• 한국세라믹학회지
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• 제31권9호
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• pp.1060-1068
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• 1994

Stable zirconia sol was prepared from zirconium butoxide Zr(OC4O9)4 as a precursor and ethylacetoacetate(EAcAc) or diethylene glycol(DEG) as a chelating agent under ambient agent under ambient atmosphere by Sol-Gel process. The sythesized sol was coated on 304 stainless steel substrate by dip coating, thereafter zirconia film could be obtained by heat-treatment at $600^{\circ}C$. The characteristics of coating film were determined by FT-IR, XRD, and ellipsometion peak represented Zr-O-Zr bonding of tetragonal phase was shown at 470cm-1. Crystallization of zirconia gel and film from amorphous state to tetragonal phase started at 40$0^{\circ}C$, and then transformed into monoclinic phase around $700^{\circ}C$. Zirconia film coated on 304 stainless steel substrate showed relatively low porosity of 16% when it was coated with 0.4M zirconia sol and thereafter heat-treated at 80$0^{\circ}C$ and the film was densified continuously up to 90$0^{\circ}C$. The zirconia film of 10 nm thick acted as a protective layer against oxidation up to $700^{\circ}C$.

• KSBB Journal
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• 제30권4호
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• pp.141-147
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• 2015

The convenient determination of methylsulfonylmethane (MSM) for a commercially available dietary supplement was developed using gas chromatography (GC)-flame ionization detector (FID). Chromatography was performed on a capillary column ($0.32mm\;I.D{\times}30m$, $0.25{\mu}m$) coated with dimethylpolysiloxane using diethylene glycol methyl ether as an internal standard. The performance characteristics of GC were evaluated in terms of selectivity, linearity, precision, accuracy, recovery, limit of detection (LOD) and limit of quantification (LOQ). The calibration curve was highly linear (the coefficient of determination: 0.9979) within the concentration range of $10.0{\sim}800.0{\mu}g/mL$ for MSM. The recoveries for three fortified concentrations were 96.7~97.1%, 96.6~97.3% and 96.8~97.2%, respectively. The LOD and LOQ of the method were $0.29{\mu}g/mL$ and $0.97{\mu}g/mL$, respectively. All obtained results were acceptable according to the guidelines of the Association of Official Analytical Chemists for dietary supplements. Thus, the validated analytical method using the GC-FID system is suitable for the determination of MSM in dietary supplement formulations for quality control.

• 한국군사과학기술학회지
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• 제27권3호
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• pp.428-435
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• 2024

The important factors in the design of the gun propellant are impetus, flame temperature and pressure. In this paper, we considered a nitrocellulose based propellant composition that replaced sensitive NG(Nitroglycerin) with RDX(Cyclotrimethylenetrinitramine) and DEGDN(Diethylene glycol dinitrate) which high energy and low sensitivity. Particle size and content of RDX are the two main factors that affect the burning stability of RDX-based propellants. Among them, the characteristics of the propellant according to the particle size of RDX were confirmed. The relative combustion rate(R.Q., Relative Quickness) of the propellant changed according to the RDX particle size, and internal ballistics of properties of propellant were also varied. The particle size of RDX can be confirmed as a major factor in the combustion and internal ballistics characteristics of the propellant.

• Elastomers and Composites
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• 제49권2호
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• pp.110-116
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• 2014

디에틸렌글리콜(DEG, 분자량 106.1)과 폴리에틸렌글리콜600(PEG600, 분자량 603.3)을 아디프산(AA)과 반응시켜 폴리(옥시에텔렌-아디페이트)-디올 공중합체를 합성하는 에스테르 반응에서, stannous 2-ethylhexanoate 촉매의 농도가 반응속도에 주는 영향을 연구하였다. 반응에 사용되는 AA의 카르복실기 당량 대비 폴리올의 히드록실기의 당량비를 2로 맞추어서 합성된 폴리(에테르-에스테르)의 양말단이 OH기로 결합되도록 유도하였다. 반응은 $170^{\circ}C$에서 촉매농도 0.15 ~ 2.0 wt.%로 수행하였다. 합성된 폴리(옥시에텔렌-아디페이트)-디올의 수평균 중합도는 약 3 이었다. DEG와 AA로부터 폴리(옥시에텔렌-아디페이트)-디올이 합성되는 반응의 겉보기속도상수($k_{app}$) 값은 촉매의 농도가 커짐에 따라 $k_{app}=0.88[C_{cat}]$의 관계를 가지며 선형적으로 증가한 반면에, PEG600과 AA의 에스테르 반응의 $k_{app}$ 값은 촉매농도와 $k_{app}=0.123[C_{cat}]^{0.55}$의 관계로 증가하며 포화되는 경향을 나타내었다. DEG와 AA사이의 합성반응에서도 반응속도의 촉매농도에 대한 의존성이 비선형 관계로 바뀌는 것이 예상되며, 이때의 촉매농도는 [$Sn(C_8H_{15}O_2)_2$ mole/mole of AA mole] 값이 0.066([$C_{cat}$]=0.22M)에 가까운 영역에 있을 것으로 추정된다.

