Anthraquinones (AQs) constitute the largest group of natural pigments, are commonly found in dyes, and are widely used in the textile industry due their photostability. They combine high absorptivity in the visible region with high excited‐state reduction potentials, making them effective acceptors of electrons and hydrogen atoms. AQs can be employed as organic catalysts in photooxidation reactions as well to produce reactive oxygen species (ROS). All these methods feature green chemistry aspects such as avoiding heavy metals, reducing waste, using inexpensive reagents, employing environmentally low‐impact solvents, and oxidizing with O2. This review covers the application of AQs in photoredox catalysis.
Abstract:The coffee processing agro-industry generates large quantities of wastewater requiring systematic treatment prior to disposal. For this reason, the aim of this study was to evaluate the hydraulic retention times (HRT) in treatment of coffee processing wastewater (CPWW) using a laboratory scale Expanded Granular Sludge Bed (EGSB) bioreactor at different HRT (3 to 9 days). The EGSB was evaluated in mesophilic condition (26 ± 2 • C) with an average pH of 7.5 ± 0.2 to determine the chemical oxygen demand (COD) removal efficiency. According to the results, the COD removal efficiency increases from 94 to 98% when the HRT increase from 3 to 9 days; the α factor remained stable (0.98) throughout the evolution of the bioreactor. The HRT´s between 7-9 days generated effluents capable to be dischargeable into water bodies with a permitted COD concentration according to World Health Organization (WHO) and Official Mexican Environmental Regulations permissible limits. Results evidenced that the HRT of 9 days was the one that greater COD removal generated, so the EGSB bioreactor can be a sustainable alternative to solve the environmental problems, compared to other conventional methods to CPWW treatment.
Uncatalyzed one-pot, three-component reactions of aldehydes, chiral α-methylamines, and dimethyl phosphite under solvent-free conditions were used for the diastereoselective synthesis of α-amino phosphonates. The reactions proceeded
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