FLAVIO KIYOSHI TOMINAGA
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Artigo IPEN-doc 30419 BDD-persulfate-based anodic oxidation process for progestin degradation2024 - JESUS, JULIANA M.S. de; ARGOLO, ALLAN dos S.; TOMINAGA, FLAVIO K.; BILA, DANIELE M.; BORRELY, SUELI I.; TEIXEIRA, ANTONIO C.S.C.Considering the increasing presence of the hormones levonorgestrel (LNG) and gestodene (GES) in wastewater, the limited effectiveness of conventional treatment methods, and the demand for advanced complementary processes, our study aimed to optimize an anodic oxidation treatment with a focus on low specific energy consumption (SEC) and costs. An electrochemical system coupled to a boron-doped diamond anode (BDD) was continuously used to treat synthetic and real pharmaceutical wastewater from contraceptive production. The central design composite and response surface methodology were the tools employed for optimization. The lowest SEC was obtained as a response to the main process variables: current density, initial pH, and the concentration of the support electrolyte ([Na2S2O8]). The optimal condition ([Na2S2O8]0 = 0.07 mol L−1; [LNG]0,RPW = 1.02±0.05 mg L−1 and [GES]0,RPW = 1.05±0.05 mg L−1; j = 37.5 mA cm−2; pH = 6.75) was established considering an SEC ≤ 3.6 ± 0.8 kWh g−1 and progestins removal ≥70%, which was the experimental condition used to evaluate acute toxicity to Daphnia similis and the effect on estrogenic activity removal using the YES assay. Notably, our study evaluated, for the first time, a comparative investigation that highlights the substantial effect of support electrolytes over the eco-compatibility assessment of the anodic oxidation process investigated. The adaptability of the operation indicates the prospective suitability for the implementation of the process in wastewater treatment facilities in the pharmaceutical industry.Artigo IPEN-doc 28433 UVA/persulfate-driven nonylphenol polyethoxylate degradation2022 - NUNES, R.F.; TOMINAGA, F.K.; BORRELY, S.I.; TEIXEIRA, A.C.S.C.UV/persulfate (UV/PS) technologies have gained increased attention as efficient alternatives for removing pollutants from different classes, although processes based on the UVA-driven S2O2−8 (PS) activation have not yet been discussed in the literature for the removal of the nonionic surfactant nonylphenol polyethoxylate (NPEO). The present study investigated the simultaneous effect of the initial persulfate concentration ([PS]0) and specific photon emission rate (EP,0) on NPEO degradation by UVA/PS following a Doehlert experimental design. The results for [NPEO]0 = (4.65 ± 0.15) mg L−1 indicated more than 97.8% NPEO removal after 2 h, with pseudo first-order specific degradation rate (kobs) of 0.0320 min−1, for [PS]0 = 7.75 mmol L−1 and EP,0 = 0.437 μmol photons L−1 s−1. Under these conditions, NPEO half-life time was about 22 min, and the EC50-48 h (% v/v) values for Daphnia similis before and after treatment did not differ significantly. Higher values of EP,0 would influence NPEO removal for [PS]0 not higher than 8–10 mmol L−1, although lower degradation efficiencies were obtained with higher [NPEO]0 or real wastewater, except for longer reaction times. Additionally, UVA/PS showed to be efficient for tensoactivity removal, despite the negligible total organic carbon (TOC) removal achieved. Finally, UVC and UVA resulted in NPEO degradation higher than 96% and similar tensoactivity removals when UVA/PS was conducted under optimal conditions ([PS]0 = 10 mmol L−1; EP,0 = 0.324 μmol photons L−1 s−1), suggesting that UVA radiation available in solar light could be advantageously employed for NPEO removal at concentrations usually found in wastewater.