Atmospheric Pressure Non-Equilibrium Plasma Deposition with Retention of Functional Group

2013 ◽  
Vol 423-426 ◽  
pp. 537-540 ◽  
Author(s):  
Jun Yan ◽  
Yuki Kondo ◽  
Xiao Yi Qian ◽  
Xiao Meng Fei ◽  
Katsuhiko Hosoi ◽  
...  

A non-equilibrium atmospheric pressure plasma was applied for the polymerization of the methacrylic monomers such as (2-hydroxyethyl methacrylate (HEMA), methacrylic acid (MAA) and butyl methacrylate (BMA)). These monomers were successfully polymerized with retaining the functional groups of ester or acid. The polymerization mechanism was discussed on the basis of the optical emission spectroscopy (OES) of the plasma. It was strongly suggested that the functional groups could be retained in the polymerization proceeds when the HOMO-LUMO gap of the monomer is close to the energy of Ar metastable atom, which initiates the polymerization.

2014 ◽  
Vol 670-671 ◽  
pp. 244-248 ◽  
Author(s):  
Jun Yan ◽  
Katsuhiko Hosoi ◽  
Shin-ichi Kuroda

The non-equilibrium atmospheric pressure Ar plasma was applied for the polymerization of maleic anhydride (MA). The deposited films were analyzed by using Fourier transform infrared spectroscopy (FT-IR) proving the monomer was successfully polymerized with retaining the functional groups. The intensity of optical emission spectroscopy (OES) of the plasma jet was found to become weaker when the monomer was introduced into the jet. This was interpreted as the result of the energy transfer from the metastable Ar to the monomer. It was proposed that the excited MA changed into π-π* transition state to produce dimer biradicals which initiate the polymerization.


2014 ◽  
Vol 13 (1) ◽  
Author(s):  
Jaroslav Hnilica ◽  
Lucia Potočňáková ◽  
Vít Kudrle

AbstractIn this paper, the effects of the power modulation on atmospheric pressure plasma jet, operated in Ar+2%N2 mixture, are studied. Time resolved optical emission spectroscopy is used for the investigation. From line and band intensities, the excitation, vibration and rotation temperatures are calculated. Their evolution during the modulation period exhibits a strong dependence on modulation frequency. For higher modulation frequencies, there is significant discrepancy in rotational temperatures calculated from OH spectra and from N2+ spectra, which indicates that thermalisation time can reach milliseconds.


Sign in / Sign up

Export Citation Format

Share Document