Organotin Compounds as Pvc Stabilizers
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Date
2008
Authors
Arkış, Esen
Journal Title
Journal ISSN
Volume Title
Publisher
Wiley
Open Access Color
Green Open Access
Yes
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Publicly Funded
No
Abstract
When poly(vinyl chloride) is fabricated, it passes between rollers (calendars) at about 200 ◦C, which causes elimination of some HCl at allylic defects in the polymer, as shown below (Figure 3.3.1). Furthermore, the released HCl induces further elimination, giving a polyolefin structure with a yellow coloration, which turns red, and then black, after which the polymer becomes brittle. This degeneration can be inhibited by organotin stabilizers, often organotin mercaptides that appear to have two principal functions. Firstly, they react with the HCl to give organotin chlorides, which do not catalyze the elimination process. Secondly, they substitute the chloride at the reactive sites, introducing other groups, such as mercaptide groups, which are not easily eliminated. Organotin maleates may also remove diene units by the Diels–Alder reaction.
Description
Keywords
CVD tin compounds, Organotin stabilizer concentration, Organotin stabilizer concentration, CVD tin compounds
Fields of Science
Citation
Arkış, E. (2008). Organotin compounds as PVC stabilizers. In A. G. Davies, M. Gielen, K. H. Pannell and E. R. T. Tiekink /Eds.), Tin Chemistry: Fundamentals, Frontiers, and Applications, (pp. 312-323). Chichester, UK : Wiley. doi:10.1002/9780470758090.ch3
WoS Q
N/A
Scopus Q
N/A

OpenCitations Citation Count
3
Source
Tin Chemistry: Fundamentals, Frontiers, and Applications
Volume
41
Issue
Start Page
312
End Page
323
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CrossRef : 2
Scopus : 19
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Mendeley Readers : 9
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11
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1113
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920
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