• 제목/요약/키워드: $H_2O$ precipitation

검색결과 502건 처리시간 0.03초

니켈 도금액의 붕산분석에 관한 연구 (Theoretical Study of Boric Acid Determination In Nickel Plating Solution)

  • 염희택
    • 한국표면공학회지
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    • 제4권1호
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    • pp.5-15
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    • 1971
  • "Rapid Determination of Boric Acid in Nickel Plating Solution" by the addition of Na$_2$C$_2$O$_4$ and thus preventing the precipitation of i(OH)$_2$ during titiration , has previously been reported. In this paper, the exact amount of glycerine and the complexing possibility of oxalate with nickel has been determined by measn of conductivity titrations. This experimental work has been supported by the mathematical application of the Debye-Huckel and mass action equitions as well as statistical analysis. The results were ; (1) Fro determining boric acid in nickel plating solution, 20 ml of 400ml/ι glycerine was sufficient, since 97% of the H$_3$BO$_3$ was dissoicated by this addition. (2) In the absence of Na$_2$C$_2$O$_4$ the continious precipitation of Ni(OH)$_2$ during titration with NaOH even past end -point for boric acid determination resulted in considerable anlaytical error. (3) In the presence of Na$_2$C$_2$O$_4$ during titration , Ni++ combined with C$_2$O$_4$-to form NiC$_2$O$_4$. The solution with this precititate of very fine, colloidal , trantsparent particles, remained quite clear for approximately 2 hours. Therefore it was shown that the presence of Na$_2$C$_2$O$_4$ prevents the formation of gross Ni(OH)$_2$ precititation by forming NiC$_2$O$_4$ instead of a complex salt with Ni++ , which did not interfere with the visible determination of the end point for boric acid with NaOH titation. This observous may be interpreted in the light of the previously published solubility ratio for NiC$_2$O$_4$ and Ni(OH)$_2$, 0.3mg/100g H$_2$O(25$^{\circ}C$), respectively. Precipitation of the less soluble , albeit transparent salt, NiC$_2$O$_4$ precluded therefore the precipitation of the Ni(OH)$_2$ salt.

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소다배소 처리된 탈질 폐촉매로부터 황산침출과 가수분해 침전반응에 의한 TiO2의 회수 (Titanium Dioxide Recovery from Soda-roasted Spent SCR Catalysts through Sulphuric Acid Leaching and Hydrolysis Precipitation)

  • 김승현;친빅하;이재령
    • 자원리싸이클링
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    • 제29권5호
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    • pp.48-54
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    • 2020
  • 소다배소 처리한 탈질폐촉매의 수침출 잔사로부터 TiO2 회수를 위하여 황산침출과 가수분해 반응을 실시하였다. Ti 성분의 황산침출은 70 ℃, 3 시간, 교반속도 500 rpm, 슬러리 농도 100 g/L로 고정하여 실시하였고, 황산농도는 4~8 M로 변화시키며 진행하였다. 침출액으로부터 Ti 성분의 침전회수는 가수분해반응을 이용하였으며, 실험조건은 100 ℃, 반응시간 2 시간으로 고정하였고, Ti 성분의 침전율은 침출액과 증류수의 혼합비와 침전반응 Seed 혼입유무에 따라 비교하였다. Ti의 침출율은 6 M에서 최대 95.2 %까지 도달 후 점차 감소하는 경향을 나타내었고, Si의 침출율은 황산농도 증가에 반비례하여 급격히 감소하여 91.7 %에서 8 M 조건에서는 3.0 %까지 억제되었다. 침출액을 이용한 가수분해는 부성분인 Si의 함량이 가장 낮은 8 M 침출액을 이용하여 진행하였다. 침출액의 혼합비에 의한 Ti의 침전회수율은 반응시간에 비례하였고 혼합비에 반비례하였다. 또한, 침전반응의 가속화를 위해 TiO2(#325~#400 mesh, 0.2 g) seed를 첨가하였을 경우에 모든 혼합조건에서 침전회수율이 상승하였으며, 혼합비(침출액:증류수) 1:9~3:7 구간에서 98.8~99.8 %의 침전율이 달성되었다. 회수된 TiO2의 순도는 침출액 혼합비 1:9~3:7 구간에서 혼합비가 낮을수록 증가하여 최대 99.46 %까지 상승함을 확인하였다.

Effects of pH on Preparation of Au-Coated $TiO_2$ Nanoparticles by Deposition-Precipitation Method

  • Nguyen, Dung The;Kim, Dong-Joo;Kim, Kyo-Seon
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2009년도 춘계학술대회 논문집
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    • pp.150-150
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    • 2009
  • We prepared the Au-coated $TiO_2$ (Au/$TiO_2$) nanoparticles by deposition-precipitation (DP) method with and without bases (urea or NaOH) and investigated the effects of pH on the preparation of Au/$TiO_2$ nanoparticles for various kinds of bases. For the DP method without bases, the Au nanoparticles in the diameter of about 50 nm were generated in the solution by the reduction reaction with trisodium citrate and they did not deposit on the surface of $TiO_2$. For the DP method with bases, Au precursors deposited on the surface of $TiO_2$ and then reduced to the Au nanoparticles in the diameter of 4-5 nm on the surface of $TiO_2$ by the reaction with trisodium citrate.

