• 대한화학회지
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• 제56권4호
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• pp.440-447
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• 2012

Heteroleptic complexes of zirconium (IV) derived from bulky Schiff base ligands containing a sulphur atom and oximes of heterocyclic ${\beta}$-diketones of the general formula ZrLL' (where $LH_2=RCNH(C_6H_4)SC:C(OH)N(C_6H_5)N:CCH_3$, $R=-C_6H_5$, $-C_6H_4Cl(p)$ and $L^{\prime}H_2=R^{\prime}C:(NOH)C:C(OH)N(C_6H_5)N:CCH_3$, $R^{\prime}=-CH_2CH_3$, $-C_6H_5$, $-C_6H_4Cl(p)$ were prepared by the reactions of zirconium tetrachloride with disodium salts of Schiff bases ($L\;Na_2$) and oximes of heterocyclic ${\beta}$-diketones ($L^{\prime}\;Na_2$) in 1:1:1 molar ratio in dry refluxing THF. The structures of these monomeric zirconium (IV) complexes were elucidated with the help of elemental analysis, molecular weight measurements, spectroscopic (IR, NMR and mass) studies. A distorted trigonal bipyramidal geometry may be suggested for these heteroleptic zirconium (IV) complexes. The ligands (bulky Schiff base ligands containing a sulphur atom and oximes of heterocyclic ${\beta}$-diketones) and their heteroleptic complexes of zirconium (IV) were screened against A. flavus, P. aeruginesa and E. coli.

• 한국환경과학회지
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• 제24권8호
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• pp.1015-1021
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• 2015

In order to establish the design parameters of adsorption for arsenic compounds with hydrotalcite including chlorine ion, the basic properties of adsorption and desorption as well as the oxidation of As (III) were examined in batch tests. The maximum adsorption capacities of arsenite and arsenate were 6.2 mg-As(III)/g and 103 mg-As (V)/g, respectively. Although 80.4% of maximum desorption was shown in 20% NaOH solution, 5~10% of NaOH was recommended considering operating benefits, where the proper condition of the desorption was in the range of 73% to 80%. The most suitable desorption condition was in the combination of NaCl (10~20%) and NaOH (5~10%). Within 2 minutes, As (III) was easily oxidized to As (V) with 0.0001 N KMnO4, where the maximum oxidization ratio was shown to 98.9%.

• 자원리싸이클링
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• 제10권5호
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• pp.36-43
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• 2001

The chlorine component in fly ash from municipal solid waste incineration ash was removed by water washing for the purpose of recycling fly ash as a raw material of ordinary portland cement. The samples were a different kind of 리y ashes using $Ca(OH)_2$and NaOH as media of wet scrubber for flue gas cleaning. The content of soluble salts of fly ash using $Ca(OH)_2$and NaOH was 32.8%, 50.1% and the content of chlorine component, 22.9% and 26.0% respectively, which was KCl, NaCl, CaC1OH mainly. When each fly ash was washed using water under conditions of a agitation speed of 300 rpm, a liquid to solid ratio of 10, most soluble salts in fly ash were dissolved within 30 minutes and the content of chlorine component in ash was diminished to the content of 4.4%, 2.O% at $20^{\circ}C$ and 1.7%, 0.8% at $50^{\circ}C$ respectively. And the main compound of residual chlorine component in ash after water washing was friedel`s salt ($3CaO.A1_2$$O_3$.$CaCl_2$.$10H2$O). From analysis results of water quality for wastewater by water washing, the components exceeding discharged wastewater standard were only Pb and Cd. But As pH was controlled to 10 with addition of $CO_2$(g) or $Na_2$$_CO3$in water, the concentration of heavy metals such as Pb and Cd was also under discharged wastewater standard.

