Mass spectroscopic study of the chemical reaction zone in detonating liquid nitromethane

被引:48
作者
Blais, NC [1 ]
Engelke, R [1 ]
Sheffield, SA [1 ]
机构
[1] LOS ALAMOS NATL LAB,LOS ALAMOS,NM 87545
关键词
D O I
10.1021/jp971928p
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report a time-of-flight mass spectroscopic study of the chemical reaction zone in base-sensitized detonating liquid nitromethane (NM-CH3NO2). Mass spectra of the reaction zone region are presented for cases where the CH3NO2, (CH3NO2)-C-13, and CD3NO2 forms of NM were detonated. In experiments in which detonation was made to occur, the detonation process was initiated by a slapper detonator system. The NM explosives were confined in steel, and the charge geometry was chosen such that the detonations were traveling steadily by the time the detonation wave reached the end of the charge. Various nondetonation control experiments were also performed and are described. Two-dimensional numerical fluid-dynamic computations that mimic the experimental system were performed in order to help in the interpretation. We estimate that, for the base-sensitized NM explosive used, the steady two-dimensional chemical-reaction zone is ca. 50 mu m in spatial extent and has a time duration of ca. 7 ns. The most important result obtained is that the new chemical species that are observed in the reaction zone are the result of condensation reactions where two or more Nhl molecules combine to form molecules more massive than NM or produce molecules in which numerous nitrogen atoms are present. A brief review of earlier work on this problem is presented to aid readers in understanding the new results.
引用
收藏
页码:8285 / 8295
页数:11
相关论文
共 36 条
[1]  
Barnard G P., 1953, MODERN MASS SPECTROM
[2]   APPARATUS FOR THE MASS-SPECTROMETRIC ANALYSIS OF DETONATION PRODUCTS QUENCHED BY ADIABATIC FREE EXPANSION [J].
BLAIS, NC ;
FRY, HA ;
GREINER, NR .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1993, 64 (01) :174-183
[3]   A MODEL OF REACTIVE DYNAMICS IN A DETONATION [J].
BLAIS, NC ;
STINE, JR .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (11) :7914-7922
[4]   IRREVERSIBLE REACTION OF NITROMETHANE AT ELEVATED PRESSURE AND TEMPERATURE [J].
BRASCH, JW .
JOURNAL OF PHYSICAL CHEMISTRY, 1980, 84 (16) :2084-2085
[5]   STRUCTURES OF METHAZONIC ACID AND ITS ANIONS [J].
BROWNSTEIN, S .
JOURNAL OF ORGANIC CHEMISTRY, 1963, 28 (10) :2919-&
[6]  
Campbell A. W., 1976, 6th symposium (international) on Detonation, P642
[7]   UV/VISIBLE ABSORPTION-SPECTRA OF SHOCKED NITROMETHANE AND NITROMETHANE-AMINE MIXTURES UP TO A PRESSURE OF 14 GPA [J].
CONSTANTINOU, CP ;
WINEY, JM ;
GUPTA, YM .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (32) :7767-7776
[8]   REACTIONS OF NITROALKANES IN GAS PHASE .1. PYROLYSIS OF NITROMETHANE [J].
CRAWFORT.CG ;
WADDINGT.DJ .
TRANSACTIONS OF THE FARADAY SOCIETY, 1969, 65 (557P) :1334-&
[9]   A STUDY OF THE STEADY-STATE REACTION-ZONE STRUCTURE OF A HOMOGENEOUS AND A HETEROGENEOUS EXPLOSIVE [J].
ENGELKE, R ;
BDZIL, JB .
PHYSICS OF FLUIDS, 1983, 26 (05) :1210-1221
[10]   Pressure driven ligand rearrangement reaction in a cobalt-chloride complex [J].
Engelke, R ;
Pettit, DR ;
Sheffield, SA .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (09) :1696-1704