Laser damage comparisons of E-beam evaporated HfO2/SiO2 antireflection coatings at 0% and 40% relative humidity for 532 nm and 1064 nm

2021 ◽  
Author(s):  
Ella S. Field ◽  
Damon E. Kletecka
2018 ◽  
Vol 18 (10) ◽  
pp. 7001-7017 ◽  
Author(s):  
Andrés Esteban Bedoya-Velásquez ◽  
Francisco Navas-Guzmán ◽  
María José Granados-Muñoz ◽  
Gloria Titos ◽  
Roberto Román ◽  
...  

Abstract. This study focuses on the analysis of aerosol hygroscopic growth during the Sierra Nevada Lidar AerOsol Profiling Experiment (SLOPE I) campaign by using the synergy of active and passive remote sensors at the ACTRIS Granada station and in situ instrumentation at a mountain station (Sierra Nevada, SNS). To this end, a methodology based on simultaneous measurements of aerosol profiles from an EARLINET multi-wavelength Raman lidar (RL) and relative humidity (RH) profiles obtained from a multi-instrumental approach is used. This approach is based on the combination of calibrated water vapor mixing ratio (r) profiles from RL and continuous temperature profiles from a microwave radiometer (MWR) for obtaining RH profiles with a reasonable vertical and temporal resolution. This methodology is validated against the traditional one that uses RH from co-located radiosounding (RS) measurements, obtaining differences in the hygroscopic growth parameter (γ) lower than 5 % between the methodology based on RS and the one presented here. Additionally, during the SLOPE I campaign the remote sensing methodology used for aerosol hygroscopic growth studies has been checked against Mie calculations of aerosol hygroscopic growth using in situ measurements of particle number size distribution and submicron chemical composition measured at SNS. The hygroscopic case observed during SLOPE I showed an increase in the particle backscatter coefficient at 355 and 532 nm with relative humidity (RH ranged between 78 and 98 %), but also a decrease in the backscatter-related Ångström exponent (AE) and particle linear depolarization ratio (PLDR), indicating that the particles became larger and more spherical due to hygroscopic processes. Vertical and horizontal wind analysis is performed by means of a co-located Doppler lidar system, in order to evaluate the horizontal and vertical dynamics of the air masses. Finally, the Hänel parameterization is applied to experimental data for both stations, and we found good agreement on γ measured with remote sensing (γ532=0.48±0.01 and γ355=0.40±0.01) with respect to the values calculated using Mie theory (γ532=0.53±0.02 and γ355=0.45±0.02), with relative differences between measurements and simulations lower than 9 % at 532 nm and 11 % at 355 nm.


2021 ◽  
Vol 114 ◽  
pp. 110995
Author(s):  
Liyuan Zhang ◽  
Shenglai Wang ◽  
Houwen Yang ◽  
Wenyong Cheng ◽  
Hui Liu ◽  
...  

2009 ◽  
Vol 36 (11) ◽  
pp. 3050-3054
Author(s):  
周明 Zhou Ming ◽  
赵元安 Zhao Yuan′an ◽  
李大伟 Li Dawei ◽  
范正修 Fan Zhengxiu ◽  
邵建达 Shao Jianda
Keyword(s):  

2019 ◽  
Author(s):  
Wenyu Zhang ◽  
Weigang Wang ◽  
Junling Li ◽  
Chao Peng ◽  
Kun Li ◽  
...  

Abstract. Secondary organic aerosol (SOA) have great impacts on air quality, climate change and human health. The composition and physicochemical properties of SOA differ a lot for they originated under different atmospheric conditions and from various precursors and oxidations. In this work, photooxidation experiments of toluene were performed under four conditions (dry, dry with SO2, wet, and wet with SO2) to investigate the effect of SO2 under different relative humidity on the composition and optical properties of SOA at the wavelength of 375 nm and 532 nm. According to our results, the increase of humidity enhances not only light absorption, but also scattering property of SOA. Highly conjugated oligomers formed through multiphase reaction might be the reasons of this phenomenon. Adding SO2 slightly lower the real part of complex refractive index (n) of SOA: ndry, SO2 


