Inelastic Neutron Scattering from Filled Elastomers

2000 ◽  
Vol 73 (5) ◽  
pp. 847-863 ◽  
Author(s):  
A. I. Nakatani ◽  
R. Ivkov ◽  
P. Papanek ◽  
H. Yang ◽  
M. Gerspacher

Abstract Inelastic neutron scattering experiments are powerful techniques for evaluating local molecular dynamics. These methods are especially sensitive to hydrogen atoms containing motions. An overview of these experimental techniques is presented. Neutron filter analyzer and time-of-flight spectroscopy methods are used to characterize the local dynamics of polymers in the presence and absence of fillers. Of particular interest is the comparison between bound rubber attached to the filler surface and the pure, unbound rubber. A commercial synthetic polyisoprene containing approximately 100% cis-1,4 isomers was compounded with three different carbon blacks: N299, G299 (graphitized N299), and N762. Soxhlet extraction on each of the samples was performed so that corresponding samples containing purely bound rubber with filler were obtained. The filter analyzer and time-of flight spectra show distinct differences between the bound and pure rubber as well as differences based on carbon black type. Correlation of the spectral differences to the type of carbon black and initial concentration of carbon black are discussed.

1994 ◽  
Vol 376 ◽  
Author(s):  
P. Papanek ◽  
J. E. Fischer ◽  
J. L. Sauvajou ◽  
A. J. Dianoux ◽  
P. M. Mcneillis ◽  
...  

ABSTRACTInelastic incoherent neutron-scattering spectra of cis-, trans- and Na-doped polyacety-lene are presented. The experiments were performed with time-of-flight and filter-analyzer spectrometers on stretch-oriented samples such that the polarization of vibrational modes could also be determined.


2005 ◽  
Vol 38 (3) ◽  
pp. 405-411 ◽  
Author(s):  
M. D. Lumsden ◽  
J. L. Robertson ◽  
M. Yethiraj

The UB matrix approach has been extended to handle inelastic neutron scattering experiments with differing k_{\rm i} and k_{\rm f}. We have considered the typical goniometer employed on triple-axis and time-of-flight spectrometers. Expressions are derived to allow for calculation of the UB matrix and for converting from observables to Q-energy space. In addition, we have developed appropriate modes for calculation of angles for a specified Q-energy position.


2017 ◽  
Vol 88 (10) ◽  
pp. 105116 ◽  
Author(s):  
J. L. Niedziela ◽  
R. Mills ◽  
M. J. Loguillo ◽  
H. D. Skorpenske ◽  
D. Armitage ◽  
...  

1994 ◽  
Vol 48 (6) ◽  
pp. 669-673 ◽  
Author(s):  
Stewart F. Parker ◽  
Kenneth P. J. Williams ◽  
Peter Meehan ◽  
Mark A. Adams ◽  
John Tomkinson

Carbon black-filled polymers are among the most challenging samples that an analyst may be called upon to identify. In this paper three novel methods of obtaining vibrational spectra from four different carbon black-filled polymers are evaluated: transmission infrared spectroscopy using a diamond anvil cell, Raman spectroscopy using 780-nm excitation, and inelastic neutron scattering. Overall, none of the three methods used in this work was totally satisfactory, but for most purposes infrared spectroscopy provides the best results in terms of spectrometer accessibility and the availability of suitable reference collections. Raman spectroscopy was successful only with one of the four polymers. Inelastic neutron scattering (INS) was successful in obtaining a spectrum with all four materials, but this success occurred only with respect to the hydrogenic part of the polymer, and, for many materials, it is the heteroelements, O, S, and halogens, that determine the important physical properties of the compound. For both Raman spectroscopy and INS, a major disadvantage is the lack of a suitable data base for identification of the materials.


2010 ◽  
Vol 58 (1) ◽  
pp. 52-61 ◽  
Author(s):  
L'ubomír Smrčok ◽  
Daniel Tunega ◽  
Anibal Javier Ramirez-Cuesta ◽  
Alexander Ivanov ◽  
Jana Valúchová

Author(s):  
Alisha L. Davidson ◽  
Paul B. Webb ◽  
Stewart F. Parker ◽  
David Lennon

AbstractA dual sodium and sulfur promoted haematite, representative of a candidate Fischer-Tropsch to olefins (FTO) catalyst, is prepared and contrasted with the performance of an unpromoted hematite sample in the ambient pressure CO hydrogenation reaction at 623 K as a function of time-on-stream (0–24 h). In-situ post-reaction temperature-programmed oxidation measurements show the carbon evolutionary phase of the catalyst conditioning process to be retarded for the FTO catalyst. Ex-situ inelastic neutron scattering measurements show the promoters perturb the formation of a previously described hydrocarbonaceous overlayer. Specifically, whilst the sp3 hybridised C–H modes of the hydrocarbonaceous overlayer are almost unaffected by the additives, the formation of the overlayer’s sp2 hybridised C–H modes are noticeably impeded. The results are discussed in terms of the Na/S promoters disturbing the formation of an ordered hydrocarbonaceous overlayer that is thought to constrain the supply of adsorbed hydrogen atoms, which favours the formation of unsaturated hydrocarbons associated with the FTO process.


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