Particle-Fluorescence Spectrometer for Real-Time Single-Particle Measurements of Atmospheric Organic Carbon and Biological Aerosol

2009 ◽  
Vol 43 (2) ◽  
pp. 429-434 ◽  
Author(s):  
Yong-Le Pan ◽  
Ronald G. Pinnick ◽  
Steven C. Hill ◽  
Richard K. Chang
2011 ◽  
Vol 11 (1) ◽  
pp. 1219-1264 ◽  
Author(s):  
C.-H. Jeong ◽  
M. L. McGuire ◽  
K. J. Godri ◽  
J. G. Slowik ◽  
P. J. G. Rehbein ◽  
...  

Abstract. Mass concentrations of particulate matter (PM) chemical components were determined from data for 0.3 to 3.0 μm particles measured by an Aerosol Time-of-Flight Mass Spectrometer (ATOFMS) data at an urban and rural site. Hourly-averaged concentrations of nitrate, sulphate, ammonium, organic carbon, and elemental carbon, estimated based on scaled ATOFMS peak intensities of corresponding ion marker species, were compared with collocated chemical composition measurements by an Aerosol Mass Spectrometer (AMS), a Gas-Particle Ion Chromatograph (GPIC), and a Sunset Lab field OCEC analyzer. The highest correlation was found for nitrate, with correlation coefficients (Pearson r) of 0.89 and 0.85 at the urban and rural sites, respectively. ATOFMS mass calibration factors, determined for the urban site, were used to calculate mass concentrations of the major PM chemical components at the rural site. Mass reconstruction using this ATOFMS based composition data agreed very well with the total PM mass measured at the rural site. Size distributions of the ten main types of particles were resolved for the rural site and the mass composition of each particle type was determined in terms of sulphate, nitrate, ammonium, organic carbon and elemental carbon. This is the first study to estimate hourly mass concentrations of individual aerosol components and the mass composition of individual particle-types based on ATOFMS single particle measurements.


2010 ◽  
Vol 5 (3) ◽  
pp. 331-341 ◽  
Author(s):  
Fan Yang ◽  
Xinning Wang ◽  
Yaping Zhang ◽  
Xiaofei Wang ◽  
Hong Chen ◽  
...  

2007 ◽  
Vol 41 (15) ◽  
pp. 5439-5446 ◽  
Author(s):  
Kerri A. Denkenberger ◽  
Ryan C. Moffet ◽  
John C. Holecek ◽  
Thomas P. Rebotier ◽  
Kimberly A. Prather

Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2826 ◽  
Author(s):  
Shangguo Hou ◽  
Courtney Johnson ◽  
Kevin Welsher

Single molecule fluorescence spectroscopy has been largely implemented using methods which require tethering of molecules to a substrate in order to make high temporal resolution measurements. However, the act of tethering a molecule requires that the molecule be removed from its environment. This is especially perturbative when measuring biomolecules such as enzymes, which may rely on the non-equilibrium and crowded cellular environment for normal function. A method which may be able to un-tether single molecule fluorescence spectroscopy is real-time 3D single particle tracking (RT-3D-SPT). RT-3D-SPT uses active feedback to effectively lock-on to freely diffusing particles so they can be measured continuously with up to photon-limited temporal resolution over large axial ranges. This review gives an overview of the various active feedback 3D single particle tracking methods, highlighting specialized detection and excitation schemes which enable high-speed real-time tracking. Furthermore, the combination of these active feedback methods with simultaneous live-cell imaging is discussed. Finally, the successes in real-time 3D single molecule tracking (RT-3D-SMT) thus far and the roadmap going forward for this promising family of techniques are discussed.


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