• 한국추진공학회지
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• 제8권1호
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• pp.1-7
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• 2004

과염소산암모늄(AP)의 N-메틸피롤리돈(NMP) 용액으로부터 초미세 크기를 갖는 과염소산암모늄(UFAP) 결정의 결정화 연구를 수행하였고, 침전된 결정들의 특성들을 scanning electron micrograph(SEM)와 X-ray diffraction(XRD) 그리고 thermogravimetric analysis(TGA)를 사용하여 분석하였다. 침전용매로 클로로포름, 염화메틸렌 그리고 톨루엔이 사용되었을 경우, 2$\mu\textrm{m}$ 이하의 크기를 갖는 결정들이 제조되었다. 제조된 UFAP의 결정학적 특성과 열분해 거동은 상용으로 사용되는 AP와 거의 유사하였다.

• 공업화학
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• 제7권1호
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• pp.118-128
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• 1996

양이온성 천연 고분자 전해질인 chitosan의 수용성 유도체를 제조하기 위해 chitosan에 먼저 Schiff's base를 형성시키고, 이를 다시 환원시키는 방법으로 chitosan에 N-methyl, N-butyl, N,N-dibutyl기를 각각 도입시킨 후, NMP중에서 methyl iodide를 이용하여 4차 ammonium 기가 도입된 chitosan 유도체를 합성하였다. 이 반응에서 선택적인 N-alkyl 유도체 뿐 아니라 O-alkyl 또한 진행됨을 확인하였다. 제조한 각 4 차 ammonium기가 도입된 chitosan 유도체의 응집성능을 검토하기 위해 제지공장 폐수를 대상으로 응집실험을 행한 결과, chitosan 에서와는 달리 거의 모든 pH 영역에서 일정하게 뛰어난 투과도와 COD 제거율을 보였으며, alkyl 기의 탄소수가 증가할수록 응집능은 증가되었고 그 중에서도 N-butyl dimethyl chitosan ammonium iodide가 가장 우수하였다. 그러나 N-dibutyl methyl chitosan ammonium iodide는 오히려 chitosan 자체보다 감소하는 경향을 나타내었다.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2017년도 춘계학술논문요약집
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• pp.419-420
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• 2017

• Elastomers and Composites
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• 제50권4호
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• pp.297-303
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• 2015

Ammonium polyphosphate-polyurethane foam composite (APP-PUF) was prepared from poly(adipate)diol/ammonium polyphosphate composite (f = 2), polyether polyol (f = 4.6), and PMDI (f = 2.5). As a blowing agent, $H_2O$ was used at various concentrations. The thermal decomposition behavior, morphology, closed-cell content, and density of APP-PUF were characterized. At the $H_2O$ concentrations lower than 3.5 php, the cell size of pure polyurethane foams (PUF) and APP-PUFs were close each other. As the $H_2O$ concentration became greater than 5.0 php, the cell size of the PUFs greatly increased compared to that of APP-PUFs. Addition of 1.5~1.9 wt% ammonium polyphosphate to the PUFs greatly enhanced the thermal stability of the PUFs, so 50 wt% residual temperature of APP-PUFs increased to $380{\sim}488^{\circ}C$, which were $30{\sim}70^{\circ}C$ higher than those of the PUFs. Thermal stability of the PUFs and APP-PUFs increased with $H_2O$ content and then decreased once $H_2O$ content exceeded 5 php.

• 한국재료학회지
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• 제31권9호
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• pp.481-487
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• 2021

ZnO particles are successfully synthesized at 150 ℃ for 30 min using zinc acetate as the Zn source and 1,4-butanediol as solvent using a relatively facile and convenient glycol process. The effect of ammonium hydroxide amounts on the growth behavior and the morphological evolution of ZnO particles are investigated. The prepared ZnO nanoparticle with hexagonal structure exhibits a quasi-spherical shape with an average crystallite size of approximately 30 nm. It is also demonstrated that the morphology of ZnO particles can be controlled by 1,4-butanediol with an additive of ammonium hydroxide. The morphologies of ZnO particles are changed sequentially from a quasi-spherical shape to a rod-like shape and a hexagonal rod shape with a truncated pyramidal tip, exhibiting preferential growth along the [001] direction with increasing ammonium hydroxide amounts. It is demonstrated that much higher OH^- amounts can produce a nano-tip shape grown along the [001] direction at the corners and center of the (001) top polar plane, and a flat hexagonal symmetry shape of the bottom polar plane on ZnO hexagonal prisms. The results indicate that the presence of NH⁴⁺ and OH^- ions in the solution greatly affects the growth behaviors of ZnO particles. A sharp near-band-edge (NBE) emission peak centered at 383 nm in the UV region and a weak broad peak in the visible region between 450 nm and 700 nm are shown in the PL spectra of the ZnO synthesized using the glycol process, regardless of adding ammonium hydroxide. Although the broad peak of the deep-level-emission (DLE) increases with the addition of ammonium hydroxide, it is suggested that the prominent NBE emission peaks indicate that ZnO nanoparticles with good crystallization are obtained under these conditions.

