Direct determination of gas velocity and gas temperature in an atmospheric-pressure argon-hydrogen plasma jet

Direct gas temperature and gas velocity measurements made in the exit plane of a subsonic argon-hydrogen thermal plasma jet from high-resolution lineshape analysis of laser light scattered by the plasma are reported. The lineshapes are in general a superposition of the ion feature of the Thomson-scattered light and the lineshape of Rayleigh scattered light. In the center of the jet Thomson scattering dominates while at larger radii Rayleigh scattering dominates. Because of the complexity of the lineshapes of light scattered by multicomponent plasmas, only those that are predominantly due to Thomson scattering can in practice be analyzed for gas temperature. Gas velocity can be determined from the Doppler shift of the lineshapes relative to the frequency of the incident laser if the velocity is greater than about 50 m s⁻¹. The maximum gas temperature measured was 14,500 K±5%. The maximum gas velocity measured was 1100 m s⁻¹±3%. Temperature values and the radial velocity profile are compared with those previously obtained from a subsonic all-argon plasma jet operated under similar conditions.     

Nickel(II) and palladium(II) complexes with α‐dioxime ligands as catalysts for the vinyl polymerization of norbornene in combination with methylaluminoxane,tris(pentafluorophenyl)borane,or triethylaluminum cocatalyst systems

Nickel(II) and palladium(II) complexes with α‐dioxime ligands dimethylglyoxime, diphenylglyoxime, and 1,2‐cyclohexanedionedioxime represent six new precatalysts for the polymerization of norbornene that can be activated with methylaluminoxane (MAO), the organo‐Lewis acid tris(pentafluorophenyl)borane [B(C₆F₅)₃], and triethylaluminum (TEA) AlEt₃. The palladium but not the nickel precatalysts could also be activated by B(C₆F₅)₃ alone, whereas two of the three nickel precatalysts but none of the palladium systems are somewhat active with only TEA as a cocatalyst. It was possible to achieve very high polymerization activities up to 3.2 · 10⁷ g_polymer/mol_metal · h. With the system B(C₆F₅)₃/AlEt₃, the activation process can be formulated as the following two‐step reaction: (1) B(C₆F₅)₃ and TEA lead to an aryl/alkyl group exchange and result in the formation of Al(C₆F₅)_nEt_3?n and B(C₆F₅)_3?nEt_n; and (2) Al(C₆F₅)_nEt_3?n will then react with the precatalysts to form the active species for the polymerization of norbornene. Variation of the B:Al ratio shows that Al(C₆F₅)Et₂ is sufficient for high activation. Gel permeation chromatography indicated that it was possible to control the molar mass of poly(norbornene)s by TEA or 1‐dodecene as chain‐transfer agents; the molar mass can be varied in the number‐average molecular weight range from 2 · 10³ to 9 · 10⁵ g · mol^?1. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 3604–3614, 2002     

Large size anion binding with iron(II) complexes of a 5,5'-disubstituted-2,2'-bipyridine ligand

Three 5,5'-substituted 2,2'-bipyridyl ligands around a metal atom form two clefts which can encapsulate sulfate, perchlorate, or nitrate anions.