• Bulletin of the Korean Chemical Society
• /
• 제29권9호
• /
• pp.1827-1830
• /
• 2008

• 한국방사성폐기물학회:학술대회논문집
• /
• 한국방사성폐기물학회 2017년도 추계학술논문요약집
• /
• pp.353-354
• /
• 2017

• 한국세라믹학회지
• /
• 제16권3호
• /
• pp.155-163
• /
• 1979

This study was to explore the characteristics of 6 mole% CaO stabilized $ZrO_2$ prepared by wet chemical methods. The results of the experiments were as follows: 1. The powder calcined at 1000$^{\circ}$-110$0^{\circ}C$ was partly agglomerated. The morphology of agglomerate was spherical of 0.5-1$\mu{m}$ in size for Hot Petroleum Drying Method, chain-like of 1-2$\mu{m}$ for Freeze Drying Method, and irreqular of 2-3$\mu{m}$ for Coprecipitation Method. 2. Optimum calcining conditions for powder prepared by wet chemical methods were found: 110$0^{\circ}C$, 2h in air for Hot Petroleum Drying Method and Freeze Drying Method, and 100$0^{\circ}C$, 2h in air for Coprecipitation Method. 3. When specimen was calcined at 1000$^{\circ}$-110$0^{\circ}C$ in air for 2h and then sintered at 1$600^{\circ}C$ in air for 4h, the specimens prepared by wet chemical methods showed a high sintered density (94% of theoretical density) and a low open porosity (<0.8%); however, the sintered density of the specimen prepared by Oxide Wet Mixing Method was 90%. 4. The amount of cubic phase of sintered body prepared by wet chemical methods was observed to be higher than the one prepared by Oxide Wet Mixing Method. 5. It was found that Hot petroleum Drying Method, Freeze Drying Method and Coprecipitation Method were nearly the same in respect of the results of stabilization grade and sintered density of CaO-stabilized $ZrO_2$.

• Applied Biological Chemistry
• /
• 제26권4호
• /
• pp.199-204
• /
• 1983

대두(大豆) 단백질에의 함유황(含硫黃) 아미노산 강화원(强化源)으로서 유청(乳淸)단백질을 사용하기 위한 목적으로 유청과 두유(豆乳)의 혼합물로부터 응고물을 만들고 유청(乳淸) 및 대두(大豆) 단백질의 공동침전 최적조건과 특성을 조사하였다. 유청과 두유는 1:1 부피비로 혼합한 다음 응고제인 $CaCl_2$의 농도를 $0.005{\sim}0.5M$, pH$1.5{\sim}8.0$, 온도를 $60{\sim}100^{\circ}C$로 조정하여 응고시키고 이 때 얻어지는 커드 여액(濾液)의 흡광도가 가장 낮은 조건을 결정하였다. 공동침전 최적조건은 여액의 흡광도가 낮고 그 때 얻어지는 커드의 조직감이 좋은 때로 하였다. 공동침전 최적조건은 $CaCl_2$농도 0.0125M, pH$6.5{\sim}7.5$, 온도 $70{\sim}80^{\circ}C$로 나타났다.

• Transactions on Electrical and Electronic Materials
• /
• 제18권1호
• /
• pp.46-50
• /
• 2017

The Zn1-xMnxO ($0.00{\leq}x{\leq}0.06$) samples have been synthesized in the form of powder by the coprecipitation method at low temperature using $Zn(CH_3COO)_2$. $2H_2O$ and $Mn(CH_3COO)_2$. $4H_2O$ powders, as well as HCl and $NH_4OH$ solutions as starting materials. Characterization was conducted using XRD, TEM, XRF, FTIR and VSM. The result shows that the $Zn_{(1-x)}Mn_xO$ ($0.00{\leq}x{\leq}0.06$) nanoparticles have the wurtzite phase with a hexagonal structure and particle sizes ranging from 17.48 to 118.83 nm. In a qualitative analysis of XRF, the peaks that confirm the existence of the manganese element in Mn-doped ZnO samples were observed. Meanwhile, FTIR test result shows that there are peaks at around $500cm^{-1}$ and $400cm^{-1}$ in the FTIR spectra for Mn doped ZnO samples which clearly reveal the existence of the (Zn, Mn)-O strain mode. The (Zn, Mn)-O absorption peak positions have shifted to a lower wave number with increasing Mn doping content. The peak intensity is also lower if compared to that of the ZnO sample without doping. From the VSM test, it is shown that $Zn_{(1-x)}Mn_xO$ ($0.00{\leq}x{\leq}0.06$) nanoparticles are all paramagnetic having monotonically increased susceptibility as increasing Mn content.

• 공업화학
• /
• 제27권6호
• /
• pp.555-564
• /
• 2016

대기 중 이산화탄소의 재활용 기술과 재생에너지에 의한 물 분해 기술의 접목이 최근 가능해지면서 메탄올은 많은 관심을 받고 있다. 경제성이 유리하도록 메탄올 경제를 실현하기 위해서는 고활성 메탄올 합성 촉매를 제조하여야 하며, 이를 위해서는 논리적인 접근법이 필요하다. 공침법을 통해 제조하는 Cu/ZnO 기반의 촉매는 침전, 숙성, 여과, 세척, 건조, 소성, 환원 등의 복잡한 단계로 제조되며, 100년의 역사를 가지고 있음에도 불구하고 최근에야 침전 화학과 촉매 나노구조에 대한 기초적인 이해가 이루어지고 있다. 이에 본 고에서는 단계별로 합성 변수가 침전, 소성, 환원상태 물질의 물성에 미치는 영향에 대한 최근 결과들을 리뷰하고, 화학적 기억 효과라고 부르는 이들 물성들과 최종 촉매의 활성 사이의 관련성을 논의하였다. 제조 변수별 설명은 메탄올 합성을 위한 Cu/ZnO 기반 고활성 촉매를 제조하는 방법에 초점이 맞추어져 있다. 논의된 합성 전략은 공침법을 기반으로 하는 타 금속 또는 금속 산화물 담지 촉매의 제조에 활용 가능할 것으로 판단된다.

