Comparative study on photooxidation of methyl orange using various UV/oxidant systems

In the present work, a comparative study of the photooxidation of an aqueous solution of Methyl Orange (MeO) has been realized using H2O2 and IO3 −, BrO3 −, ClO3 −, ClO4 −, BO3 − ions in the presence of UV low pressure mercury lamp (UV-C light at λ max = 254 nm). The initial concentration of MeO in all experiments was 6 × 10−5 mol L−1. The degradation rate of MeO follows pseudo-first-order kinetics in all UV/Oxidant systems. The highest degradation rate of MeO was in the BrO3 −/UV254nm system. Different systems were compared for an oxidant concentration of 10−2 mol L−1 and the obtained results showed that decolorization followed the decreasing order: BrO 3 − /UV 254 nm > IO 3 − /UV 254 nm > H 2 O 2 /UV 254 nm > BO 3 − /UV 254 nm > ClO 3 − /UV 254 nm = ClO 4 − /UV 254 nm = UV 254 nm . The optimization of oxidants concentration for each process was determined (10−2 mol L−1 for IO3 − which gives almost the same k app for 5 × 10−3, 10−2 mol L−1 for BO3 − and 5 × 10−2 mol L−1 for H2O2). No degradation of MeO in presence of ClO3 − and ClO4 − because these ions do not absorb at 254 nm, therefore they do not generate radical species which degrade organic pollutants. The mineralization was also studied where it was reached 97% after 5 h of irradiation for both H2O2/UV254 nm and BO3 −/UV254 nm systems.

Degradation of paraquat herbicide using hybrid AOP process: statistical optimization, kinetic study, and estimation of electrical energy consumption

Background This work studied the performance of UV/PS/TiO2NPs and UV/PI/TiO2NPs as hybrid advanced oxidation processes for degradation of paraquat in aqueous solution, because this very toxic herbicide is used third most widely. Results The effects of several factors such as UV irradiation, initial oxidant concentration, TiO2 nanoparticles dosage, and pH on the degradation efficiency were investigated. The process optimization was performed by the central composite design as a tool of response surface methodology for 30 mgL−1 of the herbicide initial concentration at 25 ℃ and 40 min of degradation process. Based on the results, a degradation efficiency of 77% and 90% were obtained for the UV/PS/TiO2NPs and UV/PI/TiO2NPs processes, respectively, in the optimum conditions. The mineralization efficiency of the paraquat solution using UV/PS/TiO2NPs and UV/PI/TiO2NPs processes are about 32% and 55%, respectively, after 40 min. The kinetic studies show that both processes follow a pseudo-first-order kinetic model, and the kinetic constants are 0.0299 min−1 for the PS process and 0.0604 min−1 for the PI process. The electrical energy consumption was estimated to be about 481.60 kWhm−3 for the PS process and 238.41 kWhm−3 for the PI process. Conclusions The degradation and mineralization efficiency of the paraquat solution using the UV/PI/TiO2NPs process was more than that of the UV/PS/TiO2NPs process at the optimum conditions after 40 min.

Structure design of multi-functional flexible electrocardiogram electrodes based on PEDOT:PSS-coated fabrics

Herein, Polyester woven fabrics as the matrices for the experimental group, while cotton knitted fabrics, cotton woven fabrics, and Polyethylene terephthalate (PET) mesh cloth used as the matrices for the control groups, at 40 °e, using 3,4-ethoxylene dioxy thiophene (EDOT)as the polymer monomer, FeCl3 as the oxidant, and poly(sodium-p-styrenesulfonate) (PSS) as the dopant, are separately coated with PEDOT:PSS polymer to prepare flexible conductive composite fabrics. The influences of the fabric pattern, oxidant concentration, and monomer concentration on the electrical performance of composite fabrics are optimized. The maximal electrical conductivity of PET-based composite fabrics (218 S/m) occurs when monomer concentration is 0.035 mol/L, the molar ratio of oxidant to monomer is 2.5, and the dopant concentration is 2.5 g/L. Moreover, bacteriostasis rate of this composite fabric reaches 71.8%. Furthermore, by electrocardiogram (ECG) simulated human body unit test as well as human body ECG test, the optimal PET-based composite fabric electrode both has a lower impedance which helps form the stabilized ECG signal. The resulting fabric electrodes retain the soft and breathable advantages from fabrics and reduce the discomfort for a long-term use of conventional electrographic gel, thereby validating the empirical evidence for mobile, portable, wearable ECG electrodes.

