scholarly journals Homogeneous Graft Copolymerization of Vinyl Monomers onto Cellulose in a Dimethyl Sulfoxide–Paraformaldehyde Solvent System III. Methyl Acrylate

1983 ◽  
Vol 15 (8) ◽  
pp. 591-596 ◽  
Author(s):  
Noboru Nishioka ◽  
Kouji Minami ◽  
Kouichi Kosai
1986 ◽  
Vol 18 (4) ◽  
pp. 323-330 ◽  
Author(s):  
Noboru Nishioka ◽  
Yoshiyuki Matsumoto ◽  
Toshiyuki Yumen ◽  
Kouji Monmae ◽  
Kouichi Kosai

2002 ◽  
Vol 10 (5) ◽  
pp. 391-404 ◽  
Author(s):  
Inderjeet Kaur ◽  
B. N. Misra ◽  
Raj Kumar ◽  
Baljit Singh

To introduce functional moieties into Tefzel® film, a copolymer of tetrafluoroethylene and ethylene, graft copolymerization of vinyl monomers such as methyl acrylate (MA) and ethyl acrylate (EA) was attempted by a pre-irradiation method in aqueous medium. Optimum conditions for obtaining the maximum grafting was evaluated for both monomers. Maximum grafting of MA (306.0%) and EA (462.1%) was obtained at a total dose of 25.4 and 31.9kGy respectively, using [MA] = 2.20 mol/L and [EA] 0.032 moles. The effect of aliphatic alcohols of varying chain length, such as methanol, ethanol, n-butanol, 1-Pentanol and cyclohexanol on the percentage grafting of MA & EA was also studied. Characterization of Tefzel® and grafted Tefzel® films was carried out by IR spectroscopy and thermogravimetric analysis. Grafted Tefzel® film was found to have improved thermal resistance.


2014 ◽  
Vol 70 (11) ◽  
pp. 1050-1053 ◽  
Author(s):  
Xiang Li ◽  
Zhi-Gang Wang ◽  
Hou-He Chen ◽  
Sheng-Gao Liu

The title compound, C18H28O3, was prepared by the reaction of 2,6-di-tert-butylphenol with methyl acrylate under basic conditions using dimethyl sulfoxide as the promoter. The structure of this antioxidant indicates significant strain between theortho tert-butyl substituents and the phenolic OH group. In spite of the steric crowding of the OH group, it participates in intermolecular hydrogen bonding with the ester carbonyl O atom.


1977 ◽  
pp. 421-428
Author(s):  
R. V. Kucher ◽  
Ju. S. Zaitsev ◽  
A. A. Kuznetsov ◽  
V. V. Zaitseva

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