Study of the spectra of silica colloidal crystals with assembled silver obtained from a photolysis method

2005 ◽  
Author(s):  
Wenjiang Li ◽  
Jinglong He ◽  
Sailing He
2010 ◽  
Vol 118 (1382) ◽  
pp. 862-866
Author(s):  
Tian-Song DENG ◽  
Jun-Yan ZHANG ◽  
Kong-Tao ZHU ◽  
Qi-Feng ZHANG ◽  
Jin-Lei WU

Nano Letters ◽  
2012 ◽  
Vol 12 (9) ◽  
pp. 4920-4924 ◽  
Author(s):  
Francisco Gallego-Gómez ◽  
Víctor Morales-Flórez ◽  
Álvaro Blanco ◽  
Nicolás de la Rosa-Fox ◽  
Cefe López

2013 ◽  
Vol 34 (5) ◽  
pp. NA-NA
Author(s):  
Robert E. Birdsall ◽  
Brooke M. Koshel ◽  
Yimin Hua ◽  
Saliya N. Ratnayaka ◽  
Mary J. Wirth

2013 ◽  
Vol 117 (29) ◽  
pp. 6244-6249 ◽  
Author(s):  
Benjamin J. Rogers ◽  
Mary J. Wirth

2016 ◽  
Vol 55 (36) ◽  
pp. 10702-10706 ◽  
Author(s):  
Yoshiyuki Kuroda ◽  
Yosuke Shimbo ◽  
Yasuhiro Sakamoto ◽  
Hiroaki Wada ◽  
Kazuyuki Kuroda

Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2329
Author(s):  
Andrey Galukhin ◽  
Guzel Taimova ◽  
Roman Nosov ◽  
Tatsiana Liavitskaya ◽  
Sergey Vyazovkin

This study investigates the kinetics of confined polymerization of bisphenol E cyanate ester in the nanopores of the three types of silica colloidal crystals that differ in the concentration and acidity of the surface-grafted proton-donor groups. In all three types of pores, the polymerization has released less heat and demonstrated a very similar significant acceleration as compared to the bulk process. Isoconversional kinetic analysis of the differential scanning calorimetry measurements has revealed that the confinement causes not only a dramatic change in the Arrhenius parameters, but also in the reaction model of the polymerization process. The obtained results have been explained by the active role of the silica surface that can adsorb the residual phenols and immobilize intermediate iminocarbonate products by reaction of the monomer molecules with the surface silanols. The observed acceleration has been quantified by introducing a new isoconversional-isothermal acceleration factor Zα,T that affords comparing the process rates at respectively identical conversions and temperatures. In accord with this factor, the confined polymerization is 15–30 times faster than that in bulk.


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