• 마이크로전자및패키징학회지
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• 제28권4호
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• pp.31-39
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• 2021

본 논문에서는 FEM(유한요소법)을 사용하여 PoP (Package on Package)용 PCB를 unit(유닛)과 substrate(서브스트레이트)로 분리한 warpage 해석과 warpage에 미치는 층별 두께의 영향도 분석과 층별 두께 조건을 다구찌법에 의한 SN비(Signal-to-Noise ratio)로 분석하였다. 해석 결과에 의하면 유닛 PCB는 회로층의 영향이 대단히 높았는데 특히 외층의 영향도가 높았다. 반면에 서브스트레이트 PCB는 회로층의 영향도가 높았으나 유닛 PCB에 비해 상대적으로 낮았으며 오히려 솔더 레지스트의 영향도가 증가하였다. 따라서 유닛 PCB와 서브스트레이트 PCB를 동시에 고려하여 PoP PCB의 층별 구조는 외부와 내부 회로층은 두껍게, 윗면 솔더 레지스트는 얇게 설계하고 바닥면 솔더 레지스트의 두께를 5 ㎛와 25 ㎛ 사이의 두께를 선정하는 바람직하다.

• 한국결정성장학회지
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• 제7권4호
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• pp.648-657
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• 1997

합성원료로써 $Mg_3(PO_4)_2$와 $MgF_2$분말을 혼합한 후 백금밀폐용기를 사용하여 $1040^{\circ}C$에서 단일상의 wagnerite$(Mg_2PO_4F)$를 합성하였으며 이 결정상의 동질이상에 대하여 연구한 결과, 이미 발표된 연구 결과들과는 달리 $1255^{\circ}C$에서 단 한번의 가역적인 상전이가 관찰되었고, $1340^{\circ}C$에서 용융될 때까지 열분해 현상은 나타나지 않았으며, 이로써 2가 금속이온의 치환에 의해 여러 종류의 고용체를 합성해 낼 경우, 유약 및 플라스틱의 색상발현을 위한 안료로 사용될 수 있는 것으로 밝혀졌다. $Zn_4P_2O_8F_2$와 $Zn_3MgP_2O_8F_2$ wagnerite의 Zn 대신 2가 금속을 치환한 경우, 전반적으로 d값이 줄어들었으며 Co는 자주색, Ni은 금색, Cu는 녹색을 나타내었다. 또한 charge-coupled 치환을 시도한 결과, $A^{1+}A_3^{2+}X^{5+}X^{6+}O_8_F2$의 경우만 wagnerite가 형성되었다.

• 한국세라믹학회지
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• 제32권7호
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• pp.858-864
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• 1995

A porous glass-ceramics body was prepared in the phosphate system. The glass composition of 47.2CaO-22.2TiO2-30.6P2O5 (mol%) containing a few weight percent of ZrO2 was suitable for a mother glass of a porous glass-ceramics. The dense glass-ceramics body was made by a two-step heat treatment of the mother glass. The crystalline phases of the glass-ceramics were $\beta$-Ca3(PO4)2 and CaTi4(PO4)6. The $\beta$-Ca3(PO4)2 phase could be selectively leached out with HCl solution and thus a crystalline $\beta$-Ca3(PO4)2 skeleton was remained. The dimension and shape of the porous glass-ceramics were nearly the same as the those of the first formed glass. The specific surface area and average proe radius of the porous glass-ceramics were 19$m^2$/g and 22 nm, respectively.

• 수산해양교육연구
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• 제26권4호
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• pp.808-822
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• 2014

