• Title/Summary/Keyword: 이산화탄소 흡수제

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Absorption Characteristics of Aqueous Sodium Glycinate Solution with Carbon Dioxide and Its Mechanistic Analysis (Sodium Glycinate 수용액의 CO$_2$ 흡수특성 및 반응 메커니즘 해석)

  • Shim, Jae-Goo;Kim, Jun-Han;Jang, Kyung-Ryong
    • Journal of Korean Society of Environmental Engineers
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    • v.30 no.4
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    • pp.430-438
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    • 2008
  • The experiments for separation and recovery of CO$_2$ were conducted by aqueous sodium glycinate solution, which is one of the amino acid salts, as an absorbent of CO$_2$ in this study. Absorption capacities of aqueous MEA and sodium glycinate solution according to partial pressure of CO$_2$ were evaluated by vapor-liquid equilibrium tests of 20 wt% and 30 wt% above-mentioned absorbents, respectively. In addition, the pilot scale(2 t-CO$_2$/day) experiments based on prior results were carried out. As a result, CO$_2$ removal efficiency of aqueous sodium glycinate solution was lower than that of aqueous MEA solution. This phenomenon means that CO$_2$ removal efficiency of aqueous sodium glycinate solution mainly depends on its molecular structure. Consequently, the first application of certain amino acid salt, as an absorbent of CO$_2$, to pilot plant of 2 t-CO$_2$/day scale was carried out in our country.

Development of a novel amino acid salt solution for $CO_2$ capture (아미노산염수용액을 이용한 이산화탄소 흡수제 개발)

  • Lim, Jin-Ah;Jo, Min;Jeong, Soon-Kwan;Nam, Sung-Chan;Yoon, Yeo-Il;Kim, Dong-Hyun
    • Proceedings of the KAIS Fall Conference
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    • 2011.05a
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    • pp.310-313
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    • 2011
  • 본 논문에서는 지구온난화의 주요원인 중의 하나인 이산화탄소를 포집하기 위한 새로운 흡수제를 연구하였다. 액상 흡수법에서 가장 중요한 핵심 기술요소는 성능과 경제성면에서 우수한 흡수제를 개발하는 것이다. 흡수평형장치인 VLE(Vapor-Liquid Equilibrium)장치를 사용하여 신규흡수제의 이산화탄소 흡수능을 평가하고 특성을 알아봄으로써 신 흡수제를 개발하고자 하였다. 기존 아민흡수제인 MEA(monoethanolamine), DEA(diethanolamine)와 비교한 결과 아미노산염 흡수제의 경우 MEA (1.108), DEA (1.105)의 이산화탄소 흡수능보다 0.15~0.2 (mol $CO_2$/mol absorbent) 더 높은 흡수능과 2.5~3배 더 빠른 겉보기 속도를 나타내는 것을 확인하였다. 본 연구를 통하여 개발된 아미노산염 흡수제가 경제적인 이산화탄소 포집공정을 구현할 수 있는 가능성을 확인하였다.

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Post-combustion CO2 capture with potassium L-lysine (Potassium L-lysine을 이용한 연소 후 이산화탄소 포집)

  • Lim, Jin Ah;Yoon, Yeo Il;Nam, Sung Chan;Jeong, Soon Kwan
    • Journal of the Korea Academia-Industrial cooperation Society
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    • v.14 no.9
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    • pp.4627-4634
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    • 2013
  • Carbon dioxide is one of the main causes of global warming. In order to develop a novel absorbent, the characteristics of amino acid salts solution as a solvent for $CO_2$ capture in continuous process were investigated. The cost of $CO_2$ capture is almost 70% of total cost of CCS (carbon dioxide capture and storage). In the carbon dioxide capture process, process maintenance costs consist of the absorbent including the absorption, regeneration, degradation, and etc. It is very important to study the characteristics of absorbent in continuous process. In this study, we have investigated the properties of potassium L-lysine (PL) for getting scale-up factors in continuous process. To obtain optimum condition for removal efficiency of $CO_2$ in continuous process by varying liquid-gas (L/G) ratio, concentration of $CO_2$ and absorbent (PL) were tested. The stable condition of absorber and regenerator (L/G) ratio is 3.5. In addition, PL system reveals the highest removal efficiency of $CO_2$ with 3.5 of L/G and 10.5 vol% $CO_2$ ($1.5Nm^3/h$).

