In this work, subabul wood biomass was used to prepare carbon adsorbents by physical and chemical activation methods at various carbonization temperatures. The properties of the carbon adsorbents were estimated through characterization techniques such as X-ray diffraction, Fourier transform infrared spectroscopy, X–ray photo electron spectroscopy, laser Raman spectroscopy, scanning electron microscopy, CHNS-elemental analysis and N2 adsorption studies. Subabul-derived carbon adsorbents were used for CO2 capture in the temperature range of 25–70 °C. A detailed adsorption kinetic study was also carried out. The characterization results indicated that these carbons contain high surface area with microporosity. Surface properties were depended on treatment method and carbonization temperature. Among the carbons, the carbon prepared after treatment of H3PO4 and carbonization at 800 °C exhibited high adsorption capacity of 4.52 m.mol/g at 25 °C. The reason for high adsorption capacity of the adsorbents was explained based on their physicochemical characteristics. The adsorbents showed easy desorption and recyclability up to ten cycle with consistent activity.

Here, we report the preparation of microporous-activated carbons from a Brazilian natural lignocellulosic agricultural waste, cupuassu shell, by pyrolysis at 500 ºC and KOH activation under different experimental conditions and their subsequent application as adsorbent for CO2 capture. The effect of the KOH:precursor ratio (wt/wt%) and the activation temperature on the porous texture of activated carbons have been studied. The values of specific surface area ranged from 1132 to 2486 m2/ g, and the overall micropore volume ranged from 0.73 to 1.02 cm3/ g. Carbons activated with 2:1 ratio of KOH and activation temperature of 700 ºC presented a CO2 adsorption at 1 bar of 7.8 and 4.4 mmol/g at 0 °C and 25 ºC, respectively. The isosteric heat of adsorption, Qst , was calculated for all samples by applying the Clausius–Clapeyron approach to CO2 adsorption isotherms at both temperatures. The values of CO2 adsorption capacities are among the highest reported in the literature, especially for activated carbons produced from biomass.

Radioactive carbon dioxide (14CO2) capture using innovative materials is desirable due to associated radiological hazards, and growing climate change. Mineral carbonation technology (MCT) is amenable to irreversibly capture CO2. Typically, MCT is attractive because capturing carbon through the chemical reaction between alkaline earth metal ions and CO2 forms insoluble and significantly stable carbonates. However, most applications of MCT have an intrinsic restriction regarding their operational conditions since no forward reaction occurs within realistic time scales. Thereby, the CO2 capture performance, such as CO2 capacity and carbonation reaction rate, of MCTs and their applications are severely restricted by the difficulty of operations under mild conditions. For example, natural minerals require aggressive carbonation reaction conditions e.g. high pressure (≥ 20 bar), high temperature (> 373 K), and pH-adjusted carrier solutions. To overcome such obstacles, the fabrication of alkaline earth oxides impregnated into an amorphous glass structure have been recently developed. They show enhanced rates of dissolution of alkaline earth metal ions and carbonation reaction due to the loosely packed glass structure and the generation of a surface coating silica gel, consequently facilitating CO2 capture under mild conditions. In this presentation, we report the synthesis and application of a crystallized glass tailored by controlled heat treatment for CO2 capture under mild conditions. The controlled heat treatment of an alkaline earth oxide-containing glass gives rise to a structural transformation from amorphous to crystalline. The structural characterizations and CO2 capture performance, including CO2 capacity, carbonation reaction rate, and the dissolution rate of alkaline earth metal ion, were analyzed to reveal the impact of controlled heat treatment and phase transformation.

Global warming and climate changes are the ultimate consequences of increased CO2 volume in the air. Physical activation was used to prepare high-throughput activated carbon from a low-cost date stone. The adsorption performance of activated carbon using fixed bed for CO2 separation was studied. The reliance of temperature, flow rate, and initial CO2 concentration levels on breakthrough behaviour was analysed. The adsorption response was explored in terms of breakthrough and saturation points, adsorption capacity, temperature profiles, utilization factor, and length of mass-transfer zone. Increased temperatures lead to vary the breakthrough periods notably. The vastly steep breakthrough curves reveal satisfactory utilization of bed capacity. LMTZ is varied positively with increased feed rates and temperatures. The high utilization factor of 0.9738 with 1.66 mmol/g CO2 uptake was acquired at 298 K and 0.25 bars. The findings recommend that the carbon prepared from date stone is encouraging to capture CO2 from CO2/ N2 mixture.

Increasing ambient carbon dioxide ( CO2) concentration from anthropogenic greenhouse gas emission has contributed to the growing rate of global land and ocean surface temperature. Various carbon capture and storage (CCS) technologies were established to mitigate this impending issue. CO2 adsorption is gaining prominence since unlike traditional chemical absorption, it does not require high energy usage for solvent regeneration and consumption of corrosive chemical solvent. In CO2 adsorption, activated carbons show high CO2 adsorption capacity given their well-developed porous structures. Numerous researches employed oil palm wastes as low-cost precursors. This paper provides a comprehensive assessment of research works available thus far in oil palm-derived activated carbon (OPdAC) for CO2 adsorption application. First, we present the desired OPdAC characteristics and its precursors in terms of their chemical properties, elemental, and proximate compositions. This is followed by an overview of various activation methodologies and surface modification methods to attain the desired characteristics for CO2 adsorption. Then the focus turned to present available OPdAC CO2 adsorption performance and how it is affected by its physical and chemical characteristics. Based on these, we identify the challenges and the potential development in different aspects such as precursor selection, process development, and optimization of parameter. A pilot scale production cost analysis is also presented to compare various activation and surface modification methods, so that the appropriate method can be selected for CO2 adsorption.