넙치 (Paralichthys olivaceus)로부터 elastase-like serine protease (PoElSp)를 암호화하는 cDNA를 클로닝하여 그 서열을 분석한 결과, PoElSp 유전자는 269 아미노산을 암호화하는 978염기쌍으로 구성되었다. PoElSp 유전자의 조직 특이적 발현 양상을 RT-PCR법으로 조사한 결과, 간, 비장 및 소장에서 그 발현이 크게 나타났다. lipopolysaccharide (LPS)로 인위적 세균감염을 유도한 후, 1시간째에 콩팥에서, 3시간째에는 근육에서, PoElSp 유전자의 발현이 크게 증가하였다. 또한, 이 유전자의 발현은 비장에서 LPS 주입 후 1-24시간동안 점차로 증가하였다. pro-mature PoElSp (proPoElSp)에 해당하는 cDNA를 pET32a 벡터 시스템을 이용하여 대장균에서 발현시켰다. 이 재조합 proPoElSp 단백질의 활성은 gelatin zymography 방법과 합성형광 Z-Phe-Arg-AMC의 분해법을 이용하여 측정하였다. 단백질 분해효소 활성을 위한 최적 pH는 7.5였다. 실험결과들을 종합하면, PoElSp 단백질은 면역 반응에서 중추적 역할을 하리라 판단된다.

• Applied Biological Chemistry
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• 제18권4호
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• pp.228-233
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• 1975

고추의 성장(成長)과 주요성분(主要成分)의 함량(含量)에 미치는 anion의 영항을 조사(調査)코져 배양액내(培養液內)의 N, S, P의 조성(組成)을 달리하여 재배(栽培) 실험(實驗)을 행하고 이 결과(結果)를 systematic variation method 중(中) binary iateraction방정식(方程式)에 적응시켜 이상조건(理想條件)을 추구(追求)한 결과(結果)는 다음과 같다. 1. 성장(成長) 이상(理想) 조건(條件) 중(中) 초장(草長)은 NS group에서 $75%\;NO_3^-+25%\;SO_4$, NP group에서는 $68.5%\;NO_3^-+31.5%\;PO_4^{--}$가 최적(最適) 조건(條件)이었으며 마디수에서는 $71.0%\;NO_3^-+29.0%\;SO_4$, $75.0%\;NO_3^-+25.0%\;PO_4^{---}$이였다. 2. 수확량(收穫量)은 최대(最大)로 하기 위한 이상(理想) 조건(條件)은 $77.5%\;No_3^-+22.5%\;SO_4$, $72.5%\;NO_3^-+27.5%\;PO_4$였으며, 이 중완숙과(中完熟果)에 대(對)하여서는 $77.0%\;NO_3^-+23.0%\;SO_4$, $73.5%\;NO_3^-+26.5%\;PO_4$이었다. 3. 각(各) 처리(處理) 별(別) free sugar와 capsaicin의 함량(含量)은 유의성이 없었다.

• Bulletin of the Korean Chemical Society
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• 제30권10호
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• pp.2223-2226
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• 2009

Pristine and sulfur-doped (LiFe$PO_{3.98}S_{0.03}$) lithium iron phosphates were synthesized by a sol-gel method. The XRD pattern of the prepared materials suggested an orthorhombic structure with a Pnma space group and an absence of impurities. The Li/LiFe$PO_4$ or LiFe$PO_{3.98}S_{0.03}$ cells were employed for cycling studies at various temperatures (25, 50 and $60\;{^{\circ}C}$). In all cases, the Li/LiFe$PO_{3.98}S_{0.03}$ cell showed an improved performance with a stable discharge behavior of ~155 mA$hg^{-1}$. Nevertheless, pristine LiFeP$O_4$ cells presented poor discharge behavior at elevated temperatures, especially $60\;{^{\circ}C}$.

• 상하수도학회지
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• 제22권6호
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• pp.641-646
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• 2008

In this research, recovery of high quality organics from excess activated sludge and its potential as a external carbon sources for BNR process was studied. By simultaneous treatment of alkali and ozone, TSS concentration was reduced by 32%, and RBDCOD fraction was increased by 76.2%, and major constitute of produced organic were acetic acid and propionic acid. Also, nitrogen and phosphorus were greatly solubilized. However, because acid-hydrolyzable phosphorus(AHP) was major part of solubilized phosphorus, $NH_4{^+}-N$ and $PO_4{^3}-P$ concentration were insufficient for effective formation of crystal like as MAP(Magnesium Ammonium Phosphate) and hydroxyapatite. By placing BPR reactor before alkali-ozone treatment reactor, $PO_4{^3}-P$ concentration in pretreated sludge was increased by 1.8 times, and improved potential of phosphorus recovery by crystallization. In experiment of crystallization, hydroxyapatite formation was more easily applied than MAP. By hydroxyapatite formation, $SCOD/PO_4-P$ ratio was greatly increased from 32.7 at control to 141.9 at $Ca^{2+}/PO{_4}^{3-}-P$ mole ratio of 2.4. The results based on this study indicated that the proposed system configuration has potential to reduce the excess sludge production, to recover phosphorus in usable forms as well as utilize organics as a external carbon source in BNR process.