• 한국응용과학기술학회지
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• 제23권3호
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• pp.207-214
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• 2006

$Y_{2-x}Gd_xO_3:Eu$, phosphors for plasma display panel(PDP), were prepared by Pechini method which use yttriun chloride, gadolinium chloride, and europium oxide as starting materials. This method is a different way to the synthesis of europium(Eu)-doped phosphors, and it consists of the formation of a polymeric resin obtained by polyesterification between metal chelate compounds and a polyfunctional alcohol. This needs lower temperature than solid-state synthetic method. The prepared $Y_{2-x}Gd_xO_3:Eu$ phosphor particles had spherical shape and coherence. The luminescence intensity of $Y_{2-x}Gd_xO_3:Eu$ phosphor particles increased according to the increase of gadolinium(Gd) content(to 0.8mol%), and $Y_{1.2}Gd_{0.8}O_3:Eu$ phosphors had the highest luminescence intensity under vacuum ultra violet(VUV) excitation. The optimum concentration of Eu in the phosphor and optimum calcination temperature was 3wt% and $1100^{\circ}C$. The prepared phosphors were consist of particle, and its size was between 100nm and 150nm. Among the different polyfunctional alcohols, diethylene glycol(DEG) improved the luminescence intensities of phosphors more than other additives. The Pechini method proved that it is demonstrated to be suitable for the synthesis of phosphors used in PDP.

• 마이크로전자및패키징학회지
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• 제18권4호
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• pp.27-32
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• 2011

Tin(II) acetate와 tin(II) chloride의 주석 precursor를 사용하여 상온에서의 강제 환원 반응으로 주석 나노 입자를 합성시켰다. 0.015 g의 동일한 PVP 양을 첨가한 조건에서 PVP의 분자량이 클수록 비정상적으로 큰 입자들의 생성율이 증가되어 입도 범위가 매우 넓은 주석 나노 입자들이 생성됨을 확인할 수 있었다. 합성된 주석 나노 입자를 함유하는 DEG 용액의 DSC 분석 결과 1차 가열에서는 35 nm 미만 특정 크기 입자들의 수가 충분한 경우에서 DEG의 증발 흡열피크 외에도 특정 크기 입자들의 융점 강하 흡열 피크가 구분되게 검출되었다. 1차 DSC 측정 중 용융된 주석 나노 입자들은 서로 접촉하며 뭉쳐지는 현상이 발생하므로 2차 가열시에는 벌크 주석의 용융 피크에 해당하는 $232^{\circ}C$ 흡열 피크만이 관찰되었다.

• 한국의류학회지
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• 제9권2호
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• pp.75-84
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• 1985

In order to improve dyeing and finishing technology of thin cloth of microfiber(super-fine fiber), the degrees of deep dyeing method, the light fastness, and the washing fastness were investiagted. 1. The thin cloth made of microfiber, $0.15^d\~0.2^d$, was conjugated type and the dyeing degree was lower at 5 to $10\%$ than that of cloth made of common fiber. The cloth of excellent dyeing fastness, light fastness, was developed by increasing the concentration of dye of high quality up to $5\~10\%$. 2. Because refractory rate of microfiber of $0.2^d$ was lower than that of $0.01^d$, the surface refractory rate of $0.2^d$ was lower than that of $0.01^d$ fiber. Therefore the surface of micro-fiber, $0.2^d$, was more rougher than that of $0.01^d$ and it belongs to separate type. 3. The higher degree of dyeing was increased by using dye of microparticle. Also the degree of textile printing was increased by adding urea solution ($20\%$) and glycerine diethylene glycol. 4. Light fastness was very excellent, marked 5 grade. However, washing fastness was 2$\~$3 grade. After dyeing, we could improve to 4 grade, through hot water washing including some organic chlorine solvent. 5. Super microfiber of $0.01^d$ will not be dyed by present dye and dyeing equipment, because right reflection light rate(white light) of fiber surface was too high and the more refraction rate higher the more surface refraction rate will be increased.

