To investigate the effects of anion replacement on NO3- concentration in Italian ryegrass. Plants weregrown hydroponically to the full vegetative stage. NO3 supply(control) was replaced with SO1- (Tl), C1-(T2) and water (T3) to during 14 days. The determi

본 연구는 붕소이온 분리를 위하여 4-Vinylpyridine-divinylbenzene(이하 4-VP-DVB라 칭함) 음이온 교환수지를 합성하고, polyethylene(이하 PE라 칭함)을 지지체로 사용하여 불균질계 음이온교환막을 제조하였다. 또한 그들의 구조와 기계적 성질 및 전기화학적 특성ㅇ르 FT-IR, conductometer와 pH meter 등의 기기로 측정하였으며, 유속과 전압의 변화에 따른 막의 성능을 평가하였다. 막의 분리성능은 PE 지지체 내에 4VP-DVB 이온교환 수지의 함량이 50wt%인 불균질막이 가장 우수하였으며, 산처리한 막이 수처리한 막의 그것보다 우수하였다. 막을 이용한 전기투석 실험에서 붕소이온 분리시 최적유속, 전압 및 시간은 각각 10mol/min, 18volt, 4시간이었다.

이온교환막을 이용하는 확산투석은 농도차가 구동력인 막공정으로서 철강 산업, 금속 제련 산업, 전기 도금 산업 등으로부터 발생되어지는 폐산으로부터 염산 및 기타 산들을 회수하는데 사용된다. 이론적으로는 초기산 농도가 증가함에 따라 구동력인 농도차가 커지므로 선형적으로 산의 투과속도가 증가하게 된다. 그러나 염산의 경우 약 3 N 이상의 고농도 범위에서는 투과속도 증가율이 농도차가 커짐에 따라 감소하였다. 본 연구에서는 막흡수 실험과 확산투석조 실험을 통해 염산을 회수하기 위한 확산투석에 산의 농도가 미치는 영향과 농도 범위에 따른 음이온 교환막 내부에서의 산의 이동 기작을 고찰하였다. 실험 결과 저농도(<2 N)산의 경우에는 산의 분자확산, 그리고 고농도 (>2 N)산의 경우에는 수소이온 투과현상 (proton leakage)이 막에서의 지배적인 이동 기작임을 알 수 있었다. 또한 고농도 범위에서는 삼투압에 의한 물분자의 이동과 막의 탈수현상이 수소이온의 이동을 방해하므로 막에서의 산 플럭스 증가율이 감소하였다.

The sodium α-sulfo fatty acid vinyl ester oligomers, which are oligomer type surfactants were prepared by polymerization with fatty acid vinyl acetate. The α-sulfonation of fatty acid vinyl ester oligomers were carried by direct addition of sulfur trioxide. The dispersing performance of oligomer type anionic surfactants and sodium dodecyl sulfate(SDS) in the aqueous suspension of iron oxide and titanium dioxide particles was evaluated by particle size distribution and zeta-potential measurement. As results, the particles of iron oxide and titanium dioxide were flocculated by addition of small amount of oligomer type anionic surfactants and sodium dodecyl sulfate(SDS), then the flocks redispersed by more addition of oligomer type anionic surfactants and SDS. The flocculation, redispersion process was observed in lower concentration range of oligomer type anionic surfactants than SDS. Especially, the dispersing action of sodium α-sulfo palmitic acid vinyl ester oligomer was better than sodium α-sulfo lauric acid vinyl ester oligomer.

A series of long chain N-acyl amino acid type anionic surfactants were prepared by treating fatty acid chlorides with three kinds of amino acids, that is, sodium N-acyl-sarcosinates, sodium N-acyl-N-methyl-β-alaninates and sodium N-acyl-N-methyl-taurates in an alkaline solution. All prepared biodegradable surfactants were purified by thin layer chromatography and column chromatography, and identified their structures by spectral analysis.

Fluorescent anionic oligo surfactants were synthesized by the condensing products of long chain alkylvinylether-maleic anhydride cooligomers and resorcinol including dye structures. Their various surface activities and dispersing action were studied on the aqueous solution. These oligo surfactants exhibited a remarkable surface tension lowering property, lower foaming and a large dispersing action for the particles of α-copper phthalocyanine blue. Further it was ascertained that the binding of oligo surfactant onto the pigment surface caused the deviation towards lower wavelengths at the maximum fluorescent intensity as compared with aqueous oligo surfactant solutions, These surface active properties of the oligo surfactants may be attributed to rigid and hydrophobic structure of dye groups, besides surface-active groups of alkylether groups and carboxylic group of the anionic oligo surfactants.

