Do Chemtrails Contain Acetone?I have been reporting for a couple years now how a new chemtrail type causes horrible symptoms and tastes like acetone.
Now we have evidence that acetone actually has been measured in air-based experiments. Was this done to collect data about acetone transport potential in aerosol spraying programs?
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| Title: |
| Observation of upper tropospheric sulfur dioxide- and acetone-pollution: Potential implications for hydroxyl radical and aerosol formation |
| Authors: |
| Arnold, F.; Schneider, J.; Gollinger, K.; Schlager, H.; Schulte, P.; Hagen, D. E.; Whitefield, P. D.; van Velthoven, P. |
| Publication: |
| Geophysical Research Letters, Volume 24, Issue 1, p. 57-60 (GeoRL Homepage) |
| Publication Date: |
| 00/1997 |
| Origin: |
| AGU |
| AGU Keywords: |
| Atmospheric Composition and Structure: Troposphere-constituent transport and chemistry, Atmospheric Composition and Structure: Pollution-urban and regional, Atmospheric Composition and Structure: Aerosols and particles, Atmospheric Composition and Structure: Chemical kinetic and photochemical properties |
| DOI: |
| 10.1029/96GL03693 |
| Bibliographic Code: |
| 1997GeoRL..24...57A |
Abstract
Aircraft-based measurements of sulfur dioxide, acetone, carbon dioxide,
and condensation nuclei (CN) were made over the north-eastern Atlantic
at upper tropospheric altitudes, around 9000 m. On October 14, 1993,
strong SO
2- and acetone-pollution (both up to 3 ppbv) were
observed, which were accompanied by a CO
2-enhancement of up
to 6 ppmv, and large CN-concentrations of up to about
1500cm
-3 (for radii>=6nm). CN, excess CO
2, and
to a lesser degree also acetone, were positively correlated with
SO
2. Air mass trajectory analyses indicate, that most of the
air masses encountered by our aircraft originated from the polluted
planetary boundary layer of the North-Eastern U.S. approximately 4-5
days prior to our measurements, and that polluted boundary layer air
experienced fast vertical transport to the upper troposphere as well as
horizontal transport across the Atlantic. From our data we conclude,
that in the polluted air mass around 9000 m altitude
HO
x-formation, photochemical SO
2-conversion to
gaseous H
2SO
4, and eventually also CN-formation by
homogeneous bimolecular (H
2SO
4-H
2O)
nucleation may have taken place with enhanced efficiency.