• Journal of the Korean Wood Science and Technology
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• 제49권5호
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• pp.453-461
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• 2021

In wood-based composite panels, low-molar ratio (LMR) urea-formaldehyde (UF) resins usually result in reduced formaldehyde emission (FE) at the expense of poor adhesion. However, the FE and adhesion of medium-density fiberboard (MDF) bonded with LMR UF resins were both improved in this study. The modified LMR UF resins with transition metal ion-modified bentonite (TMI-BNT) nanoclay simultaneously improved the FE and adhesion of MDF panels. The modified LMR UF resins with 5% TMI-BNT resulted in a 37.1% FE reduction and 102.6% increase in the internal bonding (IB) strength of MDF panels. Furthermore, thickness swelling and water absorption also significantly decreased to 13.0% and 24.9%, respectively. These results imply that TMI-BNT modification of LMR UF resins could enhance the formation of a three-dimensional network rather than crystalline domains, resulting in improved cohesion.

• Journal of Ceramic Processing Research
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• 제13권spc2호
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• pp.304-307
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• 2012

Nano-fibers of LiFePO4 were synthesized from a metal oxide precursor by adopting electrospinning method. After calcination of the above precursor nano-fibers at 800 ℃, LiFePO4 nano-fibers with a diameter of 300 ~ 800 nm, were successfully obtained. Measurement were performed using X-ray diffraction (XRD), fourier transform infrared spectrometer (FT-IR), videoscope, scanning electron microscope (SEM) and atomic force microscope (AFM), respectively, were performed to characterize the properties of the as-prepared materials. The results showed that the crystalline phase and morphology of the fibers were largely influenced the starting materials and electrospinning conditions.

• 대한의용생체공학회:의공학회지
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• 제17권1호
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• pp.11-18
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• 1996

The toxic metal ion release behaviour and the cytotoxicity of a super stainless steel (S.S.S, 22cr-20Ni -6Mo-0.25N) were investigated The measurement of the amount of static and wear- induced trace metal ion released from the steels was conducted in Hank's balanced salt solution using an electrothermal atomic absdrption spectrometry equiped with Uaphite furnace. And the in vitro cytotoxicity of the materials was assesed in cell culture. The static dissolution rates of Fe and Cr ions from the S.S.S were significantly lower than those of 316L SS. However, the Ni ion release from the S.S.S during the first 4 weeks was yester than that from 316L 55 by 15-45%. Also, the wear-in- duces dissolution rates from the steels were not correlated either with their elemental composition rates or with the static metal ion release rates. The S.S.S did not deteriorate the osteoblasts viability. And no toxic response was observed from the macrophages cultured for 7 days in RFMI 1640 medium immersed with the S.S.S specimens.

• 한국표면공학회지
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• 제49권2호
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• pp.135-140
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• 2016

In this study, we prepared magnesium ion containing oxide films formed on the Ti-6Al-4V using plasma electrolytic oxidation (PEO) treatment. Ti-6Al-4V surface was treated using PEO in Mg containing electrolytes at 270V for 5 min. The phase, composition and morphology of the Mg ion containing oxide films were evaluated with X-ray diffraction (XRD), Attenuated total reflectance Fourier transform infrared (ATR-FTIR) and filed-emission scanning electron microscopy (FE-SEM) with energy dispersive X-ray spectrometer (EDS). The biocompatibility of Mg ion containing oxide films was evaluated by immersing in simulated body fluid (SBF). According to surface properties of PEO films, the optimum condition was formed when the applied was 270 V. The PEO films formed in the condition contained the properties of porosity, anatase phase, and near 1.7 Ca(Mg)/P ratio in the oxide film. Our experimental results demonstrate that Mg ion containing oxide promotes bone like apatite nucleation and growth from SBF. The phase and morphologies of bone like apatite were influenced by the Mg ion concentration.

• Journal of Industrial and Engineering Chemistry
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• 제67권
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• pp.301-311
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• 2018