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江華地域 降水의 汚染度 評價에 關한 硏究 (A Study on the Assessment of Pollution Level of Precipitation at Kangwha, 1992)

  • 강공언;강병욱;김희강
    • 한국대기환경학회지
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    • 제11권1호
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    • pp.57-68
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    • 1995
  • Precipitation samples were collected by a wet-only automatic acid precipitation sampler at Kangwha island on the western coast in Korea, through January until December 1992. pH, electric conductivity and the concentrations of major water-soluble ion components such as N $H_{4}$$^{+}$, $Ca^{2+}$, $K^{+}$, $Mg^{2+}$, N $a^{+}$, N $O_{3}$$^{[-10]}$ , S $O_{4}$$^{2-}$ and C $l^{[-10]}$ were measured. From the result of checking the validity for assesment of pollution level of precipitation samples by pH using correlation analysis between pH and major components, and t-test of chemical composition between acid rain and non-acid rain, pH proved to be not satisfactory for its pillution level. A more comprehensive method is therefore required. In order to estimate the monthly analytical result of chemical composition of precipitation samples comprehensively, a cluster analysis was used among the various multivariate statistical analysis. As a result of making a cluster analysis for separating the monthly precipitation samples into homogeneous patterns by setting the concentrations of nine major water-soluble ion components as a variable, three homogeneous patterns were obtained. The first pattern was a group of months having average ion concentrations, the second a guoup of months having low ion concentration, and the third a group of months having high ion concentrations. Thus, it was indicated that the pollution level of precipitation was higher on February and lower on May, June, August and September than the other months. As a result, this analysis method could be estimated the chemical coposition of precipitation regionally as well as monthly.monthly.

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일산화탄소 제거를 위한 니켈 담지 흡착제 제조 (Nickel Supported Adsorbent for Removing Carbon Monoxide)

  • 손정화;김영호;윤성훈;박용기;이철위
    • Korean Chemical Engineering Research
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    • 제46권5호
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    • pp.868-874
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    • 2008
  • 실리카, 알루미늄 실리케이트, 감마 알루미나 담체에 $Ni(NO_3)_2{\cdot}6H_2O$$Ni(CH_3COO)_2{\cdot}4H_2O$를 원료로 침전제인 요소와 시트르산을 사용하여 $90^{\circ}C$에서 공침법을 사용하여 흡착제를 제조하였으며 이를 환원시켜 일산화탄소 제거 실험을 수행하였다. 흡착제는 EDS, TPR, XRD 분석을 실시하여 이를 근거로 흡착제의 성능을 해석하였다. 침전제의 종류, 니켈 금속의 담지량, 담체, 니켈 금속의 염, 수소 환원 조건을 변화시켜 최적의 흡착 성능을 보이는 흡착제를 사용하여 실험을 수행하였다. 침전제인 요소에 $Ni(NO_3)_2{\cdot}6H_2O$를 사용하여 실리카 담체에 니켈 54.8 wt%를 담지하여 제조한 흡착제를 $500^{\circ}C$에서 3시간 수소 환원 전처리 후 흡착 실험을 하였을 때 가장 효과적으로 일산화탄소를 제거함을 확인하였다.

침전연소법에 의한 $Li_2$$ZrO_3$ 분말 합성 (Synthesis of $Li_2$$ZrO_3$ Powder by a Precipitation-Combustion Process)

  • 박지연;정층환;오석진;김영석;국일현
    • 한국세라믹학회지
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    • 제35권5호
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    • pp.451-457
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    • 1998
  • $Li_2$$ZrO_3$ powder which is one of the candidates of breeding materials for the fusion reactor was syn-thesized by a precipitation-combustion process. Although precipitates from the reaction between zirconium nitrate and citric acid were existed in a precursor solution. $Li_2$$ZrO_3$ could easily be obtained by using the mixed fuel of urea and citric acid in stoichiometric composition. The phases of as-synthesized powder con-sisted of $Li_2$$ZrO_3$ and small amounts of $Li_6$$Zr_2O_3$ and $Li_2$$ZrO_3$ The latter phases disappeared after the cal-cination at $1100^{\circ}C$ for 2 h. The primary particle size and the specific surface area of as-synthesized powders were smaller than 20nm and 10-14 $M^2$/g, respectively. The primary particle size of the precipitation-combustion synthesized powders was affected by the size of precipitates present in a precursor solution.

