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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The growth of the characteristic band of the melting state was observed. The initial AO crystal structure is thus strongly modified during these thermal treatments. When the heating was quicker, as studied in one of our idganox paper, 13 only the melting of form II was observed.

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Keep it up and wish you all the best for future challenges. As no difference in stiffness and adhesion were put into evidence between form II and III, it was not possible up to now to discriminate them.

After this plasma treatment the polymer surface was more hydrophilic, but there was a hydrophobic recovery of the surface with time: No melting phenomenon occurred during this process as shown by the adhesion measurements Fig. When the heating rate was lower below 0. This website provides links to other websites owned by third parties. As for irfanox III, some initial crystalline structures disappeared see the circles on Fig.

Transition irgxnox be thus induced only locally on the AFM scanned zone. However this transition has been put into evidence by this AFM study: When only using classical tools like DSC or FTIR, it is indeed difficult to very early detect changes in structures as they appear at a nano-level on the crystal surface.


The liquid thickness Fig.

However this melting of form III is concomitant to an exothermic peak characteristic of a recrystallization as observed on DSC thermogram. However our data tend to prove that form II is converted into form I before form I melts. We observed profiles of the adhesion perpendicular to the melting front of the AO crystal.

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.

In a previous paper, 26 the aging behaviour of a catheter after a discharge nitrogen plasma treatment was studied. Free Shipping for worldwide on order above USD. We have been clients of theirs for several years and we have an excellent working relationship. Irganox Worldwide Suppliers of Irganox https: Using these results and the melting temperature of the forms, we propose an enthalpy H T and a free enthalpy G T diagram Fig.

Octadecyl DI-tert-butylhydroxyhydrocinnamate | C35H62O3 – PubChem

Idganox phenomenon was observed for the melting of the other forms which began at around Thanks allot for your support and action in time. This wider melting range might result from a premelting process which occurs because of the presence of impurities in the compound using the rate of melting of the sample, the purity analysis by DSC indicated a purity of We’re sorry, but the industry you have selected is not currently available in irgaonx chosen language.

Images correspond to the height images presented on the Fig. Clearsynth has excellent products with fantastic customer service. A band characteristic of form I was detected but only with a small absorbance.


Then the band of form I kept growing and the form II band absorbance decreased slightly with time. It should be noted that the onset of the melting temperature for form III was found at The company allows additional tests when necessary and the commercial support is helpful an fast. Polymorphism is not always easy to understand and to predict and its comprehension needs the use and association of different analytical techniques. I really commend the prompt service provided by Mr.

We normally respond within 2 hours. A before melting B at the beginning irganos melting C for an almost melt needle.

Stearyl 3- 3,5-Di-tert-butylhydroxyphenyl propionate;Stearyl 3- 3,5-Di-tert-butylhydroxyphenyl propionate;ctadcyl-3,5-di-tert-butylhydroxyhydrcinnamate.

I am satisfied with their products quality, pricing and customer service. Stearyl 3- 3,5-Di-tert-butylhydroxyphenyl propionate;Stearyl 3- 3,5-Di-tert-butylhydroxyphenyl propionate;ctadcyl-3,5-di-tert-butylhydroxyhydrcinnamate Application Notes: We may suppose it is a transition between form II and form I for the following reasons: By studying adhesion force image Fig.

In comparison, the adhesion at AO crystals is around 4 nN Fig. In the medical field and, despite its potential importance, the phenomenon of blooming was much less studied than the migration of additives in the body fluids. Increasing the temperature of several degrees had a deep impact on the phase transformation kinetics: Then isotherms were consecutively realized at Experiments with several heating rates were done with form III powder in order to explicit the transformation observed by AFM.