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催化氨氧化法制备2-氰基吡嗪的研究 被引量:11

Synthesis of 2-Cyanopyrazine by Catalytic Ammoxidation
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摘要 开发了一种由VMoOP四元素组成的氨氧化催化剂(V-II型),用该催化剂在固定床反应器内由2-甲基吡嗪为原料进行气固相接触氨氧化反应制备了2-氰基吡嗪。V-II型催化剂组分中矾、磷的比例是影响催化剂反应活性及选择性的主要因素,矾磷比为1.9时,催化活性最好。探讨了氨氧化反应机理,认为2-甲基吡嗪经过氧化、脱水分别生成了吡嗪羧酸和吡嗪酰胺中间体后最终生成2-氰基吡嗪。正交实验确定了反应的影响因素和最佳条件,结果表明:反应温度是影响产品收率的最主要因素, 当2-甲基吡嗪、氨气、空气的投料量分别为0.05mLmin-1, 200mLmin-1, 1000mLmin-1, 反应温度430C时,2-氰基吡嗪选择性大于90%, 单程收率大于87%, 产品纯度大于99%。按小试工艺条件放大100倍中试,结果与小试吻合。 A new V-II ammoxidation catalyst comprising VMoOP four elements was developed. 2-cyanopyrazine was prepared from 2-methylpyrazine with above catalyst by vapor phase catalytic ammoxidation in a fixed-bed reactor. The ratio of V to P in the catalyst is the main factor influencing the catalytic activity. When the ratio is 1.9, the activity is the highest. The ammoxidation mechanism was also studied. It could be seen that 2-methylpyrazine was oxidated and dehydrated to form intermediates pyrazinyl carboxylic acid and pyrazinamide, which then changed into 2-cyanopyrazine. The factors influencing the reaction and the optimized condition were determined by orthogonal experiments. Results show that the reaction temperature is the key factor influencing the product yield. When the flow rates of 2-methylpyrazine, ammonia and air are 0.05 mL&middotmin-1, 200 mL&middotmin-1 and 1000 mL&middotmin-1, respectively, and the temperature in 430°C, the 2-cyanopyrazine yield is 87%, and its purity is above 99%. A pilot-scale production was carried out, which scaled-up the lab oratory-scale one hundred fold. The result of the pilot-scale production was in accordance with that of the laboratorial experiments.
出处 《高校化学工程学报》 EI CAS CSCD 北大核心 2003年第4期395-399,共5页 Journal of Chemical Engineering of Chinese Universities
基金 天津市自然科学基金(013606011
关键词 2-氰基吡嗪 氨氧化 催化剂 固定床反应器 Ammonia Catalysis Catalyst activity Catalysts Chemical reactors Oxidation
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参考文献11

  • 1周立山,冯亚青,曲红梅,宋红雨,史大昕.2-甲基吡嗪的合成研究(Ⅰ)——催化剂的研究[J].化学工业与工程,2001,18(5):266-268. 被引量:6
  • 2张尚湖 冯亚青 张为红.氨氧化合成2-氰基吡嗪催化剂的研究进展[J].化学工业与工程,2002,19:339-341.
  • 3王蓉麟,冯续,杜彩霞.气相氨氧化催化合成氰基吡嗪的研究[J].天然气化工—C1化学与化工,1993,18(5):45-49. 被引量:3
  • 4陈英奇,戴立言,杨能渭.2-甲基吡啶气相催化氧化合成2-吡啶甲醛的研究[J].高校化学工程学报,2002,16(4):436-440. 被引量:6
  • 5Mitsuwaka Pure Chemicals Co. Ltd. Pyrazinamide [P]. Jp 11, 971, 1982.
  • 6Opletalova V, Patel A. 5-alkyl-2-pyrazinecarboxamldes, 5-alkyl-2-pyrazine carbonitriles and 5-alkyl-2-acetylpyrazines as syntheticintermediates for antiinflammatory agents [J]. Collect Czech Chem Commun, 1996, 61(7): 1093-1101.
  • 7Zergenyi J, Raz B. Pyrazinamide [P]. EP 0, 122, 355. 1984.
  • 8Koel Chemical Industry Co. Ltd. A process for the preparation of pyrazinamide [P]. JP 111, 971. 1987.
  • 9Forni Lucio. Ammoxidation of 2-methylpyrazine over oxide catalysts [J]. Appl Catal, 1986, 20(1-2): 219-230.
  • 10Reddy B M. Vanadium phosphorus oxide catalyst for ammoxidations of 3-picoline to nicotinonitrile and 2-methylpyrazine to 2-cyanopyrazine [J]. Chem Ind, 1995, 62: 487-491.

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