In this study, the ion-gelation method was applied to fabricate novel Fe-carbon-bentonite-alginate beads ($Fe^0$/C-BABs). $Fe^0$/C-BABs could effectively control Fe release during persulfate (PS) activation in N-acetyl-p-aminophenol (APAP) oxidation. A novel two-stage approach that combined $Fe^0$/C-BABs and an oyster-shell-filled bed (OSFB) column was developed to address the low pH and high Fe concentration of the effluent of the traditional PS process. The application of the $Fe^0$/C-BABs and OSFB column regulated pH levels and Fe release during the advanced oxidation of APAP. The characteristics of $Fe^0$/C-BABs were also investigated through scanning electron microscopy, energy dispersive spectrometry, and Fourier transform infrared spectroscopy. The long-term operation performance of $Fe^0$/C-BABs in a continuous fixed-bed reactor under simultaneous PS and APAP feeding was also evaluated. The effects of initial PS concentration, pH, fixed-bed weight, in-flow rate, and dissolved oxygen (DO) were investigated. Under selected conditions, 86.3% efficiency was achieved during the first stage of APAP degradation (effluent pH of 3.05, Fe contents: $106.25mgL^{-1}$). Water quality improved after the effluent was passed through the OSFB column (effluent pH of 6.32, Fe contents: $21.43mgL^{-1}$). Moreover, this study analyzed the free radicals and intermediates produced during APAP degradation to identify the possible routes of APAP degradation.

• 전기화학회지
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• 제24권3호
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• pp.52-64
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• 2021

Li_1+xFe_xTi_2-x(PO₄)_3-y(BO₃)_y (x = 0.2, 0.5)계 유리에서 Fe doping과 BO₃ 치환이 유리 또는 결정화유리(glass-ceramics) 전해질의 구조적, 열적 및 전기적 특성에 미치는 영향을 조사하였다. 또한, Li_1.5Fe_0.5Ti_1.5(BO₃)₃ 유리분말을 소결하고, 소결 온도에 따른 결정상과 이온전도도 영향도 검토하였다. Li_1+xFe_xTi_2-x(PO₄)_3-y(BO₃)_y 유리에서 Fe²⁺ 및 Fe³⁺ 이온은 network modifier로서 FeO₆ 팔면체를 형성하거나 network former로서 유리망목구조에 들어가 FeO₄ 유사 사면체를 형성하면서 유리의 구조를 변화시키는 것으로 확인되었다. 한편, BO₃는 BO₃ 또는 BO₄ 그룹을 형성하였는데, BO₃ 치환량이 작은 경우 boron은 (PB)O₄ 망목구조를 형성하지만, BO₃ 치환량이 증가하면 붕소이상현상(boric oxide anomaly)이 생겨나면서 BO₄는 BO₃로 변화하고 이로 인하여 비가교산소(non-bridging oxygen)가 증가하였다. BO₃ 치환은 유리전이온도와 결정화 온도를 낮추는 효과가 있으며, Fe 첨가량이 증가하면 Fe³⁺의 일부는 Fe²⁺로 환원되며, 유리전이온도와 연화온도를 낮아지게 하고 결정화온도를 높아지게 하는 것으로 확인되었다. Li_1+xFe_xTi_2-x(PO₄)_3-y(BO₃)_y (x = 0.2, 0.5) 유리에서 BO₃ 함량이 증가함에 따라 이온전도도는 증가하였으며, x = 0.2 및 0.5에서 각각 8.85×10^-4 및 1.38×10^-4S/cm의 이온전도도값을 나타내었다. 본 연구에서 얻어진 높은 이온전도도는 Fe³⁺의 산화상태 변화와 붕소이상현상에 의한 BO₃ 생성 및 이로 인한 비가교산소의 생성에 기인한 것으로 생각된다. Li_1.5Fe_0.5Ti_1.5(BO₃)₃ 유리를 800℃에서 소결한 결과 이온전도도가 급격히 저하되었는데 이는 결정화유리 분말이 고온에서 유리화되었기 때문으로 생각된다. 따라서 유리분말을 800℃에서 소결한 후, 다시 460℃에서 조핵하고, 600℃에서 결정성장을 시킨 결과, 이온전도도가 열처리전과 동등 수준으로 회복되는 것을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제16권9호
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• pp.819-823
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• 1995

Thin films of two kinds of Prussian Blue (PB)-modified, using iron(Ⅲ) complex instead of conventional FeCl3, were prepared on a gold substrate and these films were able to be electrochemically reduced in potassium nitrate solution. In case of PB-modified films prepared from Fe(Ⅲ)-ethylenediamine-N,N'-diacetic acid (FeEN3+)/K3Fe(CN)6 solution, the mid-peak potential was 0.156 V in 0.1 M KNO3 and it was found that potassium ion migrates into or out of the film during the electrolysis. These films were shown to be electrochromic. These films exhibited smaller peak separation than those formed from Fe(Ⅲ)-tartaric acid (FeTA3+)/K3Fe(CN)6 system. The diffusion coefficient of Fe(CN)63-/4- redox couple, evaluated using the fabricated Au rotating disc electrode(rde) previously reported, was in good agreement with the existing data. Two experimental procedures, including the voltammetry at relatively low scan rates and the rde study, have been used in order to characterize the electrode kinetics. The electrode kinetics of some redox couples (FeEN2+-FeEN3+ and FeTA2+-FeTA3+) on both PB-modified thin films and bare Au electrode were studied using a Au rde. In all cases the rate constants of electron transfer obtained with the PB-modified film electrodes were only slightly less than those obtained for the same reaction on bare Au disc electrodes. The conductivities, as determined from the slopes of the i-V curves for a ca. 1 mm sample for dried PB-modified potassium-rich and deficient bulk samples pressed between graphite electrodes, were 6.21 × 10-7 and 2.03 × 10-7(Ω·cm)-1, respectively.

