Removal of Reactive Green Dye from Textile Waste Water by Photo Fenton Process: Modeling, Kinetic, and Thermodynamic.

This work investigated the removal of the reactive green (R.G) dye from wastewater using the photo-Fenton process. Batch experiments were carried out to research the role of the Impacts of operating parameters. The dosage of H2O2; dosage Fe+2; pH; temperature, and irradiation time were examined. Maximum decolorization efficiencies green dye were achieved at the [H2O2]=100 ppm; [Fe2+]=20 ppm; pH 3; temperature=56 °C and irradiation time=90 min. This research focuses on modeling, kinetics and thermodynamics of the removal of pollutant (reactive green dye) of water. The results showed that the decolorization kinetic of R.G followed pseudo-first-order reaction kinetic. Also the thermodynamic parameters ∆G˚, ∆H˚ and ∆S˚ were determined using the Van't Hoff equation for the oxidation processes. The changes in Gibbs free energy showed the oxidation process under normal conditions is non-spontaneous.

Adsorption Kinetics of NO2 Gas on Pt/Cr-TiO2/Pt-Based Sensors

Metal oxides are excellent candidates for the detection of various gases; however, the issues such as the limited operating temperature and selectivity are the most important ones requiring the comprehensive understanding of gas adsorption kinetics on the sensing layer surfaces. To this context, the present study focuses mainly on the fabrication of a Pt/Cr-TiO2/Pt type sensor structure that is highly suitable in reducing the operating temperature (from 400 to 200 °C), extending the lower limit NO2 gas concentration (below 10 ppm) with fast response (37 s) and recovery (24 s) times. This illustrates that the sensor performance is not only solely dependent on the nature of sensing material, but also, it is significantly enhanced by using such a new kind of electrode geometry. Moreover, Cr doping into TiO2 culminates in altering the sensor response from n- to p-type and thus contributes to sensor performance enhancement by detecting low NO2 concentrations selectively at reduced operating temperatures. In addition, the NO2 surface adsorption kinetics are studied by fitting the obtained sensor response curves with Elovich, inter-particle diffusion, and pseudo first-order and pseudo second-order adsorption models. It is found that a pseudo first-order reaction model describes the best NO2 adsorption kinetics toward 7–170 ppm NO2 gas at 200 °C. Finally, the sensing mechanism is discussed on the basis of the obtained results.

Tailoring g-C3N4 with Lanthanum and Cobalt Oxides for Enhanced Photoelectrochemical and Photocatalytic Activity

Herein, the synthesis, characterization, and photoelectrochemical and photocatalytic characteristics of hydrothermally prepared La2O3–g-C3N4, CoO–g-C3N4, and La2O3–CoO–g-C3N4 are discussed. The XRD analysis and crystalline phases unveiled the impregnation of La2O3 and CoO into g-C3N4. The microscopic analysis supports the formation of g-C3N4 nanoflakes and La2O3 and CoO nanoparticles embedded homogeneously in the La2O3–CoO–g-C3N4 nanocomposite, whereas the EDX comprehended their respective elemental composition and ratios. A bandgap energy of 2.38 eV for La2O3–CoO–g-C3N4 was calculated using the Tauc plot method, complementing high visible-light activity. The solar-driven water-splitting reaction exhibited significant photocurrent efficiency (~3.75 mA/cm2), augmenting the hydrogen generation by La2O3–CoO–g-C3N4 compared to that by pure g-C3N4, La2O3–g-C3N4, and CoO–g-C3N4 in 0.5 M Na2SO4 electrolyte. The synergistic effect of La2O3 and CoO impregnation with g-C3N4 led to effective division of the photogenerated charge transporters, enhancing the photocatalytic hydrogen generation by the photocatalysts. Furthermore, photocatalytic pollutant removal, namely greater than 90% decomposition of methylene blue (MB) from water, was investigated with a pseudo-first-order reaction kinetics under 1 sun visible-light irradiation. Thus, La2O3–CoO–g-C3N4 nanocomposite was found to be a prospective material for harnessing solar energy.

