In Situ1H NMR Studies of High-Temperature Nitroxide-Mediated Polymerization ofn-Butyl Acrylate

2011 ◽  
Vol 44 (18) ◽  
pp. 7100-7108 ◽  
Author(s):  
Lebohang Hlalele ◽  
Bert Klumperman
2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Yuzhu Zheng ◽  
Deli Xu ◽  
Shiyou Tian ◽  
Manli Li ◽  
Wenwen Wang ◽  
...  

AbstractIn this work, graft copolymer poly (n-butyl acrylate)-g-polyacrylonitrile with poly (n-butyl acrylate) as backbones and polyacrylonitrile as side chains (PnBA-g-PAN) was synthesized by macromonomer method and emulsion polymerization. The macromonomer was synthesized by atom transfer radical polymerization and end-group modification. The chemical structures and thermal properties of macromonomer and graft copolymer were investigated by FTIR, GPC, NMR and TGA, etc. The mechanical properties of graft copolymer elastomer was also measured by uniaxial tensile test. Rheological properties at different temperature and mechanical property demonstrated that graft copolymer elastomer possessed elasticity until 180 oC because of cyclization of cyano groups. Ag nanowires@PnBA-g-PAN composite elastomer was developed, and the resulted material exhibited autonomic healing property on account of segments’ flexibility and dynamic interaction between Ag nanowires (AgNWs) and cyano groups. This is a general method for generation of elastomer with high temperature elasticity and fast self-healing. The composite elastomer has potential application in flexible electronic conductor.


2021 ◽  
pp. 096739112110245
Author(s):  
Amrita Sharma ◽  
PP Pande

It has been observed that acrylate monomers are very difficult to polymerize with the low cost nitroxide catalyst 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO). Therefore, costly acyclic nitroxides such as N-tert-butyl-N-(1-diethylphosphono-2,2-dimethyl)-N-oxyl, (SG1), 2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide (TIPNO) and TIPNO derivatives have to be used for the polymerization of the acrylic acid derivatives. There are very few reports on the use of TEMPO-derivatives toward the polymerization of n-butyl acrylate. Generally different reducing agents viz. glucose, ascorbic acid, hydroxyacetone etc. have been used to destroy excess TEMPO during the polymerization reaction. The acrylate polymerizations fail in the presence of TEMPO due to the strong C–O bond formed between the acrylate chain end and nitroxide. To the best of our knowledge, no literature report is available on the use of TEMPO without reducing agent or high temperature initiators, toward the polymerization of n-butyl acrylate. The present study has been carried out with a view to re-examine the application of low cost nitroxide TEMPO, so that it can be utilized towards the polymerization of acrylate monomers (e.g. n-butyl acrylate). We have been able to polymerize n-butyl acrylate using the nitroxide TEMPO as initiator (via a macroinitiator). In this synthesis, a polystyrene macroinitiator was synthesized in the first step from TEMPO, after this TEMPO end-capped styrene macroinitiator (PSt-TEMPO) is used to polymerize n-butyl acrylate monomer. The amount of macroinitiator taken was varied from 0.05% to 50% by weight of n-butyl acrylate monomer. The polymerization was carried out at 120°C by bulk polymerization method. The experimental findings showed a gradual increase in molecular weight of the polymer formed and decrease in the polydispersity index (PDI) with increase in amount of PSt-TEMPO macroinitiator taken. In all experiments conversion was more than 80%. These results indicate that the polymerization takes place through controlled polymerization process. Effect of different solvents on polymerization has also been investigated. In the following experiments TEMPO capped styrene has been used as macroinitiator leading to the successful synthesis of poly n-Butyl acrylate. It has been found that styrene macroinitiator is highly efficient for the nitroxide mediated polymerization, even in very small concentration for the synthesis of poly n-butyl acrylate. High concentration of macroinitiator results in the formation of block copolymers of polystyrene and poly ( n-butyl acrylate) viz. polystyrene-block-poly-( n-butyl acrylate). The use of TEMPO toward controlled polymerization is of much importance, because it is the nitroxide commercially available at the lowest cost.


