• 제목/요약/키워드: 염소화 반응

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Effect of Reacting Gas Injection Rate and Reductant Quantity on Preparation of Uranium Tetrachloride in Chlorination of Uranium Dioxide (이산화우라늄의 염소화반응에서 반응가수 주입량과 환원제의 양이 사염화우라늄 제조에 미치는 영향)

  • Yang, Yeong-Seok
    • Korean Journal of Materials Research
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    • v.6 no.9
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    • pp.919-924
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    • 1996
  • 사염화우라늄을 제조하기 위한 가장 효율적인 반응계는 이산화우라늄, 염소가스와 탄소분말이다. 여러 가지 실험변수 가운데 이산화우라늄의 염소화반응에 사용된 염소가스 주입량과 탄소의 양이 사염화우라늄 제조에 미치는 영향에 관하여 연구하였다. 각각의 실험변수들에 대한 전화율과 휘발률 계산을 통해 효율적인 반응을 위한 적정 염소가스 주입량과 탄소의 양을 구하였고, 이산화우라늄의 증가함에 따라 직접접촉에 의한 기체-고체반응에서는 전화율과 휘발률은 증가했으나 이후 과량을 첨가함에 따라 감소하였고, 용융염내의 기체-액체반응에서는 전화율의 미미한 증가와 휘발률의 감소를 확인하였가. 염소주입량이 증가함에 따라 전화율과 휘발률이 증가했으며, 과량의 염소가수 주입시 고이온가 염화물의 생성량이 증가하였다.

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Selective Chlorination of Iron from Titaniferrous Magnetite in a Fluidized Bed Reactor (유동층 반응기에서 함티탄자철광의 선택염소화 반응)

  • Lee, Sang-Soon;Lee, Chul-Tae
    • Applied Chemistry for Engineering
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    • v.3 no.3
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    • pp.451-463
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    • 1992
  • A selective chlorination of titaniferrous magnetite in a fluidized bed reactor was investigated to find the optimum condition for selective removal of Fe component from low grade titaniferrours magnetite ore and to produce a rutile substitute from titaniferrous magnetite ore. The optimum chlorination condition was determined to be a temperaure of $950^{\circ}C$, 2hr of reaction time, reducting agent(petroleum coke) to titaniferrous magnetite weight ratio of 0.12, and $Cl_2$ gas velocity of 5cm/sec. Under the above mentioned condition, 99% of Fe in titaniferrous magnetite was removed and the reaction residue which became rutile substitute was identified as rutile by x-ray diffraction and was found to contain 70% $TiO_2$.

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Chlorination of Galena with Ammonium Chloride (염화암모늄에 의한 방연광의 염소화 반응)

  • Song, Yon-Ho;Oh, Chi-Hoon;Lee, Chul-Tae
    • Applied Chemistry for Engineering
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    • v.7 no.3
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    • pp.453-463
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    • 1996
  • The chlorination of reagent PbS and natural ore galena with $NH_4Cl$ was investigated to find a new extraction metallurgical process of lead. The proper conditions for the chlorination of galena were that reaction temperature ; $425^{\circ}C$, $NH_4Cl$ weight ratio to galena ; 4.0 and reaction time ; 2hrs. Under these conditions, PbS was successfully chlorinated to $PbCl_2$ and the conversion was 90%. And also $NH_4Cl$ was effectively decomposed and was separated $NH_3$ and HCl. HCl was a chlorinating agent and 90% of $NH_3$ was recovered through this chlorination reaction.

