The pitch-based activated carbon fibers (ACFs) were prepared from ethylene tar-derived pitches containing nickelocene (CNi) or nickel nitrate (NiN). The effects of different anions and contents of metal salts on the microstructure and surface chemical properties of fibers were investigated. The results revealed that Ni2+ from CNi mainly remained its pristine molecule in the organometal salt-derived pitch (OP-xCNi), while Ni2+ from NiN occurred complexation reaction with polycyclic aromatic hydrocarbons (PAHs) in the inorganic metal salt-derived pitch (IP-xNiN) due to the weaker binding ability between anions and Ni2+ of CNi than CNi. The XRD and SEM results confirmed that IP-3NiN-ACF contained Ni, NiO, Ni2O3 nanoparticles with different size distributions, while OP-3CNi-ACF only contained more uniformly distributed Ni nanoparticles with small size. Furthermore, OP-3.0CNi-ACF presented higher specific surface area of 1862 m2/ g and a pore volume of 1.69 cm3/ g than those of IP-3.0NiN-ACF due to the formation of pore structure during the in-situ catalytic activation of different metal nanoparticles. Therefore, this work further pointed out that the desired pore structure and surface chemistry of pitch-based ACFs could be obtained through regulating and controlling the interaction of anion species, metal cations and PAHs during the synthesis of pitch precursors.

Abstract In this study, we investigated that the activated carbon (AC)-based supercapacitor and introduced SIFSIX-3-Ni as a porous conducting additive to increase its electrochemical performances of AC/SIFSIX-3-Ni composite-based supercapacitor. The AC/SIFSIX-3-Ni composites are coated onto the aluminum substrate using the doctor blade method and conducted an ion-gel electrolyte to produce a symmetrical supercapacitor. The electrochemical properties of the AC/SIFSIX-3-Ni composite-based supercapacitor are evaluated through cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge/discharge tests (GCD). The AC/SIFSIX-3-Ni composite-based supercapacitor showed reasonable capacitive behavior in various electrochemical measurements, including CV, EIS, and GCD. The highest specific capacitance of the AC/SIFSIX-3-Ni composite-based supercapacitor was 129 F g−1 at 20 mV s−1.

In this research, Pb (II), Co (II), and Ni (II) toxic heavy metal ions adsorption from synthetic aqueous system have been studied using the activated carbon prepared from Citrus limetta leaves. Therefore, the relationship between the adsorption parameters (solution pH, dosage of adsorbent, temperature, initial concentration of the ions, and adsorption time) and the removal percentage of the prepared adsorbent have been investigated. Additionally, the adsorbent was analyzed through BET, SEM, EDX, FTIR, and XRD analyses. According to the results, the maximal adsorption efficiencies for heavy metal ions were achieved in pH = 6, the adsorbent dosage of 1 g/L, temperature = 25 °C, the ion initial concentration of 5 mg/L, and contact time of 60 min, which were 99.53%, 98.63%, and 97.54% for Pb, Co, and Ni ions, respectively. Based on Kinetic studies, the performance of pseudo-second-order kinetic model was better than pseudo-first-order model for the description of time-dependent behavior of the process. Additionally, the equilibrium data were fitted by Langmuir and Freundlich isotherms, while the former performed better than the latter. The maximum adsorption capacity values for Pb, Co, and Ni ions were achieved equal to 69.82, 60.60, 58.139 mg/g, respectively. Considering the thermodynamic data, the studied processes were exothermic and spontaneous.

본 연구에서는 다공성 활성탄소와 금속유기골격체 복합재료 기반의 전극 재료와 “이온젤” 이라고 불리는 고분자 고체 전해질을 이용하여 슈퍼커패시터를 제작 하였으며, 금속유기골격체의 함량에 따른 전기화학적 거동을 관찰하여 보았다. 슈퍼커패시터의 전기화학적 특성은 순환전압전류법(CV), 전기화학적 임피던스 분광법(EIS) 및 전정류 충·방전법(GCD)으로 분석하였으며, 그 결과로, 다공성 활성탄소 대비 금속유기골격체를 0.5 wt% 첨가 하였을 때 가장 높은 전기용량값을 확인 할 수 있었으며, 0.5 wt% 이상의 금속유기골격체의 함유량은 전기화학적 특성 감소에 영향을 주는 것으로 사료되며, 이러한 결과를 바탕으로 제조된 다공성 활성탄소/금속유기골격체 복합재료 기반의 슈퍼커패시터는 다양한 분야에 활용이 가능 할 것으로 판단된다.

