Styrene/Methacrylic Acid Monomer Reactivity Ratio Estimation in Bulk and Solution at High Temperatures

2005 ◽  
Vol 44 (4) ◽  
pp. 771-782 ◽  
Author(s):  
Nahla Sahloul ◽  
Alexander Penlidis
RSC Advances ◽  
2017 ◽  
Vol 7 (17) ◽  
pp. 10175-10182
Author(s):  
Zhen Yao ◽  
Da-Feng Ma ◽  
Zhi-xian Xiao ◽  
Wen-long Yang ◽  
Yu-Xia Tu ◽  
...  

Salicylaldiminato-derived [O-NS]TiCl3 is used in the copolymerization of ethylene and propylene in toluene solution with methylaluminoxane as the co-catalyst.


2021 ◽  
Vol 29 (9_suppl) ◽  
pp. S1432-S1445
Author(s):  
Ibrahim Erol ◽  
Bayram Gencer ◽  
Zeki Gurler

In this study, 2-{[(2H-1,3-benzodioxol-5-yl)methyl]amino}-2-oxoethyl 2-methylprop-2-enoate (BMAOME) monomer was synthesized, and copolymers were prepared with glycidyl methacrylate (GMA). Structural characterizations of the compounds were performed using FTIR, 1H-, and 13C-NMR techniques. Monomer reactivity ratio values were calculated by Finemann–Ross (FR) and Kelen–Tudos (KT) methods. The Tg value of the polymers was determined by differential scanning calorimetry (DSC) and their thermal stability was determined by thermogravimetric analysis (TGA). The molecular weights (w and n) and polydispersity index of the polymers were determined by gel permeation chromatography. The Ea value of thermal decomposition was determined by using the Ozawa and Kissinger methods. The photo-stability of the copolymers was investigated. Furthermore, the photo-stability of the copolymers and the biological activity of polymers against different types of bacteria and fungi were investigated.


Processes ◽  
2019 ◽  
Vol 7 (7) ◽  
pp. 444 ◽  
Author(s):  
Scott ◽  
Gabriel ◽  
Dubé ◽  
Penlidis

Multi-component polymers can provide many advantages over their homopolymer counterparts. Terpolymers are formed from the combination of three unique monomers, thus creating a new material that will exhibit desirable properties based on all three of the original comonomers. To ensure that all three comonomers are incorporated (and to understand and/or predict the degree of incorporation of each comonomer), accurate reactivity ratios are vital. In this study, five terpolymerization studies from the literature are revisited and the ‘ternary’ reactivity ratios are re-estimated. Some recent studies have shown that binary reactivity ratios (that is, from the related copolymer systems) do not always apply to ternary systems. In other reports, binary reactivity ratios are in good agreement with terpolymer data. This investigation allows for the comparison between previously determined binary reactivity ratios and newly estimated ‘ternary’ reactivity ratios for several systems. In some of the case studies presented herein, reactivity ratio estimation directly from terpolymerization data is limited by composition restrictions or ill-conditioned systems. In other cases, we observe similar or improved prediction performance (for ternary systems) when ‘ternary’ reactivity ratios are estimated directly from terpolymerization data (compared to the traditionally used binary reactivity ratios). In order to demonstrate the advantages and challenges associated with ‘ternary’ reactivity ratio estimation, five case studies are presented (with examples and counter-examples) and troubleshooting suggestions are provided to inform future work.


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