A cationic polymer surface with extensive capacity for adsorption of anionic surfactants was prepared by graft polymerization of vinyl pyridine onto a plasma-treated polypropylene surface. The nitrogen was quaternized in order to obtain the cationic sites. The concentration dependence of adsorption
Microstructure of polymers obtained by cationic polymerization of endo-dicyclopentadiene
β Scribed by Yu Xing Peng; Jia Lin Liu; Lin Feng Cun
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 274 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
SYNOPSIS
endo-Dicyclopentadiene (DCPD) was polymerized by various cationic initiating systems in different solvents. IR and 'H NMR results show that four types of structural units are formed due to the corresponding addition modes: the addition on the norhornenic (NB) double bond generates unit I and rearranged unit 11, while the addition on the cyclopentenic (CP) double bond produces unit I11 and rearranged unit IV. The reaction medium has a stronger effect on the microstructure of the polymer (PDCPD) than initiating systems. The polymers prepared in toluene and n-hexane contain all four structural units, while the polymer produced in methylene chloride is composed of structural units I1 and IV.
π SIMILAR VOLUMES
Poly(hydrogenmethylsiloxane-co-dimethylsiloxane)s of various compositions have been prepared by cationic ring-opening polymerization of octamethylcyclotetrasiloxane (D 4 ) and 1,3,5,7-tetramethylcyclotetrasiloxane (D 4 H ) in the presence of hexamethyldisiloxane as end-blocker or by rearrangement of