FT-IR Standoff Detection of Thermally Excited Emissions of Trinitrotoluene (TNT) Deposited on Aluminum Substrates

2013 ◽  
Vol 67 (2) ◽  
pp. 181-186 ◽  
Author(s):  
John R. Castro-Suarez ◽  
Leonardo C. Pacheco-Londoño ◽  
Miguel Vélez-Reyes ◽  
Max Diem ◽  
Thomas J. Tague ◽  
...  

A standoff detection system was assembled by coupling a reflecting telescope to a Fourier transform infrared spectrometer equipped with a cryo-cooled mercury cadmium telluride detector and used for detection of solid-phase samples deposited on substrates. Samples of highly energetic materials were deposited on aluminum substrates and detected at several collector-target distances by performing passive-mode, remote, infrared detection measurements on the heated analytes. Aluminum plates were used as support material, and 2,4,6-Trinitrotoluene (TNT) was used as the target. For standoff detection experiments, the samples were placed at different distances (4 to 55 m). Several target surface temperatures were investigated. Partial least squares regression analysis was applied to the analysis of the intensities of the spectra obtained. Overall, standoff detection in passive mode was useful for quantifying TNT deposited on the aluminum plates with high confidence up to target–collector distances of 55 m.

2017 ◽  
Vol 2017 ◽  
pp. 1-11 ◽  
Author(s):  
John R. Castro-Suarez ◽  
Leonardo C. Pacheco-Londoño ◽  
Joaquín Aparicio-Bolaño ◽  
Samuel P. Hernández-Rivera

Two standoff detection systems were assembled using an infrared telescope coupled to a Fourier transform infrared spectrometer, a cryocooled mercury-cadmium telluride detector, and a telescope-coupled midinfrared excitation source. Samples of the highly energetic materials (HEMs) 2,4,6-trinitrotoluene (TNT) and pentaerythritol tetranitrate (PETN) were deposited on aluminum plates and detected at several source-target distances by carrying out remote infrared spectroscopy (RIRS) measurements on the aluminum substrates in active mode. The samples tested were placed at 1–30 m for the RIRS detection experiments. The effect of the angle of incidence/collection of the IR beams on the vibrational band intensities and the signal-to-noise ratios (S/N) were investigated. Experiments were performed at ambient temperature. Surface concentrations from 50 to 400 μg/cm2 were studied. Partial least squares regression analysis was applied to the spectra obtained. Overall, RIRS detection in active mode was useful for quantifying the HEMs deposited on the aluminum plates with a high confidence level up to the target-collector distances of 1–25 m.


2015 ◽  
Vol 69 (5) ◽  
pp. 535-544 ◽  
Author(s):  
Nataly J. Galán-Freyle ◽  
Leonardo C. Pacheco-Londõno ◽  
Amanda M. Figueroa-Navedo ◽  
Samuel P. Hernandez-Rivera

2000 ◽  
Author(s):  
V. James Cannaliato ◽  
Bruce W. Jezek ◽  
Larry Hyttinen ◽  
John B. Strawbridge ◽  
William J. Ginley

Separations ◽  
2020 ◽  
Vol 7 (4) ◽  
pp. 64
Author(s):  
Ryan Thompson ◽  
John D. Perry ◽  
Stephen P. Stanforth ◽  
John R. Dean

Development of a rapid approach for universal microbial detection is required in the healthcare, food and environmental sectors to aid with medical intervention, food safety and environmental protection. This research investigates the use of enzymatic hydrolysis of a substrate by a microorganism to generate a volatile organic compound (VOC). One such enzyme activity that can be used in this context is nitroreductase as such activity is prevalent across a range of microorganisms. A study was developed to evaluate a panel of 51 microorganisms of clinical interest for their nitroreductase activity. Two enzyme substrates, nitrobenzene and 1-fluoro-2-nitrobenzene, were evaluated for this purpose with evolution, after incubation, of the VOCs aniline and 2-fluoroaniline, respectively. Detection of the VOCs was done using headspace-solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) with obtained limits of quantitation (LOQ) of 0.17 and 0.03 µg/mL for aniline and 2-fluoroaniline, respectively. The results indicated that both enzyme substrates were reduced by the same 84.3% of microorganisms producing the corresponding volatile anilines which were detected using HS-SPME-GC-MS. It was found that nitroreductase activity could be detected after 6–8 h of incubation for the selected pathogenic bacteria investigated. This approach shows promise as a rapid universal microbial detection system.


