In order to treat groundwater containing high levels of nitrate, nitrate reduction by nano sized zero-valent iron (nZVI) was studied using batch experiments. Compared to nitrate removal efficiencies at different mass ratios of nitrate/Fe0, the removal efficiency at the mass ratio of 0.02% was the highest(54.59%). To enhance nitrate removal efficiency, surface modification of nZVI was performed using metallic catalysis such as Pd, Ni and Cu. Nitrate removal efficiency by Cu-nZVI (at catalyst/Fe0 mass ratio of 0.1%) was 66.34%. It showed that the removal efficiency of Cu-nZVI was greater than that of the other catalysts. The observed rate constant (kobs) of nitrate reduction by Cu-nZVI was estimated to 0.7501 min-1 at the Cu/Fe mass ratio of 0.1%. On the other hand, TEM images showed that the average particle sizes of synthetic nZVI and Cu-nZVI were 40~60 and 80~100 nm, respectively. The results imply that catalyst effects may be more important than particle size effects in the enhancement of nitrate reduction by nZVI.

The surface modified activated carbons (SMACs) were prepared with various P2O5 concentrations using two activated carbons (ACs: waste citrus peel-based activated carbon and coconut-based activated carbon). The characteristics and adsorptivity of bisphenol A (one of phenolic endocrine disrupting chemicals) were compared between ACs and SMACs. The contents of C, H and N of SMACs were similar to those of ACs, but the content of P2O5 for the former increased greatly than for the latter, due to the impregnation of P2O5 into the pores. The specific surface area, total pore volume, average pore diameter and iodine adsorptivity for the former decreased due to the impregnation of P2O5 into the pores, compared to those for the latter. The adsorptivity of bisphenol A for the former were higher than that for the latter, although specific surface area, total pore volume, average pore diameter and iodine adsorptivity for the former were lower than those for the latter.

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.

The purpose of this study is to evaluate the effect of improvement on the impact resistance and strength properties of cement composites by surface modification of aramid fiber. For aramid fiber reinforced cement composites, therefore, dispersion capability and the bonding efficiency between the fibers and the cement composite material need to be improved. It is possible by modifying surface properties to hydrophobic, it is considered that oiling agent ratio of 1.2 % and improvement of performance is in need to be investigated. In this study, short aramid fibers were mixed by different fiber length and oiling agent ratio. And improvement of strength properties and impact resistance performance of hybrid cement composites were evaluated under the influence of steel fiber. As a result, strength properties of aramid fiber reinforced cement composites are different by mixing ratio of fiber, oiling agent ratio and length of fiber. In case of cement composites which have same volume fraction and fiber length, tensile strength and flexural strength were improved with increase of the emulsions throughput of the fiber surface. The results of evaluation on the static strength properties had effects on impact resistance performance by high-velocity impact. And it was observed that the scabbing of rear was suppressed with increase of the oiling agent ratio.

Experiments were divided into two parts; one part is to understand the basic properties of high flowable VA/VeoVa-modified cement mortar with different polymer cement ratio (P/C) and the weight ratio of fine aggregate to cement (C:F) and the other part is to investigate the effect of surface water spread on the concrete substrate on adhesion in tension. To understand the basic performance, the specimens were prepared with proportionally mixing VA/VeoVa redispersible powder, ordinary portland cement, silica sand, superplasticizer and viscosity enhancing agent. Here, P/C were 10, 20, 30, 50 and 75% and C:F were 1:1 and 1:3. As the change of P/C and C:F unit weight, flow test, crack resistance and adhesion in tension were measured. Three specimens with good adhesion properties were selected among specimens with different P/C and C:F. The effect of surface water evenly sprayed on concrete substrate on adhesive strength is investigated. The results show that surface water on concrete substrate increases the adhesion in tension of high flowable VA/VeoVa-modified cement mortar and additionally improves the flowability compared to the non-sprayed case.

