Activation properties of ambient aerosol in the Netherlands

A cloud chamber has been used to study the cloud activation of ambient aerosol in The Netherlands. The large dimensions and throughput of the chamber allowed unperturbed collection of aerosol and droplets with cascade impactors and on-line measurements with cloud monitors (FSSP) inside the facility....

Full description

Bibliographic Details
Main Authors: Khlystov, A, Kos, GPA, Ten Brink, HM, Kruisz, C, Berner, A
Format: Article in Journal/Newspaper
Language:unknown
Published: Elsevier BV 1996
Subjects:
Online Access:https://hdl.handle.net/10161/6421
id ftdukeunivdsp:oai:localhost:10161/6421
record_format openpolar
spelling ftdukeunivdsp:oai:localhost:10161/6421 2023-11-12T04:13:52+01:00 Activation properties of ambient aerosol in the Netherlands Khlystov, A Kos, GPA Ten Brink, HM Kruisz, C Berner, A 1996 application/pdf https://hdl.handle.net/10161/6421 unknown Elsevier BV ATMOSPHERIC ENVIRONMENT 1352-2310 https://hdl.handle.net/10161/6421 Journal article 1996 ftdukeunivdsp 2023-10-17T09:44:55Z A cloud chamber has been used to study the cloud activation of ambient aerosol in The Netherlands. The large dimensions and throughput of the chamber allowed unperturbed collection of aerosol and droplets with cascade impactors and on-line measurements with cloud monitors (FSSP) inside the facility. The study provided maxima for the number of man-made aerosol acting as cloud nuclei in marine clouds in The Netherlands. Emphasis was given to the investigation of cloud formation in marine air, since sensitivity studies had shown that such clouds are most effectively influenced by the (extra) anthropogenic aerosol particles. For this reason the supersaturations in the study were low (on average 0.12\%), similar to those in actual marine stratus. The effect of the anthropogenic aerosols on cloud formation was determined by comparing the number of droplets formed in `'clean'' arctic marine air to the number of droplets formed in `'polluted'' marine air (air which had travelled over the U.K.). Air masses with the total aerosol number concentration of the order of 100 cm(-3) were considered as `'clean'' marine air. Air masses with higher aerosol concentrations were divided into `'moderately'' and `'heavily'' polluted with total aerosol concentrations of the order of 1000 and 10,000 cm(-3), respectively. In the clean marine air all potential cloud nuclei (particles lar er than the threshold size of the smallest reference particles that were activated al given supersaturation) were activated and the number of cloud droplets formed was on average 45 cm(-3). In the moderately polluted air 72\% of potential cloud nuclei were activated and the average droplet number was 190 cm(-3). The difference in the actual cloud droplet number and the number of potential cloud nuclei could be explained by the presence of water-insoluble particles which do not activate. In the heavily polluted air the average droplet concentration was around 320 cm(-3) which is, on average, 24\% of the number of potential cloud nuclei. Copyright (C) 1996 ... Article in Journal/Newspaper Arctic Duke University Libraries: DukeSpace Arctic
institution Open Polar
collection Duke University Libraries: DukeSpace
op_collection_id ftdukeunivdsp
language unknown
description A cloud chamber has been used to study the cloud activation of ambient aerosol in The Netherlands. The large dimensions and throughput of the chamber allowed unperturbed collection of aerosol and droplets with cascade impactors and on-line measurements with cloud monitors (FSSP) inside the facility. The study provided maxima for the number of man-made aerosol acting as cloud nuclei in marine clouds in The Netherlands. Emphasis was given to the investigation of cloud formation in marine air, since sensitivity studies had shown that such clouds are most effectively influenced by the (extra) anthropogenic aerosol particles. For this reason the supersaturations in the study were low (on average 0.12\%), similar to those in actual marine stratus. The effect of the anthropogenic aerosols on cloud formation was determined by comparing the number of droplets formed in `'clean'' arctic marine air to the number of droplets formed in `'polluted'' marine air (air which had travelled over the U.K.). Air masses with the total aerosol number concentration of the order of 100 cm(-3) were considered as `'clean'' marine air. Air masses with higher aerosol concentrations were divided into `'moderately'' and `'heavily'' polluted with total aerosol concentrations of the order of 1000 and 10,000 cm(-3), respectively. In the clean marine air all potential cloud nuclei (particles lar er than the threshold size of the smallest reference particles that were activated al given supersaturation) were activated and the number of cloud droplets formed was on average 45 cm(-3). In the moderately polluted air 72\% of potential cloud nuclei were activated and the average droplet number was 190 cm(-3). The difference in the actual cloud droplet number and the number of potential cloud nuclei could be explained by the presence of water-insoluble particles which do not activate. In the heavily polluted air the average droplet concentration was around 320 cm(-3) which is, on average, 24\% of the number of potential cloud nuclei. Copyright (C) 1996 ...
format Article in Journal/Newspaper
author Khlystov, A
Kos, GPA
Ten Brink, HM
Kruisz, C
Berner, A
spellingShingle Khlystov, A
Kos, GPA
Ten Brink, HM
Kruisz, C
Berner, A
Activation properties of ambient aerosol in the Netherlands
author_facet Khlystov, A
Kos, GPA
Ten Brink, HM
Kruisz, C
Berner, A
author_sort Khlystov, A
title Activation properties of ambient aerosol in the Netherlands
title_short Activation properties of ambient aerosol in the Netherlands
title_full Activation properties of ambient aerosol in the Netherlands
title_fullStr Activation properties of ambient aerosol in the Netherlands
title_full_unstemmed Activation properties of ambient aerosol in the Netherlands
title_sort activation properties of ambient aerosol in the netherlands
publisher Elsevier BV
publishDate 1996
url https://hdl.handle.net/10161/6421
geographic Arctic
geographic_facet Arctic
genre Arctic
genre_facet Arctic
op_relation ATMOSPHERIC ENVIRONMENT
1352-2310
https://hdl.handle.net/10161/6421
_version_ 1782331666746834944