Valorization of Lignin Waste: Carbons from Hydrothermal Carbonization of Renewable Lignin as Superior Sorbents for CO2 and Hydrogen Storage

被引:163
作者
Sangchoom, Wantana [1 ]
Mokaya, Robert [1 ]
机构
[1] Univ Nottingham, Nottingham NG7 2RD, England
关键词
Lignin hydrochar; Hydrothermal carbonization; CO2; capture; Hydrogen storage; Activated carbon; Lignin waste; Activation; Biomass; HIGH-SURFACE-AREA; ZEOLITE-TEMPLATED CARBONS; ACTIVATED CARBON; MICROPOROUS CARBONS; CHEMICAL ACTIVATION; DIOXIDE CAPTURE; POROUS CARBON; PORE-SIZE; KRAFT LIGNIN; GAS-STORAGE;
D O I
10.1021/acssuschemeng.5b00351
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This report presents the preparation of renewable carbons from hydrothermally carbonized lignin waste. The hydrothermally carbonized mineral-free lignin-derived hydrochar was activated with KOH to yield carbons with surface area of 11573235 m(2) g-(1) and pore volume of 0.59-1.77 cm(3) g-(1). Activation at KOH/carbon = 2, generates highly microporous carbons (>= 97% micropore surface area and 93% micropore volume), which exhibit excellent CO2 uptake capacity; up to 4.6 mmol g-(1) at 1 bar and 25 degrees C, and 17.3 mmol g-(1) at 20 bar and 25 degrees C, whereas at 0 degrees C and 1 bar, they store up to 7.4 mmol g-(1). Activation at KOH/carbon = 4 can generate carbons with surface area and pore volume of up to 3235 m(2) g-(1) and 1.77 cm(3) g-(1), respectively, which have hydrogen uptake of up to 6.2 wt % at -196 degrees C and 20 bar. The simplicity of hydrothermal carbonization in generating hydrochars suitable for activation from readily available lignin waste, without the need for a demineralization step, makes these carbons attractive as gas storage materials for energy related applications. Furthermore, the lignin-derived carbons offer advantages with respect to attainable porosity and gas storage capacity compared to other forms of biomass (e.g., cellulose)-derived carbons.
引用
收藏
页码:1658 / 1667
页数:10
相关论文
共 96 条
[1]   Low temperature synthesized carbon nanotube superstructures with superior CO2 and hydrogen storage capacity [J].
Adeniran, Beatrice ;
Mokaya, Robert .
JOURNAL OF MATERIALS CHEMISTRY A, 2015, 3 (09) :5148-5161
[2]   A family of microporous carbons prepared via a simple metal salt carbonization route with high selectivity for exceptional gravimetric and volumetric post-combustion CO2 capture [J].
Adeniran, Beatrice ;
Masika, Eric ;
Mokaya, Robert .
JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (35) :14696-14710
[3]   The effect of Al content of zeolite template on the properties and hydrogen storage capacity of zeolite templated carbons [J].
Alam, Nurul ;
Mokaya, Robert .
MICROPOROUS AND MESOPOROUS MATERIALS, 2011, 144 (1-3) :140-147
[4]   Characterisation and hydrogen storage of Pt-doped carbons templated by Pt-exchanged zeolite Y [J].
Alam, Nurul ;
Mokaya, Robert .
MICROPOROUS AND MESOPOROUS MATERIALS, 2011, 142 (2-3) :716-724
[5]   Evolution of optimal porosity for improved hydrogen storage in templated zeolite-like carbons [J].
Alam, Nurul ;
Mokaya, Robert .
ENERGY & ENVIRONMENTAL SCIENCE, 2010, 3 (11) :1773-1781
[6]   Porosity modulation of activated ZIF-templated carbons via compaction for hydrogen and CO2 storage applications [J].
Almasoudi, A. ;
Mokaya, R. .
JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (28) :10960-10968
[7]   Preparation and hydrogen storage capacity of templated and activated carbons nanocast from commercially available zeolitic imidazolate framework [J].
Almasoudi, A. ;
Mokaya, R. .
JOURNAL OF MATERIALS CHEMISTRY, 2012, 22 (01) :146-152
[8]   A CVD route for the preparation of templated and activated carbons for gas storage applications using zeolitic imidazolate frameworks (ZIFs) as template [J].
Almasoudi, Afaf ;
Mokaya, Robert .
MICROPOROUS AND MESOPOROUS MATERIALS, 2014, 195 :258-265
[9]  
Brebu M, 2010, CELL CHEM TECHNOL, V44, P353
[10]   Adsorbent Materials for Carbon Dioxide Capture from Large Anthropogenic Point Sources [J].
Choi, Sunho ;
Drese, Jeffrey H. ;
Jones, Christopher W. .
CHEMSUSCHEM, 2009, 2 (09) :796-854