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Chlorination of Uranium Dioxide for the preparation of Uranium Tetrachloride (사염화우라늄 제조를 위한 이산화우라늄의 염소화반응)

  • Yang, Yeong-Seok;Hwang, Seong-Chan;Ju, Geun-Sik;Lee, Hong-Gi;Gang, Yeong-Ho
    • Korean Journal of Materials Research
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    • v.7 no.4
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    • pp.317-321
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    • 1997
  • 사염화우라늄 제조를 위해 염소가스와 탄소를 이용한 이산화우라늄의 염소화반응에 대하여 연구하였다. 이론적측면에서 열화학적 자료를 이용한 계산을 통하여 일어날 수 있는 반응들을 확인하였으며, 염소화반응이 진행되는 동안 초래될 현상에 대하여 검토하였다. 실험결과로 부터 반응온도, 반응시간 및 질소가스 주입비율이 사염화우라늄 제조에 미치는 영향을 정량적으로 평가하였다. 순수한 이산화우라늄을 사용한 사염화우라늄 제조공정에서의 적절한 반응시간과 반응온도는 각각 약 2시간과 50$0^{\circ}C$-$700^{\circ}C$범위였으며, 질소가스의 적정 주입량은 염소가스의 약 50%로 나타났다.

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A Convenient Preparation of Polychloroanisidine and Fluorochloroanisole Derivatives (Polychloroanisidine 및 Fluorochloroanisole 유도체의 간편한 합성)

  • Kim, Yu Seon;Kim, Tae Yeong;Kim, Yun Hui
    • Journal of the Korean Chemical Society
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    • v.18 no.4
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    • pp.278-288
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    • 1974
  • Starting from p-dichlorobenzene, 2-amino-4-chloroanisole could be prepared via a nitration, a methoxylation, and subsequent reduction. The repeated chlorination of 2-amino-4-chloroanisole resulted 2-amino-3,4,5-trichloroanisole without any isomeric products. The chlorination of 4-chloro-2-nitroanisole could easily give 2,4-dichloro-6-nitroanisole but polychlorination of the product could not be achieved at the atmospherical pressure. The repeated chlorination of 2-amino-4,6-dichloroanisole could give 2-amino-3,4,5,6-tetrachloroanisole, The Schiemann reaction of 2-amino-4-chloroanisole and 2-amino-4,6-dichloroanisole could give 2-fluoro-4-chloroanisole and 2-fluoro-4,6-dichloroanisole, respectively. The repeated chlorination of these fluorochloroanisoles could give 2-fluoro-3,4,5,6-tetrachloroanisole. In each chlorination process, the components of products were examined by means of NMR spectrometry and the chlorination reaction was repeated without isolating each isomeric product. The feasibility of the present routes of preparations was discussed in respects to the conveniency of reaction conditions and respective overall yields of the processes.

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Chlorination of the scheelite concentrate in a fluidized bed reactor (유동층 반응기에서 회중석 정광의 염소화반응)

  • Um, Myeong-Heon;Park, Yong-Sung;Lee, Chul-Tae
    • Applied Chemistry for Engineering
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    • v.4 no.3
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    • pp.591-600
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    • 1993
  • Chlorination of tungsten from scheelite ore in a fluidized bed reactor has been investigated to develope tungsten extractive metallurgical process by the chlorination. All of the results in this experiment showed tungsten component could be sucessively chlorinated in a fluidized bed reactor. The proper conditions are as follows; reaction temperature $900^{\circ}C$, reaction time : 20min, $Cl_2$ gas velocity : 3.2cm/sec and petroleum coke-to-scheelite ore weight ratio : 0.2. Also the mean diameters of scheelite and petroleum coke were $150.5{{\mu}m}$ and $750.9{{\mu}m}$ respectively. Under these conditions, over 95% of tungsten component in scheelite was chlorinated.

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The Effects of Cross-Section Openings on the Chlorination Reaction Rate of ZIRLO Cladding Hulls (단면 개방이 ZIRLO 피복관의 염소화 반응 속도에 미치는 영향)

  • Jeon, Min Ku;Choi, Yong Taek;Lee, Chang Hwa;Kang, Deok Yoon;Hur, Jin-Mok;Ahn, Do-Hee
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.13 no.3
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    • pp.211-218
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    • 2015
  • The reaction rates of ZIRLO cladding hulls with cross-section openings were investigated using a thermo-gravimetric analysis system in order to identify whether selective recovery of Zr from oxidized cladding hulls is possible. The experimental results showed that an oxidized ZIRLO cladding hull was not reactive with chlorine gas at 400℃. However, providing fresh cross-sections on one or both ends of the ZIRLO hulls enabled a chlorination reaction. This reaction was completed after 8 hours; a 14% increase on the 7 hours seen with a bare ZIRLO cladding hull. The Sharp-Hancock plot analysis results revealed that the contracting volume model is the best for describing the reaction between the cross-section opened ZIRLO hulls and chlorine gas under the condition of this work. It was concluded that the chlorination process can be employed for oxidized ZIRLO cladding hulls by providing cross-section openings.

