Ernst-Berl-Institut für Technische und Makromolekulare Chemie, Technische Universität Darmstadt, Petersenstrasse 20, 64287 Darmstadt, Germany.
ChemSusChem. 2010;3(1):85-90. doi: 10.1002/cssc.200900154.
Nitriles act as important intermediates for the chemical industry and are accessible on a large scale through hydrocyanation or ammonoxidation. Nitrile hydrolysis yields amides and acids used in various applications. The conventional nitrile hydrolysis process relies on stoichiometric amounts of mineral acid or base which inherently deliver great amounts of waste brine. Improving this process towards green chemistry would require reaction conditions which can provide technically significant results without the use of catalysts. Under these conditions, the hydrolysis of valeronitrile in pure supercritical water was investigated. The experiments were performed in a continuous high pressure laboratory-scale apparatus at a temperature between 400 and 500 degrees C, 30 MPa pressure and maximal residence time of 100 s. Nitrile conversion and valeric acid selectivity greater than 90% were achieved.
腈类化合物作为化学工业的重要中间体,可以通过氢氰化或氨氧化大规模获得。腈水解生成酰胺和酸,用于各种应用。传统的腈水解工艺依赖于化学计量的矿物酸或碱,这不可避免地产生大量的废盐水。为了使这一过程朝着绿色化学方向发展,需要在不使用催化剂的情况下提供具有技术意义的结果的反应条件。在这些条件下,在纯超临界水中研究了戊腈的水解。实验在 400 到 500 摄氏度、30 MPa 压力和最长 100 秒停留时间的连续高压实验室规模装置中进行。腈的转化率和戊酸的选择性大于 90%。