A Topologically Interpenetrating Elastomeric Network

1970 ◽  
Vol 43 (4) ◽  
pp. 883-886 ◽  
Author(s):  
H. L. Frisch ◽  
D. Klempner ◽  
K. C. Frisch

Abstract While chemically different monomers can be mixed, the mixing of the corresponding polymers in the solid state usually results in (multiphase) polyblends. Even the mixing of two different polymer solutions generally produces two liquid phases. This difficulty can be overcome, without resorting to grafting, by producing interpenetrating polymer networks (IPN). By crosslinking an initially linear polymer in the presence of a crosslinked network we can produce a polymeric catenane or an IPN held together predominantly by “permanent” entanglements, assuming chain transfer reactions can be suppressed. Several workers have made IPN's from either chemically identical or chemically similar polymers and have studied their properties. In this work, two different elastomers, a crosslinked polyether-based poly(urethane-urea) and a linear poly(butadiene-acrylonitrile), as aqueous emulsions, are mixed, together with crosslinking agents and stabilizers, films cast, and subsequently cured to form the IPN. A partial chemical structure proof is obtained by separating the crosslinked poly(butadiene-acrylonitrile) from the IPN by essentially total hydrolysis of the interpenetrating poly(urethane-urea) network.

1995 ◽  
Vol 385 ◽  
Author(s):  
Barry J. Bauer ◽  
Catheryn L. Jackson ◽  
Da-Wei Liu

ABSTRACTInterpenetrating polymer networks have been synthesized by performing sol-gel chemistry and conventional organic polymerizations in mixtures of the monomers. The organic polymers were acrylates, and the inorganic phase was SiO2 formed by hydrolysis of orthosilicates. Polymerizations were conducted at a variety of relative rates, and the chemistry was designed to allow different amounts of grafting between the components. The morphology was characterized by transmission electron microscopy and small angle neutron and x-ray scattering. Wide variations in morphology were observed depending on the polymerization conditions, ranging from grossly phase separated to dendritic to finely divided structures (at a 100Å size scale). The phases ranged from mixtures of the two components to relatively pure phases. The interface between the phases ranged from very narrow to relatively broad.


e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Xiaozhen Chen ◽  
Shimei Xu ◽  
Shun Feng ◽  
Jide Wang ◽  
Xin Li

AbstractA novel amphoteric hydrogel with semi-interpenetrating polymer networks (semi-IPNs), was prepared by entrapping linear poly[2-[(methacryloyloxy) ethyl]trimethylammonium] chloride (PDMC) into lightly crosslinked starch phosphate- graft-acrylic acid (St-OPO3-g-AA) network in aqueous solution. The influences including the degree of substitution (DS) of starch phosphate, the doses of crosslinker, AA and PDMC were investigated with respect to the swelling capacity. The swelling capacity of hydrogel reached 2016 g/g in deionized water and 121 g/g in 0.9 wt% NaCl solutions, respectively. The swelling behaviors of hydrogel in various salt solutions and different pH buffer solutions were discussed. The amphoteric semi-IPN hydrogels exhibited pH-sensitivity and salt-resistance.


Polymer ◽  
2021 ◽  
Vol 224 ◽  
pp. 123671
Author(s):  
Gregory N. Smith ◽  
Erik Brok ◽  
Martin Schmiele ◽  
Kell Mortensen ◽  
Wim G. Bouwman ◽  
...  

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