본 연구에서는 “이온젤” 이라고 불리는 고분자 기반의 PVA(polyvinyl alcohol) 기반의 고체 전 해질에 이온성 액체 BMIMBF4 (1-buthyl-3-methylimidazolium tetrafluoroborate)를 첨가하여 제조한 전 고체 전해질과 활성탄소와 금속유기골격체 복합재료 기반의 전극 재료를 이용하여 슈퍼커패시터를 제작 하였으며, 유기골격체의 유 무에 따른 전기화학적 특성을 분석하여 보았다. 슈퍼커패시터의 전기화학적 특 성은 순환전압전류법(CV), 전기화학적 임피던스 분광법(EIS) 및 전정류 충·방전법(GCD)을 통하여 비교 및 분석하여 보았다. 그 결과로, 금속유기골격체가 함유되지 않은 슈퍼커패시터의 전기용량값은 380 F/g 으로 확인 할 수 있었고, 이 값은 금속유기골격체를 첨가하였을 때 340 F/g로 감소하는 현상을 확인할 수 있었 다. 이러한 결과로 1 wt%의 금속유기골격체의 함유량은 전기화학적 특성 감소에 영향을 주는 것으로 사료 되며 이러한 결과를 바탕으로 금속유기골격체의 첨가량을 최적화 할 필요가 있다고 판단된다

실 산성 도금폐수를 입상활성탄(GAC)이 유동메디아로 첨가된 유동상 멤브레인 반응기를 이용하여 처리하였다. GAC 유동조건에서 적용 투과플럭스에 대해 시간에 따른 흡입압의 증가는 관찰되지 않았다. 폐수의 중성 pH에서 파울링 속도는 산성 조건에 비해 GAC 유동조건에서 크게 감소하였다. 해당 폐수의 용액 pH 증가는 입자크기의 증가를 가져왔고 이는 멤브레인 표면에서 상대적으로 성긴 구조의 케이크층 형성을 야기시켰다. 유동상 멤브레인 반응기에서 GAC 유동 하에 95% 이상의 COD 제거율이 관찰되었으며 총부유물질은 거의 완벽하게 제거되었다. 실 도금폐수의 pH에서, 유동상 멤브레인 반응기의 구리 및 크롬의 제거는 거의 관찰 되지 않았다. 그러나 pH를 중성으로 증가 시켰을 시 구리와 크롬의 제거율은 각각 99%와 94%까지 증가를 하였다. 적용해 준 pH에 상관 없이, 시안의 경우 95% 이상의 제거율을 달성하였다. 이는 유기물과 시안 착물 형성으로 인해 유동상 멤브레인 반응기 내 GAC의 강한 흡착으로 제거된 것으로 사료된다.

In this study, composite PAN-based ACNFs embedded with MgO and MnO2 were prepared by the electrospinning method. The resultant pristine ACNFs, ACNF/MgO and ACNF/MnO2 were characterized in terms of their morphological changes, SSA, crystallinity and functional group with FESEM-EDX, the BET method, XRD and FTIR analysis, respectively. Results from this study showed that the SSA of the ACNF/MgO composite (1893 m2 g–1) is significantly higher than that of the pristine ACNFs and ACNF/MnO2 which is 478 and 430 m2 g–1, respectively. FTIR analysis showed peaks of 476 and 547 cm–1, indicating the presence of MgO and MnO2, respectively. The FESEM micrographs analysis showed a smooth but coarser structure in all the ACNFs. Meanwhile, the ACNF/MgO has the smallest fiber diameter (314.38±62.42 nm) compared to other ACNFs. The presence of MgO and MnO2 inside the ACNFs was also confirmed with EDX analysis as well as XRD. The adsorption capacities of each ACNF toward CH4 were tested with the volumetric adsorption method in which the ACNF/MgO exhibited the highest CH4 adsorption up to 2.39 mmol g–1. Meanwhile, all the ACNF samples followed the pseudo-second order kinetic model with a R2 up to 0.9996.

