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Polymer surface area

A vacuum system, made of stainless steel, has an internal surface area of 3 m2. In the chamber, there are several electrical connections insulated with PTFE. The polymer surface area is 0.3 m2. If the outgassing constants alh and a are 3 x 10 7 mbar L s 1 cm-2 and 1, respectively, for stain-... [Pg.132]

The synthesis process for the sponges is well established, can be accomplished at room temperature, and the incorporated enzymes have been shown to be stable for over 3 years in a dry state and over 3 months if wet. A large-scale deployment of these sponges is currently limited by the amount of available enzyme. Use of a high-specificity enzyme is desirable but not a necessity because so much enzyme can be integrated into the polyurethane polymer surface area. [Pg.621]

The following phenomena have been proposed to describe the mechanism of PET glycolysis 14,15 glycol diffusion into the polymer, polymer swelling which increases the diffusion rate, and reaction of the glycol with an ester bond in the chain. Because the reaction rate is proportional to the polymer surface area, it is advisable to first reduce the size of the raw PET waste to small particles by grinding, cutting, etc. [Pg.33]

Porapak Polymer Surface area (m g- ) Polarity RI benzene RI 1-butanol Applications... [Pg.206]

It reduces the total surface energy of the system by reducing polymer surface area. [Pg.971]

Generation rate of product j per unit polymer surface area (g/m s) Hydrogen atom... [Pg.486]

Nanoclay is the term generally used when referring to a clay mineral with a phyllosilicate or sheet structure with dimensions of the order of 1 nm thick and surfaces of perhaps 50-150 nm. The mineral base can be natural or synthetic and is hydrophilic. The clay surfaces can be modified with specific chemistries to render them organophilic and therefore compatible with organic polymers. Surface areas of nanoclays are very large, about 750 m /g. When small quantities are added to a host polymer, the resulting product is called a nanocomposite. [Pg.177]

As the particle continues to grew and polymer surface area Increases, more surface active agent Is absorbed from micelles vdilch have not yet been activated, until micelles have either been converted to polymerization sites or the surfactant from v ch they were formed has been absorbed on the e q>andlng polymer surface This point determines the total number of polymer particles that are formed In the dispersion and, consequently, the average size of the particles vhen polymerization Is complete ... [Pg.164]

Typically, the MIPs prepared at lower temperature displayed much smoother surfaces. This was anticipated, as it is known that polymerisation temperature has a direct influence on the polymer particle size and porosity (Lu et al., 2004 Kotrotsiou et al., 2009 Li et al., 2007 Rajaram Hudson, 19%). Interestingly, no fixed correlation between polymer surface area and porosity has been reported for polymers formed in CHCI3, with character dependent upon the nature of the template, functional monomer and cross linker used (Li et al., 2007 Kotrotsiou et al., 2009). [Pg.205]


See other pages where Polymer surface area is mentioned: [Pg.112]    [Pg.585]    [Pg.100]    [Pg.1]    [Pg.97]    [Pg.63]    [Pg.649]    [Pg.100]    [Pg.390]    [Pg.657]    [Pg.420]    [Pg.3146]    [Pg.100]    [Pg.266]    [Pg.26]    [Pg.246]    [Pg.22]    [Pg.1750]    [Pg.234]   


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