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Photocatalytic Degradation of Oxytetracycline Using Co-precipitation Method Prepared Fe2O3/TiO2 Nanocomposite

  • Jia, Yuefa;Liu, Chunli;Li, Rong
    • Journal of Magnetics
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    • 제21권1호
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    • pp.46-50
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    • 2016
  • $Fe_2O_3/TiO_2$ nanocomposite were successfully synthesized by co-precipitation method using $Fe(NO_3)_3{\cdot}9H_2O$ and $Ti(SO_4)_2$ as raw materials. Structural and textural features of the mixed oxide samples were characterized by X-ray diffractometer, field emission scanning electron microscopy and energy-dispersive X-ray. The effects of initial concentration of oxytetracycline (OTC), different competitive ions and organics on the photocatalytic degradation rate of OTC by the $Fe_2O_3/TiO_2$ nanocomposite were analyzed under UV and visible light irradiation. The results indicate that the optimized initial concentration of OTC was 50 mg/L to achieve the best photocatalytic efficiency. $Cu^{2+}$, $NH_4{^+}$, $C_3H_8O$ and EDTA in the aqueous suspension were found to suppress the degradation rate of OTC, whereas the effect of $NO_3{^-}$ and $H_2C_2O_4$ can be ignored.

Studies on Pollution Characteristics and Sources of Precipitation in Jeiu Island

  • Kang, Chang-Hee;Kim, Won-Hyung
    • Journal of Korean Society for Atmospheric Environment
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    • 제18권E4호
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    • pp.191-201
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    • 2002
  • The pH, electric conductivity. and the major ionic components were analyzed for the precipitation samples collected at 1100 Site of Mt. Halla and Jeju city. The quality of analytical data was verified by the comparison of ion balances, conductivities and acid fractions, all of which correlation coefficients were over 0.952. The ionic strengths lower than 10$^{-4}$ M were found in 57 and 28% at 1100 Site and Jeju city respectively. The precipitation in Jeju city was influenced more by the oceanic effect than those in 1100 Site. The acidification of precipitation was caused mostly by S $O_4$$^{2-}$and N $O_3$$^{[-10]}$ in both areas, and the organic acids have contributed to the acidity with only 7~8%. The neutralization factors by N $H_3$ were about 44 and 47% at the 1100 site and the Jeju city, respectively, whereas those by CaC $O_3$were 21 and 24%, and the free acidity were about 38 and 28% at two sites. From the investigation of seawater and soil enrichment factors, the S $O_4$$^{2-}$, N $O_3$$^{[-10]}$ and N $E_4$$^{+}$ were immigrated by other sources rather than from the seawater or soil origins. but not in the case of $Mg^{2+}$, C $l^{[-10]}$ , N $a^{+}$, and $K^{+}$. Factor analysis has shown that the precipitation at the 1100 site had been influenced mostly by anthropogenic sources, followed by soil and sea-water sources. On the other hand, the precipitation at the Jeju city was mainly influenced by oceanic sources, followed by anthropogenic and soil sources.urces.

TiOCl2 수용액의 균일침전반응에 의한 나노크기의 브루카이트상 TiO2 분말제조 (Synthesis of Nanosized Brookite-type Titanium Dioxide Powder from aqueous TiOCl2 Solution by homogeneous Precipitation Reaction)

  • 이정훈;양영석
    • 한국재료학회지
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    • 제12권12호
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    • pp.947-954
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    • 2002
  • HCl concentration and reaction time are the decisive factors in determining the structure of precipitates in the process of synthesis of $TiO_2$ particles from aqueous $TiOCl_2$ solution by precipitation and the volumetric proportion of brookite phase in $TiO_2$ particles can be controlled by these two factors. As reaction rate increases with increase of reaction temperature, the reaction time, at which maximum volumetric proportion of brookite phase in $TiO_2$ particles was obtained, was reduced. The brookite was transformed directly to rutile phase with only increase of reaction time. And precipitation was delayed with increase of HCl concentration because the amount of $H_2$O, which is necessary source of oxygen for conversion of $Ti^{+4}$ to $TiO_2$, was relatively reduced with increase of that. Brookite in the mixture phase powder was finally transformed to rutile phase via anatase through heat-treatment.

수산화물과 옥살산염의 열분해에 의한 $SnO_2$미분말의 합성 ($SnO_2$ Powder Preparation from Hydroxide and Oxalate and its Characterization)

  • 이종흔;박순자
    • 한국세라믹학회지
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    • 제27권2호
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    • pp.274-282
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    • 1990
  • SnO2 powder was prepared by hydroxide method and oxalate method. In hydroxide method, the pH dependence of powder characteristics was investigated by using buffer solution. As increasing the pH of solution, SnO2 powder size was decreased because nucleation rate was inctreased by more supersaturation of solution. Also, we found that the powder by our method has larger specific surface area in comaprison with other method. And the degree of agglomeration of precipitate with the change of precipitation temperature was investigated in oxalate method. The SnC2O4 was angular shape precipitate, and the size of the SnC2O4 was increased with the increase of precipitation temperature in methanol solvent.

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