2012 ◽  
Vol 12 (23) ◽  
pp. 11695-11721 ◽  
Author(s):  
P. J. Sheridan ◽  
E. Andrews ◽  
J. A. Ogren ◽  
J. L. Tackett ◽  
D. M. Winker

Abstract. Between June 2006 and September 2009, an instrumented light aircraft measured over 400 vertical profiles of aerosol and trace gas properties over eastern and central Illinois. The primary objectives of this program were to (1) measure the in situ aerosol properties and determine their vertical and temporal variability and (2) relate these aircraft measurements to concurrent surface and satellite measurements. The primary profile location was within 15 km of the NOAA/ESRL surface aerosol monitoring station near Bondville, Illinois. Identical instruments at the surface and on the aircraft ensured that the data from both platforms would be directly comparable and permitted a determination of how representative surface aerosol properties were of the lower column. Aircraft profiles were also conducted occasionally at two other nearby locations to increase the frequency of A-Train satellite underflights for the purpose of comparing in situ and satellite-retrieved aerosol data. Measurements of aerosol properties conducted at low relative humidity over the Bondville site compare well with the analogous surface aerosol data and do not indicate any major sampling issues or that the aerosol is radically different at the surface compared with the lowest flyby altitude of ~ 240 m above ground level. Statistical analyses of the in situ vertical profile data indicate that aerosol light scattering and absorption (related to aerosol amount) decreases substantially with increasing altitude. Parameters related to the nature of the aerosol (e.g., single-scattering albedo, Ångström exponent, etc.), however, are relatively constant throughout the mixed layer, and do not vary as much as the aerosol amount throughout the profile. While individual profiles often showed more variability, the median in situ single-scattering albedo was 0.93–0.95 for all sampled altitudes. Several parameters (e.g., submicrometer scattering fraction, hemispheric backscattering fraction, and scattering Ångström exponent) suggest that the fraction of smaller particles in the aerosol is larger near the surface than at high altitudes. The observed dependence of scattering on size, wavelength, angular integration range, and relative humidity, together with the spectral dependence of absorption, show that the aerosol at higher altitudes is larger, less hygroscopic, and more strongly absorbing at shorter wavelengths, suggesting an increased contribution from dust or organic aerosols. The aerosol profiles show significant differences among seasons. The largest amounts of aerosol (as determined by median light extinction profile measurements) throughout most of the sampled column were observed during summer, with the lowest amounts in the winter and intermediate values in the spring and fall. The highest three profile levels (3.1, 3.7, 4.6 km), however, showed larger median extinction values in the spring, which could reflect long-range transport of dust or smoke aerosols. The aerosols in the mixed layer were darkest (i.e., lowest single-scattering albedo) in the fall, in agreement with surface measurements at Bondville and other continental sites in the US. In situ profiles of aerosol radiative forcing efficiency showed little seasonal or vertical variability. Underflights of the CALIPSO satellite show reasonable agreement in a majority of retrieved profiles between aircraft-measured extinction at 532 nm (adjusted to ambient relative humidity) and CALIPSO-retrieved extinction, and suggest that routine aircraft profiling programs can be used to better understand and validate satellite retrieval algorithms. CALIPSO tended to overestimate the aerosol extinction at this location in some boundary layer flight segments when scattered or broken clouds were present, which could be related to problems with CALIPSO cloud screening methods. The in situ aircraft-collected aerosol data suggest extinction thresholds for the likelihood of aerosol layers being detected by the CALIOP lidar. In this study, aerosol layers with light extinction (532 nm) values > 50 Mm−1 were detected by CALIPSO ~ 95% of the time, while aerosol layers with extinction values lower than 10 Mm−1 had a detection efficiency of < 2%. For all collocated comparison cases, a 50% probability of detection falls at an in situ extinction level of 20–25 Mm−1. These statistical data offer guidance as to the likelihood of CALIPSO's ability to retrieve aerosol extinction at various locations around the globe.


2011 ◽  
Vol 50 (9) ◽  
pp. C340 ◽  
Author(s):  
John Bellum ◽  
Damon Kletecka ◽  
Patrick Rambo ◽  
Ian Smith ◽  
Jens Schwarz ◽  
...  

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