INTRODUCTION-MARINE AEROSOL

Roger J. CHENG, ASRC-SUNY-UALBANY

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纽约州立大学,大气科学研究中心 郑均华研究员主持的科研项目
  • The generation of maritime cloud condensation nuclei (CCN) through the ejection of jet and film droplets from bursting whitecap-produced bubbles on the ocean surface has been well documented. The processes involved in the transformation (evaporation and crystallization) of these liquid droplets into their solid form under varying conditions, however, has not previously attracted much attention from researchers. A set of laboratory investigations and field observations of the characteristics, both physical and chemical of sea water droplets during phase change in a controlled environment has revealed the following startling and very significant phenomena:

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海洋中云凝结核(CCN)的显微观察,测试研究报告
  • 1,附带硫化物(CaSO/4,MgSO/4)的气溶胶的测定
• 2,海盐颗粒空心球体的发现。
• 3,氯化物(MgCl/2和KCl)在凝结核表面的证实
纽约州立大学,大气科学研究中心郑均华研究员主持的科研项目

 

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OBSERVATION of MARINE AEROSOL-ROGER J CHENG ASRC UALBANY SUNY USA.htm

1,附带硫化物(CaSO/4,MgSO/4)的气溶胶的测定
• 2,海盐颗粒空心球体的发现。
• 3,氯化物(MgCl/2和KCl)在凝结核表面的证实

纽约州立大学,大气科学研究中心郑均华研究员主持的科研项目

  • The FORMATION of HOLLOW SEA-SALT PARTICLES

from the EVAPORATION of DROPS of SEAWATER

  • Roger J. Cheng, Duncan C. Blanchard and Ramon J. Ciprianoa
    Atmospheric Sciences Research Center
    State University of New York

    ASRC UALBANY SUNY

Atmospheric Research
Volume 22, Issue 1, Pages 15-25,
June 1988

Abstract

Some non-volatile materials dissolved in water drops will, upon evaporation of the water, produce a hollow shell of the material. Though known for years in the chemical engineering literature, this fact was not appreciated by those working with the marine sea-salt aerosol. Our laboratory experiments show that a majority of seawater drops in free fall in air with a relative humidity less than about 60% evaporate, become salt-saturated, and change phase to produce hollow sea-salt particles. Some hollow salt particles have been found in marine air, though further investigation is required to show the extent of this phenomenon. Expressions have been derived from which both the size of the original drop of seawater and its salt supersaturation at the time of phase change can be calculated from the inner and outer radii of the salt shell. If hollow particles are common in the marine aerosol, then instruments that measure particle size -(TSP) cannot be used to obtain particle mass.

Résumé

Certaines substances non volatiles dissoutes dans les gouttes d'eau produisent, à l'évaporation de l'eau, des coquilles creuses. Ce processus est bien connu en génie chimique, et pourtant il n'en est pas tenu compte dans les travaux sur les aérosols salins océaniques. Nos expériences de laboratoire montrent que lorsque des gouttes du de mer tombent en chute libre dans de l'air à moins de 60% d'humidité relative, la plupart d'entre elles arrivent à saturation et changent de phase pour produire des particules salines creuses. On a d'ailleurs trouvé des particules creuses de sel dans de l'air marin, mais d'autres recherches sont nécessaires pour connaître l'étendue du phénomène. On présente des relations qui donnent la dimension de la goutte originale d'eau de mer, ainsi que la sursaturation au changement de phase, à partir des rayons intérieurs et extérieurs de la coquille de sel. S'il est prouvé que les particules creuses sont courantes dans l'aérosol marin, on ne pourra pas utiliser les appareils qui mesurent les dimensions des particules pour évaluer la masse de l'aérosol.

 

    Atmospheric Research
  • Volume 22, Issue 1, Pages 15-25, June 1988
  • Received 12 December 1986; accepted 31 July 1987.

 
 

 

CITATION by: DR. H.K. PRUPPACHER'S TEAM of GERMANY

 

  • The FORMATION of HOLLOW
  • SEA-SALT PARTICLES

from the EVAPORATION of DROPS of SEAWATER

Roger J. Cheng, Duncan C. Blanchard and Ramon J. Ciprianoa

  • Atmospheric Sciences Research Center
  • State University of New York at Albany
  • Received 12 December 1986; accepted 31 July 1987.
A, "A Wind Tunnel Study on the Drop-to-Particle Conversion"
JOURNAL of AEROSOL SCIENCES,
Vol.23, No.3, 1992.

by Dr. Pruppacher's term at Institute of Atmospheric Physics, Germany)

 

B, MICROPHYSICS OF CLOUDS AND PRECIPITATION ;
By Dr. Pruppacher and Dr. Klett,
Second Revised and Enlarged Edition.
Kluwer Academic Publishers, 1997
 
