Exploring the activity of chemical-activated carbons synthesized from peach stones as metal-free catalysts for wet peroxide oxidation

• Autor(a) principal: Martin-Martinez, Maria
• Data de Publicação: 2018
• Outros Autores: Álvarez-Torrellas, Silvia, García, Juan, Silva, Adrián, Faria, Joaquim, Gomes, Helder
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/10198/14483
• topic: Activated carbon; Chemical activation; Metal-free CWPO; Peach stone

Peach stones were used as raw material for the synthesis of activated carbons with different properties. Firstly, peach stones were chemically activated using a 12M H3PO4 solution and carbonized under flowing air (400 °C). The obtained activated carbon, named as PS, is characterized by a high surface development (SBET=1262m2 g−1) and acidic character (pHPZC=4.2). A fraction of PS was further carbonized under N2 atmosphere at 800 °C to remove surface functionalities and to increase its basicity (PS-800). In addition, a Pt catalyst supported on PS (3% w/w Pt/PS) was synthesized by incipient wetness impregnation, resulting in a considerable hydrophilicity increasing. The synthesized materials were tested in the catalytic wet peroxide oxidation (CWPO) of highly concentrated solutions of 4-nitrophenol (4-NP, 5 g L−1) during 24 h experiments, conducted at relatively mild operating conditions (T=50–110 °C, pH=3, catalyst load=2.5 g L−1 and [H2O2]0=17.8 g L−1, corresponding to the stoichiometric amount of H2O2 needed for the complete mineralization of 4-NP). It was observed that the increase of electron-donating functionalities in PS-800 promotes the generation of reactive HO% radicals, being the activity towards CWPO twice higher than that obtained with the pristine PS. Besides, increasing operating temperature substantially enhances CWPO, finding a 80% of 4-NP removal at 110 °C. On the other hand, despite the sharp increment in H2O2 decomposition due to the presence of Pt particles in Pt/PS catalyst, this decomposition is inefficient in all cases, with a consequent poor pollutant removal. This can be attributed to the recombination of HO% radicals into non-reactive species −scavenging effects, promoted by the hydrophilicity of the catalyst.