Author(s):  
O. B. Lapina ◽  
V. V. Terskikh ◽  
B. S. Bal’Zhinimaev ◽  
K. M. Eriksen ◽  
R. Fehrmann

Polymers ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1897
Author(s):  
Hui Yang ◽  
Haijun Ji ◽  
Xinxin Zhou ◽  
Weiwei Lei ◽  
Liqun Zhang ◽  
...  

A novel elastomer poly(diethyl itaconate-co-butyl acrylate-co-ethyl acrylate-co-glycidyl methacrylate) (PDEBEG) was designed and synthesized by redox emulsion polymerization based on bio-based diethyl itaconate, butyl acrylate, ethyl acrylate, and glycidyl methacrylate. The PDEBEG has a number average molecular weight of more than 200,000 and the yield is up to 96%. It is easy to control the glass transition temperature of the PDEBEG, which is ranged from −25.2 to −0.8 °C, by adjusting the monomer ratio. We prepared PDEBEG/CB composites by mixing PDEBEG with carbon black N330 and studied the oil resistance of the composites. The results show that the tensile strength and the elongation at break of the composites with 10 wt% diethyl itaconate can reach up to 14.5 MPa and 305%, respectively. The mechanical properties and high-temperature oil resistance of the composites are superior to that of the commercially available acrylate rubber AR72LS.


2002 ◽  
Vol 602-603 ◽  
pp. 89-103 ◽  
Author(s):  
Koji Saito ◽  
Moriaki Hatakeyama ◽  
Ikuo Komaki ◽  
Kenji Katoh

Polymer ◽  
2010 ◽  
Vol 51 (21) ◽  
pp. 4806-4813 ◽  
Author(s):  
Azhar Juhari ◽  
Jaroslav Mosnáček ◽  
Jeong Ae Yoon ◽  
Alper Nese ◽  
Kaloian Koynov ◽  
...  

2010 ◽  
Vol 63 (8) ◽  
pp. 1237 ◽  
Author(s):  
Jessica Marchand ◽  
Laurent Autissier ◽  
Yohann Guillaneuf ◽  
Jean-Luc Couturier ◽  
Didier Gigmes ◽  
...  

Due to a specific balance between steric, polar, and stabilization effects, SG1 nitroxide and its corresponding alkoxyamine BlocBuilder MA are now well recognized as two of the most potent compounds in nitroxide-mediated polymerization (NMP). In this work, alternatives to SG1, based on various aldehydes, were targeted using structure–reactivity relationships already developed by our group. Compared with SG1, we show that the substitution of the tert-butyl group on the carbon α to the aminoxyl function by a 2-ethylhexyl group led to a new nitroxide (ETHEXNO), which exhibited an half-life time at 120°C similar to SG1 and a slightly slower kd for the alkoxyamine (2–3 times lower than the SG1). The styrene polymerization mediated by the ETHEXNO nitroxide has a similar behaviour to the one mediated by the SG1 in terms of livingness and control but the kinetics is affected (2–3 times lower). Concerning the n-butyl acrylate polymerization, an unexpected overheating occurred at 120°C, which led us to perform the polymerization in toluene at 100°C. The slow kinetics impedes the use of this nitroxide as a good alternative to SG1 and shows that the structure of the SG1 nitroxide is already delicately optimized and finding good alternatives is not straightforward.


2019 ◽  
Vol 10 (15) ◽  
pp. 1956-1967 ◽  
Author(s):  
Marco Drache ◽  
Maria Stehle ◽  
Jonas Mätzig ◽  
Katrin Brandl ◽  
Marcel Jungbluth ◽  
...  

Unsaturated low molar mass species were identified via ESI-MS after fractionation of poly(butyl acrylate) from high temperature radical polymerization.


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