음이온 교환막은 수전해 시스템에서 매우 중요한 역할을 하며, 생성된 수소와 산소 기체를 물리적으로 분리할 뿐 만 아니라 전극 사이에서 수산화 이온의 선택적인 전달을 용이하게 한다. 음이온 교환막에 요구되는 특성은 수산화 이온에 대한 높은 전도도와 알칼리 환경에서의 화학적/기계적 안정성 등이 있다. 본 연구에서는 셀룰로오스 나노 크리스탈이 포함된 poly(terphenyl piperidinium) (qPTP/CNC) 복합매질분리막을 제조하였다. 고분자 매질로 사용된 poly(terphenyl piperidinium) 은 super-acid 중합법을 통해 제조되었으며 이온전도성과 알칼라인 내구성이 뛰어난 소재로 알려져 있다. qPTP/CNC 분리막 의 구조는 고분자와 나노 입자 계면의 공극이나 큰 응집체가 없는 조밀하고 균일한 형태를 나타냈다. CNC 나노 입자가 2 wt% 첨가된 qPTP/CNC 분리막은 높은 이온교환용량(1.90 mmol/g)과 낮은 함수율(9.09%) 및 팽윤도(5.56%)를 보였다. 또한, 복합막은 수전해 작동 환경인 50°C 1 M KOH에서 상용 FAA-3-50 분리막에 비해 월등히 낮은 저항과 우수한 알칼라인 내구 성(384시간)을 달성했다. 이러한 결과는 친수성 첨가제인 CNC가 음이온 교환막의 이온 전도 특성과 알칼라인 내구성 향상에 기여할 수 있음을 보고하였다.

A carbon matrix for high-capacity Li/Na/K-alloy-based anode materials is required because it can effectively accommodate the variation in the volume of Li/Na/K-alloy-based anode materials during cycling. Herein, a nanostructured porous polyhedral carbon (PPC) was synthesized via a simple two-step method consisting of carbonization and selective acid etching, and their electrochemical Li/Na/K-ion storage performance was investigated. The highly uniform PPC, with an average particle size of 800 nm, possesses a porous structure and large specific surface area of 258.82 cm2 g– 1. As anodes for Li/Na/K-ion batteries (LIBs/NIBs/KIBs), the PPC matrix exhibited large initial reversible capacity, fast rate capability (LIB: ~ 320 mAh g– 1 at 3C; NIB: ~ 140 mAh g– 1 at 2C; KIB: ~ 110 mAh g– 1 at 2C), better cyclic performance (LIB: ~ 550 mAh g– 1; NIB: ~ 210 mAh g– 1; KIB: ~ 190 mAh g– 1 at 0.2C over 100 cycles), high ionic diffusivity, and excellent structural robustness upon cycling, which demonstrates that the PPC matrix can be highly used as a carbon matrix for high-capacity alloy-based anode materials for LIBs/NIBs/KIBs.

To improve the thermophysical properties of Al alloy for thermal management materials, the Cu-coated carbon fibers (CFs) were used as reinforcement to improve the thermal conductivity (TC) and the coefficient of thermal expansion (CTE) of Al-12Si. The CFs reinforced Al matrix (CFs/Al) composites with different CFs contents were prepared by stir casting. The effects of the CFs volume fraction and Cu coating on the microstructure, component, TC and CTE of CFs/Al composites were investigated by scanning electron microscopy with EDS, X-ray diffraction, thermal dilatometer and thermal dilatometer. The results show that the Cu coating can effectively improve the interface between CFs and the Al-12Si matrix, and the Cu coating becomes Al2Cu with Al matrix after stir casting. The CFs/Al composites have a relative density greater than 95% when the volume fraction of CFs is less than 8% because the CFs uniform dispersion without agglomeration in the matrix can be achieved by stir casting. The TC and CTE of CFs/Al composites are further improved with the increased CFs volume fraction, respectively. When the volume fraction of CFs is 8%, the CFs/Al composite has the best thermophysical properties; the TC is 169.25 W/mK, and the CTE is 15.28 × 10– 6/K. The excellent thermophysical properties of CFs and good interface bonding are the main reasons for improving the thermophysical properties of composites. The research is expected to improve the application of Al matrix composites in heat dissipation neighborhoods and provide certain theoretical foundations.

The flaw of low dispersibility in the metal matrix brought on by graphene's full crystal structure can be improved by the application of ion beam radiation to the surface of the material. Copper atoms are uniformly dispersed on the modified graphene oxide ( GOM) surface after being irradiated to a copper ion beam, and during the sputtering modification, the valence state of copper is changed, resulting in the formation of a new CuO phase on the graphene oxide (GO) surface. Therefore, after copper ion beam irradiation of graphene, the interfacial adhesion between GOM and copper matrix is enhanced, and the wear resistance is significantly improved. When the GOM content is low, it can withstand most of the load during the friction and wear test, which reduces the wear of the copper matrix and the occurrence of fatigue cracks at the interface of the composite material.