 

 

    SHELL STRUCTURED MARINE AEROSOL:
    • A LABORATORY OBSERVATION
  • Roger J. CHENG -ASRC UALBANY SUNY

  • Atmospheric Sciences Research Center
  • State University of New York

 

Laboratory investigation revealed that a shell structure of chlorides (MgCl/2 and KCl) is always present on the surface of marine aerosol. Close examination by a polarizing microscope of an individual seawater droplet has resulted in the following observations: Evaporation of water increased the salt concentration. At first, a thin layer of brine formed at the surface of the evaporating droplet; this was followed by clearly sequential precipitations of numerous microcystals of sulfates (CaSO/4, MgSO/4), and by a crust of many relatively larger cubic NaCI crystals correspondent with their individual solubility and concentrations.

During this process solution of chlorides (MgCl/2, KCl) mixed with microciystals of sulfates or NaCl were situated beneath the surface of the droplet. Finally, a seasalt particle with chloride film on the surface was formed. The shell structure of chlorides film present on the surface of the marine aerosol confirmed via optical and scanning electron microscopy is of extreme importance to understanding the fundamental nucleation processes in the atmosphere.

The chloride film presents a highly hygroscopic surface and was found to initiate the condensation of water vapor in an environment with RH as low as 40%. Sodium chloride (NaCI) crystals, on the other hand play only a minor role in initiating condensation (RH 75%) for cloud droplets formation in the atmosphere.

  • To be presented at:
  • the Annual Meeting of the American Associationfor Aerosol Research (AAAR),
  • Oak Brook, ILL. October 11-15, 1993
 

 

 

A NEW MECHANISM for the GENERATION of

HIGH SULFATE ENRICHED AEROSOLS

in the MARINE ATMOSPHERE

(CaSO/4, MgSO/4---NOT DMS)

Roger J. CHENG: ASRC SUNY UALBANY

****大气中的微观世界 系列****

纽约州立大学,大气科学研究中心 郑均华研究员主持的科研项目

 

A NEW MECHANISM for the GENERATION of

HIGH SULFATE ENRICHED AEROSOLS

in the MARINE ATMOSPHERE

 

***********************************************************************************************************************

Roger J. CHENG, ASRC SUNY UALBANY

The high concentration of sulfate in marine aerosols has long been suggested to be the products of atmospheric oxidation of gaseous dimethyl sulphide (DMS) emitted by phytoplankton and the photo chemical reaction of S02 originated from contented and distance anthropogenic sources. But these mechanisms cannot explain for observed high concentration of sulfate in remote marine atmosphere

Recent macroscopically investigation and field observation revealed that high enriched sulfate aerosols were ejected from seawater droplets, generated by whitecaps at the oceanic surface, during their phase transition.

Close examination of an individual seawater droplet in an environment of relative humidity less than 75% and temperature of 25 C have resulted in the following observations: Evaporation of water increased the salt concentration- At first, a thin layer of brine formed at the surface of the evaporating droplet; this was followed by clearly sequential precipitations of numerous microcrystal of sulfates, and of a crust of many relatively larger cubic NaCl crystals beneath the surface correspondent with their individual solubilities and concentrations in the droplet During this process, solution of chlorides (MgCl/2, KCI) mixed with microcrystals of sulfates and/or NaCl were expelled from the surface of the droplet. Brine film bursting at the interstices of cubic NaCl crystals was also observed and was followed by the formation of a hollow sphere of sea-salt particle with many holes. A larger number of aerosols were generated from rapid evapom6on followed by crystalline of seawater droplets on a hot (35-40 C) rock surface. A secondary ejection of sulfate aerosols was also detected during melting by the bursting of air bubbles which formed when hollow particle was moved into a high-moisture environment or dissolved into another water droplet.

The concentration and chemical composition of the ejected aerosols. identified by the techniques of scanning electron microscopy and energy dispersive x-ray spectroscopy, were dependent on the rate of droplet evaporation; aerosols were composed predominantly of sulfate particles (CaSO/4, MgSO/4) with a size range of 0.1 um to I0 um. High concentration of [S04=] and (CI-] from the ejected aerosols were also measured by ion chromatographic analysis. The shell structure of chlorides (MgCl/2, KCI) present on the surfaces of the ejected aerosols was detected and confirmed via polarizing microscopy.