• 한국표면공학회지
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• 제52권5호
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• pp.265-274
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• 2019

Formation behavior of PEO (Plasma Electrolytic Oxidation) films on AZ31 Mg alloy was investigated under application of 310 Hz AC as a function of $Na_3PO_4$ concentration from 0.02 M to 0.2 M. Film formation voltage and in-situ observation of arcs generated on the specimen surface were recorded with time, and surface morphologies of the PEO films were investigated using optical microscopy, confocal scanning laser microscopy and scanning electron microscopy. PEO film formation voltage decreased linearly with increasing $Na_3PO_4$ concentration which is attributed to the increase of solution pH. PEO films were grown uniformly over the entire surface in $Na_3PO_4$ solutions between 0.05 M and 0.1 M. However, non-uniform PEO films with white spots were formed in $Na_3PO_4$ solutions containing more than 0.1 M. Thickness and roughness of PEO films on AZ31 Mg alloy increased linearly with increasing $Na_3PO_4$ concentration and their increasing rates appeared to be much higher under 1 M than above 1 M. The experimental results suggest that phosphate ions can contribute to the formation of PEO films but higher $Na_3PO_4$ concentration more than 1 M results in local damages of PEO films due to repeated generation of white arcs at the same surface site of AZ31 Mg alloy.

• 방사선산업학회지
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• 제4권4호
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• pp.313-317
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• 2010

The struvite crystallization was applied to remove $NH_4{^+}$ in livestock wastewater. The ammonium ions can be very toxic to the aquatic creatures. In this experiments, the livestock wastewater from Gongju livestock wastewater treatment plant was used. The behaviors of various parameters such as pH, mole ratio of $Mg^{2+}$ : $NH_4{^+}$ : $PO{_4}^{3-}$ and reaction temperature for struvite crystallization of livestock wastewater and the effect of gamma ray irradiation were evaluated. As results, for the pH variation, the $NH_4{^+}$ removal efficiency showed the highest, 88%, at pH 9~9.25. The removal efficiency of $NH_4{^+}$, $Mg^{2+}$ and $PO{_4}^{3-}$ was showed highest when same molar ratio of $Mg^{2+}$ and $PO{_4}^{3-}$ were applied. The $NH_4{^+}$ removal efficiency showed 82% at $7^{\circ}C$, and 90% at $30^{\circ}C$ with temperature. When the wastewater was irradiated with 20 kGy of gamma ray, $NH_4{^+}$ was removed as much as 83%.

• 한국세라믹학회지
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• 제28권1호
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• pp.46-52
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• 1991

The hydroxyapatite powders were prepared by the reaction of Ca(CH3COO)2$.$H2O and H3PO4 in aqueous solution. Effect of Ca/P mole ration and pH value on the powder characteristics were investigated. For phosphoric acid was dissociated to PO43- ion above pH 10, the preparation condition of hydroxyapatite by H3PO4 solution had this value. Dried powders were agglomerated each other. The mean agglomerate particle diameter was minimum when the condition was pH 11, Ca/P=1.75 and its specific surface area was 97㎡/g. All powders had poor crystallinity and small CO2. It prevented CaCO3 from using aspirator in preparation and maturing time. In most cases, hydroxyapatite was decomposed into ${\beta}$-TCP at more than 800$^{\circ}C$, into ${\alpha}$-TCP at 1200$^{\circ}C$. However non-decomposed hydroxyapatite was remained in Ca/P=1.85.