Thermoelectric (TE) energy harvesting, which converts available thermal resources into electrical energy, is attracting significant attention, as it facilitates wireless and self-powered electronics. Recently, as demand for portable/wearable electronic devices and sensors increases, organic-inorganic TE films with polymeric matrix are being studied to realize flexible thermoelectric energy harvesters (f-TEHs). Here, we developed flexible organic-inorganic TE films with p-type Bi0.5Sb1.5Te3 powder and polymeric matrices such as poly(3,4-eethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and poly (vinylidene fluoride) (PVDF). The fabricated TE films with a PEDOT:PSS matrix and 1 wt% of multi-walled carbon nanotube (MWCNT) exhibited a power factor value of 3.96 μW ‧ m-1 ‧ K-2 which is about 2.8 times higher than that of PVDF-based TE film. We also fabricated f-TEHs using both types of TE films and investigated the TE output performance. The f-TEH made of PEDOT:PSS-based TE films harvested the maximum load voltage of 3.4 mV, with a load current of 17.4 μA, and output power of 15.7 nW at a temperature difference of 25 K, whereas the f-TEH with PVDF-based TE films generated values of 0.6 mV, 3.3 μA, and 0.54 nW. This study will broaden the fields of the research on methods to improve TE efficiency and the development of flexible organic-inorganic TE films and f-TEH.

Volatile organic compounds (VOCs) are a paramount factor in air pollution of the environment. VOCs are vastly present in the wastewater discharged by the pharmaceutical industries. As it is evaporative in nature, it enters the environment spontaneously and causes air pollution, global warming, acid rain and climate change. VOCs must be treated before discharging or any other aerobic methods using an efficient catalyst. As the catalytic oxidation in the liquid phase is facile compared to the gas phase, this study investigated on catalytic liquid-phase oxidation of VOCs in model and real pharmaceutical wastewater. The model compounds of toluene-, ethylbenzene- and chlorobenzene-contaminated waters were treated separately along with the VOCs present in real pharmaceutical wastewater using a tungsten-based carbon catalyst. The tungsten was impregnated on the low-cost activated carbon matrix as it has good selectivity and catalytic property toward VOCs for facile catalytic operations. The metal catalysts were characterised by Fourier transform infrared spectroscopy, X-ray diffraction studies, and scanning electron microscopy with elemental and mapping analysis. The treatability was monitored by total organic carbon, ultra-violet spectroscopy and high-pressure liquid chromatography analysis. The tungsten-impregnated activated carbon matrix (WACM) has a catalytic efficiency toward toluene by 85.45 ± 1.78%, ethylbenzene by 93.9 ± 1.16%, chlorobenzene by 85.9 ± 2.26% and pharmaceutical VOCs by 85.05 ± 1.73% in 20 treatment cycles. The results showed that WACM worked efficiently in VOCs treatment, preventing the environment from air pollution. Furthermore, liquid-phase oxidation could easily be implementable on an industrial scale.

To analyze the activity concentration of radionuclides in radioactive sludge samples generated from low- and intermediate-low-level radioactive waste from domestic nuclear power plant, a pretreatment process that dissolves and homogenizes the sample is essential. However, this pretreatment process requires the use of hydrofluoric acid, which makes analysis difficult and challenges users to handle harmful chemicals. Therefore, we aim to minimize the use of hydrofluoric acid by measuring gamma nuclides in the sludge sample without pretreatment process and compare the differences of measurement results according to the sample matrix with and without pretreatment process. We will collect about 0.1 g of the sludge sample, and dissolve it using an acid treatment process after using microwave decomposition. We will then use gamma spectroscopy to check the concentration of nuclides present in the sludge before and after dissolution and consider the effect of the sample matrix.

본 연구에서는 PEBAX 2533에 합성된 PEI-GO@ZIF-8의 함량을 달리 첨가하여 혼합막을 제조하고 N2와 CO2의 투과 특성을 연구하였다. PEBAX/PEI-GO@ZIF-8 혼합막의 N2 투과도는 PEI-GO@ZIF-8 함량이 증가함에 따라 감소하였고, CO2 투과도는 PEI-GO@ZIF-8 함량에 따라 다른 경향을 보였는데 순수 PEBAX 막에서 PEI-GO@ZIF-8 0.1 wt%까지 CO2 투과도는 증가하다가 그 이후의 함량에서는 감소하였다. PEI-GO@ZIF-8 0.1 wt% 혼합막은 CO2 투과도 221.9 Barrer, CO2/N2 선택도는 60.0으로, 제조된 혼합막들 중 CO2 투과도와 CO2/N2 선택도가 향상되어 가장 높은 투과 특성을 보였고 Robeson upper-bound에 도달하는 결과를 얻었다. 이는 충진물이 PEBAX 내에 고루 분산되면서 CO2와 친화적인 상호작용을 하는 GO의 -COOH, -O-, -OH 작용기와 PEI에 결합된 아민기 그리고 CO2에 대해 gate-opening 현상이 일어나는 ZIF-8의 영 향 때문이다.