To be presented at: 9th World Clean Air Congress
August 30 - September 4, 1992, Montreal , Quebec, Canada

 

 

 

Presented at: 9th WORLD CLEAN AIR CONGRESS

AUGUST 30- SEPTEMBER 4, 1992

MONTREAL, QUEBEC, CANADA

 

SCIENCE EDUCATION-- SLIDE SHOW PRESENTATION

Roger J. CHENG, ASRC UALBANY SUNY USA

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POWER-POINT SLIDE SHOW for STUDENT, TEACHER & GENERAL PUBLIC

 

The MICRO-WORLD in the ATMOSPHERE

MARINE AEROSOL PROJECT:

REFERENCES and CITATIONS

Roger J. CHENG: ASRC UALBANY SUNY

****大气中的微观世界 系列--4.海洋****

纽约州立大学,大气科学研究中心 郑均华研究员主持的科研项目

  •  

    REFERENCES and CITATIONS

    • 1. "The Formation of Hollow Sea-Salt Particles from the Evaporation of Drops of Seawater"
    • ATMOSPHERIC RESEARCH,
    • Vol. 22, No. 1. June 1988 (Cheng, Blanchard & Cipriano).
    • 2. "The Generation of Secondary Marine Aerosols: The Crystallization of Seawater Droplets"
    • A. LECTURE NOTES IN PHYSICS, 309, Atmospheric Aerosols and Nucleation,
    • Ed: P.E Wagner and G. Vail, Springer-Verlag. 1988.
    • B. International Conference on Atmospheric Aerosols and Nucleation,
    • Vienna, Austria. August 22-27, 1988
    • 3. "Sulfate Aerosols Generation in the Marine Atmosphere: The Evaporation of SeawaterDroplets"
    • International Conference on Global and Regional Environmental Atmospheric Chemistry,
    • Beijing, China. May 1989.
    • 4. "A New Mechanism for the Generation of High Sulfate Enriched Aerosol in the Marine Atmosphere"
    • 9th World Clean Air Congress, Montreal, Quebec, Canada. 1992.
    • 5. "Shell Structured Marine Aerosol: A Laboratory Observation"
    • Annual Meeting of American Association for Aerosol Research,
    • Oak Brook, Illinois. October 11-15, 1993.
    • 6. "On the Phenomenon of Nuclei Enhancement During the Evaporative Stage of a Cloud"
    • ATMOSPHERIC RESEARCH, Vol. 47, No. 48, 1998. ( DeFelice and Cheng )
    • CITATIONS:
    • A. AN INTRODUCTION TO METEOROLOGICAL INSTRUMENTATION AND MEASUREMENT
    • By Dr.Thomas P. DeFelice, Prentice Hall, 1998.
    • B. "A Wind Tunnel Study on the Drop-to-Particle Conversion"
    • JOURNAL of AEROSOL SCIENCES, Vol.23, No.3, 1992.
    • (Confirmation by Dr. Pruppacher's term at Institute of Atmospheric Physics, Germany)
    • C. MICROPHYSICS OF CLOUDS AND PRECIPITATION ;
    • By Dr. Pruppacher and Dr. Klett, Second Revised and Enlarged Edition.
    • Kluwer Academic Publishers, 1997
    • .
    • D. " Microscopic Investigation of Marine Aerosol "
    • ALBANY-Fall 1996-University at Albany Magazine.
     

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The MICRO-WORLD in the ATMOSPHERE series

SCIENCE EDUCATION---WEB SITE PRESENTATION

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WHO want to KNOW MORE the SECRETS of the ATMOSPHERE and
WHO wish to SEE the LIFE CYCLE of A WATER DROP in A THUNDERCLOUD
SCIENCE EDUCATION and GENERAL PUBLIC EDITION
 
1, The MICRO-WORLD in the ATMOSPHERE
SCIENTIFIC and PROFESSIONAL EDITION
 
2, The MICRO-WORLD in the THUNDERSTORM
  • www.RogerCheng.com
  • "The STORY of The LIFE CYCLE of A WATER DROP in a THUNDERCLOUD"
  • NEWLY PUBLISHED: FEB.2011--under TESTING and REVISION
3, The MICRO-WORLD in our ENVIRONMENT
  • A, CHARACTERIZATION of POWER PLANT EMISSION--OIL and COAL
  • B, ACID RAIN FORMATION-CATALYTIC SO/2 OXIDATION in A WATER DROP
  • C, ECOLOGICAL EFFECTS- MARBLE DETERIORATION and PLANT DAMAGE
  • in preparation

4, The MICRO-WORLD in the MARINE ATMOSPHERE

  • A, DISCOVERY of HOLLOW SEA SALT PARTICLES
  • B, TRANSFER of MARINE SULFATE from OCEAN into the ATMOSPHERE
  • C, SHELLED (CHLORIDES) MIRINE-CCN (CLOUD CONDENSATION NUCLEI)
  • in preparation
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The MICRO-WORLD in the ATMOSPHERE series

Roger J. CHENG-ASRC-SUNY-UALBANY

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