Formation Kinetics of Polymer Vesicles from Spherical and Cylindrical Micelles Bearing the Polyelectrolyte Complex Core Studied by Time-Resolved USAXS and SAXS

2022 ◽  
Author(s):  
Rintaro Takahashi ◽  
Theyencheri Narayanan ◽  
Shin-ichi Yusa ◽  
Takahiro Sato
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.


1994 ◽  
Vol 9 (2) ◽  
pp. 275-285 ◽  
Author(s):  
V. Milonopoulou ◽  
K.M. Forster ◽  
J.P. Formica ◽  
J. Kulik ◽  
J.T. Richardson ◽  
...  

The YBa2Cu3O7−x formation kinetics from a spray-roasted precursor powder containing Y2O3, BaCO3, and CuO was followed via in situ, time-resolved x-ray diffraction as a function of gas atmosphere and temperature. In inert atmospheres, BaCO3 and CuO form BaCu2O2 which subsequently reacts with Y2O3 to form YBa2Cu3O6. However, YBa2Cu3O6 decomposes at temperatures exceeding 725 °C with Y2BaCuO5 being one of the decomposition products. In oxidizing atmospheres, YBa2Cu3O7−x formation involves the BaCuO2. At high temperatures (800–840 °C), oxygen increases the yield of YBa2Cu3O6. A nuclei growth model assuming two-dimensional, diffusion-controlled growth with second-order nucleation rate fits the experimental data.


2015 ◽  
Vol 17 (2) ◽  
pp. 1070-1076 ◽  
Author(s):  
Hyojung Yoon ◽  
Aoran Xu ◽  
George E. Sterbinsky ◽  
Dario A. Arena ◽  
Ziying Wang ◽  
...  

In situ time resolved XAS measurements are applied to investigate the phase formation kinetics of metastable cobalt carbide nanoparticles using polyol reduction chemistry. The resulting material exhibits an energy product of greater than 20.7 kJ m−3 at room temperature before compaction, a vastly improved coercivity compared to pure bulk material.


1993 ◽  
Vol 311 ◽  
Author(s):  
J. Sariel ◽  
Haydn Chen ◽  
J. F. Jongste ◽  
S. Radelaar

ABSTRACTAmorphous Si/Ti multilayers transform at high temperatures (above 700°C) to TiSi2-C54. This phase is important for microelectronics applications because of its low resistivity, stability up to 900°C, and compatibility with silicon processing. However, an unfavorable metastable TiSi2-C49 phase is usually formed at lower temperatures. Thus, an understanding of the C49 phase formation kinetics is useful to the device processing strategy. The kinetics of the transformation of TiSi2-C49 phase can be characterized as a process of nucleation and growth, using the well known Johnson Mehl Avrami (JMA) equation. In the present work the formation kinetics of the C49 phase has been studied by an in situ x-ray diffraction technique. Isothermal annealing in vacuum was done at four temperatures, in the range of 275"C to 310°C. A position sensitive detector (PSD) was used to simultaneously collect the diffracted beams of (131) and (150) peaks of the C49 phase. From the data, the Avrami exponent, n, was determined to be 2.0±0.1. The reaction rate constant k follows a familiar Arrhenius-type equation with a measured activation energy of 2.5eV. Comparison of our x-ray results with kinetic data obtained by other means will be discussed.


2020 ◽  
Author(s):  
Hao Wu ◽  
Jeffrey Ting ◽  
Boyuan Yu ◽  
Nicholas Jackson ◽  
Siqi Meng ◽  
...  

We have directly observed the in situ 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. A synthesized neutral-charged diblock polycation and homopolyanion that we have previously investigated as a model charge-matched, core-shell micelle system were selected for this work. The initial micellization of the oppositely charged polyelectrolytes was completed within the dead time of mixing of 100 ms, followed by micelle growth and equilibration up to several seconds. By combining the structural evolution of the radius of gyration (Rg) and aggregation number (N) with complementary molecular dynamics simulations, we develop new information on how the self-assemblies evolve incrementally in size over time through a two-step kinetic process: first, oppositely-charged polyelectrolyte chains pair to form nascent aggregates that immediately assemble into spherical micelles, and second, these PEC micelles grow into larger micellar entities. This work has determined one possible kinetic pathway for the initial formation of PEC micelles, which provides useful physical insights for increasing fundamental understanding self-assembly dynamics driven by polyelectrolyte complexation that occur on ultrafast timescales.


Author(s):  
Hao Wu ◽  
Jeffrey Ting ◽  
Boyuan Yu ◽  
Nicholas Jackson ◽  
Siqi Meng ◽  
...  

We have directly observed the in situ 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. A synthesized neutral-charged diblock polycation and homopolyanion that we have previously investigated as a model charge-matched, core-shell micelle system were selected for this work. The initial micellization of the oppositely charged polyelectrolytes was completed within the dead time of mixing of 100 ms, followed by micelle growth and equilibration up to several seconds. By combining the structural evolution of the radius of gyration (Rg) and aggregation number (N) with complementary molecular dynamics simulations, we develop new information on how the self-assemblies evolve incrementally in size over time through a two-step kinetic process: first, oppositely-charged polyelectrolyte chains pair to form nascent aggregates that immediately assemble into spherical micelles, and second, these PEC micelles grow into larger micellar entities. This work has determined one possible kinetic pathway for the initial formation of PEC micelles, which provides useful physical insights for increasing fundamental understanding self-assembly dynamics driven by polyelectrolyte complexation that occur on ultrafast timescales.


2000 ◽  
Vol 104 (17) ◽  
pp. 3964-3973 ◽  
Author(s):  
Sergey A. Nizkorodov ◽  
Warren W. Harper ◽  
Bradley W. Blackmon ◽  
David J. Nesbitt

Sign in / Sign up

Export Citation Format

Share Document