IRGANOX 1076 PDF

Irganox is a high molecular weight phenolic antioxidant. CAS# Click here for quote or sample. Irganox® highly efficient, non-discoloring, sterically hindered primary phenolic antioxidant stabilizer that protects organic substrates against. Get instant access to Irganox® technical datasheet. It is a highly efficient sterically hindered phenolic primary antioxidant which provides processing and.

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A irgznox melting B at the beginning of melting C for an almost melt needle. However irgahox data tend to prove that form II is converted into form I before form I melts. Received 21st OctoberAccepted 8th December For others the transition needs the forming of critical nuclei of the new phase, such as local defects: A band characteristic of form I was detected but only with a small absorbance.

As shown by the adhesion measurement, no liquid areas were detected during the first moments of the process images 1—13 from Fig. As evidenced in Fig. We considered more specifically in this paper the case of additives contained in a polymer used as a medical device. The company allows additional tests when necessary and the commercial support is helpful an irganod.

You may choose a language below to continue to this industry or close this dialog above. Irgamox the band of form I kept growing and the form II band absorbance decreased slightly with time. We estimated the transition temperature using the following relationship, which was used quite successfully by other authors: It allows to distinguish between the crystallized AO regions from the rest of the sample: AFM is proved to be a powerful method for evidencing the slow speed phase transitions.

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We might thus explain the recrystallization into form I from the melt after the melting of forms IV and III by the fact the free enthalpy of form I is below that of the liquid but higher than those of form II 1067 form III at least up to the form III melting temperature.

Using these results and the melting temperature of the forms, we propose an enthalpy H T and a free enthalpy G T diagram Fig. The growth of the characteristic band of the melting state was observed. However, UL assumes no responsibility or liability for the accuracy of the information contained on this website and strongly encourages that upon final product or material selection information is validated with the manufacturer.

Octadecyl DI-tert-butylhydroxyhydrocinnamate | C35H62O3 – PubChem

It should be noted that the onset of the melting temperature for form III was found at The heating rate used was a quick one till the form III melted. For a quick heating Fig. Our innovative products also help manufacturers in the adhesives, nonwovens and fiber bonding industries meet functional and performance demands. This may be the high-temperature stable form before melting; however, as the forms I and II have very close enthalpies of fusion, it is thus not trivial to conclude about a monotropic or enantiotropic transition between them.

We’re sorry, but the industry you have selected is not currently available in your chosen language. From using DSC enthalpy of fusion of the forms, this transition is irganx an enantiotropic irganoxx between the low temperature stable form III and the form II. The enthalpy of fusion of form II is a little higher than that of form I and its melting point a little lower, what would be consistent with the fact that form I is the stable form at high temperature. As a consequence, two samples with form III were evaluated by using two relevant heating rates as deduced from the DSC experiments.

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Irganox® by BASF Dispersions & Resins – Paint & Coatings

Irganox an antioxidan primarily used to stabilize various polymers, especially polyamides. Images correspond to the height images presented on the Fig. However it was difficult to exclude the previous melting of the form II because it was shown that, at this heating rate, forms I and II have very close melting temperature and enthalpies of fusion.

It is indeed well known that surface properties will condition the device biocompatibility and the bioadhesion on it.

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Isotherms were realized during hours at different temperatures between 42 and The initial AO crystal structure is thus strongly modified during these thermal treatments. After this plasma treatment the polymer surface was more hydrophilic, but there was a hydrophobic recovery of the surface with time: Stearyl 3- 3,5-Di-tert-butylhydroxyphenyl propionate;Stearyl 3- 3,5-Di-tert-butylhydroxyphenyl propionate;ctadcyl-3,5-di-tert-butylhydroxyhydrcinnamate.

Transition might be thus induced only locally on the AFM scanned zone. Experiments with several heating rates were done with form III powder in order to explicit the transformation observed by AFM.