• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2009년도 추계학술대회 논문집
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• pp.262-262
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• 2009

최근 리튬이차전지가 전지자동차, hybrid car, PHEV, Ev, UPS 저장장치로 사용되기 시작함에 따라 고용량화, 고출력화가 요구되고 있다. 현재까지 주로 사용 되어왔던 carbon으로는 작동전압이 낮고, 고용량화, 고출력화가 어려워 금속산화물, 금속 비정질 금속 및 금속산화물을 carbon과 혼합 사용 함으로써 차세대 전지로서 특성을 달성하고 있다. 따라서 본 연구에서는 음극 소재로서 안정성이 뛰어난 금속산화물로 $Li_4Ti_5O_{12}$를 합성할 때 저가의 $TiCl_4$를 이용 $Li_4Ti_5O_{12}$가 고밀도를 갖게끔 $TiCl_4$를 이용 구형의 Ti-precursor(전구체)를 합성한 후 구형의 $Li_4Ti_5O_{12}$를 합성하였다. Ti전구체는 $TiCl_4$로부터 합성하였는데 이때 구형을 제조하고자 Hydroxypropyl cellulose(이하 HPC)를 사용하여 반응을 진행하였다. 이때 반응 조건 및 HPC의 몰수 변화에 따른 입자 형상의 변화에 관하여 관찰한 결과, $TiOCl_2$ 0.4mol, 반응온도 $10^{\circ}C$, 유지시간 6시간, HPC양 0.02mol일 때 $0.6{\mu}m$ 정도의 구형 Ti-전구체를 합성하였다. 합성된 Ti-전구체와 리튬수화물을 사용하여 $Li_4Ti_5O_{12}$를 합성 하였고, 상기 물질로 전지특성을 평가하였다.

• 한국물환경학회지
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• 제34권1호
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• pp.77-83
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• 2018

This paper aims to evaluate the results of toxicity testing with Daphnia magna and Vibrio fischeri on wastewater samples which might be influenced by ion imbalance. The effluents from factories were found to be more toxic with high salinity levels than those from public wastewater treatment plant (WTP) and sewage treatment plant (SWP). Clion composition was highest in the effluent, in terms of percentage, which was followed by $Na^+$, $SO_4^{2-}$ and $Ca^{2+}$. $K^+$ and $Mg^{2+}$ ion was relatively low. The sensitivity of D. magna test results was higher than V. fischeri. Among samples which were proved by V. fischeri testing to be nontoxic, the composition ratio of each ion whether toxic samples or nontoxic samples which were decided by D. magna toxicity testing, were compared. $Na^+$, $K^+$, $Ca^{2+}$, $Mg^{2+}$ ion composition ratio showed high level in nontoxic samples whereas $SO_4^{2-}$ and $Cl^-$ ion composition ratio was high in toxic samples. Accordingly, $SO_4^{2-}$ and $Cl^-$ ion seemed to be considered the ions causing toxicity in effluent. Toxicity from some categories of industries (Mining of non-metallic minerals, Manufacture of basic organic petrochemicals, Manufacture of other basic organic chemicals, Manufacture of other chemical products etc.) seemed to be influenced by salinity. The Ion concentration in influent and effluent were similar. Concentration of $Na^+$, $Cl^-$, $K^+$, $Ca^{2+}$ ions were high in influent, however $Mg^{2+}$ and $SO_4^{2-}$ ions were high in effluent.

• 한국입자에어로졸학회지
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• 제14권1호
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• pp.17-24
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• 2018

Since the motion of the charged particle strongly depends on its charge characteristics, information on charge distributions of target particles is one of the important variables in aerosol research. In this study, charged distribution of atomized NaCl particles were measured using a Gerdien type ion counter. Two kinds of particle charging conditions were used in this study. First, atomized NaCl particles were passed through an aerosol neutralizer to have a Boltzmann charge distribution, and then its charge distribution was measured. In this case, the portion of uncharged particles was compared with the portion obtained from the Boltzmann charge distribution for verifying the suggested experimental method. Second, same experiment was conducted without the aerosol neutralizer to measure the charge distribution of atomized and un-neutralized NaCl particles. In the conclusion, the portion of uncharged, negatively charged and positively charged particles were 19%, 62% and 20%, respectively, for neutralized particles. The atomized particles, which was generated without the aerosol neutralizer, also had almost a zero charge state, but the standard deviation in charge distribution was larger than that of neutralized particles. The test method proposed in this study is expected to be used in various aerosol research fields because it can obtain simple information on the particle charge characteristics more easily and quickly than the existing test methods.