• 멤브레인
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• 제24권4호
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• pp.292-300
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• 2014

내염소성을 갖는 염제거공정용 술폰화 폴리아릴렌 에테르 술폰 랜덤 공중합체(SPAES) thin film composite (TFC)막이 모노글라임 용매를 이용하여 제조되었다. 모노글라임은 선택층인 SPAES만을 용해시키며, 다공성 폴리술폰(예 : Udel$^{(R)}$)층에 대해 비용해성을 지녀, TFC 제조를 위한 선택적 용매로 사용될 수 있다. 또한 개미산이나 디에틸글리콜과는 달리, 환경적으로 무해하며, 매우 낮은 끊는점을 지녔다는 점이 또 다른 장점이 될 수 있다. 다공성 Udel$^{(R)}$ 지지체 위에 코팅시, 코팅용액이 기공구조에 침투하여 유수량을 감소시키는 기공투과현상이 발생하는데, 이를 최소화하기 위해 지지체를 이소프로필알콜과 글리세린 혼합액에서 전처리 후에, 코팅-건조 공정을 통해 결함이 없는 SPAES TFC로 제조된다. 또한, SPAES 선택층의 술폰화도, 고정이온의 염상태 및 물리-화학적 가교효과를 SPAES TFC막을 통한 투과거동과 관련하여 관찰하였다.

• 청정기술
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• 제22권4호
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• pp.225-231
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• 2016

본 연구에서는 2중 효용 증발관을 이용하여 21.0 wt%의 NaCl 수용액에서 고형물의 NaCl을 $1,524.58kg\;h^{-1}$만큼 석출시키는 공정에 대해서 증기 재압축을 활용하여 스팀 소모량을 $3,139kg\;h^{-1}$에서 $496kg\;h^{-1}$로 줄이는 공정에 대한 전산모사 및 최적화 작업을 수행하였다. 디에틸렌 글리콜(diethylene glycol)을 포함한 NaCl 수용액을 농축시키기 위한 증발농축 공정의 전산모사를 위해서는 AspenTech사의 Aspen Plus V8.8을 활용하였으며, 중간에 냉각기를 가지는 증기 재압축 공정의 전산모사를 위해서는 Schneider Electric사의 PRO/II with PROVISION V9.4를 이용하였다. 증기 재압축 공정에 대해서는 1기의 압축기를 사용한 공정과 중간에 냉각기를 가지는 2단 압축 공정을 상호 비교하였다.

• 한국재료학회지
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• 제21권6호
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• pp.327-333
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• 2011

Nanostructured cobalt materials have recently attracted considerable attention due to their potential applications in high-density data storage, magnetic separation and heterogeneous catalysts. The size as well as the morphology at the nano scale strongly influences the physical and chemical properties of cobalt nano materials. In this study, cobalt nano particles synthesized by a a polyol process, which is a liquid-phase reduction method, were investigated. Cobalt hydroxide ($Co(OH)_2$), as an intermediate reaction product, was synthesized by the reaction between cobalt sulphate heptahydrate ($CoSO_4{\cdot}7H_2O$) used as a precursor and sodium hydroxide (NaOH) dissolved in DI water. As-synthesized $Co(OH)_2$ was washed and filtered several times with DI water, because intermediate reaction products had not only $Co(OH)_2$ but also sodium sulphate ($Na_2SO_4$), as an impurity. Then the cobalt powder was synthesized by diethylene glycol (DEG), as a reduction agent, with various temperatures and times. Polyvinylpyrrolidone (PVP), as a capping agent, was also added to control agglomeration and dispersion of the cobalt nano particles. The optimized synthesis condition was achieved at $220^{\circ}C$ for 4 hours with 0.6 of the PVP/$Co(OH)_2$ molar ratio. Consequently, it was confirmed that the synthesized nano sized cobalt particles had a face centered cubic (fcc) structure and with a size range of 100-200 nm.