scholarly journals The Emulsion Polymerization of Each of Vinyl Acetate and Butyl Acrylate Monomers Using bis (2-ethylhexyl) Maleate for Improving the Physicomechanical Properties of Paints and Adhesive Films

2009 ◽  
Vol 2009 ◽  
pp. 1-6 ◽  
Author(s):  
K. A. Shaffei ◽  
A. B. Moustafa ◽  
A. I. Hamed

Improving the water sensitivity of polyvinyl acetate PVAc films as well as pressure sensitivity, adhesion and washability of polybutyl acrylate were achieved by using bis (2-ethylhexyl) maleate (BEHM). The emulsion polymerization kinetics of vinyl acetate and butyl acrylate in presence of BEHM was studied. The order of the polymerization reaction with respect to the BEHM in presence of each of vinyl acetate and butyl acrylate was studied. The physicomechanical properties of the polyvinyl acetate films and vinyl acetate-butyl acrylate copolymer films were studied in presence of BEHM and the obtained results were matched with those prepared in the presence of pluronic F 108 and showed superior values. The obtained mean average molecular weights were found to be smaller in presence of BEHM assuring the presence of chain transfer reaction.

2021 ◽  
Vol 1028 ◽  
pp. 263-268
Author(s):  
Rafly Aprilian ◽  
Mas Ayu Elita Hafizah ◽  
Azwar Manaf ◽  
Andreas

Synthesis of Polyvinyl Acetate (PVAc) through the conversion of Vinyl Acetate Monomer (VAM) was carried out by emulsion polymerization method assisted by thermal initiator Ammonium persulfate (APS) under reaction temperature was kept at 70 °C – 80 °C with 5 hours of reaction time and agitation speed at 300 rpm. The polymerization reaction was running used batch process technique where is all components were mixed all together simultaneously. A set of polymerization reactions was conducted when the absence of surfactant and cationic and amphoteric surfactant presence. The monomer chain's double bond was found at 1645 cm-1 was measured by FTIR Spectrophotometer did not disappear after polymerization reaction was utterly done. The spectrum FTIR of Polyvinyl acetate did not explicitly found at 1644 cm-1. During the reaction, characterization was conducted by measuring the solid content value where the maximum solid content was achieved was 6,1 % when using Amphoteric surfactant while the lowest solid content was obtained when the absence of surfactant. Other parameters were conducted to observe the acidity value by pH Meter.


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):  
M. S. El-Aasser ◽  
T. Makgawinata ◽  
S. Misra ◽  
J. W. Vanderhoff ◽  
C. Pichot ◽  
...  

Materials ◽  
2020 ◽  
Vol 13 (4) ◽  
pp. 865 ◽  
Author(s):  
Yifu Zhang ◽  
Wenkai Bei ◽  
Zhiyong Qin

The soap-free emulsion of vinyl acetate (VAc)/butyl acrylate (BA) copolymer was prepared by a semi-continuous and pre-emulsification polymerization method, using ammonium sulfate allyloxy nonylphenoxy poly(ethyleneoxy) (10) ether (DNS-86) as a reactive emulsifier. The effects of DNS-86 on the stability of the emulsion and the properties of the latex film were investigated. The infrared spectrum, thermal stability, glass transition temperature and micromorphology of latex were also studied. The results showed that the emulsion had the best stability and the conversion rate reached a maximum of 98.46% when the DNS-86 amount was 4 wt % of the total amount of monomers. Compared with the PVAc latex synthesized with octylphenol polyoxyethylene ether (10) (OP-10), the latex prepared with DNS-86 has higher thermal stability and ionic stability, whereas the latex film has better water resistance.


AIChE Journal ◽  
1988 ◽  
Vol 34 (5) ◽  
pp. 840-848 ◽  
Author(s):  
Chan H. Lee ◽  
Richard G. Mallinson

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