이산화탄소 포집 및 저장기술(CCS)은 인류발생적 요인에 의한 이산화탄소 배출 증가와 그로 인한 기후변화를 완화시킬 수 있는 기술 중 하나이다. 그 중, 매체 순환식 연소(chemical looping combustion, CLC)와 칼슘루핑(calcium looping) 기술은 현재 아민 스크러빙(amine scrubbing)을 대체할 수 있는 유망한 기술로 주목받고 있다. 두 방법 모두 금속 산화물을 이용한 연속적인 순환 사이클 반응에 의한 것이다. 전체적인 이산화탄소 포집 및 저장 성능의 향상을 위해서는 사이클을 거듭 하며 발생하는 소결(sintering)로 인한 안정성 저하 문제를 해결하고 금속 산화물의 구조 또한 최적화해야 한다. 금속 산화물 표면에 얇은 박막을 형성하는 것은 소결로 인한 손상을 막을 수 있는 방법이다. 이러한 박막 제조 기술로 잘 알려진 기술에는 화학기상증착법(chemical vapor deposition)과 원자층증착기술(atomic layer deposition)이 있다. 본 총설에서는 CVD, ALD 기술을 비롯하여 효과적인 반응 안정성 향상을 위한 안정제 첨가 방법, 금속 산화물 구조 개선에 대한 다양한 최근 기술들을 다루었다.

천연가스, 산업공정, 화석연료의 연소과정과 같은 대규모 고정 배출원에서 발생하는 온실가스인 CO2를 포집하기 위한 기술 개발이 전 세계적으로 활발하게 수행되고 있다. 특히, 습식 흡수 법은 비교적 낮은 CO2분압에서도 높은 제거 효율을 달성할 수 있어 많은 개발이 이루어져온 포집 기술이다. 하지만 흡수제의 재생에 필요한 에너지가 과다한 문제가 있으며, 충분한 부지가 확보되어야하기 때문에 공정 상용화에는 큰 걸림돌이 있다. 이러한 문제를 극복하고 공정 효율을 개선 할 수 있는 접촉분리막 공정 기술이 최근 주목받고 있다. 본 연구에서는 접촉분리막과 화학적 습식 아민 흡수제를 이용한 이산화탄소 제거 특성을 분석하였다.

The stereotype of flexible MOFs(Amino-MIL-53) and carbonized porous carbon prepared from renewable resources is successfully synthesized for CO2 reduction application. The textural properties of these microporous materials are investigated, and their CO2 storage capacity and separation performance are evaluated. Owing to the combined effects of CO2-Amino interaction and its flexibility, a CO2 uptake of 2.5 mmol g−1 is observed in Amino-MIL-53 at 20 bar 298 K. In contrast, CH4 uptake in Amino-MIL-53 is very low up to 20 bar, implying potential sorbent for CO2/CH4 separation. Carbonized samples contain a small quantity of metal residues(K, Ca, Mg, S), resulting in naturally doped porous carbon. Due to the trace metal, even higher CO2 uptake of 4.7 mmol g−1 is also observed at 20 bar 298 K. Furthermore, the CH4 storage capacity is 2.9 mmol g−1 at 298 K and 20 bar. To evaluate the CO2 separation performance, the selectivity based on ideal adsorption solution theory for CO2/CH4 binary mixtures on the presented porous materials is investigated.

배가스의 이산화탄소 농도인 14%를 기준으로 실험실규모에서 벤치스케일로 격상하였고, 랩스케일에서는 모사가스로 진행한 반면 벤치스케일에서는 실제 보일러에서 나오는 배가스로 실험을 진행하였다. 배가스의 높지않은 압력조건을 감안하여 본 연구에서는 1단 분리막 공정실험에서는 주입부 압력 2 bar, 투과부압력 0.2 bar에서 실험을 진행 하였고, 2단 막 공정에서는 1단 분리막은 동일하게, 2단 분리막 주입부 압력 1 bar, 투과부 압력 0.05 bar에서 진행하였다. 결론적으로 랩스케일에서 벤치스케일로 격상했을 경우 같은 경향성을 볼 수 없었으며 이는 실제 발전소 및 보일러에서 연소되는 배가스를 분리막공정으로 포집하는 것은 사전연구가 더욱 필요하다는 것을 확인하였다.

본 연구에서는 이산화탄소 포집 및 물 재이용을 위한 통합 시스템으로서 정삼투 공정의 적용 가능성에 대한 평가를 수행하였다. 해당 통합 공정은 이산화탄소 배출 저감을 위해 화력발전소에 적용되고 있는 습식 이산화탄소 포집설비에 정삼투 기반 공정을 추가함으로써 이산화탄소 포집뿐만 아니라 물 재이용 및 냉각수 생산을 동시에 달성할 수 있다. CO2를 흡수한 5M의 모노에탄올아민(습식용매)을 유도용액으로 적용한 결과 40 LMH (FO mode) 및 85 LMH (PRO mode)라는 매우 높은 수투과도를 얻을 수 있었다.