Manganese Dioxide-Based Chlorination of Alcohols Using Silicon Tetrachloride (이산화망간 존재하에서 사염화규소를 이용한 알코올의 염소화반응)

  • Ha, Dong Soo;Yoon, Myeong Jong
    • Journal of the Korean Chemical Society
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    • v.41 no.10
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    • pp.541-546
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    • 1997
  • Manganese dioxide may react with silicon tetrachloride to form manganese(Ⅳ) oxodichloride which reacts subsequently with another molecule of silicon tetrachloride leading to manganese tetrachloride eventually in chlorinated solvents. This in situ generated manganese(Ⅳ) oxodichloride or manganese tetrachloride were found to be very effective for the chlorination of a wide variety of alcohols to the corresponding chlorides. Primary, secondary and benzylic alcohols were converted into corresponding chlorides when treated with silicon tetrachloride in the presence of manganese dioxide at room temperature.

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Chlorination Reaction Behavior of Zircaloy-4 Hulls: A Preliminary Study on the Effect of the Oxidation Process on the Reaction Rate (Zircaloy-4 피복관의 염소화 반응 거동: 산화 공정이 반응 속도에 미치는 영향에 대한 기초 연구)

  • Jeon, Min Ku;Lee, Chang Hwa;Heo, Chul Min;Lee, You Lee;Choi, Yong Taek;Kang, Kweon Ho;Park, Geun Il
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.11 no.1
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    • pp.69-75
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    • 2013
  • The recovery of Zr from Zircaloy-4 (Zry-4) cladding hulls was demonstrated to investigate the effect of the oxidation process on the reaction rate of the chlorination reaction. In chlorination reaction experiments performed for 6 h, where reaction products were collected every 2 h, it was observed that a significant decrease in the reaction rate was caused by the oxidation process ($500^{\circ}C$, 10 h under an air atmosphere) within the reaction period of 0 - 2 h. The amount of reaction residue increased from 0.95 to 1.65wt% of initial weights in the fresh and Zry-500-10 (Zry-4 hulls oxidized at $500^{\circ}C$ for 10 h under an air atmosphere) hulls, respectively. The purity of the recovered Zr was identical at 99.61wt% for the fresh Zry-4 and Zry-500-10 hulls. Quantitative analysis of the chlorination reaction rate was performed by varying the reaction time from 0.5 to 1.0, 2.0, and 4.0 h. The fitting results showed that the relationship between weight loss and reaction time can be interpreted by a linear line with a slope of 23.35wt%/h for the fresh Zry-4 case, while two linear lines were necessary to fit the results of Zry-500-10. In addition, the slope values were 17.12 and 27.16wt%/h for (0 - 20) and (20 - 100)wt% loss regions, respectively.

Chlorination of Alcohols Using Potassium Carbonate and Silicon Tetrachloride (탄산칼륨 존재하에서 사염화규소를 이용한 알코올의 염소화반응)

  • Ha, Dong Soo;Kim, Hyeung Ae
    • Journal of the Korean Chemical Society
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    • v.41 no.10
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    • pp.535-540
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    • 1997
  • Potassium carbonate reacts with silicon tetrachloride to form trichlorosilyloxy carbonylchloride which reacts subsequently with another molecule of silicon tetrachloride leading to phosgene eventually in chlorinated solvents. This in situ generated trichlorosilyloxy carbonylchloride or phosgene were found to be very effective for the chlorination of a wide variety of alcohols to the corresponding chlorides. Primary, secondary and benzylic alcohols were converted into corresponding chlorides when treated with silicon tetrachloride in the presence of potassium carbonate at room temperature.

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