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Process for the manufacture of nitroguanidine using guanidine nitrate under the action of an aqueous sulfuric acid.

机译:在硫酸水溶液的作用下使用硝酸胍制备硝基胍的方法。

摘要

P process by which the reaction is carried out with the implementation of 2,5 to 3,5 mole of sulfuric acid per mole of guanidine nitrate with the impurity-depleted acid from each of the working cycle of the preceding / p & & p & process characterized in that the dehydration is carried out with sulphuric acid at 82 - 85% at a temperature of 40 to 80°C. for one to three hours, it is subsequently diluted sulphuric acid recovered with the washing water at 0 to 5°C. from the preceding cycle, and after separation of nitroguanidine precipitated, it recovers the acid diluted to 25 - 35% for a new cycle of the reaction. / p & & p & method applicable to a continuous production cost and high efficiency. / p
机译:

方法,通过上述过程中的每个工作循环中的每摩尔硝酸胍与贫杂质酸实施2.5至3.5摩尔硫酸进行反应 & &所述方法的特征在于,所述脱水是在40-80℃的温度下用82-85%的硫酸进行的。 1-3小时,然后用0-5℃的洗涤水回收稀硫酸。从前一个循环中分离出硝基胍后,将回收到稀释至25-35%的酸回收用于新的反应循环。 & &该方法适用于连续生产成本高,效率高。

著录项

  • 公开/公告号FR2405929B1

    专利类型

  • 公开/公告日1983-12-23

    原文格式PDF

  • 申请/专利权人 INDUSTRIE CHEMIE THOMA;

    申请/专利号FR19780014995

  • 发明设计人

    申请日1978-05-11

  • 分类号C07C129/10;

  • 国家 FR

  • 入库时间 2022-08-22 08:46:26

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