• 자원리싸이클링
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• 제22권1호
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• pp.42-47
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• 2013

페로니켈 슬래그는 페로니켈 제조 공정의 부산물이다. 페로니켈 슬래그가 마그네슘 산화물 및 규소 산화물 등 유용 성분을 갖는데도 불구하고 대부분이 폐기되거나 골재로 사용된다. 이 연구는 $H_2SO_4$ 용액을 사용하여 Mg 이온을 추출하고, NaOH 용액을 사용하여 불순물 제거 및 고순도의 $Mg(OH)_2$를 얻으려고 하였다. $H_2SO_4$ 용액에 의해 Mg 이온은 Fe 이온 및 기타 페로니켈 슬래그 구성 성분과 함께 추출되었다. 불순물을 제거하고 고순도의 $Mg(OH)_2$를 얻기 위해서는 침출액의 pH 조절이 중요하다. 불순물은 가수분해에 의한 수산화물 침전으로 제거하였다. 이 과정 후, 여과액에 NaOH를 첨가하여 고순도의 $Mg(OH)_2$을 얻었다.

• 대한환경공학회지
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• 제38권11호
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• pp.618-626
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• 2016

상온조건($25^{\circ}C$)에서 하수슬러지처리를 위한 생물전기화학 혐기성소화조의 성능에 미치는 제2철 이온($Fe^{+3}$)의 영향을 연구하였다. 생물전기화학 혐기성소화조를 상온에서 운전하였을 때 pH, 알카리도, COD 및 VFAs 등의 상태변수들은 안정하였으며, VS 제거율과 비메탄발생율은 각각 65.9% 및 370 mL/L/d이었다. 생물전기화학 혐기성소화조에 제2철 이온(200 ppm)을 주입한 후 상태변수들의 안정도는 더욱 향상되었으며, VS 제거율 및 비메탄발생량은 각각 69.8%, 396 mL/L/d로 증가하였다. 그러나, 제2철 이온을 주입 이후에 바이오가스의 메탄함량은 76.6%로 주입 이전의 77.3%에서 비하여 약간 감소하였다. 부유슬러지의 미생물 군집을 변화를 분석한 결과 공생 혐기성미생물(Cloacamonas) 및 가수분해균(Saprospiraceae, Ottowia pentelensis) 등의 우점균의 비율이 제2철 이온의 주입으로 증가하였다. 이것은 철이온의 주입으로 부유혐기성미생물(planktonic anaerobic bacteria, PAB)의 활성이 증가하였음을 나타낸다. 제2철 이온은 상온조건에서 하수슬러지처리를 위한생물전기화학 혐기성소화조의 성능을 향상시킨다.

• Bulletin of the Korean Chemical Society
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• 제27권10호
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• pp.1597-1600
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• 2006

The mononuclear iron complex 1, $Fe^{III}$(Hbida)Cl($H_2O$), was synthesized using a tripodal tetradentate ligand, N-(benzimidazol-2-ylmethyl)iminodiacetic acid (H3bida), which has two carboxylate groups, one benzimida- zoyl group, and one tertiary amine where it serves as a tetradentate chelating ligand for the octahedral Fe(III) ion. The four equatorial positions of the octahedral complex are occupied by two monodentate carboxylates, a benzimidazole nitrogen, and an oxygen of a water molecule. One of the axial positions is occupied by an apical nitrogen of the Hbida and the other by a chloride anion. The mononuclear octahedral complex 1 mimics the geometry of the key intermediate structure of the catalytic reaction cycle proposed for the FeSODs, which is a distorted octahedral geometry with three histidyl imidazoles, an aspartyl carboxylate, a superoxide anion, and a water molecule. The redox potential of complex 1, $E_{1/2}$ is -0.11V vs. Ag/AgCl (0.12 V vs. NHE), which is slightly lower than those reported for the most FeSODs. The magnetic susceptibility of complex 1 at room temperature is 5.83 $\mu$B which is close to that of the spin only value, 5.92 $\mu$B of high-spin d5 Fe(III).