In this study the degradation of Methyl Orange, using Fenton reaction was studied and optimized using central composite design as a response surface methodology. The effects of various experimental parameters in this reaction were investigated using central composite design. 28 experiments, with 4 factors and 5 levels for each factor were designed. These factors (or variables) were: initial concentration of Fe (II), initial concentration of H2O2, initial concentration of oxalate and the reaction time. A full-quadratic polynomial equation between the percentage of dye degradation (as a response) and the studied parameters was established. After removing the non-significant variables from the model, response surface method was used to obtain the optimum conditions. The optimum ranges of variables were: 0.25 - 0.35 mM for initial concentration of Fe (II), 5-17 mM for initial concentration of H2O2, 4-9 mM for initial concentration of oxalate, and 50-80 min for the reaction time. Also the results of extra experiments showed that these optimized values can be used for real samples and yield to a high value for the response

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In this study the degradation of an azo dye, Methyl Red, which is used in textile industry, using Fenton reaction was studied and optimized by a chemometrics method. Fenton oxidation is one of the Advanced Oxidation Processes (AOPs), in which hydroxyl radicals are generated from Fenton's reagents (Fe

Heteroatom doping is regarded as a promising method for controlling the optoelectronic properties of carbon nanodots (CNDs), notably their fluorescence and antioxidation activities. In this study, phosphorous (P) and boron (B) are doped at different quantities in the CNDs’ structures to investigate their effects on the optical and antioxidation properties. Both the dopants can enhance light absorption and fluorescence, yet via different approaches. After doping, the UV–vis absorption of high P%-CNDs demonstrated a slight blue shift (348–345 nm), while the high B%-CNDs showed a minor red shift (348–351 nm), respectively. The fluorescence emission wavelength of doped CNDs changes marginally while the intensity increases significantly. Structural and composition characterizations show elevated levels of C=O on the surface of high P%-CND compared to low P%-CNDs. In B-doped CNDs, more NO 3 – functional groups and O–C=O bonds and fewer C–C bonds form at the surface of high B%-CNDs compared to the low B%-CNDs. A radical scavenging study using 2,2-diphenyl-1-picrylhydrazyl (DPPH) was carried out for all CNDs. It was found that the high B%-CNDs exhibited the highest scavenging capacity. The effects of the atomic properties of dopants and the resulting structures of CNDs, including atomic radius, electronegativity, and bond lengths with carbon, on the optoelectronic property and antioxidative reactions of CNDs are comprehensively discussed. It suggests that the effect of P-doping has a major impact on the carbogenic core structure of the CNDs, while the B-doping mainly impacts the surface functionalities.

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