CO2 separation technology for carbon capture, which is one of the hot issues to reduce greenhouse gases from industrial flue gas, has been intensively investigated so far. Despite of several benefits, the membrane technology has some obstacles like large-scale module fabrication, membrane durability, need of pre-treatment or high pressure drive for its industrial application. Also, the power plant flue gas with normally 10~20% of CO2 content should be concentrated upto 99% for being compressed and liquefied to transportable CO2 by pipeline, indicating the need of high selective membrane process as well as high recovery. In this work, the possibility of membrane process for post-combustion treatment in terms of recent technology will be announced. The practically applicable process for CO2 capture also be suggested briefly.

The carbon capture and storage (CCS) technology from industrial flue-gas has been an important environmental issue in these days. However, membrane process has a number of breakthrough-point to commercialization in scale-up. In this work, process optimization for high purity and high CO2 recovery with lower the capture cost has been investigated. Lab-made membrane pilot process using real flue gas has been also set up to derive industrial factor.

Membrane is a relatively new industrial gas separation technology and has been studied as an alternative CO2 capture technologies to amine absorption. Membrane processes have a merit such as low energy use, small footprint, no by-products formation, and simple operating condition. When applied to flue gas CO2 capture, low CO2 concentration and normal pressure of flue gas stream places a practical limits on the membrane operation. The up-to-date membranes should allow module performance to rise to levels practical for fossil-fuel power station use. In this talk, membrane module is being evaluated for flue gas treatment. Membrane processes using several membranes, which are now being studied under the R&D projects granted by KCRC, are investigated to capture CO2 from the simulated gas.

Flat sheet membranes consisting of a selective layer and a porous support usually require gutter layer to reduce the bulk pores of the substrates. The gutter layer mitigates the geometric restrictions of support, which enables selective layer to have defect-free morphology with thin thickness (< 100 nm). For this reason, the gutter layer has been introduced to many industrial membranes, and the systematical studies of the effects of the gutter layer properties on membrane performance should be needed. Herein, we introduced several gutter layers with different thicknesses into graphene oxide intercalated polymer TFC membranes to determine the relationship between gutter layer properties and total membrane performances. This study provides more practical insight to determine the optimum gutter layer properties in designing TFC membranes.

연소 후 생성되는 연소가스 중 CO2는 온실가스 기체중 하나로, CO2를 처리하기 하기 위해 CCS 기술 개발이 세계적으로 주목 받고 있다. 하지만 단일막을 이용한 CO2 포집 공정에서는 약 14%의 CO2를 포함한 연소 배기가스로부터 고 순도, 고회수율을 달성하기란 매우 어렵다. 본 연구에서는 다단막 공정 디자인 및 다양한 운전 변수를 통하여 14%의 CO2를 가지고 있는 혼합모사가스로부터 순도 73% 회수율 74%의 포집 효율을 얻을 수 있었다.

The carbon capture and storage (CCS) technology from industrial flue-gas is an important environmental issue these days. Membrane process can be competitive technology for its relatively small footprint and eco-friendly system. Many membrane modules with high selectivity and excellent flux have been developed so far. However, the high purity and recovery for CO2 capture can be achieved by optimization of operating conditions such as membrane area, feed/permeate pressure ratio and humidity of flue gas as well as membrane permeance or selectivity. In this study, we discuss the effect of operating parameters for high CO2 purity and recovery at permeate side. Using polymeric hollow fiber membrane, the single membrane process was tested to figure out the effect of feed flow rate, pressure ratio, membrane area and moisture content.

이산화탄소는 온실가스로써 대기 중에 축적되어 지구의 온도를 지속적으로 상승시킨다. 화석 연료 기반의 전력 생산에서 발생되는 이산화탄소는 상당량을 차지하며, 향후 수십 년간 화석연료 의존도 는 지속적으로 증가할 것으로 예상된다. 따라서 대기 중으로 배출되는 이산화탄소를 분리하는 기술개발 은 매우 시급하다. 이산화탄소 분리 기술은 크게 전처리, 후처리, 순산소 연소 방식으로 나뉘며, 본 연구 에서는 후처리 제거 공정을 중심으로 제올라이트, 활성탄, MOF 소재의 이산화탄소 분리 특성을 비교하 고, 공정기술에 대해 분석하였다.

We produced cylindrical porous TiNi bodies by Self-propagating High-temperature Synthesis (SHS) process, varying the heating schedule prior to ignition of a loose preform compact made from (Ti+Ni) powder mixture. To investigate the effect of the heating schedule on the behaviour of combustion wave propagation and the structure of porous TiNi shape-memory alloy (SMA) body, change of temperature in the compact during SHS process was measured as a function of time and used for determining combustion temperature and combustion wave velocity. Microstructure of produced porous TiNi SMA body was observed and the results were discussed with the combustion characteristics. From the results it was concluded that the final average pore size could be controlled either by the combustion wave velocity or by the average temperature of the preform compact prior to ignition.

Ni and NiO particles were made by a combustion synthesis process. The characteristics of synthesized powders were investigated with various kinds and amounts of fuels such as urea, citric acid and glycine. Ni phase particles without NiO phase were obtained through combustion synthesis process in air atmosphere with-out further calcinations process, when the content of glycine was 2.44 times of the stoichiometric ratio in the precursor solution. Primary particle sizes of synthesized Ni and NiO particles were about 20∼30 nm.

This is a study on the volatile organic compounds(VOCs) concentrator with zeolite adsorptive honey rotor and catalytic combustion system for abating VOCs emitted from printing industry. VOCs emitted from the printing industry is mainly caused by organic solvent of printing ink. The content of organic solvents in printing ink varies from 40% to 75% and its content in the gravure ink is higher than that in any other ink. The average concentrations of each VOCs are 139 ppm for toluene, 152.1 ppm for MEK, 256.9 ppm for methanol and 42.9 ppm for isopropyl alcohol. We used zeolite honeycomb for absorbent of VOCs concentrator and palladium for catalyst combustion system. This system abated over 96% of emitted total VOCs, 98% of toluene, 100% of MEK, 92% of methanol and 100% of isopropyl alcohol. It is concluded that the low-leveled high-volume VOCs emitted from printing process were removed almost by concentrator with zeolite adsorptive honey rotor and catalytic combustion system.