Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
Thermal decomposition of polystyrene-b-poly(2-vinylpyridine) coordinated to co nanoparticles
Date
2009-11-01
Author
Elmaci, Ayşegül
Hacaloğlu, Jale
Kayran, Ceyhan
Sakellariou, Georgios
Hadjichristidis, Nikos
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
283
views
0
downloads
Cite This
Direct pyrolysis mass spectrometry analyses of polystyrene-block-poly(2-vinylpyridne), PS-b-P2VP, indicated that the thermal degradation of each component occurred independently through the decomposition pathways proposed for the corresponding homopolymers; depolymerization for PS and depolymerization and loss of protonated oligomers for P2VP by a more complex degradation mechanism. On the other hand, upon coordination to cobalt nanoparticles, thermal decomposition of the P2VP blocks was initiated by loss of pyridine units, leaving an unsaturated and/or crosslinked polymer backbone that degraded at relatively high temperatures.
Subject Keywords
Metal nanoparticles coordinated to block polymers
,
Metal polystyrene-b-poly(2-vinylpyridine)
,
Thermal degradation
,
Pyrolysis mass spectrometry
URI
https://hdl.handle.net/11511/31346
Journal
Polymer Degradation and Stability
DOI
https://doi.org/10.1016/j.polymdegradstab.2009.07.026
Collections
Graduate School of Natural and Applied Sciences, Article
Suggestions
OpenMETU
Core
Thermal decomposition of glycidyl azide polymer by direct insertion probe mass spectrometry
Fazlioǧlu, Hatice; Hacaloğlu, Jale (2002-01-01)
Thermal decomposition reactions and products of glycidyl azide polymer (GAP), have been investigated by direct insertion mass spectrometry and evolved gas analyses by FTIR spectroscopy techniques. It has been observed that thermal degradation of GAP begins with cleavage of the side groups. Although the main decomposition started with the elimination of molecular nitrogen from the azide functional group, degradation initiated by loss of N-3 and CH2N3, depolymerization type reactions were also identified. Rea...
Thermal degradation of poly(p-phenylene-graft-ε-caprolactone) copolymer
Nur, Yusuf; Yurteri, Seda; Cianga, Ioan; Yagci, Yusuf; Hacaloğlu, Jale (2007-01-01)
The thermal degradation of poly (p-phenylene-graft-epsilon-caprolactone) (PPP), synthesized by Suzuki polycondensation of poly(E-caprolactone) (PCL) with a central 2,5-dibromo-1,4-benzene on the chain with 1,4-phenylene-diboronic acid, has been studied via direct pyrolysis mass spectrometry. The thermal degradation occurred mainly in two steps. In the first step, decomposition of PCL chains occurred. A slight increase in thermal stability of PCL chains was noted. In the second stage of pyrolysis, the decomp...
Thermal degradation of polystyrene composites. Part I. The effect of brominated polyepoxy and antimony oxide
Kaya, Hatice; Hacaloğlu, Jale (2014-01-01)
Thermal degradation of polystyrene (PS) involving brominated polyepoxy (BA) and antimony oxide (PS/BE/Sb2O3) was studied systematically via direct pyrolysis mass spectrometry. Thermal decomposition of brominated polyepoxy was started by loss of end groups. The relative yields of high mass thermal degradation products of PS and the product distribution of brominated polyepoxy and antimony oxide were changed noticeably during the pyrolysis of PS/BE/Sb2O3 composite. Its thermal decomposition was initiated by t...
Thermal degradation of poly(propylene oxide) and polyepichlorohydrin by direct pyrolysis mass spectrometry
Uyar, T; Hacaloğlu, Jale (2002-09-01)
The thermal degradation of poly(propylene oxide), (PPO) and polyepichlorohydrin, (PECH) were studied with the use of direct pyrolysis mass spectrometry. The effects of heating rate and dissociative ionization on fragmentation pattern have also been investigated. It has been determined that PPO degrades via a random cleavage mechanism, the labile C-O bond scissions being preferred, An analogous degradation mechanism can be proposed for PECH. Yet, the elimination of side chains, evolution of HCl and the loss ...
Thermal degradation of poly(isobornyl acrylate) and its copolymer with poly(methyl methacrylate) via pyrolysis mass spectrometry
Ozlem, Suriye; Aslan-Guerel, Evren; Rossi, Rene M.; Hacaloğlu, Jale (2013-03-01)
In this work, the thermal degradation characteristics of poly(isobornyl acrylate) (PIBA), and its copolymer with PMMA, P(MMA-co-IBA) were investigated via direct pyrolysis mass spectrometry. Thermal degradation behavior of poly(isobornyl methacrylate) (PIBMA) was also studied for a better understanding of thermal degradation mechanism of PIBA. For both PIBA and PIBMA, gamma-H transfer from the isobornyl ring to the carbonyl group was predominantly effective in thermal degradation. As a consequence of evolut...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
A. Elmaci, J. Hacaloğlu, C. Kayran, G. Sakellariou, and N. Hadjichristidis, “Thermal decomposition of polystyrene-b-poly(2-vinylpyridine) coordinated to co nanoparticles,”
Polymer Degradation and Stability
, pp. 2023–2027, 2009, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/31346.