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Silicone networks

The types of polymers that are used as release coatings include silicone networks, silicone containing copolymers, polymers with long alkyl or fluoroalkyl side chains, fluoropolymers, and polyolefins. These polymers have surface energies that are less than the surface energies of commonly used PSAs, an important feature of release materials. [Pg.536]

Silicone release coatings are the workhorses of the easy release industry because the very nature of the molecule fulfills most requirements for low adhesion. When well cured, silicone networks are fairly inert and present a very low sur-... [Pg.546]

Fluorosilicones consist of PDMS backbones with some degree of fluoro-aliphatic side chains. The fluorinated group can be trifluoropropyl, nonafluorohexylmethyl, or fluorinated ether side group [78,28,79]. These polymers differ not only in substituent group, but also in the amount of fluoro-substitution relative to PDMS, the overall molecular weight and crosslink density, and the amount of branching. In most commercially available cases, these polymers are addition cure systems and the reactions are those discussed previously for silicone networks. [Pg.550]

Yamamoto and Minamizaki [159] disclose the use of a curable silicone based release agent blended with resin particles which swell or are soluble in organic solvent. Coatings made with such blends can be written on with solvent based inks. For example, an addition cure silicone network containing 20 wt% 0.1 p,m diameter PMMA particles exhibited both good writeability (no ink dewetting and smear free) and a low release force of 10 g/cm for a PSA tape. [Pg.565]

A chemical property of silicones is the possibility of building reactivity on the polymer [1,32,33]. This allows the building of cured silicone networks of controlled molecular architectures with specific adhesion properties while maintaining the inherent physical properties of the PDMS chains. The combination of the unique bulk characteristics of the silicone networks, the surface properties of the PDMS segments, and the specificity and controllability of the reactive groups, produces unique materials useful as adhesives, protective encapsulants, coatings and sealants. [Pg.681]

Silicone adhesives are generally applied in a liquid and uncured state. It is therefore the physical and chemical properties of the polymers, or more precisely of the polymer formulation, that guide the various processes leading to the formation of the cured silicone network. The choice of the cure system can be guided by a variety of parameters that includes cure time and temperature, rheological properties in relation with the application process, substrates, the environment the adhesive joints will be subjected to and its subsequent durability, and of course, cost. [Pg.681]

Once cured, PDMS networks are essentially made of dimethylsiloxane polymeric chains crosslinked with organic linkages. The general and inherent molecular properties of the PDMS polymers are therefore conferred to the silicone network. Low surface energy and flexibility of siloxane segments are two inherent properties very useful in adhesion technology. [Pg.688]

It is noteworthy that an important industrial application is based on pure silicone network [9]. This is the organic PSA release technology where an uncured silicone is deposited as a thin coating to a flexible substrate. Strong adhesion develops at the silicone-substrate interface whilst the coating cures. [Pg.688]

In silicone adhesives used to bond structural glazing assemblies, the silicone network is made of very long PDMS chains and is filled with silica that improves the elastomeric properties of the adhesive. The strength of such an adhesive is strongly enhanced through various mechanisms of energy absorption. [Pg.694]

Silicone networks that form the matrix of the adhesives are not susceptible to degrade or to depolymerize when exposed to a wide range of conditions of temperature and relative humidity. Therefore, the cohesive strength will not change, as... [Pg.698]

The second class of models was formulated by Winer [441] and Street [442, 443]. Here the notion that hydrogen atoms are more mobile than silicon atoms forms the basis of the model. The silicon network is fixed up to a temperature... [Pg.130]

Equilibrium Tensile Behavior of Model Silicone Networks of High Junction Functionality... [Pg.329]


See other pages where Silicone networks is mentioned: [Pg.889]    [Pg.47]    [Pg.49]    [Pg.49]    [Pg.537]    [Pg.543]    [Pg.547]    [Pg.547]    [Pg.549]    [Pg.558]    [Pg.559]    [Pg.566]    [Pg.566]    [Pg.682]    [Pg.682]    [Pg.688]    [Pg.691]    [Pg.691]    [Pg.694]    [Pg.10]    [Pg.11]    [Pg.86]    [Pg.128]    [Pg.129]    [Pg.331]    [Pg.333]    [Pg.335]    [Pg.337]    [Pg.339]    [Pg.341]    [Pg.343]    [Pg.345]    [Pg.347]    [Pg.397]    [Pg.398]   
See also in sourсe #XX -- [ Pg.682 ]

See also in sourсe #XX -- [ Pg.682 ]




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Carbon and Silicon Network Atomic Solids

Incorporation into silicone network

Network atomic solids silicon

Network solids silicon

Networks Silicon Resin network

Silicon networks

Silicon oxide network

Silicon-based interpenetrating polymer network materials

Silicon-based interpenetrating polymer networks

Silicone networks behavior

Silicone networks formation

Silicone networks functionality

Silicone networks high junction

Silicone networks nanocomposites

Silicone networks organic-inorganic hybrids

Silicone resin network

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