A Multi-Criteria Decision-Making Approach to Evaluate Different UVC/H2O2 Systems in Wastewater Treatment

High azoxystrobin (AZO), difenoconazole (DFZ), and imidacloprid (IMD) pesticide removal rates in sixteen bench-scale experiments concerning tomato washing water treatment were obtained through a UVC/H2O2 advanced oxidative process. Experimental conditions ([H2O2]0) and irradiance (EUVC) were optimized for higher degradation rates (pseudo-first-order reaction). To consider both economic aspects and environmental impacts when defining the treatment technology, as well as technological requirements, this study applied a multi-criteria decision-making method (MCDM) to assess and differentiate similar UVC/H2O2 process configurations. This allowed for the identification of the cheapest experimental arrangement with the lowest associated environmental impacts, coupled to the highest degradation rate (kIMD). After consulting experts to determine the importance of the applied criteria and measuring alternative performances, experiment E7 ([H2O2]0 = 43.5 mg L−1; EUVC = 15.0 W m−2; kIMD = 0.236 s−1) was determined as meeting the three criteria in a balanced manner. Although E7′s technological performance regarding degradation rate did not achieve the best individual result, it presented the lowest impacts and costs among the analyzed series, although alternatives are sensitive to decision-maker priorities. This study considered different factors of a process displaying potential industrial applications still in the design stage to achieve a more efficient and balanced solution.

Degradation Characteristics of Carbon Tetrachloride by Granular Sponge Zero Valent Iron

Granular sponge zero valent iron (ZVI) was employed to degrade carbon tetrachloride (CCl4). The effects of acidic washing, initial solution pH, and ZVI dosage on CCl4 degradation were investigated. Results showed that CCl4 was effectively removed by ZVI and approximately 75% of CCl4 was transformed into chloroform through hydrogenolysis. The rate of chloroform transformation was slower compared to that of CCl4, resulting in chloroform accumulation. CCl4 degradation was a pseudo first-order process. The observed pseudo first-order reaction rate constant (kobs) for CCl4 and chloroform were 0.1139 and 0.0109 h−1, respectively, with a ZVI dosage of 20 g/L and an initial CCl4 concentration of 20 mg/L. Surface acidic washing had a negligible effect on CCl4 degradation with ZVI. The kobs for CCl4 degradation increased linearly with increasing ZVI dosage and the optimal dosage of ZVI was 20 g/L based on the surface area-normalized rate constants. The negative relationship between kobs and the solution pH indicated that the degradation of CCl4 by ZVI performed better under weakly acidic conditions.

The Kinetics Investigation of CO2 Absorption into TEA and DEEA Amine Solutions Containing Carbonic Anhydrase

Tertiary amines have been used as alternative absorbents for traditional primary and secondary amines in the process of carbon capture. However, the carbon dioxide (CO2) absorption rates in these kinds of amine are relatively slow, which implies greater investment and construction costs and limits the large-scale application of carbon capture. Carbonic anhydrase (CA) is considered to be an ideal homogeneous catalyst for accelerating the rate of CO2 into aqueous amine solution. In this work, CO2 absorption combining CA with two single aqueous tertiary amines, namely triethanolamine (TEA) and 2-(diethylamino)ethanol (DEEA), was studied by use of the stopped-flow apparatus over temperature ranging from 293 to 313 K. The concentrations of selected aqueous amine solution and CA used in the experiment were ranging among 0.1–0.5 kmol/m3 and 0–50 g/m3 , respectively. Compared to the solution without the addition of CA, the pseudo first-order reaction rate in the presence of CA (k0,withCA) is significantly increased. The values of k0,withCA have been calculated by a new kinetics model. The results of experimental and calculated k0,amine and k0,withCA in CO2-amine-H2O solutions were also investigated,respectively.

In-Situ FTIR Study of Heterogeneous Oxidation of SOA Tracers by Ozone

Secondary organic aerosols (SOA) play an important role in global climate change and air quality, and SOA tracers can directly characterize the source and reaction mechanism of SOA. However, it is not well known that whether the tracers can be oxidized or how the instability of the tracers in the atmosphere. In this paper, in-situ FTIR was used to analyze the chemical structure changes of erythritol, analogue of 2-methyl erythritol (AME) that is, a tracer of isoprene SOA, and 2, 3-dihydroxy-4-oxopentanoic acid (DHOPA), a tracer of toluene SOA, when exposed to high concentration of ozone for short periods. Under the condition of 20 ppm ozone exposure for 30 min, the change rate of absorption area of AME at 3,480 and 1700 cm−1 was −0.0134 and 0.00117 int.abs/s, respectively, and the change rate of the absorption area of DHOPA at 1,640 and 3340cm−1 was −0.00191 and 0.00218 int.abs/s, respectively. The pseudo-first-order reaction rate constant kapp were 1.89 × 10−8 and 2.12 × 10−7 s−1, and the uptake coefficients of ozone on the surface of AME and DHOPA were (1.3 ± 0.8) × 10−8 and (4.5 ± 2.7) × 10−8, respectively. These results showed the oxidation processes of AME and DHOPA were slow in the presence of high concentrations of ozone, which implied that AME and DHOPA could be considered to be stable in the atmospheric environment with ozone as the main oxidant.

