Two- and three-body dissociation dynamics of temporary negative ion NF3(-).

Dissociation dynamics of temporary negative ion NF3(-) formed in the low-energy (0.5 to 4.5 eV) electron attachment is investigated by the anion velocity slice imaging spectroscopy. The kinetic and angular distributions of the F(-) fragment indicate that this fragment is produced via two distinctly different dissociation channels, namely, two-body and three-body fragmentations, at the higher electron attachment energies. The anisotropic distributions of the fast F(-) ions are interpreted as the two-body dissociations relevant to the (2)E resonant state of NF3(-), whereas the slow F(-) can be produced via various three-body dissociations with the products of NF(X (3)Σ(-)) + F + F(-), NF(b (1)Σ(+)) + F + F(-), or N + F2 + F(-), depending on the electron attachment energy.

Communication: Imaging the indirect dissociation dynamics of temporary negative ion: N2O- → N2 + O-.

We reported an imaging study of the dissociation dynamics of temporary negative ion N(2)O(-) formed in the low-energy electron attachment, e(-) + N(2)O → N(2)O(-) → N(2) + O(-). With the help of ab initio molecular dynamics calculations, the evolution of momentum distributions of the O(-) fragment in terms of the electron attachment energy is identified as the result of a competition between two distinctly different indirect pathways, namely, climbing over and bypassing the energy ridge after the molecular structure bending. These two pathways prefer leaving the N(2) fragment at the high vibrational and rotational states, respectively.

Positive/negative ion velocity mapping apparatus for electron-molecule reactions.

In molecular dissociative ionization by electron collisions and dissociative electron attachment to molecule, the respective positively and negatively charged fragments are the important products. A compact ion velocity mapping apparatus is developed for the angular distribution measurements of the positive or negative fragments produced in the electron-molecule reactions. This apparatus consists of a pulsed electron gun, a set of ion velocity mapping optic lenses, a two-dimensional position detector including two pieces of micro-channel plates, and a phosphor screen, and a charge-coupled-device camera for data acquisition. The positive and negative ion detections can be simply realized by changing the voltage polarity of ion optics and detector. Velocity sliced images can be directly recorded using a narrow voltage pulse applied on the rear micro-channel plate. The efficient performance of this system is evaluated by measuring the angular distribution of O(-) from the electron attachments to NO at 7.3 and 8.3 eV and O(+) from the electron collision with CO at 40.0 eV.

[Major, minor and trace-elemental contents analysis in northeast soybeans by ICP-AES].

Major, minor and trace elemental contents in northeast China soybeans were determined by using inductively coupled plasma atomic emission spectrometry (ICP-AES). Three different sample digestion methods including two wet digestions, HNO3-HClO4 and HNO3-H2SO4 and a dry ash method were compared. Owing to the high oil content in soybeans, long time is needed and access acid should be added with mixed acid digestion methods, which may result in higher sample blank. Therefore, the dry ask method would be more proper for the pre-treatment of soybean samples. Potassium and phosphorus are major elements in soybeans, so the effect of potassium and phosphorus on the other elements was investigated. Results showed that the potassium and phosphorus did not affect the determination of other trace elements. There are not significant differences in trace elemental contents for the eleven northeast China soybeans.