The treatment of piggery wastes was carried out at pilot scale using a multilayered metal-activated carbon system followed by carbon bed filtration. The physicochemical properties were obtained from treated samples with aqueous solutions containing metallic ions such as Ag+, Cu2+, Na+, K+ and Mn2+, which main obsevations are subjected to inspect surface properties, color removal properties by Uv/Vis and EDX. Multilayered metal-activated carbons were contacted with waste water to investigation of the simultaneous catalytic effect for the COD, BOD, T-N and T-P removal. The removal results for the piggery waste using multilayered metal-activated carbon bed was achieved the satisfactory removal performance under permitted values of Ministry of Environment of Korea. The high efficiency of the multilayered metal-activated carbon bed was determined by the performance of this material for trapping, catalytic effect and adsorption of organic solid particles.

Antibacterial behaviors of PAN-based activated carbon fibers (ACFs) containing silver metal were investigated. The effects of surface and pore structures of the ACFs were studied by N2/77 K adsorption and D-R plot as a function of silver loading content. The antibacterial activities were investigated by a dilution test against Staphylococcus aureus (S. aureus; gram positive) and Klebsiella pnemoniae (K. pnumoniae; gram negative). As experimental results, the ACFs showed some decreases in specific surface areas, micropore volumes, and total pore volume with an increase of silver content. However, the antibacterial activities of the ACFs were strongly increased against S. aureus as well as K. pnumoniae, which could be attributed to the presence of antibacterial metal in the ACFs system.

A series of micro- and mesoporous activated carbons were prepared from two kinds of phenolic resin using a metal treated chemical activation methodology. N2-adsorption data were used to characterize the surface properties of the produced activated carbons. Results of the surface properties and pore distribution analysis showed that phenolic resin can be successfully converted to micro- and mesoporous activated carbons with specific surface areas higher than 973 m2/g. Activated carbons with porous structure were produced by controlling the amount of metal chlorides (CuCl2). Pore evolvement depends on the amount of additional metal chloride and precursors used. From the SEM and EDX data, copper contents were shown to be most effected by the incremental addition of metal chloride.

In this work, the effect of anodic oxidation treatment on Cr(VI) ion adsorption behaviors of activated carbon fibers (ACFs) was investigated. The aqueous solutions of 10 wt% H3PO4 and NH4OH were used for acidic and basic electrolytes, respectively. Surface characteristics and textural properties of ACFs were determined by XPS and N2 adsorption at 77 K. The heavy metal adsorption of ACFs was conducted by ICP. As a result, the adsorption amount of the anodized ACFs was improved in order of B-ACFs 〉 A-ACFs 〉 pristine-ACFs. In case of the anodized treated ACFs, the specific surface area was decreased due to the pore blocking or pore destroying by acidic electrolyte. However, the anodic oxidation led to an increase of the Cr(VI) adsorption, which can be attributed to an increase of oxygen-containing functional groups, such as, carboxylic, lactonic, and phenolic groups. It was clearly found that the Cr(VI) adsorption was largely influenced by the surface functional groups, in spite of the reduced specific surface area of the ACFs.

Based on the previous results of the equilibrium and batch adsorptions, the removal efficiency of the two-step surface-modified activated carbon (2ndAC) for heavy metal ions such as Pb, Cd, and Cr in fixed column was evaluated by comparing with that of the as-received activated carbon (AC) and the first surface-modified activated carbon (1stAC). The order of metal removal efficiency was found as 2ndAC 〉 1stAC 》 AC, and the efficiency of the 2ndAC maintained over 98% from the each metal solution. Increase of the removal efficiency by the second surface modification was contributed to maintain favorable pH condition of bulk solution during adsorption process. The removal of the heavy metals on the 2ndAC was selective with Pb being removed in preference to Cr and Cd in multicomponent solutions and slightly influenced by phenol as the organic material.