To developed new process for obtaining maximum molecular weight of anionic acrylamide and acrylic acid copolymer by inverse emulsion polymerization. Concentration of initiator, reducing agent, surfactant and mole ratio of acrylamide-acrylic acid were studied for the process. Semi-batch processes with method of redox, control of reaction temperature, feeding method of monomer and reaction time, was suitable for maximum molecular weight of P(AMAC) from this process obtained 3.09 × 106(Mn.) and 4.41 × 106(Mw.) in molecular weight measured by the intrinsic viscosity method. inverse emulsion polymerization mechanism of P(AMAC) does not followed the Smith-Ewart and Medvedev theory, but selected for concentration of initiator, reducing agent, surfactant, water solubility of monomer.

山地草地開發파 聯關된 草地士爆改良 및 施R巴法 改善올 薦하여 Homes의 Systematic variations 方法으로 多量要素 ΣAnion : ΣCation 適正施服比率 및 適正總養分(ΣA+ ΣC) 施肥量을 決定코자 Grass-clover 混播我培條件에서 山地土壞을 供試한 Pot 試驗으로 遂行한 結果는 1. 混播條件에서 各構成草種別 收量提高를 위한 ΣA/Σ

산지초지개발과 聯關된 草地士壞개랑 및 施肥法改攻善을 馬하여 Homes의 Systematic variations 方法으로 多量要素 anions N : S : P 및 Cations K : Ca Ca:Mg 적정비료비율J인比率 (當量基準) 을 決定코자 山地 土爆을 공시한 Pot試驗으로 Orchardgrass-Ladino clover混播條件에서 수행한 결과는 1. 混播條件에서 各構成훌種別 最高收量을 얻기 위한 적정비료比率을 求하였다(Table 4), 大略的으로

자로사이트 내의 SO4는 다른 산화음이온으로 치환될 수 있는데 자로사이트가 침철석으로 전이되는 과정은 공침된 산화음이온의 거동에 중요한 역할을 하게 된다. 본 연구에서는 다양한 산화음이온과 함께 공침된 자로사이트가 환원성 용해에 의하여 상변화를 거칠 때 산화음이온 종에 따른 상변화의 양상과 이와 수반된 산화음이온의 거동을 광물학적 및 지구화학적으로 연구하였다. 다섯 가지의 산화음이온이 SO4를 5 몰% 치환한 자로사이트가 본 연구에 사용되었다. 본 연구에서는 암모늄 옥살레이트를 이용한 환원성 용해 시 일어나는 자로사이트의 광물상의 변화를 측정하였으며 자로사이트의 침철석으로의 전이 속도는 MoO4-자로사이트 ≥ SeO4-자로사이트 ≥ CrO4-자로사이트 > 순수한 자로사이트 > SeO3-자로사이트 > AsO4-자로사이트의 순서를 보여 치환된 산화음이온에 따라서 자로사이트의 상전이 속도가 다름을 보여주었다. 이에 따른 Fe의 용출은 시간과 산화음이온의 종류에 따라 큰 차이를 보이지 않았다. 광물의 변화에 따라 용출되어져서 나온 각 산화 음이온의 농도는 전체적으로 Mo > Se(SeO3) > As > Se(SeO4) > Cr의 농도 순위를 보였으며 시간에 따라 약 간의 증가를 보였다. 이러한 경향은 광물상의 변화보다는 산화음이온 종류의 특성에 의한 것으로 파악된다. 본 연구 결과는 산화음이온의 종류에 따라 자로사이트의 침철석으로의 변화는 영향이 있었으나 이러한 경향이 용출되는 산화음이온의 농도에 영향을 미치지 않음을 보여주었다.

