Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Ethylene lonomers

The crystallinity levels in ethylene ionomers are generally low due to their high levels of branching and the clustering of the metal salts. At high temperatures, the clusters dissociate and the individual chains can move independently in the molten state, permitting them to be molded. When the ionomer is cooled clusters reform, crosslinking the chains [Pg.281]

As cast or blown films we encounter polyethylene in packaging films, bags, cling film, greenhouse skins, diaper back sheets, and high altitude scientific balloons. In these applications [Pg.281]

Rotationally molded objects include kayaks and agricultural chemical storage tanks, which are lightweight and tough, especially when crosslinked. Other large items, such as pick up truck bed liners and panels for portable sanitation facilities, are made by thermoforming. [Pg.282]

Ultrahigh molecular weight ultra-oriented fibers have outstanding tensile strength and modulus, which suits them for use in bullet proof vests. [Pg.282]

Describe the seven different classes of polyethylene and explain how the structural differences affect the tensile strength, crystallinity and flexural modulus of each of the materials. [Pg.283]


New lonomer Types. There is a continuing interest in new ionomers within the academic community, since novel and unexpected phenomena are frequently being discovered. However, there are still many unanswered questions with respect to the ethylene ionomers, especially the influence of ionic bonding on crystalline stmcture. Continued study of these interesting polymers will close the gaps in knowledge of this area of polymer science. [Pg.409]

Property lonomer Ethlene-vinyl acetate Ethylene-ethyl acrylate Units... [Pg.277]

Sulfonated-Styrene(Ethylene-Co-Butylene)-Styrene Triblock lonomer... [Pg.116]

Fluorinated ethylene propylene (FEP) Pol y tet raftuoroe th ylene (FTFE) Polyvinyl fluoride (PVF) Polyvinylidene fluoride (PVDF) lonomer Ketone... [Pg.5]


See other pages where Ethylene lonomers is mentioned: [Pg.232]    [Pg.402]    [Pg.406]    [Pg.647]    [Pg.651]    [Pg.295]    [Pg.299]    [Pg.232]    [Pg.402]    [Pg.406]    [Pg.647]    [Pg.651]    [Pg.836]    [Pg.1208]    [Pg.620]    [Pg.625]    [Pg.270]    [Pg.277]    [Pg.281]    [Pg.409]    [Pg.232]    [Pg.402]    [Pg.406]    [Pg.647]    [Pg.651]    [Pg.295]    [Pg.299]    [Pg.232]    [Pg.402]    [Pg.406]    [Pg.647]    [Pg.651]    [Pg.836]    [Pg.1208]    [Pg.620]    [Pg.625]    [Pg.270]    [Pg.277]    [Pg.281]    [Pg.409]    [Pg.1021]    [Pg.12]    [Pg.154]    [Pg.378]    [Pg.574]    [Pg.587]    [Pg.611]    [Pg.805]    [Pg.909]    [Pg.1087]    [Pg.452]    [Pg.280]    [Pg.199]    [Pg.217]    [Pg.228]    [Pg.229]    [Pg.693]    [Pg.378]    [Pg.869]    [Pg.869]    [Pg.869]    [Pg.473]    [Pg.9]   


SEARCH



Lonomer

Lonomers

© 2024 chempedia.info