ranging from 0 to -20degC. Ice generated on the aircraft can vary between clear/glaze, rime, and mixed (Fig. 1) depending on air temperature (-5 to -20degC), liquid water content (0.3-0.6 g/m3), and droplet size (median volumetric diameter of 15-40 m). Current strategies to remove ice are based on active technologies such as pneumatic boots, heated surfaces, and deicing agents (i.e., ethylene- and propylene-based glycols). The latter have potential environmental concerns. A passive approach to mitigate accreting ice that is actively being investigated are protective coatings. An ice mitigating coating could potentially be used as a stand-alone material, but more likely in combination with an active approach. In the latter scenario, potential reduction in power consumption by the active approach may be realized. To determine the ice adhesion strength of impact ice that is representative of the aircraft environment is not a trivial matter. Test methods utilizing slowly formed ice (i.e., freezer ice) do not accurately simulate this environment. Likewise, some testing methodologies involve sample relocation from the icing environment to the test chamber that can result in thermal shock to the sample, thus affecting the results. The Adverse Environment Rotor Test Stand (AERTS) located at Pennsylvania State University (PSU) has been demonstrated to simulate impact icing conditions within the icing envelope for the determination of ice adhesion shear strength (IASS) without removal/relocation of the sample.2 Due to the confidence in results obtained from AERTS, this instrument is in high demand and requires a significant amount of lead time and capital investment to obtain IASS results. As a solution for quickly and economically screening coatings in a controlled manner under impact icing conditions, a laboratory-scale ice adhesion test and dead blades were then removed from the rotor/blade assembly to obtain the final mass. The IASS of the live blade was determined from the difference in mass (before and after testing) of the live and dead blades, the ice shed area, and the rpm of the shed event. The same live blade sample was tested in triplicate at all three test temperatures. Surface roughness was determined using a Bruker Dektak XT Stylus Profilometer. Measurements were conducted using a 12.5 m tip at a vertical range of 65.5 m with an applied force of 3 mg. Data were collected over a 1.0 mm length at a resolution of 0.056 m/point. Five single line scans at different locations were collected and processed using a two-point leveling subtraction. The resultant Ra (arithmetic roughness) and Rq (root mean square roughness) average values were calculated

Ultrafast Energy Transfer In Oligofluorene-aluminum Bis(8-hydroxyquinoline)acetylacetone Coordination Polymers

Understanding the excited-state dynamics in conjugated systems can lead to their better utilization in optical sensors, organic photovoltaics (OPVs), and organic light-emitting diodes (OLEDs). We present the synthesis of self-assembled coordination polymers comprising two types of fluorescent moieties: discrete fluorene oligomers of a well-defined length (n = 1-9) connected via aluminum(III) bis(8-quinolinolate)acetylacetone joints. Due to their well-defined structure, these materials allowed for a detailed study of energy migration processes within the materials. Thus, femtosecond transient spectroscopy was used to study the ultrafast energy transfer from the oligofluorene to the quinolinolate moieties, which was found to proceed at a rate of 10(11) s(-1). The experimental results were found to be in agreement with the behavior predicted according to the Beljonne\u27s improved Forster model of energy transfer. In addition, the solid-state and semiconductor properties of these coordination polymers allowed for the fabrication of OLEDs. Preliminary experiments with simple two- and three-layer devices fabricated by spin-coating yield bright yellow electroluminescence with maximum brightness of 6000 cd/m(2), with a turn-on voltage of similar to 6 V and a maximum external quantum efficiency of up to 1.2%, suggesting their potential for use in PLED applications