본 연구에서는 고유동성의 SBR 개질 시멘트 모르타르의 기초적 성능을 바탕으로 콘크리트의 보수용 재료에 매우 중요한 요구성능인 부착강도에 대한 피착체의 표면에 존재하는 표면수량의 영향을 검토하는 연구가 수행하였다. 고유동성 SBR 개질 시멘트 모르타르의 기초적인 성능을 토대로 부착강도, 잔갈림성, 재료분리 저항성이 좋은 시험체를 선택하였다. 시험체는 C:F=1:1인 경우 P/C=20%, 30%의 시험체 2개, C:F=1:3인 경우 P/C=50%의 시험체 1개, 총 3개가 선택되었으며 이 3개의 배합에 대하여 피착체의 표면수량에 따른 고유동성 SBR 개질 시멘트 모르타르의 특성을 파악하였다. 표면수는 콘크리트 피착면의 단위 면적 (cm2) 당 각각 0, 0.006, 0.012, 0.017, 0.024 g이 균등하게 살포되었으며, 이에 따른 연도변화, 플로우값, 부착강도, 부착파괴형상, 내균열성 및 재료분리여부를 파악하였다. 본 연구를 통해 콘크리트 피착체에 살포된 표면수는 고유동성 SBR 개질 시멘트 모르타르의 부착강도를 증진하는 효과가 있다는 결론을 얻었다.

본 연구를 통해 반도체 산업에서 유래된 마이크로웨이브 증폭 에칭기술(MEE)을 이용하여, 마이카의 표면 구조를 변화시키고 오일 흡유량을 조절할 수 있었다. 마이크로웨이브 에너지가 마이카에 조사되면, 마이카 표면이 몇 분 이내에 에칭이 된다. 에칭의 결과로 마이카의 오일 흡유량이 증가되고, 마이카 SiO2층의 표면 변화에 의해 백색도가 증가한다. 추가적으로, 땀을 흡수한 이후에도 높은 백색도가 유지된다. 마이카의 표면구조의 변화는 불산에 슬러리화된 마이카에 마이크로웨이브 조사를 통해서 이루어졌다. 에칭의 정도는 산의 농도, 조사 시간, 조사 에너지의 양, 슬러리의 농도에 의해 조절되었다. 에칭된 마이카의 표면 구조는 ‘달' 표면 모양과 유사하게 보인다. 표면적과 거칠기 등의 특성은 Brunauer-Emmett-Teller (BET), atomic force microscopy (AFM), scanning electron microscopy (SEM), Spectrophotometer, goniophometer로 측정되었다.

The surface properties and adsorption rates of activated carbon modified with acid and base were compared. The distribution ratio of C and C-H on the surface of activated carbon were decreased by modification with acid and base, but the distribution ratio of C-O, C=O, and O=C-O were increased. Base modification damaged the surface of activated carbon more than acid modification, it caused the effect of 6 percent increments of surface area. Adsorption rate model was more suitable to second order equation than first order equation. Adsorption rate was controlled by adsorption in pore better than in surface.

The surface properties of activated carbon modified by acids and base were studied. The influence of the surface chemistry on the adsorption of benzene and acetone vapor on modified activated carbons has been investigated The modified activated carbons were obtained by treatment with acetic acid (CH3COOH), nitric acid (HNO3) and sodium hydroxide (NaOH). The modified activated carbons had similar porosity but different surface chemistry and adsorption characteristics. The total surface acidity (sum of functional groups) of activated carbon (AC-AN) treated by nitric acid was 2.6 times larger than that of activated carbon (AC) before the acid treatment. Especially, carboxyl group was much developed by nitric acid treatment. The benzene equilibrium adsorption capacity of AC-AN decreased 20% more than that of AC. However, the acetone equilibrium adsorption capacity of AC-AN increased 20% more than that of AC because of the large increase of carboxyl group and acidity.