Absorption Characteristics of Carbon Dioxide by Water-lean Diethylenetriamine Absorbents Mixed with Physical Solvents (물리 흡수제를 포함한 디에틸렌트리아민(Diethylenetriamine) 저수계 흡수제에서의 이산화탄소 흡수 특성)

  • Lee, Hwa Young;Seok, Chang Hwan;You, Jong-Kyun;Hong, Yeon Ki
    • Clean Technology
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    • v.24 no.1
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    • pp.50-54
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    • 2018
  • In this work, N-methyl-2-pyrrolidone (NMP) was added into diethylenetriamine (DETA) aqueous solution for high $CO_2$ loading via phase splitting of absorbents during $CO_2$ absorption. Immiscible two phases were formed in the range of more than 30 wt% of NMP in 2 M DETA + NMP + water absorbents because of low solubility of DETA-carbamate in NMP solution. As the composition of NMP in the absorbents increased, the difference of $CO_2$ loading between each phase increased and the volume of bottom phase decreased. In $CO_2$ absorption in packed column by 2 M DETA + NMP + water absorbents, the absorption rate decreased in the range of more than 40 wt% of NMP. It is due to the increasing of mass transfer resistance in liquid film of absorbents at the high concentration of NMP. DETA + NMP + water absorbent is expected as the promising one for reducing the regeneration energy of absorbents according to volume reduction of $CO_2-rich$ phase.

Carbon Dioxide Absorption in a Packed Column Using Guanidine-based Superbase Solution (구아니딘계 초염기 흡수제에 의한 충진탑에서의 이산화탄소 포집 특성)

  • Choi, Young Min;Hong, Yeon Ki;You, Jong Kyun
    • Korean Chemical Engineering Research
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    • v.54 no.5
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    • pp.648-652
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    • 2016
  • The study of $CO_2$ absorption in a packed column by 1,1,3,3-tetramethylguanidine (TMG) dissolved in ethylene glycol is presented. Absorption column of inner diameter 1 in and 0.6 m length was filled with Protruded-packing $0.16in{\times}0.16in$. We investigated the effect of operating conditions on overall mass transfer coefficients as well as on $CO_2$ removal efficiency. The loading values reached at about $1.0mol_{CO2}/mol_{TMG}$. In case of absorbent with lean $CO_2$ loading, the overall mass transfer coefficient was proportional to the concentration of TMG. However, in the range of more than ${\alpha}=0.5molCO_2/molTMG$, the overall mass transfer coefficients decreased with the concentration of TMG. It is due to the increasing of mass transfer resistance in liquid phase as increasing of viscosity at higher loading values.

A Study on the Absorption of Carbon Dioxide using PVDF/Plasma Membrane Contactor (PVDF/플라즈마 막접촉기를 이용한 이산화탄소의 흡수에 관한 연구)

  • Choi, Seung-Hak;Gao, Tongzhai;Oh, Sae-Joong
    • Korean Chemical Engineering Research
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    • v.43 no.1
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    • pp.161-169
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    • 2005
  • Numerical simulation and experiments were carried out on the absorption of carbon dioxide using PVDF hollow-fiber membrane contactor. Water or monoethanolamine (MEA) aqueous soluton was used as absorbents. Simulation results showed that the concentration profile of carbon dioxide was less affected by the flow rate of MEA than that of water absorbent. The absorption rate and mass transfer coefficient of carbon dioxide increased as the concentration of MEA increased. The mass transfer coefficients obtained by experiments coincided with those obtained by numerical simulation and theoretical results for $CO_2-water$ system. However, for $CO_2-MEA$ system, the mass transfer coefficients obtained by experiments were lower than those obtained by simulation, while the simulation results agreed well with theoretical results. The durability of plasma-treated hollow fiber membranes was better than that of no plasma-treated ones.

Degradation Characteristics of Carbon Dioxide Absorbents with Different Chemical Structures (상이한 화학적 구조를 가진 이산화탄소 흡수제의 열화특성)

  • Kim, Jun-Han;Lee, Ji-Hyun;Jang, Kyung-Ryong;Shim, Jae-Goo
    • Journal of Korean Society of Environmental Engineers
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    • v.31 no.10
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    • pp.883-892
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    • 2009
  • We evaluated the degradation properties of various alkanolamine absorbents (MEA, AMP, DEA, and MDEA) having different chemical structures for $CO_2$ capture. The degradation of $CO_2$ absorbent in general was known to be caused by oxygen which is in flue gas and by heat source, respectively. To analyze the effect of $CO_2$ and $O_2$ on degree of degradation, we conducted a variety of experiments at $30^{\circ}C$ and $60^{\circ}C$ (oxidative degradation) and $130^{\circ}C$ and $150^{\circ}C$ (thermal degradation), respectively. DEA showed the worst property for oxidative degradation in the presence of oxygen among the alkanolamine absorbents. In the case of thermal degradation, the degradation of absorbent was occurred for most of absorbents at $150^{\circ}C$. Among these absorbents, MEA and DEA gave the worst results. As a result, AMP which is a primary amine and having a steric hindrance showed the best result through the degradation test. But, the degradation of absorbent proceeded easily in the case of DEA which is a secondary amine and having 2 OH groups in terminal position. Consequently, we have evaluated the degree of degradation of various absorbents having different chemical structures to give the basic data for the development of alkanolamine absorbent.

