Insight into Asphaltene Nanoaggregate Structure Inferred by Small Angle Neutron and X-ray Scattering

2011 ◽  
Vol 115 (21) ◽  
pp. 6827-6837 ◽  
Author(s):  
Joëlle Eyssautier ◽  
Pierre Levitz ◽  
Didier Espinat ◽  
Jacques Jestin ◽  
Jérémie Gummel ◽  
...  
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Joanna Korpanty ◽  
Lucas R. Parent ◽  
Nicholas Hampu ◽  
Steven Weigand ◽  
Nathan C. Gianneschi

AbstractHerein, phase transitions of a class of thermally-responsive polymers, namely a homopolymer, diblock, and triblock copolymer, were studied to gain mechanistic insight into nanoscale assembly dynamics via variable temperature liquid-cell transmission electron microscopy (VT-LCTEM) correlated with variable temperature small angle X-ray scattering (VT-SAXS). We study thermoresponsive poly(diethylene glycol methyl ether methacrylate) (PDEGMA)-based block copolymers and mitigate sample damage by screening electron flux and solvent conditions during LCTEM and by evaluating polymer survival via post-mortem matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI-IMS). Our multimodal approach, utilizing VT-LCTEM with MS validation and VT-SAXS, is generalizable across polymeric systems and can be used to directly image solvated nanoscale structures and thermally-induced transitions. Our strategy of correlating VT-SAXS with VT-LCTEM provided direct insight into transient nanoscale intermediates formed during the thermally-triggered morphological transformation of a PDEGMA-based triblock. Notably, we observed the temperature-triggered formation and slow relaxation of core-shell particles with complex microphase separation in the core by both VT-SAXS and VT-LCTEM.


Soft Matter ◽  
2019 ◽  
Vol 15 (41) ◽  
pp. 8372-8380 ◽  
Author(s):  
Harald Rennhofer ◽  
Sven F. Plappert ◽  
Helga C. Lichtenegger ◽  
Sigrid Bernstorff ◽  
Michael Fitzka ◽  
...  

In this article we report on the nanostructural changes of a cellulose II aerogel network during compressive strain of up to 80%, which are investigated by in situ small angle X-ray scattering and linked to the corresponding stress–strain curves.


2016 ◽  
Vol 18 (16) ◽  
pp. 11497-11502 ◽  
Author(s):  
Umme Salma ◽  
Paolo Ballirano ◽  
Marianna Usula ◽  
Ruggero Caminiti ◽  
Natalia V. Plechkova ◽  
...  

In this paper, small angle X-ray scattering has been used to study a series of ionic liquids, alkylammonium alkanoates ([N0 0 0 n][CmCO2]), with varying alkyl chain lengths in the cation and the anion.


2020 ◽  
Vol 17 (8) ◽  
pp. 2809-2820
Author(s):  
Lasse Sander Dreyer ◽  
Jesper Nygaard ◽  
Leila Malik ◽  
Thomas Hoeg-Jensen ◽  
Rasmus Høiberg-Nielsen ◽  
...  

2006 ◽  
Vol 62 (a1) ◽  
pp. s141-s141
Author(s):  
A. V. Sokolova ◽  
L. Kreplak ◽  
L. P. Kurochkina ◽  
D. I. Svergun ◽  
T. Wedig ◽  
...  

2019 ◽  
Author(s):  
Christian Prehal ◽  
Aleksej Samojlov ◽  
Manfred Nachtnebel ◽  
Manfred Kriechbaum ◽  
Heinz Amenitsch ◽  
...  

<b>Here we use in situ small and wide angle X-ray scattering to elucidate unexpected mechanistic insights of the O2 reduction mechanism in Li-O2 batteries.<br></b>


2019 ◽  
Author(s):  
Hao Wu ◽  
Jeffrey Ting ◽  
Siqi Meng ◽  
Matthew Tirrell

We have directly observed the <i>in situ</i> self-assembly kinetics of polyelectrolyte complex (PEC) micelles by synchrotron time-resolved small-angle X-ray scattering, equipped with a stopped-flow device that provides millisecond temporal resolution. This work has elucidated one general kinetic pathway for the process of PEC micelle formation, which provides useful physical insights for increasing our fundamental understanding of complexation and self-assembly dynamics driven by electrostatic interactions that occur on ultrafast timescales.


Sign in / Sign up

Export Citation Format

Share Document