Use of monolithic silicon carbide aerogel as a
reusable support for development of regenerable
CO
2
adsorbent†
Yong Kong,
ab
Xiaodong Shen,
*
ab
Sheng Cui
ab
and Maohong Fan
*
cd
Monolithic silicon carbide aerogel (MSiCA) was firstly used as a reusable support to develop a novel CO
2
adsorbent, i.e. amine functionalized monolithic silicon carbide aerogel (AFMSiCA). Used or exhausted
AFMSiCA was separated, treated and re-functionalized by amine to form RF-MSiCA. CO
2
capture
performance of the resulting adsorbents was investigated in a 1% CO
2
flow stream. The results revealed
that CO
2
adsorption capacities of AFMSiCA at different temperatures ranging from 25 to 75
C showed
little change, indicating that the resulting adsorbent is well-adapted to temperature. The adsorption rate
is affected by the combined effect of CO
2
adsorption and desorption. Benefiting from the highly unique
properties of the aerogel (e.g. high surface area and large pore volume), MSiCA-based adsorbents are
dynamic in their CO
2
adsorption process. MSiCA could be readily recovered and reused at least 12 times
without significant loss of CO
2
adsorption performance. The resulting adsorbents presented good
stability during cyclic adsorption–regeneration tests. MSiCA is exceptional in practical application for
CO
2
capture due to its excellent reusability and the regenerability of its amine functionalized counterparts.
Introduction
Concentrations of CO
2
in the atmosphere are increasing at an
accelerating rate, a phenomenon that has drawn signicant
attention because of its link to climate change. CO
2
capture and
sequestration (CCS) is a promising way to control CO
2
emis-
sions.
1
Among available techniques, amine scrubbing is the
current state-of-the-art technology for CO
2
capture on an
industrial scale. However, this approach shows signicant
shortcomings, including corrosion, oxidative degradation, high
energy consumption for regeneration, and secondary pollution
resulting from its high volatility.
2
Hence, porous adsorbents
functionalized with amines have been extensively studied for
CO
2
capture because they can overcome the shortcomings of an
aqueous amine scrubbing technique.
3
Recent investigations
have focused on using aerogels as new CO
2
capture materials,
due to their unique physical properties such as low densities,
high surface areas and porosities.
4
Moreover, the
microstructures and elemental compositions of aerogels can be
tailored using solution chemistry via a process known as the
sol–gel method.
5
Therefore, aerogel-based CO
2
adsorbents have
been extensively developed recently. Cui et al. achieved a high
CO
2
adsorption capacity in 10% CO
2
mixture stream by using
silica aerogel modied with 3-aminopropyltriethoxysilane
(APTES).
6
Begag et al. developed hydrophobic amine function-
alized aerogels by graing amine groups onto silica backbone
and achieved 1.43 mmol g
1
CO
2
sorption capacity in simulated
ue gas.
7
Linneen et al. found that 1 g silica aerogel immobi-
lized with tetraethylenepentamine (TEPA) could adsorb 3.5
mmol CO
2
under a dry 10% CO
2
/Ar stream.
8
Wang et al. found
that 1 g silica aerogel can adsorb 3.3 mmol CO
2
from pure CO
2
at 25
C and 1 atm.
9
Masika developed a carbon aerogel for CO
2
capture, the CO
2
adsorption capacity obtained in pure CO
2
at 25
C and 1 bar was only 2.2 mmol g
1
although the carbon aerogel
has a high surface area of 1100 m
2
g
1
.
10
Alhwaige et al. devel-
oped chitosan hybrid aerogels for CO
2
capture, the CO
2
adsorption capacity in pure CO
2
at 25
C is up to 4.15 mmol
g
1
.
11
Lin et al. successfully developed hydrophobic silica aer-
ogel membranes for CO
2
capture.
12
We have developed a novel
aerogel adsorbent based on amine hybrid silica aerogel via
facile sol–gel route and supercritical drying, its CO
2
adsorption
capacity of at 25
C and 1 atm in a 1% CO
2
mixture stream is as
high as 5.55 mmol g
1
.
13
All these reports indicate that aerogels
have a promising prospect in CO
2
capture.
Silicon carbide (SiC) has high hardness, excellent thermal
stability and superior chemical inertness,
14
therefore, its aerogel
counterpart can be promisingly used for CO
2
capture. Bhatia
a
College of Materials Science and Engineering, Nanjing Tech University, Nanjing
210009, P. R. China. E-mail: xdshen@njtech.edu.cn; Tel: +86-25-8358-7234
b
State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing Tech
University, Nanjing 210009, P. R. China. E-mail: xdshen@njtech.edu.cn; Tel: +86-
25-8358-7234
c
Department of Chemical and Petroleum Engineering, University of Wyoming, Laramie,
WY 82071, USA. E-mail: mfan@uwyo.edu; Tel: +1-307-766-5633
d
School of Civil and Environmental Engineering, Georgia Institute of Technology,
Atlanta, GA 30332, USA. E-mail: mfan3@mail.gateche.edu; Tel: +1-404-385-4577
† Electronic supplementary information (ESI) available. See DOI:
10.1039/c4ra11261j
Cite this: RSC Adv. , 2014, 4, 64193
Received 26th September 2014
Accepted 10th November 2014
DOI: 10.1039/c4ra11261j
www.rsc.org/advances
This journal is © The Royal Society of Chemistry 2014 RSC Adv. , 2014, 4, 64193–64199 | 64193
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