Effect of Active Master Packaging System on Preservation of Fresh Shiitake Mushrooms in Supply Chain (유통과정에서 생표고버섯에 대한 Active 마스터 포장 시스템의 적용 효과)

  • An, Duck Soon
    • Journal of the Korean Society of Food Science and Nutrition
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    • v.45 no.3
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    • pp.402-408
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    • 2016
  • Master packaging system consists of an inner individual package and secondary outer package. During the stages of chilled transport and distribution, the combination of primary individual package and secondary package was used to maintain a modified atmosphere for shiitake mushrooms. During the retail stage at higher temperature ($25^{\circ}C$), the primary individual package was exposed to display conditions after dismantling of the secondary packaging. The master packaging system was constructed to contain eight individual $30-{\mu}m$ thick polypropylene film bags of 500 g shiitake mushrooms inside a $40-{\mu}m$ low-density polyethylene bag. Carbon dioxide absorbent material [$Ca(OH)_2$] and/or moisture absorbent (superabsorbent polymer) were designed in their required amounts based on respiration characteristics and then applied to the outer secondary packaging in sachet form. Gas concentration of the packaging, temperature, and humidity were monitored throughout transport and storage. The quality of shiitake mushrooms was measured at the retail stage to determine the packaging effect. During the distribution stage of 108 h, $O_2$ and $CO_2$ concentrations in the master packaging system were maintained at 9~11% and 1~4% in the inner packaging, respectively, which are good for quality preservation. Compared to the control, the master packaging with $CO_2$ and/or moisture absorbents improved mushroom preservation and particularly reduced decay.

Characteristics of Solid Regenerable $CO_2$ sorbents for Pre-combustion $CO_2$ Capture (연소전 $CO_2$ 포집용 분무건조 고체 흡수제의 물성 및 $CO_2$ 흡수 특성)

  • Baek, Jeom-In;Ryu, Jungho;Lee, Joong Beom;Eom, Tae-Hyoung;Kim, Ji-Woong;Jeon, Eon-Sik;Ryu, Chong Kul
    • 한국신재생에너지학회:학술대회논문집
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    • 2010.06a
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    • pp.110.2-110.2
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    • 2010
  • 현재 상용가능한 연소전 $CO_2$ 포집 기술은 습식 스크러빙 방식으로 고온의 합성가스를 상온 수준으로 온도를 낮춘 후 $CO_2$를 포집해야 하고 포집된 $CO_2$의 압력이 낮아 재압축하여 저장소로 보내야 함에 따라 큰 폭의 열효율 손실이 불가피하다. 고온 고압에서 이산화탄소를 포집할수 있는 고체 흡수제를 이용할 경우 이산화탄소 포집 치 저장 추가에 따른 시스템 효율 저하를 최소화할 수 있다. 고체 $CO_2$ 흡수제는 서로 연결된 두 개의 유동층 반응기를 순환하면서 흡수탑에서는 합성가스 중의 $CO_2$를 흡수하고 재생탑에서는 고온의 수증기와 접촉하여 흡수된 $CO_2$를 다시 배출함으로써 재생된다. 따라서 건식 재생 $CO_2$ 흡수제는 유동층 공정에 응용가능한 물성과 함께 높은 $CO_2$ 흡수능과 빠른 반응성이 요구된다. 본 연구에서는 유동층 공정에 적합한 물성을 가진 연소전 $CO_2$ 포집용 고체 흡수제를 분무건조법으로 제조하였으며, 모사 합성가스를 이용하여 열중량분석기와 기포유동층반응기를 이용하여 $200^{\circ}C$ 흡수, $400^{\circ}C$ 재생, 압력 20 bar 조건으로 반응성을 측정하였다. 개발된 고체 $CO_2$ 흡수제는 열중량분석기에서는 반응 후 10-13 wt%의 무게증가를 나타내었고 기포유동층반응기에서는 8-10 wt%의 $CO_2$ 흡수능을 보여주었다. 특히 수증기의 함량이 10% 이상에서 높은 흡수능을 나타내어 수증기가 반응에 크게 작용하고 있음을 알 수 있었다.

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Solubility Measurement of Carbon Dioxide in Alkylcarbonates and Triacetin at High Pressure (고압에서 알킬카보네이트와 트리아세틴의 이산화탄소 용해도 측정)

  • Kim, Ji Won;Hong, Won Hi;Hong, Yeon Ki
    • Clean Technology
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    • v.21 no.2
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    • pp.124-129
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    • 2015
  • The constant-volume method was used to determine the solubility of CO2 in various physical absorbents such as DMPEG (dimethyl ether of polyethylene glycol), DEC (diethyl carbonate), DMC (dimethyl carbonate), and TAT (triacetin) in the total pressure range from 5 to 30 bar. The Peng-Robinson equation of state has been used to describe the equilibrium behavior of these mixtures. It was found that the solubility of absorbents was in the of DMPEG250 > TAT > DEC > DMC at the same temperature. Futhermore, the solubiity of blended absorbent of DMPEG250 and DEC is higher than that of DMPEG 250 alone. Therefore, blended absorbent of DMPEG250 and DEC is expected to be an effective and low cost absorbent for physical absorption in precombustion CO2 capture.