• 한국수산과학회지
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• 제49권5호
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• pp.665-670
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• 2016

A three-dimensional ecological model (EMT-3D) was used to simulate the behavior of PFOA in Gwangyang Bay, Korea. The results of sensitivity analysis showed that partition rate, adsorption rate, and settling rate were important factors in the variation in PFOA in particulate organic matter. Bioconcentration was the most significant factor for PFOA in phytoplankton, with the largest effect size. These parameters must therefore be carefully considered when modeling PFOA behavior. In simulations, 30% and 50% reductions in loads from land-based sources of PFOA resulted in concentrations of dissolved PFOA lower than 4 ng/L and 2 ng/L, respectively, in the central part of the bay.

• 한국환경과학회지
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• 제16권5호
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• pp.641-647
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• 2007

The phase transfer catalysis(PTC) reagent, ethyl tri-octyl ammonium bromide(ETABr), strongly catalyzes the reaction of p-nitrophenyi diphenyl phosphinate(p-NPDPIN) with benzimidazole(BI) and its anion($BI^{\theta}$). In ETABr solutions, the dephosphorylation reactions exhibit higher first order kinetics with respect to the nucleophile, BI, and ETABr, suggesting that reactions are occuring in small aggregates of the three species including the sub-strate(p-NPDPIN), whereas the reaction of p-NPDPIN with $OH^{\theta}$ is not catalyzed by ETABr. This behavior for the drastic rate-enhancement of the dephosphorylation is referred as 'aggregation complex model' for reaction of hydrophobic organic phosphinates with benzimidazole(BI) in hydrophobic quarternary ammonium salt(ETABr) solutions.

• 한국산학기술학회:학술대회논문집
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• 한국산학기술학회 2001년도 춘계학술대회 발표논문집
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• pp.287-289
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• 2001

The morphology of silica supported MoO$_3$ catalysts, which was prepared by impregnation of ammonium heptamolybdate with various weight loadings up to 35 wt%, was studied using x-ray diffraction. In addition to the orthorhombic phase, the behavior of the rarely studied hexagonal phase was characterized. For high loading catalysts, excess ammonium ions present in the monoclinic and triclinic precursors are capable of occupying interstitial sites of microcrystalline MoO$_3$ during moderate temperature calcinations and in doing so enhance the MoO$_3$-SiO$_2$ interaction. This results in a "well dispersed" morphology at high loadings. Sintering at high temperature is due to loss of ammonium from the oxide framework. Ammonia reimpregnation, which leads back to the well dispersed hexagonal phase, may offer a simple regeneration process for spent Mo containing catalysts.

• Bulletin of the Korean Chemical Society
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• 제21권5호
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• pp.465-470
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• 2000

The conformations and energies of p-tert-butylcalix[4] crown-6-ether (1) and its alkyl ammonium complexes have been simulated by AM1 semi-empirical quantum mechanics and molecular mechanics calculations using a variety of forcefields (MM2, MM+, CVFF). We performed molecular dynamics calculations to simulate the behavior of these coplexes primartily focusing on the three representative conformations (cone, partial cone, 1,3-alternate) of host molecule 1. When we performed AM1 semi-empirical and molecular mechanics calculations, the one conformation was generally found to be most stable for all the employed calculation methods. The primary binding site of host 1 for the recognition of alkyl ammonium guests was confirmed to be the central part of the crown moiety. The complexation enthalpy calculations revealed that the alkyl amonium cations having smaller and linear alkyl group showed the better complexation efficiencies when combined with p-tert-butylcalix[4]crown-6-ether, that is in satisfactory agreement with the experimental results.

• 대한화학회지
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• 제17권3호
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• pp.182-187
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• 1973