Solid-State Methylamine VUV Irradiation Study Using Carbon Monoxide as an H Radical Scavenger

2012 ◽  
Vol 65 (2) ◽  
pp. 129 ◽  
Author(s):  
Jean-Baptiste Bossa ◽  
Fabien Borget ◽  
Fabrice Duvernay ◽  
Grégoire Danger ◽  
Patrice Theulé ◽  
...  

Solid-phase methylamine (CH3NH2) was vacuum ultraviolet (VUV) photoprocessed at low temperature (20 K) using a hydrogen flow discharge lamp, which allows irradiation down to 120 nm. Methanimine (CH2=NH), the methylammonium cation (CH3NH3+) and the counterion CN–, as well as the amino radical (NH2), methane (CH4) and ammonia (NH3), were identified as the photoproducts by using FTIR spectroscopy. So far, the branching ratios of the photodissociation pathways of methylamine in the solid phase remain unknown. The methylamine molecule holds two non-equivalent hydrogen atoms on the methyl and the amino group, so we can expect the formation of two distinct radicals via a carbon–hydrogen or a nitrogen–hydrogen bond cleavage, namely CH2NH2 and CH3NH. These radicals are highly reactive and may reform methylamine with hydrogen atom recombination. Their direct infrared spectroscopic detection is therefore tricky. To solve that problem, we use carbon monoxide (CO) as an H radical scavenger, forming the intermediate species HCO. After the irradiation of a CH3NH2 : CO binary ice mixture, formamide (NH2CHO) and N-methylformamide (CH3NHCHO) were identified as the main photoproducts using both infrared and mass spectrometry. We give a rough approximation of the branching ratios, which are in agreement with previous studies in the gas phase.

2016 ◽  
Vol 94 (4) ◽  
pp. 265-272 ◽  
Author(s):  
R. Toukabri ◽  
Y.J. Shi

The elimination of H2 from the dissociation of four methyl-substituted silane molecules, including monomethylsilane (MMS), dimethylsilane (DMS), trimethylsilane (TriMS), and tetramethylsilane (TMS), on a heated tungsten or tantalum filament surface has been studied using laser ionization mass spectrometry. Two complementary ionization methods, i.e., single photon ionization (SPI) using a vacuum ultraviolet wavelength at 118 nm (10.5 eV) and a dual ionization source incorporating both 10.5 eV SPI and laser-induced electron ionization, were employed to detect the production of H2. Examination of the intensity of the H2+ peak from the four molecules has shown that it increases with temperature until reaching a plateau at around 2000−2100 °C on both tungsten and tantalum filaments. These methyl-substituted silanes are dissociatively adsorbed on tungsten and tantalum surfaces by Si−H bond cleavage, and as the temperature is raised, by C−H bond rupture. Experiments with the isotopomers of MMS, DMS, and TriMS have shown that the formation of H2 follows the Langmuir−Hinshelwood mechanism where two adsorbed hydrogen atoms on metal surfaces recombine to produce H2. The determined activation energy (Ea) for H2 formation from MMS, DMS, and TriMS, in the range of 58.2−93.4 kJ mol−1, has been found to increase with the number of methyl substitutions in the precursor molecule. Comparison of these Ea values with the reported values of 51.1−78.8 kJ mol−1 for the methyl radical formation from the same three precursor molecules has led to the conclusion that the initial Si−H bond cleavage in the dissociative adsorption of MMS, DMS, and TriMS is the rate-limiting step for the formation of both H2 molecules and ·CH3 radicals.


2021 ◽  
Author(s):  
Clemens Krempner ◽  
Chamila Manankandayalage ◽  
Daniel K Unruh

Utilizing an intramolecular frustrated Lewis pair (FLP) decorated with a strongly donating guanidino moiety enabled the formation of a thermally remarkably stable FLP-CO adduct, which at 120°C underwent CO migration...


2019 ◽  
Vol 141 (2) ◽  
Author(s):  
Silvan Siegrist ◽  
Henrik von Storch ◽  
Martin Roeb ◽  
Christian Sattler

Three crucial aspects still to be overcome to achieve commercial competitiveness of the solar thermochemical production of hydrogen and carbon monoxide are recuperating the heat from the solid phase, achieving continuous or on-demand production beyond the hours of sunshine, and scaling to commercial plant sizes. To tackle all three aspects, we propose a moving brick receiver–reactor (MBR2) design with a solid–solid heat exchanger. The MBR2 consists of porous bricks that are reversibly mounted on a high temperature transport mechanism, a receiver–reactor where the bricks are reduced by passing through the concentrated solar radiation, a solid–solid heat exchanger under partial vacuum in which the reduced bricks transfer heat to the oxidized bricks, a first storage for the reduced bricks, an oxidation reactor, and a second storage for the oxidized bricks. The bricks may be made of any nonvolatile redox material suitable for a thermochemical two-step (TS) water splitting (WS) or carbon dioxide splitting (CDS) cycle. A first thermodynamic analysis shows that the MBR2 may be able to achieve solar-to-chemical conversion efficiencies of approximately 0.25. Additionally, we identify the desired operating conditions and show that the heat exchanger efficiency has to be higher than the fraction of recombination in order to increase the conversion efficiency.


1981 ◽  
Vol 55 (1-2) ◽  
pp. 9-15 ◽  
Author(s):  
A. Jówko ◽  
S. U. Pavlova ◽  
H. Baj ◽  
B. G. Dzantiev ◽  
M. Foryś

1970 ◽  
Vol 52 (5) ◽  
pp. 2205-2221 ◽  
Author(s):  
John P. Appleton ◽  
Martin Steinberg ◽  
David J. Liquornik

Sign in / Sign up

Export Citation Format

Share Document