Enhanced Photocatalytic Activity of Spherical Nd3+ Substituted ZnFe2O4 Nanoparticles

In this study, nanocrystalline ZnNdxFe2−xO4 ferrites with x = 0.0, 0.01, 0.03 and 0.05 were fabricated and used as a catalyst for dye removal potential. The effect of Nd3+ ions substitution on the structural, optical and photo-Fenton activity of ZnNdxFe2−xO4 has been investigated. The addition of Nd3+ ions caused a decrease in the grain size of ferrites, the reduction of the optical bandgap energies and thus could be well exploited for the catalytic study. The photocatalytic activity of the ferrite samples was evaluated by the degradation of Rhodamine B (RhB) in the presence of H2O2 under visible light radiation. The results indicated that the ZnNdxFe2−xO4 samples exhibited higher removal efficiencies than the pure ZnFe2O4 ferrites. The highest degradation efficiency was 98.00%, attained after 210 min using the ZnNd0.03Fe1.97O4 sample. The enhanced photocatalytic activity of the ZnFe2O4 doped with Nd3+ is explained due to the efficient separation mechanism of photoinduced electron and holes. The effect of various factors (H2O2 oxidant concentration and catalyst loading) on the degradation of RhB dye was clarified.

Relationship between Changes over Time in Factors, Including the Impact of Meteorology on Photochemical Oxidant Concentration and Causative Atmospheric Pollutants in Kawasaki

To clarify the relationship between changes in photochemical oxidants’ (Ox) concentrations and their precursors in Kawasaki, a series of analyses were conducted using data on Ox, their precursors, nitrogen oxides (NOx) and volatile organic compounds (VOCs), and meteorology that had been monitored throughout the city of Kawasaki for 30 years from 1990 to 2019. The trend in air temperature was upward, wind speed was downward, and solar radiation was upward, indicating an increasing trend in meteorological factors in which Ox concentrations tend to be higher. Between 1990 and 2013, the annual average Ox increased throughout Kawasaki and remained flat after that. The three-year moving average of the daily peak increased until 2015, and after that, it exhibited a slight decline. The amount of generated Ox is another important indicator. To evaluate this, a new indicator, the daytime production of photochemical oxidant (DPOx), was proposed. DPOx is defined by daytime averaged Ox concentrations less the previous day’s nighttime averaged Ox concentrations. The trend in DPOx from April to October has been decreasing since around 2006, and it was found that this indicator reflects the impact of reducing emissions of NOx and VOCs in Kawasaki.

Health Risk of Increased O3 Concentration Based on Regional Emission Characteristics under the Unusual State of the COVID-19 Pandemic

Photochemical oxidant concentration increases with the decrease in nitrogen oxide (NOx) concentration in volatile organic compound (VOC)-sensitive areas with several automobiles and factories. We aimed to quantify the changes in health risks from ozone (O3) and nitrogen dioxide (NO2) using disability-adjusted life years (DALY) in Osaka City, which is one of the major cities in Japan. ADMER-PRO version 1.0, an atmospheric model for secondary products, was used to estimate the concentration distribution of NO2, VOC, and O3 using the year-on-year change of traffic during the declaration of the state of emergency in response to the coronavirus disease 2019 (7 April to 21 May 2020). NO2 concentration decreased by an average of 0.962 ppb in 88.9% of the grids in Osaka City, whereas O3 concentration increased by an average of 1.00 ppb in all the grids with a 26–28% reduction of traffic volume due to the pandemic. We also found three intensities for the VOC-sensitive condition depending on the different regional emission characteristics, with the DALYs of health risks from the decrease in NO2 exceeding those from the increase in O3, reaching 811.4 and 55.90 total DALYs in the city, respectively.

Investigating the synergistic effect of UV/PS/TiO2 and UV/PI/TiO2 processes on paraquat herbicide degradation in media aqueous: statistical optimization, kinetic study, and estimation of electrical energy consumption

In this paper, the performance of UV/PS/TiO2 and UV/PI/TiO2 as hybrid AOPs for degradation of paraquat (PQ) herbicide in aqueous solution has been studied. The effect of several factors such as UV irradiation, initial oxidant concentration, nano-TiO2 (TiO2NPs) dosage, and pH on the degradation efficiency was investigated. Process optimization was performed by Central Composite Design (CCD) and response surface methodology (RSM) for 30 mgL− 1 of herbicide at 25 ˚C and 40 min. Based on the results, for UV/PS/TiO2 process a degradation efficiency of 83% was obtained in the optimum condition of initial PS concentration of 400 mgL− 1, initial TiO2NPs concentration of 150 mgL− 1, and pH = 6.3. Also for UV/PI/TiO2 process, 87% degradation efficiency was achieved in the optimum condition of initial PI concentration of 88 mgL− 1, initial TiO2NPs dosage of 125.5 mgL− 1, and pH of 7.5. Mineralization efficiency of the PQ solution by using PS and PI were about 47.5% and 57%, respectively after 80 min. Kinetic studies showed that both process follow pseudo-first-order kinetic model and their kinetic constants were 0.0299 min− 1 for PS process and 0.0604 min− 1 for PI process. Electrical energy consumption was estimated about 481.60 kWh/m3 for PS process and 238.41 kWh/m3 for PI process.