• 한국환경보건학회지
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• 제24권1호
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• pp.32-37
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• 1998

The Carbon Dioxide is the gas, which causes green house effects, unusual changes in the weather, destruction of the life. Almost every nation in the world is trying to search the countermeasure to this poisonous gas. I synthesized $Fe_3O_4$ and NaOH, in order to decompose the Carbon Dioxide. Among the particles synthesizing $Fe_3O_4$, I chose the equivalent ratio 1.00 which can decompose the Carbon Dioxide best, and fixed that equivalent ratio and added the 0.005-3.00 mole percentage of NiCl$_2$ and synthesized $Fe_3O_4$. I studied the decomposition of the Carbon Dioxide and methanized reaction, by measuring its crystal structure, thermochemistrical character and specific surface area. In decomposing the Carbon Dioxide, I used oxygen-deficit Magnetite which I produced by injecting the hydrogen gas into the synthesized sample. I observed the methanization reaction by raising the temperature of sample up to 650$\circ$C and having it reacted with the hydrogen gas. The decomposition of the Carbon Dioxide was added 0.005, 0.03, 0.05 mole percentage of NiCl$_2$ was more effective than pure $Fe_3O_4$. All sample in which the decomposition of the Carbon Dioxide took place produced the methane gas.

• 한국콘크리트학회:학술대회논문집
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• 한국콘크리트학회 1994년도 가을 학술발표회 논문집
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• pp.87-92
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• 1994

The main objective of this study is to determine the critical chloride ion concentrations in the pore solutions causing depassivation of steel reinforcement in concrete made with cements of different $C_3A$ contents. Cement pastes with water-ratio of 0.5 were prepared using four cements with $C_3A$ contents of 0.46, 5.97, 9.14, and 9.65 percent. The pastes were allowed to hydrate in sealed containers for 28days and then objected to pore solution expression. The expressed pore fluids were analyzed for chloride and hydroxyl ion concentrations. It was found that the free cholride concentration in the pore solution decreases significantly with an increase in the $C_3A$ content of the cement. With increasing level of chloride addition, although the alsolute amount of bound chloride increase, the ratio of bound to total chlorides decreases.

• 센서학회지
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• 제17권3호
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• pp.217-222
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• 2008

$BaCl_2$ crystals were grown by using the Czochralski method, and their scintillation properties were measured. The emission spectrum was located in the range of $370{\sim}450$ nm, peaking at about 400 nm. The fluorescence decay time was approximately 75.9 ns for 662 keV ${\gamma}$-rays excitation. The energy resolution was about 24.4 % for $^{137}Cs$ 662 keV ${\gamma}$-rays, and the ${\alpha}/{\beta}$ ratio to $\alpha$ particles from a $^{210}Po$ 5.4 MeV was about 0.25.

• 한국세라믹학회지
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• 제35권2호
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• pp.185-195
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• 1998

This experiment carried out in order to investigate the effect of the chemical activators for acceleration of hydration the system of Fly ash-Cao The paste was consisted of 80wt% Fly ash and 20wt% CaO with 1. 3. 5wt% of 4 activators(N{{{{ alpha _2 }}S{{{{ OMICRON _4 }}, CaC{{{{ {l }_{2 } }}, NaOH, Ca(N{{{{ OMICRON _3 {)}_{2 } }} and W/S ratio of 0.42 After curing for 1, 3, 7, 14, 28 days the paste hydration was characterized by the measurement of compressive strength XRD analysis SEM observation the combined water and the reaction amount of Ca(OH)2 determination. As a result of this ex-periment all of the system which involved Na2SO4 or NaOH had a god compressive strength. In the case of 7 days curing a system which added CaCl2 showed the highest compressive strength among all especially NaOH system showed a high increase in strength as a dosage of it increased. Hydration products were different according to activatores added. Only C-S-H was observed in NaOH system. As the reaction amount of Ca(OH)2 and combined water were increased the compressive strength increased. There were few differences in the comparision of strength between ignited loss 3.1% and loss 9.3% of fly ash.

• 공업화학
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• 제31권4호
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• pp.390-397
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• 2020

To synthesize non-corrosive metallic gold colored α-Al₂O₃ nanoplate-TiO₂ core-shell pigments with controlled roughness, we systematically checked the morphological variation of the TiO₂ shell with the mole ratio of TiCl₄ and NaOH from 1 : 1 to 1 : 1.5, 1 : 2, 1 : 2.5, 1 : 3, 1 : 3.5, and 1 : 4. The more increased mole ratio of TiCl₄ and NaOH resulted in the smoother TiO₂ shell due to the promoted formation of anatase TiO₂ than that of the rutile one. By the heat-treatment of pigments at 500 ℃, we could improve the adhesiveness between TiO₂ shell and α-Al₂O₃ nanoplates without changing their topology and roughness. In addition, the α-Al₂O₃ nanoplate with the robust TiO₂ by heat-treatment exhibited comparable photo-stability against photo-catalytic degradation by UV exposure compared with the commercially available α-Al₂O₃/TiO₂ lustering pigment.

