Associate Professor
Supervisor of Doctorate Candidates
Supervisor of Master's Candidates
Open time:..
The Last Update Time:..
Date of Publication:2022-10-06
Journal:物理化学学报
Affiliation of Author(s):化工学院
Volume:34
Issue:3
Page Number:247-255
ISSN No.:1000-6818
Abstract:Nitriles are very important for the synthesis of fine chemicals and
medicines. However, many nitriles are not widely available, as their
synthesis processes pose a serious risk to the environment. Herein, we
report that a spontaneous CH_3OH/NH_3 coupling reaction can directly
synthesize N,N-dimethyl cyanamide[(CH_3)_2NCN],amino acetonitrile
[NH_2CH_2CN], and N,N-dimethyl amino acetonitrile [(CH_3)_2NCH_2CN],when
a mixture of methanol and ammonia is transferred into the plasma state
via a dielectric barrier discharge. The effects of the plasma reactor
configuration, discharge conditions, reaction conditions, and packing
materials on the methanol conversion as well as the product selectivity
were systematically investigated. Experimental results indicate that,
under optimized conditions, a nitrile compound selectivity of 22.1% with
a methanol conversion of 51.5% could be achieved. Analysis by optical
emission spectroscopy indicates that the C=N species in CH_3OH/NH_3
plasma could be a key reactive intermediate aiding in the synthesis of
nitrile compounds. The CH_3OH/NH_3 plasma coupling reaction process is
an environment-friendly methodology for the synthesis of (CH_3)_2NCN,
NH_2CH_2CN, and (CH_3)_2NCH_2CN,and is a potential novel pathway for the
synthesis of fine chemicals like methanol and ammonia.
Note:新增回溯数据