Thanks for the support, but I now think any thought of commercial fight use is 
just wildly premature at the moment.

For now we need to concentrate on the practical, one off, development of the 
ways of distributing particles at the heights required.

Trivial amounts of research money are required for this but so far I cant get 
any. Grant proposal attached again.

johngorman


----- Original Message ----- 
  From: Veli Albert Kallio 
  To: David Keith ; [email protected] ; [email protected] 
  Cc: [email protected] ; [email protected] ; Geoengineering FIPC ; 
[email protected] ; Climateintervention FIPC 
  Sent: Thursday, October 21, 2010 3:24 PM
  Subject: RE: [clim] RE: [geo] The problem with stratospheric SRM


   
   

  Note that Gorman has proposed direct formation of silicates in commercial 
aircraft exhaust, following earlier suggestions of sulfur in jet fuel. 
Commercial aircraft don’t flight at the right height or location to efficiently 
deliver materials to the stratosphere. You need to be in the tropical 
stratosphere get reasonably long lifetimes, this requires altitudes beyond 
about 18 km. 

   
  I think it is a very important fact to bear in mind that the stratospheric 
flights are specialist flights, whereas the commerical flights to certain 
extent will have a free-ride. One could argue equipment added on same basis as 
catalysators on cars through regulatory directive. This would effectively 
ensure a free ride, even though the flotation half-life would be very much 
shorter. 
   
  This recalls my experience at Farnborough Air Show where we were looking 
Locheed Martin F-130 Hercules aircraft and Sikorsky Helicopters. At the end of 
the meeting, some of the staff suggested a Sikorsky ride home to take down the 
stuff at the air show by chopper. But then the manager said no, we pack all 
stuff to packet vans and drive back and forth several hours to-and-fro (even 
though immensely multiplying the task of taking stuff home.)
   
  As per the above experience, I have doubts about the practicality any 
specialist stratospheric flight programme by specialist aircraft: (even if it 
delivers ten or twenty times longer flotation half-times in stratosphere to the 
commercial flights). If spraying carbon tetrasilicate, sulphur dioxide, or H2S, 
or H2SO2 the cost of speciality flights may count against the ideal delivery 
such a way in quantities. 
   
  Have anyone look at cost / half-life ratios if the startospheric flights 
would still end up as more expensive?
   
  A commercial air craft flies at 11,000 metres: Wouldn't it make more sense to 
say that planes flying above, say, troposphere would be required by law to have 
an injector installed in them, which should be switched on when above say 
8,000, 9,000, 10,000 or 11,000 metres? Any feedback from this pragmatist 
viewpoint?
   
  Kind regards,

  Albert

   

------------------------------------------------------------------------------
  From: [email protected]
  To: [email protected]; [email protected]
  CC: [email protected]; [email protected]; 
[email protected]; [email protected]; 
[email protected]
  Date: Thu, 21 Oct 2010 07:04:06 -0600
  Subject: [clim] RE: [geo] The problem with stratospheric SRM


  A few comments on microphysics of stratospheric aerosols.



  We have examine the microphysics in a recent GRL paper. We confirmed earlier 
findings that the standard SO2 injection can be surprisingly ineffective 
because most of the sulfur is deposited on existing particles making them too 
large.



  We proposed a solution, injecting H2SO4 directly and showed that in the same 
modeling framework it worked far better than SO2. (Better=less sulfur mass to 
get same forcing, plus weak ozone surface-area benefits). This can be 
generalized to other condensable vapors.



  The paper is enclosed along with slides that may be helpful. N.B., we have 
reexamine assumptions and discovered an minor error in the original 
calculation, as it happens the new results make the direct H2SO4 scheme look a 
bit better, the figure on the slide is the new version. 



  We also reexamined ozone loss, this effort was directed by Thomas Peter, one 
of the collaborators on the paper who runs a major stratospheric chemistry 
group. 



  We have examine the engineering with an aircraft engineering group and found 
no first-order problems (that report will be released soon).



  I don’t think H2S would help. It has the same disadvantage as SO2.



  Note that Gorman has proposed direct formation of silicates in commercial 
aircraft exhaust, following earlier suggestions of sulfur in jet fuel. 
Commercial aircraft don’t flight at the right height or location to efficiently 
deliver materials to the stratosphere. You need to be in the tropical 
stratosphere get reasonably long lifetimes, this requires altitudes beyond 
about 18 km. 