Kinetics of DPPH• scavenging by bacterioruberin from Haloferax alexandrinus GUSF-1 (KF796625)

This is the first account of the kinetics of free radical scavenging by bacterioruberin obtained from cells of Haloferax alexandrinus GUSF-1(KF796625), grown at optimum conditions of 25% NaCl, pH 7, 42 °C, 150 rpm in NaCl Tryptone yeast extract medium and light. Bacterioruberin separated from methanolic extract displayed characteristics absorption peaks at 368, 386, 463, 492 and 525 nm and gave an m/z value of 740.4 (C50H76O4) in Liquid Chromatography-Mass Spectroscopy validating its purity. Bacterioruberin (13 µM) decolorized and decayed 0.2 mM 1,1-diphenyl-2-picrylhydrazyl radicals (DPPH•) monitored at 517 nm and reached a steady state within 30 min. An EC50 of 6.50 µM ± 0.27 (4.81 µg/mL ± 0.2) was deduced for the 0.2 mM DPPH•-bacterioruberin reaction using the GraphPad Prism 9 statistical software and employing the right-angled triangle technique. The study also revealed a comprehensive information of the total kinetic activity of bacterioruberin with DPPH•: the antioxidant activity index was 16.38 ± 0.67; time needed to reach the steady state with the added EC50—30 min; the antiradical power 30.77 ± 1.27 and the antiradical efficiency of 54.7 × 10–3 ± 2.24, thus reflecting the strong antioxidant nature of bacterioruberin. Scavenging of DPPH• by bacterioruberin was a pseudo-first-order reaction with a rate constant k2 of 2.76 × 10–5 ± 0.001 µM−1 s−1 calculated at t = 0 or initial time and t = 30 min. The knowledge of the kinetics of bacterioruberin to scavenge DPPH• adds to its effective application as an antioxidant in medicinal use, pharmaceutical products and others. Additionally, the use of simple conventional method of DPPH• free radical scavenging, monitored using an easily available laboratory spectrophotometer, will certainly help in the effective use of any antioxidant compound.

Photocatalytic Performance of a Novel Sr-Ce-TiO2/HAp for Degradation of Methylene Blue Dye in the Presence of Visible Light

In this study, Sr-Ce-TiO2/HAp as a novel and efficient nanocomposite was synthesized and characterized by Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), scanning electron microscopy (SEM), and surface area determination of porous using the Brunauer–Emmett–Teller (BET) method and degradation of methylene blue under visible radiation was investigated. Evaluations showed that doped with metal cations and the presence of hydroxyapatite reduced energy gap, increased surface area, increased adsorption and decreased electron-hole recombination. The results also showed that more than 92% of methylene blue was removed within 100 min. The pseudo-first order reaction synthetic was obtained.

Enhanced Photocatalytic Efficiency of Soft Chemically Synthesized MAl2O4 / Activated Carbon Based Composite in the Removal of Toxic Malachite Green Dye Under Visible Light

Composites of spinel aluminate (MAl2O4) based materials having activated carbon (AC) as the base materials were synthesized using chemical precipitation method. The as synthesized photocatalyst was characterized using X-Ray Diffractometry (XRD), Fourier transform Infrared Spectrophotomatry (FTIR), Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Analysis (EDS) and UV- DRS studies. The XRD confirms the presence of amorphous phase along-with crystalline spinel phase. The bonds related to tetrahedral and octahedral sites of the spinel were confirmed by FTIR. EDS confirmed the presence of appropriate elements. The presence of pores in the sample was shown by SEM. The UV-Visible spectra of the spinel – AC composites exhibited λmax in the range of 365–400 nm. The composites were very effective in the photo-degradation of MG dye from water. The photocatalytic degradation of MG follows pseudo first order reaction mechanism i.e., Langmuire and Hinshelwood kinetic model. Among the photocatalysts studied, Co0.85Ni0.15Al2O4−δ /AC exhibited excellent degradation efficiency in removing MG completely within 90 minutes under visible light irradiation.