Chain-branching activation energy in acetylene-oxygen flames

1955 ◽  
Vol 5 (1) ◽  
pp. 637-641 ◽  
Author(s):  
J. Van Wonterghem ◽  
A. Van Tiggelen

The effect of the magnitude of activation energy on reaction rates has been examined. The conclusions suggest that a valid approximation to combustion mechanisms should be obtainable from a consideration of a single rate-controlling chain-branching and a single rate-controlling chain-breaking step. This concept has been applied in turn to homogeneous auto-ignition, ignition lags, limits of inflammability, flame propagation and burning velocities, resulting in a simple co-ordinating scheme. The formulae derived imply methods of identification of the rate-controlling processes from measurable flame properties.


2012 ◽  
Vol 550-553 ◽  
pp. 736-741
Author(s):  
Peng Peng Li ◽  
Shi Yuan Yang ◽  
Shan Xue

Dynamic rheological results of 17 commercial and noncommercial metallocene-catalyzed polyethylenes, such as shear thinning index(SHI), modulus of crossover point of store modulus and loss modulus (Gco) and flow activation energy(Ea), are presented. The effects of molecular weight distribution(MWD), and degree of short chain branching (SCB) determined by gel permeation chromatography (GPC) and FTIR, were analyzed. Plots of SHI versus MWD revealed the influence of branching level on the shear thinning behavior of polyethylenes. Gcowas observed scaling with MWD for metallocene-catalyzed polyethylenes and the correlation between them was generated by MWD=193378*Gco. Correlation between flow activation energy measured by dynamic temperature sweep at low frequency and short chain branch-0.9038was also established for metallocene polyethylenes as SCB=7*10-8*Ea6.024. Thus, an alternative single rheological method, based on the effect of molecular structural parameters on dynamic rheological behaviors, was proposed to evaluate the polydispersity and short chain branching of metallocene-catalyzed polyethylene.


2003 ◽  
Vol 762 ◽  
Author(s):  
A. Gordijn ◽  
J.K. Rath ◽  
R.E.I. Schropp

AbstractDue to the high temperatures used for high deposition rate microcrystalline (μc-Si:H) and polycrystalline silicon, there is a need for compact and temperature-stable doped layers. In this study we report on films grown by the layer-by-layer method (LbL) using VHF PECVD. Growth of an amorphous silicon layer is alternated by a hydrogen plasma treatment. In LbL, the surface reactions are separated time-wise from the nucleation in the bulk. We observed that it is possible to incorporate dopant atoms in the layer, without disturbing the nucleation. Even at high substrate temperatures (up to 400°C) doped layers can be made microcrystalline. At these temperatures, in the continuous wave case, crystallinity is hindered, which is generally attributed to the out-diffusion of hydrogen from the surface and the presence of impurities (dopants).We observe that the parameter window for the treatment time for p-layers is smaller compared to n-layers. Moreover we observe that for high temperatures, the nucleation of p-layers is more adversely affected than for n-layers. Thin, doped layers have been structurally, optically and electrically characterized. The best n-layer made at 400°C, with a thickness of only 31 nm, had an activation energy of 0.056 eV and a dark conductivity of 2.7 S/cm, while the best p-layer made at 350°C, with a thickness of 29 nm, had an activation energy of 0.11 V and a dark conductivity of 0.1 S/cm. The suitability of these high temperature n-layers has been demonstrated in an n-i-p microcrystalline silicon solar cell with an unoptimized μc-Si:H i-layer deposited at 250°C and without buffer. The Voc of the cell is 0.48 V and the fill factor is 70 %.


Diabetes ◽  
2018 ◽  
Vol 67 (Supplement 1) ◽  
pp. 1897-P
Author(s):  
HISASHI YOKOMIZO ◽  
ATSUSHI ISHIKADO ◽  
TAKANORI SHINJO ◽  
KYOUNGMIN PARK ◽  
YASUTAKA MAEDA ◽  
...  

Author(s):  
А. А. Горват ◽  
В. М. Кришеник ◽  
А. Е. Кріштофорій ◽  
В. В. Мінькович ◽  
О. А. Молнар

Sign in / Sign up

Export Citation Format

Share Document