The two-step surface modifications of activated carbon was carried out to improve the adsorption capacity of toxic heavy metal ions in liquid phase. Physical and chemical properties of the as-received activated carbon (AC) and two kinds of surface-modified activated carbons (1stAC and 2ndAC) were evaluated through the BET analysis, surface acidity, and oxides measurements. Specific surface area and pore volume did not significantly change, but surface oxide-group remarkably increased by the surface modification. Equilibrium and batch adsorptions of the various metals, such as Pb, Cd, and Cr, using AC, 1stAC, and 2ndAC were performed at initial pH 5. The adsorption capacity and rate of 2ndAC were higher than those of AC and 1stAC. The carboxylic/sodium carboxylate complex groups were developed from the two-step surface modification of activated carbon, which strongly affected the adsorption of metal ions.

In this work, activated carbon fibers (ACFs) were plated with copper metal using electroless plating method and the effects of surface properties and pore structures on chromium adsorption properties were investigated. Surface properties of ACFs have been characterized using pH and acid/base values. BET data with N2 adsorption were used to obtain the structural parameters of ACFs. The electroless copper plating did significantly lead to a decrease in the surface acidity or to an increase in the surface basicity of ACFs. However, all of the samples possessed a well-developed micropore. The adsorption capacity of Cr(III) for the electroless Cu-plated ACFs was higher than that of the as-received, whereas the adsorption capacity of Cr(VI) for the former was lower than that of the latter. The adsorption rate constants (K1, K2, and K3) were also evaluated from chromium adsorption isotherms. It was found that K1 constant for Cr(III) adsorption depended largely on surface basicity. The increase of Cr(III) adsorption and the decrease of Cr(VI) adsorption were attributed to the formation of metal oxides on ACFs, resulting in increasing the surface basicity.

This study evaluates heavy metal(Cu and Cr) adsorption characteristics produced from food waste charcoal extracted in an optimal operation condition after analyzing activated charcoal of iodine adsorption and heavy metals that derived from an activation process of carbide by the developed by-products of food waste treatment facility using the methods from previous studies. As experiment apparatus, this study used a tube-shaped high temp furnace. The mixing ratio of by-products of food waste treatment facility, carbide, and activation component(ZnCl2) was 1:1. The experiment was proceeded as adjusting the activation temperature from 400 to 800℃ and activation time from 30 to 120 minutes. The optimal activation condition for iodine absorption was 90 minutes at 700℃ and by using the produced food waste charcoal, this study conducted an experiment on absorption of heavy metals (Cu and Cr) as changing pH of artificial wastewater and stirring time. As a result, pH 7 showed the highest heavy metal decontamination ratio and in terms of stirring time, it revealed balance adsorption after 10 minutes. This result can be particularly applied as basic data for recyclability of high concentration organic waste, by-products of food waste treatment facility, as an food waste charcoal.

본 연구에서는 표면개질 활성탄을 이용하여 수용액상에서 혼합 중금속(Cr6+, As3+)의 흡착능을 평가하였고 또한 표면개질 활성탄을 안정화제로 활용하여 해양오염퇴적물 내 As 및 Cr에 대하여 중금속 안정화 실험을 수행하였다. 실험결과, 흡착평형은 약 120분 후에 도달하였다. 또한, 중금속 등온 흡착 특성은 Freundlich 및 Langmuir 방정식을 이용하여 해석하였으며, 평형흡착 실험결과는 Langmuir 모델에 잘 부합되었고 As3+ (28.47 mg/g)가 Cr6+ (13.28 mg/g)보다 평형 흡착량이 많았다. Cr6+인 경우, 용액의 pH가 6에서 10으로 증가함에 따라서 흡 착량은 감소하는 것으로 나타났다. 하지만 pH 증가 변화에서 As3+의 흡착량은 미미한 증가를 보였다. 안정화 방법은 오염퇴적물에 표면 개질한 활성탄 첨가 후 120일간 습윤 양생하였다. 연속추출 실험결과로부터, 미처리 오염퇴적물과 비교해서 Cr 및 As의 이온교환, 탄산염, 산화물 및 유기물 존재 형태 합의 비는 각각 5.8% 및 7.6% 감소하였다.