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Featured researches published by Stanley A. Johnson.


Aerosol Science and Technology | 1982

Airborne Detection of Acidic Sulfate Aerosol Using an ATR Impactor

Stanley A. Johnson; Romesh Kumar; Paul T. Cunningham

As a first step in determining how aerosol acidity varies with altitude, studies were conducted using a new instrument called an ATR impactor installed aboard the Battelle Pacific Northwest Laboratorys DC-3 aircraft. This instrument combines collection of the aerosol by inertial impaction with infrared spectroscopic analysis by the highly sensitive ATR technique. Results from several series of flights have revealed the occurrence of acidic sulfate aloft, while simultaneously collected ground-level samples contained only neutral ammonium sulfate. Acidic sulfate was detected in aerosol samples collected on four of the five flights conducted in the Chicago area during the spring of 1981.


Aerosol Science and Technology | 1985

The Influence of Humidity on Fine-Particle Aerosol Dynamics and Precipitation Scavenging

D. L. Sisterson; Stanley A. Johnson; Romesh Kumar

Precipitation chemistry and the chemical composition and mass loading of atmospheric fine-particle aerosols were examined for 25 individual precipitation events during a 12-month period. Aerosol and precipitation data were used (a) to determine the influence of the precipitation event on the mass loading and the chemical composition of the fine-particle aerosol, and (b) to calculate the apparent scavenging ratios for sulfate and ammonium ions. Two distinct types of aerosol behavior were observed. In one, the concentration of aerosol particles were observed to decrease during the rain but to recover quickly after the event. In the other, the aerosol particle concentration in the 0.3–1.0 μm size range was found to increase either during or just after the rain. The meteorology associated with each precipitation event was examined in detail to determine the factors responsible for the observed behavior of the aerosol particles. Particle mass concentration decrease in the first type of behavior was attributed ...


Journal of Geophysical Research | 1991

Composition and spectral characteristics of ambient aerosol at Mauna Loa observatory

Stanley A. Johnson; Romesh Kumar

Ambient aerosol particles were sampled continuously with a time resolution of {approximately}4 hours for a period of 8 days at the Mauna Loa Observatory, Hawaii, in August 1986. The samples were analyzed on-site for their chemical composition by attenuated total internal reflection infrared spectroscopy. The infrared absorption spectra of the samples also provided data on aerosol light absorbance characteristics at 9.1 and 10.6 {mu}m - wavelengths of interest in determining aerosol backscatter coefficients for CO{sub 2} lidars. The chemical species in the ambient aerosol varied considerably during this 8-day period. The aerosol was acidic ((NH{sub 4}){sub 3}H(SO{sub 4}){sub 2},NH{sub 4}HSO{sub 4}, or H{sub 2}SO{sub 4}) rather than neutral ((NH{sub 4}){sub 2}SO{sub 4}) for a major fraction of the sampling time. The samples generally showed much higher absorbance at 9.1 {mu}m than at 10.6 {mu}m. Changes in the chemical composition between (NH{sub 4}){sub 2}SO{sub 4} and the more acidic forms were accompanied by substantial changes in the samples absorbance at 9.1 {mu}m but lesser changes in the absorbance at 10.6 {mu}m. These variations could have a profound effect on backscatter coefficients of atmospheric aerosol particles at CO{sub 2} wavelengths.


MRS Proceedings | 1991

Formation and characterization of sulfide clusters in molecular sieve zeolite materials

Markus Winterer; Lennox E. Iton; Stanley A. Johnson; Victor A. Maroni

The incorporation of molybdenum into the faujasite pore system via reaction of molybdenum pentachloride with H-Y zeolite results in dealumination of the zeolite framework and formation of MoO{sub 3} species. These species are readily sulfided by H{sub 2}S, but MoS{sub 2} clusters are not produced. A sulfur-bridged dimeric molybdenum cluster, of proposed composition HO-Mo-(S){sub 3}-Mo-OH, is formed, which can strongly chemisorb CO. Sulfidation of niobium in this manner is not readily accomplished. 19 refs.


Environmental Science & Technology | 1974

Variations in Chemistry of Airborne Particulate Material with Particle Size and Time

Paul T. Cunningham; Stanley A. Johnson; Ralph T. Yang


Archive | 1990

Real time infrared aerosol analyzer

Stanley A. Johnson; Gerald T. Reedy; Romesh Kumar


Journal of Geophysical Research | 1984

Vertical distribution of aerosol strong acid and sulfate in the atmosphere

Roger L. Tanner; Romesh Kumar; Stanley A. Johnson


Environmental Science & Technology | 1982

Quantitative analysis of nitrate ion in ambient aerosols by fourier-transform infrared spectroscopy

James S. Bogard; Stanley A. Johnson; Romesh Kumar; Paul T. Cunningham


Unknown conference | 1975

Kinetics of the reaction of half calcined dolomite with sulfur dioxide

Ralph T. Yang; Paul T. Cunningham; W. I. Wilson; Stanley A. Johnson


Environmental Science & Technology | 1978

Regional oxygen-18 variations in particulate sulfate and water vapor at three sampling sites about 100 km apart

Ben D. Holt; Romesh Kumar; Paul T. Cunningham; Margo Bouchard; Antoinette G. Engelkemeir; Stanley A. Johnson; Eugene L. Nielsen; Jack D. Shannon

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Romesh Kumar

Argonne National Laboratory

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Paul T. Cunningham

Argonne National Laboratory

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W. I. Wilson

Argonne National Laboratory

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Ben D. Holt

Argonne National Laboratory

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Lennox E. Iton

Argonne National Laboratory

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Markus Winterer

Argonne National Laboratory

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Roger L. Tanner

Tennessee Valley Authority

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Victor A. Maroni

Argonne National Laboratory

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