• 한국토양비료학회지
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• 제24권4호
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• pp.272-277
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• 1991

채소(菜蔬) 재배지(栽培地)에서 붕소(硼素) 시용량(施用量)에 따른 토양중(土壤中) 유효붕소(有效硼素) 및 붕소(硼素)의 형태별함량변화(形態別含量變化)를 구명(究明)하기 위(爲)하여 토양특성(土壤特性)이 상이(相異)한 광질사양토(鑛質砂壤土), 석회질토양(石灰質土壤), 유기물(有機物)이 많은 토양(土壤) 및 비닐하우스 토양(土壤) 등 4개(個) 토양(土壤)에 조생미호 배추를 공시품종(供試品種)으로 하여 1/2,000a pot에서 시험(試驗)을 실시(實施)하여 얻은 결과(結果)는 다음과 같다. 1. 붕소(硼素) 시용량(施用量)에 따른 토양중(土壤中) 유효붕소(有效硼素) 증가(增加)는 비닐하우스 토양(土壤)>유기물(有機物)이 많은 토양(土壤)>광질(鑛質) 사양토(砂壤土)>석회질(石灰質) 토양(土壤) 순(順)이었다. 2. 붕소(硼素)의 전체함량(全體含量)에 대(對)한 토양중(土壤中) 형태별(形態別) 붕소함량(硼素含量)중 Ammonium Oxalate ext.-B 가 19.1%로 가장 많았으며 Water Sol.-B및 $CaCl_2$ ext.-B는 각각(各各) 0.7%로 가장 적었다. 3. 붕소(硼素) 시용량(施用量)에 따른 붕소(硼素)의 형태별(形態別) 붕소함량(硼素含量)의 증가(增加) 정도(程度)는 $NH_2-Oxalate$ ext.-B>Mannitol exah.-B> $CaCl_2$ ext.-B> $NH_4OH{\cdot}HCl$ ext.-B>Water sol.-B 순(順)이었다. 4. 토양중(土壤中) 석회함량(石灰含量)이 증가(增加)하면 Water sol.-B는 감소(減少)하고 다른 형태(形態)의 붕소(硼素)는 증가(增加)하였으나 유기물(有機物) 함량(含量)이 증가(增加)하면 Water sol.-B와 Ammonium Oxalate ext.-B는 증가폭(增加幅)이 컸으나 다른 형태(形態)의 붕소(硼素)는 경미(輕微)하게 증가(增加) 되거나 감소(減少)하는 경향(傾向)이었다.

• Korean Chemical Engineering Research
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• 제55권4호
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• pp.535-541
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• 2017

Ag 200 ppm과 총유량 120 l/h의 기준으로 이온 교환 섬유 시스템을 제작하였다. 이 시스템은 이온교환 섬유로서 강염기성인 FIVAN A-6을 이용하였고, 이온교환 섬유의 교환이 용이하고 고정틀이 필요 없도록 고안된 이중관 형 이온 교환 섬유조로 구성되어있다. 이 시스템의 이온교환섬유의 Ag에 대한 이온교환 용량은 4.6 meq/g 이었으며, 공정조건별로는 다음과 같은 결과를 얻었다. 흡착공정의 경우 유속의 영향을 확인한 후 40~90 l/h의 범위에서 운전하였으며, pH 7~12 범위에서는 Ag의 착이온 형성에 대한 pH의 영향이 없는 것으로 나타났다. 역세공정의 경우 60~120 l/h의 범위에서 Ag 회수율 실험을 수행하였으며, 역세용 화학물질로는 NaOH, $NH_4Cl$, NaCl을 이용하여 비교실험을 하였고, 역세 화학물질이 고농도 일수록 탈착시간은 짧아지지만 몰당 탈착 효율은 저하되는 경향이었으므로 탈착시간과 농도의 균형을 잘 맞추어 운전해야 경제적 운전이 될 수 있음을 확인하였다. 강염기성 음이온 섬유인 FIVAN A-6와 이중관형 이온교환 섬유조를 이용하여 Ag 흡착율은 99.5% 이상, 총 Ag회수율은 96% 이상의 결과를 얻을 수 있었으며 상용화 가능함을 확인할 수 있었다.