scholarly journals Kinetics of ascorbic acid loss during thermal treatment in different pH buffer solutions and the presence of oxygen

Food Research ◽  
2020 ◽  
Vol 4 (5) ◽  
pp. 1513-1519
Author(s):  
N.M. Thuy ◽  
H.T.N. Ha ◽  
N.V. Tai

Ascorbic acid stability is greatly influenced by temperature, oxygen content. Both exposures to oxygen and prolonged heating in the presence of oxygen destroy ascorbic acid. Thermal degradation kinetics of ascorbic acid in sodium acetate buffer (0.2 M, pH 5.0) and sodium phosphate buffer (0.1 M, pH 7.0) were studied at the temperature range of 80 to 100°C and the different molar ratio between oxygen and ascorbic acid. The obtained results showed that the decrease in AA concentration as a function of time at constant temperature occurred in two phases. The biphasic model was used to describe the loss of AA in aqueous solution due to thermal treatment. The AA degradation had occurred during thermal processing probably due to oxidation (aerobic degradation). When the oxygen was totally used up, the anaerobic degradation dominated and took place much more slowly than aerobic degradation. At low AA concentration (≈0.28 mM) and an oxygen concentration of 0.25 mM, most of the degradation of AA occurred under aerobic conditions, however, AA was further degraded through an anaerobic pathway at a higher ratio of AA to oxygen concentration [0.57:0.25 (mM:mM) and 1.42:0.25 (mM:mM)]. The estimated activated energy Ea values, the temperature sensitivity of the kvalues was lower at pH 7.0 than at pH 5.0. Studying the degradation of ascorbic in a model system is essential in order to fully understood and applied effectively in food products processing.

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1597
Author(s):  
Iman Jafari ◽  
Mohamadreza Shakiba ◽  
Fatemeh Khosravi ◽  
Seeram Ramakrishna ◽  
Ehsan Abasi ◽  
...  

The incorporation of nanofillers such as graphene into polymers has shown significant improvements in mechanical characteristics, thermal stability, and conductivity of resulting polymeric nanocomposites. To this aim, the influence of incorporation of graphene nanosheets into ultra-high molecular weight polyethylene (UHMWPE) on the thermal behavior and degradation kinetics of UHMWPE/graphene nanocomposites was investigated. Scanning electron microscopy (SEM) analysis revealed that graphene nanosheets were uniformly spread throughout the UHMWPE’s molecular chains. X-Ray Diffraction (XRD) data posited that the morphology of dispersed graphene sheets in UHMWPE was exfoliated. Non-isothermal differential scanning calorimetry (DSC) studies identified a more pronounced increase in melting temperatures and latent heat of fusions in nanocomposites compared to UHMWPE at lower concentrations of graphene. Thermogravimetric analysis (TGA) and derivative thermogravimetric (DTG) revealed that UHMWPE’s thermal stability has been improved via incorporating graphene nanosheets. Further, degradation kinetics of neat polymer and nanocomposites have been modeled using equations such as Friedman, Ozawa–Flynn–Wall (OFW), Kissinger, and Augis and Bennett’s. The "Model-Fitting Method” showed that the auto-catalytic nth-order mechanism provided a highly consistent and appropriate fit to describe the degradation mechanism of UHMWPE and its graphene nanocomposites. In addition, the calculated activation energy (Ea) of thermal degradation was enhanced by an increase in graphene concentration up to 2.1 wt.%, followed by a decrease in higher graphene content.


Materials ◽  
2017 ◽  
Vol 10 (11) ◽  
pp. 1246 ◽  
Author(s):  
Samson M. Mohomane ◽  
Tshwafo E. Motaung ◽  
Neerish Revaprasadu

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