• 한국결정성장학회지
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• 제21권6호
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• pp.274-279
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• 2011

연소 반응기를 이용하여 고분자 물질에 함유된 할로겐 원소인 브롬과 염소를 정량하기 위한 조건을 연구하였다. 염소농도 측정의 경우, Mohr법이나 전위차 적정법을 이용한 경우가 산-염기 적정법을 이용한 경우보다 분석 데이터 간 편차가 낮게 나타났다. 또한, 연소 반응기에서 단계별로 포집한 용액에 대한 염소와 브롬 측정 결과, 두 원소 모두 증류수를 흡수액으로 사용할 때, 0.3 M NaOH 수용액을 사용할 때보다 더 높은 회수율을 보였으며, 흡수액/세척액에서의 농도가 가스상의 형태로 배출되는 농도에 비해 높은 것으로 나타났다. 한편, 브롬 함량을 측정할 때, 연소 반응기를 이용한 경우가 XRF나 연소-이온크로마토그래피를 이용한 경우에 비해 농도가 상대적으로 낮게 평가되는 것으로 나타났다.

• KSBB Journal
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• 제30권6호
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• pp.291-295
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• 2015

The limited productivity of natural shell matrix proteins has hampered the investigation of their biochemical properties and practical applications, although biominerals in nature obtained by organic-inorganic assemblies have attractive mechanical and biological properties. Here, we prepared a vector for the expression of a fusion protein of a shell matrix protein from Pinctada fucata (named as GRP_BA) with the GRGDSP residue. The fusion protein of BA-RGD was simply produced in E. coli and purified through sequential steps including the treatment with $CaCl_2$ and EDTA solution for cell membrane washing, mechanical cell disruption and the application of non-ionic surfactant of Triton X-100 for BA-RGD inclusion body washing. The production yield was approximately 60 mg/L, any other protein band was not observed in SDS-PAGE and it was estimated that above 97% endotoxin was removed compared to the endotoxin level of whole cell. This study showed this simple and easy purification approach could be applied to the purification of BA-RGD fusion protein. It is expected that the protein could be utilized for the preparation of biominerals in practical aspects.

• 한국대기환경학회지
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• 제25권1호
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• pp.46-56
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• 2009

The main purpose of this study was to investigate air quality trends of ambient aerosol with obtaining size-fractionated information. The suspended particulate matters were continuously collected on membrane filters and glass fiber filters by an 8-stage cascade impactor for 2 years (Sep. 2005 $\sim$ Sep. 2007) in Kyung Hee University-Global Campus. 8 ionic species ($Na^+$, ${NH_4}^+$, $K^+$, $Mg^{2+}$, $Ca^{2+}$, $Cl^-$, ${NO_3}^-$, and ${SO_4}^{2-}$) were analyzed by an IC after performing proper pretreatments of each sample filter. The average concentration levels of each ion were $9.24{\mu}g/m^3$ of ${SO_4}^{2-}$, $7.35{\mu}g/m^3$ of ${NO_3}^-$, $2.81{\mu}g/m^3$ of ${NH_4}^+$, $2.11{\mu}g/m^3$ of $Ca^{2+}$, $1.65{\mu}g/m^3$ of $Cl^-$, $1.87{\mu}g/m^3$ of $Na^+$, $0.80{\mu}g/m^3$ of $Mg^{2+}$, and $0.54{\mu}g/m^3$ of $K^+$, respectively. The distribution pattern of $Na^+$, $Mg^{2+}$, $Ca^{2+}$, $Cl^-$, and ${NO_3}^-$ was bi-modal and two peaks appeared in the range of $0.4{\sim}0.7{\mu}m$ and $3.3{\sim}4.7{\mu}m$, respectively. On the other hand, ${SO_4}^{2-}$, ${NH_4}^+$, and $K^+$ showed patterns of uni-modal distribution, mostly abounded in the fine mode group.

• 한국환경과학회지
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• 제20권6호
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• pp.687-700
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• 2011

A new $N_3-O_2$ pentadentate ligand, H-BHPT, was synthesized. Hydrochloric acid salts of Br-BHPT, Cl-BHPT, $CH_3O$-BHPT and $CH_3$-BHPT, having Br-, Cl-, $CH_{3-}$ and $CH_3O-$ substituents at the para position of the phenol hydroxyl group of H-BHPT were synthesized. Hydrochloric acid salts of 3OH-BHPT and 4OH-BHPT, having different position of the phenol hydroxyl group of H-BHPT were also synthesized. The synthesis of each ligand was confirmed by C. H. N. atomic analysis and $^1H$ NMR, $^{13}C$ NMR, UV-visible, and mass spectra. The calculated proton dissociation constants ($log{K_n}^H$) of the phenol hydroxyl group and secondary amine group of the synthesized $N_3-O_2$ ligands showed five steps of the proton dissociations. The order of the overall proton dissociation constants ($log{\beta}_p$) of the ligands was Br-BHPT < Cl-BHPT < H-BHPT < $CH_3O$-BHPT < $CH_3$-BHPT. The order agreed with that of Hammett substituent constants (${\delta}_p$). However, dissociation steps of 3OH-BHPT were four and that of 4OH-BHPT was three. The calculated stability constants ($logK_{ML}$) between the ligands and transition metal ions agreed with the order of $log{\beta}_p$ values of the ligands. The order of the stability constants between the transition metal ions with the synthesized ligands was Co(II) < Ni(II) < Cu(II) > Zn(II) > Cd(II) > Pb(II). The order agreed well with that of the Iriving-Williams.