  Yours,

  David







  From: [email protected] 
[mailto:[email protected]] On Behalf Of Oliver Wingenter
  Sent: Sunday, October 17, 2010 7:39 PM
  To: [email protected]
  Cc: Ken Caldeira; [email protected]; geoengineering; Wingenter
  Subject: [geo] The problem with stratospheric SRM



  Dear Ken,

  The problem is after the initial injections, i.e. the second yea of GE, can 
we even create new particles with a background now 15 to 25 times higher with 
or with out nucleation sites?  Under the present sulfate schemes it appears 
not. in order to "tune in" particle size and number ternary nucleation of 
sulfate, water and perhaps ammonia (NH3) will probably need top be invoked.  
Let us remember that water vapor is not finite in the stratosphere and as more 
particles are produced additional sulfate will be needed to reduce the vapor 
pressure of the aerosols.  An additional species such as NH3 could help over 
come this limitation.

  Injection of H2S would lead to greater dispersion of sulfur, allowing more 
particle growth but is not considered in stratospheric SRM paper to date 
because the microphysics involved in most modeling studies has not yet been 
considered.

  The actual formation of particles in models of the stratosphere as a result 
of geoengineering has yet to be established.  This is it greatest priority of 
SSRM at this time.

  Sincerely,

  Oliver Wingenter


  On 10/17/2010 3:41 PM, Ken Caldeira wrote: 

  Yes, you could produce even more new particles yourself which would inhibit 
new particle production from someone else's emissions, but presumably the total 
particle count would be higher at the end of all of this than if you did not 
intervene.

  Would it be possible to act on someone else's particle production in a way 
that would lower overall particles counts?




  On Sun, Oct 17, 2010 at 1:50 PM, Oliver Wingenter 
<[email protected]> wrote:

  Dear Josh,

  If the concentration of background particle were large enough, a few hundred 
particle per cm3, then this would inhibit new particle production.  At least 
this is case in the marine boundary layer.  I understand that stratospheric 
microphysical models are having trouble making new particles.  However, adding 
NH3 would allow ternary nucleation tens of thousands of times faster than 
sulfuric acid and water alone as is seen in the free troposphere.

  In terms of a volcanic eruptions like Pinatubo, I wonder how much ash made it 
to the stratosphere and provided nucleation sites?

  Sincerely, 

  Oliver Wingenter 



  On 10/17/2010 12:29 PM, Ken Caldeira wrote: 

    Multiple, independent injections would decrease the likelihood of 
coagulation relative to injecting it all in one place.

    Of course, there is potential for coordinated injections to decrease 
coagulation (aggregation) relative to uncoordinated injections.

    There is no evidence that I know of that one injection could "cancel out" 
the effects of another injection. It seems that the main case is that the 
climate effect of A+B would be less than the climate effects of A plus the 
climate effects of B.

    It is an interesting research question to understand whether there are 
countermeasures that would decrease the effectiveness of injection by injecting 
something upwind from an injection site that would promote aggregation of the 
injected material.

    ___________________________________________________
    Ken Caldeira

    Carnegie Institution Dept of Global Ecology
    260 Panama Street, Stanford, CA 94305 USA
    +1 650 704 7212 [email protected] 
    http://dge.stanford.edu/labs/caldeiralab  @kencaldeira



    On Sun, Oct 17, 2010 at 10:43 AM, Josh Horton <[email protected]> 
wrote:



    Hi everyone,

    I am finalizing a chapter on geoengineering policy for publication and
    would greatly appreciate informed feedback on the following paragraph:

    "The aerosol most commonly suggested for stratospheric injection is
    sulfuric acid.   Plans call for delivering sulfate aerosols by
    dispersing gas-phase precursor materials.  Precursor oxidation and
    aerosol formation involve complex processes with the potential to
    reduce the effectiveness of stratospheric insertion.  For instance,
    coagulation could lead to excessively large sulfuric acid particles
    that sediment out of the stratosphere, neutralizing the effect of the
    initial dispersion.   Multiple, independent injections would increase
    the likelihood of such unintended consequences.  Unsynchronized
    staging, scheduling, and delivery of sulfate aerosol injections would
    magnify the potential for perverse particulate interactions, and might
    jeopardize the success of geoengineering deployment.  Lack of policy
    coordination may result in separate injection schemes that effectively
    cancel each other out."

    For those with scientific/technical backgrounds, is this a sound
    argument?  Is the basic science correct?  I am outside my comfort zone
    with this and want to be sure I don't miss the mark.  Thanks to anyone
    who can offer insight.

    Josh Horton
    [email protected]
    http://geoengineeringpolitics.blogspot.com/

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