This study analyzes the effect of negative air ions on the concentration of airborne particulate matter and evaluates the expected purification efficiency of open spaces for particulate matter by investigating the amount of negative air ions generated by plants. This study establishes a negative air ion generation treatment environment, plant environment, and control environment to measure the purification efficiency of particulate matter under the conditions of each, analyzing the expected purification efficiency by designing a particulate matter purification model. Results show that the amount of generated negative air ion according to environment was negative air ion generation treatment environment > plant environment > control environment; this order also applies to the particulate matter purification efficiency. Moreover, it took 65 min for the negative ion generation treatment environment, 90 min for the plant environment, and 240 min for the control environment to reach the standard expected purification efficiency of particulate matter concentration of 960 mg/m³ for PM10. For PM2.5, with the designated maximum concentration of 700 mg/m³, it took 60 min for the negative ion generation treatment environment, 80 min for the plant environment, and more than 240 min for the control environment. Based on these results, the expected purification efficiency compared to the control environment was quadrupled in the negative ion generation treatment environment and tripled in the plant environment on average.

The purpose of this study is to understand the formation of internal wind paths of open space and its effect on meteorological factors and the generation of negative air ions. Various types of internal wind paths of open space were formed. Subsequently, changes in meteorological factors in each type were measured and the generated negative air ions were analyzed. The four key findings of the study are summarized as follows. First, the average wind speed formed inside the open space was analyzed such that the difference in wind speed was dependent on the difference in the composition of the wind path. Second, the negative air ion generation was observed to have the same trend as the average wind speed difference. Third, changes to the meteorological factors were more evident depending on the difference in wind path formation patterns. Solar radiation was expected to be highly affected by the physical structure (direction) of the target site. The relative humidity was found to show large difference depending on the different wind path type; however, this difference was significantly reduced when converting to absolute humidity. Fourth, it was found that the wind path formation type of open space affects meteorological factors through path analysis, and the changed meteorological factors affect the amount of generated negative air ions. Two conclusions can be obtained based on these results. First, the changes in internal wind speed formation of open space directly reduced the amount of generated negative air ions. Second, the changes in wind speed affect meteorological factors as well as the amount of generated negative air ions.

When the reinforced concrete structure is in a high salinity environment, chlorine ions penetrate from the surroundings, resulting in corrosion of the reinforcing bars, resulting in low durability. Therefore, studies on the immobilization of chlorine ions are underway, and anion exchange resin, one of them, was used in this study. In this study, chloride ion fixing ability was confirmed by replacing OPC, conventional bead anion exchange resin, and powder anion exchange resin with mortar and then using an electron probe X-ray micro-analyzer. The bead anion exchange resin replaced 3% of the fine aggregate volume and the powder anion exchange resin 5% of the cement volume. The fabricated specimens were cured for 28 days, immersed in NaCl solution for 28 days, and confirmed by electron probe X-ray micro-analyzer.

Recently, self-healing concrete has been researched as maintenance and repair of concrete structures are important challenges we face. This paper focused on possibility of ion exchange resin as a novelty material directly and actively controlling harmful ions of concrete, whereas most self-healing concrete researches have been focused on methods to automatically filling and repairing internal crack of concrete. Because equilibrium properties between ion exchange resin and harmful ion is important before design of cement mixing proportion, it was conducted to remove chloride or sulfate in saturated Ca(OH)2 solutions containing NaCl or Na2SO4. The removal performance was analyzed using kinetic equation and isothermal equation. Consequently, the removal properties of anion exchange resin were relatively more dependent on pseudo second reaction equation and Langmuir equation than pseudo first reaction equation and Freundlich equation. And it was concluded that each chloride and sulfate can be removed to the maximum 1068 ppm and 1314 ppm.

Adsorption using highly porous and highly functionalized sorbents is a straightforward removal technology currently being employed, however the range of contaminants is limited. A novel sorbent was synthesized from activated carbon and Zr-based UiO66 metal organic framework to remove both cationic and oxyanionic metals from aqueous solutions. The composite was characterized using FSEM-EDS, FT-IR, XRD, and TGA, and showed successful integration of UiO66 on the surface of activated carbon. Batch adsorption tests with ICP-OES reveal that the composite has removal efficiency >95% for Pb (II), Cu (II), Se (IV), and As (V). The hybrid material is a promising sorbent for the removal of both cationic and oxyanionic metals for wastewater purification.

