Thanks, Andrew, for the recent updates on DAC. I remain puzzled, however, by 
the continuing interest in artificial air CO2 capture when we've got in gross 
some 700+ GT of air CO2 capture/yr naturally going on, in net consuming 55-60% 
of our CO2 emissions.  Contrary to one of the articles*, air capture is not a 
"concept", it's what is currently saving our bacon right now. Wouldn't it make 
a lot more sense (and save a lot of cents) figuring out how to enhance/exploit 
these natural CO2 absorption and conversion processes (e.g, BECCS,  CROPS, 
ocean alkalization, enhance mineral weathering, etc.) rather than trying to 
reinvent the wheel from the ground up, competing on a cost basis with what 
nature already does for free?  How about investing in improving on the global 
scale "engineering" that's already in place?
Regards,
Greg 

*http://pubs.acs.org/doi/abs/10.1021/ie300691c?prevSearch=air%2Bcapture&searchHistoryKey=
 
________________________________________
From: [email protected] [[email protected]] On 
Behalf Of Andrew Lockley [[email protected]]
Sent: Wednesday, July 25, 2012 11:59 AM
To: geoengineering
Subject: [geo] Air capture: Modification of the Mg/DOBDC MOF with Amines to 
Enhance CO2 Adsorption from Ultradilute Gases

http://pubs.acs.org/doi/abs/10.1021/jz300328j

Modification of the Mg/DOBDC MOF with Amines to Enhance CO 2 Adsorption from 
Ultradilute Gases

Sunho Choi, Taku Watanabe, Tae-Hyun Bae, David S. Sholl, Christopher W. Jones

J. Phys. Chem. Lett., 2012, 3 (9), pp 1136–1141 DOI: 10.1021/jz300328j

The MOF Mg/DOBDC has one of the highest known CO 2 adsorption capacities at the 
low to moderate CO 2 partial pressures relevant for CO 2 capture from flue gas 
but is difficult to regenerate for use in cyclic operation. In this work, 
Mg/DOBDC is modified by functionalization of its open metal coordination sites 
with ethylene diamine (ED) to introduce pendent amines into the MOF micropores. 
DFT calculations and experimental nitrogen physisorption and thermogravimetric 
analysis suggest that 1 ED molecule is added to each unit cell, on average. 
This modification both increases the material’s CO 2 adsorption capacity at 
ultradilute CO 2 partial pressures and increases the regenerability of the 
material, allowing for cyclic adsorption–desorption cycles with identical 
adsorption capacities. This is one of the first MOF materials demonstrated to 
yield significant adsorption capacities from simulated ambient air (400 ppm CO 
2 ), and its capacity is competitive with the best-known adsorbents based on 
amine–oxide composites.

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