• 대한화학회지
• /
• 제62권2호
• /
• pp.118-123
• /
• 2018

The hexagonal tungsten bronze $Cs_xWO_3$ nanoparticle was synthesized by a chemical coprecipitation method of ammonium tungstate and $Cs_2CO_3$ in acidic condition. This synthetic method for cesium tungsten bronze is reported for the first time as far as we know. The synthesized $Cs_xWO_3$ as precipitated showed a weak crystallinity of hexagonal unit cell with a crystallite size of about 4 nm without annealing. When the synthesized $Cs_xWO_3$ was annealed in $N_2$ atmosphere, the crystallinity and crystallite size systematically increased maintaining the typical hexagonal tungsten bronze structure as the annealing temperature increased. The analyzed Cs content in the bronze was about 0.3 vs W, which is very close to the theoretical maximum value, 1/3 in cesium tungsten bronze. According to XPS analysis, the reduced tungsten ions existed as both the forms of $W^{5+}$ and $W^{4+}$ and the contents systematically increased as the annealing temperature increased up to $800^{\circ}C$. The $Cs_xWO_3$ thin films on PET substrate were also prepared by a wet-coating method using the ball-milled solution of the annealed $Cs_xWO_3$ nanoparticles at various temperatures. The near-infrared shielding property of these thin films increased systematically as the annealing temperature increased up to $800^{\circ}C$ as expected with the increased contents of reduced tungsten ions.

• 한국세라믹학회지
• /
• 제38권5호
• /
• pp.401-404
• /
• 2001

Barium ferrite powders were synthesized by the coprecipitation method using iron-pickling waste acid (IPWA) and BaCl$_2$$.$2H$_2$O as raw materials. Fe$\^$2+/ ions in the IPWA, which contains both Fe$\^$2+/ and Fe$\^$3+/ ions, were oxidized into Fe$\^$3+/ ions using H$_2$O$_2$. Proper amount of BaCl$_2$$.$2H$_2$O was dissolved into the oxidized IPWA. Using NaOH, Ba$\^$2+/ and Fe$\^$3+/ ions were coprecipitated as Ba(OH)$_2$and Fe(OH)$_3$. The coprecipitated Ba(OH)$_2$and Fe(OH)$_3$were washed and dried. Barium ferrite powders were obtained by calcining the dried Ba(OH)$_2$and Fe(OH)$_3$mixture from 400$\^{C}$ to 1000$\^{C}$ with a 100$\^{C}$ interval. Barium ferrite powders were characterized by X-ray diffraction, SEM, and VSM. It was found that barium ferrite powders could be synthesized at around 630$\^{C}$. The synthesized barium ferrite powders showed hexagonal plate shapes with a fairly uniform size. The barium ferrite powder calcined at 900$\^{C}$ showed good magnetic properties, saturation magnetization of 67emu/g and maximum coercivity of 5000 Oe.

• 자원리싸이클링
• /
• 제17권1호
• /
• pp.66-72
• /
• 2008

폐알칼리망간전지로부터 침출과 공침반응을 이용하여 Mn-Zn ferrite 분말을 제조하기 위한 기초실험을 수행하였다. 100g/L 광액 농도 3.0M $H_2SO_4$, $60^{\circ}C$ 및 교반속도 200 rpm의 조건에서 과산화수소 30ml를 첨가하여 얻어진 아연과 망간의 침출율은 각각 97.9%, 93.9% 이상이었으며, 침출용액을 가지고 반응시간, 반응온도, $O_2$ 가스량을 조절하며 공침반응을 진행하였다. 공침반응 결과 pH 12, $80^{\circ}C$, $O_2$ 1.3L/min, 교반속도 400 rpm의 조건에서 Mn-Zn ferrite를 저온 합성할 수 있었다. 합성된 Mn-Zn ferrite분말은 $0.143{\mu}m$의 구형 ferrite로서 80 emu/g의 포화자화값을 가지고 있었다.

• 한국재료학회지
• /
• 제32권4호
• /
• pp.216-222
• /
• 2022

The capacity of high nickel Li(Ni_xCo_yMn_1-x-y)O₂ (NCM, x ≥ 0.8) cathodes is known to rapidly decline, a serious problem that needs to be solved in a timely manner. It was reported that cathode materials with the {010} plane exposed toward the outside, i.e., a radial structure, can provide facile Li⁺ diffusion paths and stress buffer during repeated cycles. In addition, cathodes with a core-shell composition gradient are of great interest. For example, a stable surface structure can be achieved using relatively low nickel content on the surface. In this study, precursors of the high-nickel NCM were synthesized by coprecipitation in ambient atmosphere. Then, a transition metal solution for coprecipitation was replaced with a low nickel content and the coprecipitation reaction proceeded for the desired time. The electrochemical analysis of the core-shell cathode showed a capacity retention of 94 % after 100 cycles, compared to the initial discharge capacity of 184.74 mA h/g. The rate capability test also confirmed that the core-shell cathode had enhanced kinetics during charging and discharging at 1 A/g.