2019 ◽  
Vol 3 (2) ◽  
Author(s):  
K. Wall ◽  
C. Kerth

ObjectivesThe objective of this study was to utilize mass spectrometry (MS) instrumentation to define flavor differences in beef strip loin steaks cooked on five different surface temperatures.Materials and MethodsUSDA Select strip loins (n = 30) were selected from carcasses at a commercial major packing plant in Texas. After aging 14d, the loins were cut into 2.54 cm thick steaks, randomly assigned a grill surface temperature of 149, 177, 204, 232, or 260°C, individually vacuum-packaged and frozen at –10°C until analysis. Steaks were cooked on an electric flat top grill pre-heated to the corresponding temperature treatment. Steaks were turned at an internal temperature of 35°C and removed at 71°C (medium degree of doneness). Cubes (1.3cm × 1.3cm × steak thickness) representative of those served to a trained sensory panel were frozen and held at –80°C until further analysis. For GC/MS analysis, the samples were weighed and placed in a 473 mL glass jar with a Teflon lid held in a water bath at 60°C for 2h. The collection of volatiles from the headspace was done with a solid phase micro-extraction (SPME) sampler and a multi-dimensional GC/MS. For HPLC/MS-QTOF analysis, frozen samples were homogenized in a blender and 2 g were mixed with 8 mL acidified acetonitrile (0.1% formic acid). The supernatant was exposed to dSPE Enhanced Matrix Removal and dried with 3.5 g MgSO4. Samples were analyzed at a 1:5 dilution using reverse-phase chromatography on an Agilent 6545 LC/MS-QTOF with a gradient mobile phase in both positive and negative ion modes. Data were analyzed as linear and/or quadratic effects (P < 0.05) with grill surface temperature as the independent variable. Least squares means, discriminant analyses, and partial least squares regression analyses for compounds were calculated.ResultsBoth octane (gasoline aroma) and undecane (allspice aroma) increased (P < 0.02) linearly with grill temperature. With the exception of pentanal (fermented wine aroma), which decreased (P = 0.027) as grill temperature increased, all other aldehyde compounds increased (P < 0.05) linearly as the grill temperature increased. Pyrazines (roasted, coffee, and nutty aromas) and ketones (fruity, fatty aromas) generally increased (P < 0.03) as grill temperature increased. 2,3,5-trimethyl-6-ethyl pyrazine, 2,3-diethyl-5-methyl pyrazine, 2,5-dimethyl pyrazine and 3,5,-diethyl-2-methyl-pyrazine were only present when the grill temperature reached 260°C. Nonvolatile compounds (n = 247 positive ion and 140 negative ions) were identified. Significant (P < 0.05) patterns of increasing intensity with increased grill temperature were observed in sugar-amino derivatives such as betaine, 2-dimethylamino-5,6-dimethylpyrimidin-4-ol, and (S)-N-(4,5-dihydro-1-methyl-4-oxo-1H-imidazol-2-yl) alanine. A point of inflection was observed at a grill temperature of 232°C across a majority of increasing compounds, suggesting a critical temperature for the regulation of flavorful products from the Maillard reaction.ConclusionVolatile and nonvolatile compounds known to contribute to positive flavor attributes associated with the Maillard reaction are considerably influenced by grill surface temperature. It appears that a grill temperature from 204 to 232°C is optimal for generation of volatile and nonvolatile flavor compounds.


Sensors ◽  
2020 ◽  
Vol 20 (9) ◽  
pp. 2524 ◽  
Author(s):  
Lea Fellner ◽  
Marian Kraus ◽  
Florian Gebert ◽  
Arne Walter ◽  
Frank Duschek

Laser-induced fluorescence (LIF) is a well-established technique for monitoring chemical processes and for the standoff detection of biological substances because of its simple technical implementation and high sensitivity. Frequently, standoff LIF spectra from large molecules and bio-agents are only slightly structured and a gain of deeper information, such as classification, let alone identification, might become challenging. Improving the LIF technology by recording spectral and additionally time-resolved fluorescence emission, a significant gain of information can be achieved. This work presents results from a LIF based detection system and an analysis of the influence of time-resolved data on the classification accuracy. A multi-wavelength sub-nanosecond laser source is used to acquire spectral and time-resolved data from a standoff distance of 3.5 m. The data set contains data from seven different bacterial species and six types of oil. Classification is performed with a decision tree algorithm separately for spectral data, time-resolved data and the combination of both. The first findings show a valuable contribution of time-resolved fluorescence data to the classification of the investigated chemical and biological agents to their species level. Temporal and spectral data have been proven as partly complementary. The classification accuracy is increased from 86% for spectral data only to more than 92%.


1988 ◽  
Vol 34 (8) ◽  
pp. 1640-1644 ◽  
Author(s):  
M J Khosravi ◽  
R C Morton ◽  
E P Diamandis

Abstract In this new immunofluorometric method for quantification of lutropin in serum, the "sandwich" principle is combined with time-resolved fluorescence measurements, with the europium chelate 4,7-bis(chlorosulfophenyl)-1,10-phenanthroline-2,9-dicarboxylic acid (BCPDA) used as label. A monoclonal antibody to the alpha-subunit of lutropin is adsorbed onto the walls of white-opaque microtiter wells to form the solid-phase capture antibody, and a biotin-labeled soluble monoclonal antibody is used for antigen quantification. The detection system is completed with streptavidin, which has been linked to a protein bulking agent labeled with multiple BCPDA residues. In the presence of excess europium, the fluorescence of the final complex attached to captured lutropin molecules is measured on the dried solid phasse with an automated time-resolved fluorometer. The assay can be performed as a rapid (less than 60 min incubation) or regular (150 min incubation) procedure. The rapid assay is well-suited for routine daily monitoring of increasing or ovulatory lutropin concentrations; the regular assay, with its greater sensitivity (0.5 int. unit/L), is a practical procedure for lutropin measurements in hyposecretory states. The assay measures up to 240 int. units/L, and results compare well with those by a commercially available radioimmunoassay, an immunoradiometric assay, and another time-resolved immunofluorometric procedure.


2018 ◽  
Vol 18 (10) ◽  
pp. 5713-5726 ◽  
Author(s):  
Chaoyang Zhang ◽  
Fangbao Jiao ◽  
Hongzhen Li

Sign in / Sign up

Export Citation Format

Share Document