제올라이트 함유 폴리에틸렌 필름의 최대응력, 파단신율 및 인열강도를 측정한 결과 전반적으로 금속이온으로 치환한 제올라이트 필름에 비해 계면활성제로 치환한 제올라이트를 함유한 필름의 물성이 순수 LDPE필름의 물성에 비해 큰 감소 없이 일정하게 유지되는 사실을 확인하였다. 한편 선도유지기능 실험 결과 일부의 양이온성(Al 및 Ag) 또는 계면활성제로 개질된 제올라이트 필름들이 시험된 과채류에 대하여 일반 LDPE 포장용 필름보다 우수한 선도유지기능

Waterborne fluorinated acrylate copolymer (WFAC) for surface modification of textile was synthesized from perfluoroalkyl ethyl acrylate, octadecyl acrylate, glycidyl methacrylate, surfactant and 3,3 methyl-methoxy butanol. The structures of the synthesized WFAC were determinated by FT-IR and 19F-NMR analysis. The thermal stability investigated with DSC and TGA was decreased with increasing the content of fluorinated acrylate in the copolymer. However, the particle sizes of WFAC were increased with increasing the content of fluorinated acrylate in the copolymer. The surface energies calculated by contact angles of WFAC were in the range of 29.80～13.41 dyne/cm. On the observing SEM of the textile surface treated with WFAC, the textile was swollen and compacted with increasing the concentration of water repellency agent. WFAC synthesized in this study showed a good water repellency.

The high speed elimination process of suspended solid was investigated to treat the pulp waste water by using surface modified magnetite particle and magnetic power. The effects of the various aluminum salts such as Al(NO3)3·9H2O, AlCl3·6H2O, Al2(SO4)3·13～14 on the COD, BOD and suspended solid were systematically studied. It has been found that the 2.0 wt% of Al was most effective for the modification of Fe3O4 powder and then best for the treatment of pulp waste water. Optimum quantity of modified magnetite in this study was 12 wt%, and aging time was found to be 12 hours. Comparing with the conventional process, the required time for SS removal was drastically decreased. BOB and COD were also effectively removed when applied to the pulp wastewater.

For the purpose of surveying any possibility of anchoring titanium dioxide on activated carbons to promote their activities as catalysts and/or adsorbents, two activated carbons were oxidized with ammonium peroxydisulfate and followed by anchoring titanium dioxide. The anchoring of titanium dioxide on the oxidized activated carbons were performed via the adsorption of tetrabutyltitanate, hydrolysis with deionized water, and calcination. The effect of oxidizing and anchoring treatment on the surface element composition, surface area, and pore texture were analyzed by XPS, BET and TPD. The oxidation of activated carbons with ammonium peroxydisulfate introduced carboxyl groups on the surface of activated carbons and these carboxyl groups promoted the anchoring of titanium oxide on the activated carbons. However, the treatments affected the surface area and the porosity of activated carbons.

Since the enzymatic degradation of microbial poly[(R)-3-hydroxybutyrate-co-3-hydroxyvalerate] (P(3HB-co- 3HV)) initially occurs by a surface erosion process, a degradation behavior could be controlled by the change of surface property. In order to control the rate of enzymatic degradation, plasma gas discharge and blending techniques were used to modify the surface of microbial P(3HB-co-3HV). The surface hydrophobic property of P(3HB-co-3HV) film was introduced by CF3H plasma exposure. Also, the addition of small amount of polystyrene as a non-degradable polymer with lower surface energy to P(3HB-co-3HV) has been studied. The enzymatic degradation was carried out at 37 ºC in 0.1 M potassium phosphate buffer (pH 7.4) in the presence of an extracellular PHB depolymerase purified from Alcaligenes facalis T1. Both results showed the significant retardation of enzymatic erosion due to the hydrophobicity and the enzyme inactivity of the fluorinated- and PS-enriched surface layers.

To improve CO2 permselectivity, a modified silica membrane was prepared by chemical vapor deposition with tetraethoxysilane(TEOS)-ethanol-water, and TEOS-ethanol-water-HCI solution at 300-600℃. The silica was effectively deposited in the mesopores of a γ-alumina film coated on a porous α-alumina tube by evacuating the reactants through the porous wall. In this membrane, CO2 interacts, to some extent, with the pore wall, and CO2/N2 selectivity then exceeds the value of the Knudsen diffusion mechanism, while the membrane derived from TEOS alone has no CO2 selectivity. The silica membrane prepared from TEOS-ethanol-water-HC1 solution showed that CO2 permeance was 2.5×10-7㏖/s-1. m-2. Pa-1 at 30℃ and CO2/N2 selectivity was approximately 3. The CO2 permeance and selectivity was improved by enlarging the surface diffusion with modification of chemical affinity of the silica pores.