• 한국환경과학회지
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• 제19권7호
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• pp.849-860
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• 2010

A new $N_3O_2$ pentadentate ligand, N,N'-Bis(2-hydroxybenzyl)-ethylenetriamine(H-BHET 3HCl) was synthesized. The hydrochloric acid salts of Br-BHET 3HCl, Cl-BHET 3HCl, $CH_3O$-BHET 3HCl and $CH_3$-BHET 3HCl containing Br-, Cl-, H-, $CH_3O-$ and $CH_3-$ groups at the para-site of the phenol group of the H-BHEP were synthesized. The structures of the ligands were confirmed by C. H. N. atomic analysis and $^1H$ NMR, $^{13}C$ NMR, UV-visible and mass spectra. The calculated stepwise protonation constants(${\logK_n}^H$) of the synthesized $N_3O_2$ ligands showed six steps of the proton dissociation. The orders of the overall protonation constants($\log{\beta}_p$) of the ligands were Br-BHET < Cl-BHET < H-BHET < $CH_3O$-BHET < $CH_3$-BHET. The orders agreed well with that of para Hammett substituent constants(${\delta}_p$). The calculated stability constants($\logK_{ML}$) between the ligands and heavy metal ions (Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Pb(II)) agreed well with the order of the overall proton dissociation constants of the ligands but they showed a reverse order in para Hammestt substituent constants(${\delta}_p$). The order of the stability constants between the heavy metal ions with the synthesized ligands were Co(II) < Ni(II) < Cu(II) > Zn(II) > Cd(II) > Pb(II).

• 한국작물학회지
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• 제62권4호
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• pp.293-303
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• 2017

벼 식물체에 규소, 질소, 칼슘을 단독 및 혼합 처리할 경우 무기이온의 흡수와 식물호르몬 $GA_1$과 JA 함량변화에 미친 결과는 아래와 같다. 1. 질소와 칼슘이온은 규소처리에 의해 흡수가 억제된 것으로 조사됐고, 마그네슘 함량은 규소, 질소, 칼슘 단독 및 혼합처리에서 무처리보다 증가하였다. 2. 식물호르몬 ABA의 함량은 모든 처리에서 무처리와 차이가 없었다. 3. 식물호르몬 $GA_1$의 함량은 질소와 규소 혼합처리에서 가장 높았고, 다음으로 질소 단독처리 규소 단독처리 순으로 높았다. 반면 칼슘 단독처리 및 칼슘과 규소 혼합처리에서 $GA_1$함량은 차이가 없었고, 이러한 결과는 규소, 질소 및 칼슘 처리 후 12시간 및 24시간에서도 동일한 양상을 보였다. 4. 규소, 질소, 칼슘 단독 및 혼합처리 후 6시간 뒤 식물호르몬 JA 함량은 모든 처리에서 무처리보다 증가하였고, 특히 규소와 질소 혼합처리에서 가장 높게 조사되었다. 그러나 처리 후 12시간과 24시간 후 조사에서는 칼슘 단독처리에서 JA 함량이 무처리와 차이가 없었고, 이외의 처리에서는 무처리보다 높았다.

• 분석과학
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• 제10권4호
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• pp.231-239
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• 1997

역상 이온쌍 고성능 액체크로마토그래피에 의해 3차 아민들과 4차 암모늄염들을 분리하고 정량하였다. 시료들은 간접분광광도법에 의해 검출하였다. 검출 시약과 이온쌍 시약으로는 염화벤질 트리메틸암모늄(BTMACl)과 도데실황산나트륨(DDSANa)을 사용하였다. 전해커패시터의 전해액 중에 포함되어 있는 이들 아민과 암모늄염의 분리 및 정량은 메탄올-물(40:60) 용액에 DDSANa를 0.010M, BTMACl을 0.004M 되게 용해시키고 염화암모늄-암모니아 완충용액(0.05M)으로 pH를 8.5되게 만든 용리액으로 Supelco LC-18이나 ${\mu}$-Bondapak phenyl 컬럼을 통하여 용리시킴으로써 가능하였다. 전해 커패시터들의 전해액을 분석하여 얻은 분석 값의 4차 암모늄염을 첨가하여 만든 커패시터는 임피던스 0.08~0.13의 성능이 우수한 커패시터가 됨도 발견함으로써 분석이 잘 이루어 졌음을 확인하였다.