이온교환법 또는 흡착법은 기존의 생물학적 처리공정과 연계한 고도처리시스템을 구축하는데 있어 가장 단순하고 안정적인 단위공정의 하나가 되고 있다. 이에 따라 다기능성, 고효율성, 이온 선택성 및 경제성을 갖춘 흡착소재를 개발하기 위해 많은 노력이 이루어지고 있다. 리그노셀룰로오스계 천연 고분자 물질은 자연에 풍부하면서도 저가라는 점에서 다양한 기능성의 흡착소재로 활용되고 있다. 이 중 정미산업의 주요 부산물인 왕겨는 기계적 강도가 높고 일정한 형상과 넓은 비표면적을 가지고 있다는 장점이 있어 생체흡착제 제조 원료로 적합한 특성을 가지고 있다. 우리나라에서는 매년 60만톤 이상의 왕겨가 발생하고 있으며, 이들의 95% 이상이 축산분뇨와 혼합하여 퇴비로 사용되고 있는 실정이다. 본 연구에서는 왕겨의 새로운 재활용 방안으로 생체흡착제 제조를 위한 기질물질로 왕겨의 활용 가능성과 효율성을 검토하기 위해 potassium peroxydisulphate(K2S2O8)를 산화-환원 개시제로 하는 그라프트 중합반응을 통해 왕겨표면에 glycidyl methacrylate(GMA)를 화학적으로 결합시켜 에폭시기(-COC-)를 도입하고, Diethylenetriamine(DETA)과 반응을 통해 에폭시기에 아민기(-NH)를 도입하는 방법으로 음이온 흡착기능성 왕겨흡착제(RH-g-GMA-DETA)를 제조한 다음, 회분식 흡착실험을 통해 아민형 왕겨흡착제의 NO3-N와 PO4-P에 대한 흡착효율 및 흡착특성을 평가하였다. 아민형 왕겨흡착제 RH-g-GMA-DETA의 NO3-N와 PO4-P에 대한 흡착은 Fruendlich 흡착등온식보다는 Langmuir 흡착등온식과 잘 일치하였으며, Langmuir흡착등온식으로부터 구한 최대 단일층 흡착량은 NO3- 68.5 mg/g, PO43- 129.8 mg/g이었다. 흡착은 NO3- 와 PO43- 모두 20분 이내에 평형에 도달할 정도로 빠르게 진행되었으며, 2차 흡착속도식과 잘 부합하는 특성을 보여 chemisorption이 속도결정단계에서 중요한 역할을 함을 알 수 있었다. D-R모델로부터 추산한 흡착에너지는 NO3- 가 9.3 kJ/mol, PO43- 가 140 kJ/mol로 각각 이온교환과 화학적 흡착이 주된 흡착메카니즘으로 작용하였음을 나타내었다. 공존 음이온간 흡착선택성과 흡착에 미치는 pH 영향을 동시에 살펴 본 결과 RH-g-GMA-DETA의 흡착선택성은 SO4>PO4>NO3≥NO2>F의 순이었으며, SO4는 pH의 영향을 거의 받는 흡착특성을 보이는 반면, PO4는 pH가 증가할수록 흡착량이 증가하는 특성을, NO3, NO2 및 F는 pH 5 이상에서는 흡착량이 급격히 감소하는 특성을 보였다.

This study is mainly focused on micellar effect of tetradecyltrimethyl ammonium bromide(TTABr) solution including alkylbenzimidazole(R-BI) on dephosphorylation of diphenyl-4-nitrophenylphosphinate(DPNPIN) in carbonate buffer(pH 10.7). Dephosphorylation of DPNPIN is accelerated by BI⊖ ion in 10-2 M Carbonate buffer(pH 10.7) of 4×10-4 M TTABr solution up to 80 times as compared with the reaction in Carbonate buffer by no benzimidazole(BI) solution of TTABr. The value of pseudo first order rate constant(kψ) of the reaction in TTABr solution reached a maximum rate constant increasing micelle concentration. The reaction mediated by R-BI⊖ in micellar solutions are obviously slower than those by BI⊖, and the reaction rate were decreased with increase of lengths of alkyl groups. It seems due to steric effect of alkyl groups of R-BI⊖ in Stern layer of micellar solution. The surfactant reagent, TTABr, strongly catalyzes the reaction of DPNPIN with R-BI and its anion(R-BI⊖) in Carbonate buffer(pH 10.7). For example, 4×10-4 M TTABr in 1×10-4 M BI solution increase the rate constant(kψ=99.7×10-4 1/sec) of the dephosphorylation by a factor ca. 28, when compared with reaction(kψ=3.5×10-4 1/sec) in BI solution(without TTABr). And no TTABr solution, in BI solution increase the rate constant(kψ=3.5×10-4 1/sec) of the dephosphorylation by a factor ca. 39, when compared with reaction (kψ=1.0×10-5 1/sec) in water solution(without BI).