Study of Kinetics and the Working Mechanism of Silica-Coated Amino-Functionalized CoFe2O4 Ferrite Nanoparticles to Treat Wastewater for Heavy Metals.

This study used a simple coprecipitation method to produce pristine, silica-coated, and amino-functionalized CoFe2O4 nanoadsorbents. Amino-functionalization was done to increase the active surface area and metal ion removal efficiency. Both pristine and functionalized adsorbents were employed to recover Pb(II), Zn(II), and Cu(II) ions from wastewater. The adsorption tests were performed by varying the initial concentration of metal ions and contact time at a fixed pH of 6.5. Atomic adsorption spectroscopy was utilized to detect the proportion of metals removed from water. Additionally, the pseudo-first-order, pseudo-second-order, Freundlich, and Langmuir models were employed to compute the kinetic and isothermic data from metal ion adsorption onto the adsorbents. The amino-functionalized adsorbent showed adsorption capacities of 277.008, 254.453, and 258.398 mg/g for Cu(II), Pb(II), and Zn(II) ions, respectively. According to the adsorption results, the Langmuir isotherm and the pseudo-second-order model best suit the data. The best fitting of the pseudo-second-order model with the data indicates that coordinative interactions between amino groups and metal ions are responsible for chemisorption. The metal ions bind with -NH2 groups on the adsorbent surface through chelate bonds. Chelate bonds are extremely strong and stable, indicating the effectiveness of the CoFe2O4@SiO2-NH2 adsorbent in adsorbing heavy-metal ions. The tested adsorbent exhibited good performance, batter stability, and good reusable values around 77, 81, and 76% for Cu(II), Pb(II), and Zn(II) ions, respectively, after five adsorption cycles.

Nanofiltration PVP Membrane with Gradient Cross-Linking for Efficient Polycyclic Aromatic Hydrocarbons Removal.

Polycyclic aromatic hydrocarbons (PAHs) are persistent organic pollutants that may contaminate various water sources and pose serious dangers to human health and the environment. Due to their capacity for size-based separation, nanofiltration membranes have become efficient instruments for PAH removal. However, issues such as membrane fouling and ineffective rejection still exist. To improve PAH rejection while reducing fouling problems, this work created a new gradient cross-linking poly(vinylpyrrolidone) (PVP) nanofiltration membrane. The gradient cross-linking technique enhanced the rejection performance and antifouling characteristics of the membrane. The results demonstrated that the highest membrane flow was achieved at a 0.15% SDS-PVP membrane. There is a trade-off between membrane flux and salt rejection since salt rejection increases with SDS owing to the growth of big pores. The membrane flux was reduced for the 0.25% SDS-PVP membrane owing to poor SDS dispersion. The prepared membrane showed enhanced removal efficiencies for the removal of the PAH compounds. The PVP membrane has the potential to be used in several water treatment applications, improving water quality, and preserving the environment.

Assessing spatiotemporal trends of total and extreme precipitation in a subtropical highland region: A climate perspective.

This study used a dataset of 30 years (1990-2020) of daily observations from 24 meteorological stations in the northern highlands of Pakistan to assess trends in extreme precipitation indices. The RClimDex model was used to analyze the indices, and the Modified Mann-Kendal test and the Theil-Sen slope estimator were applied to determine trends and slopes, respectively. The results showed a significant decrease in total annual precipitation amount (PRCPTOT) with varying rates of negative trend from -4.44 mm/year to -19.63 mm/year. The total winter and monsoon precipitation amounts were also decreased during the past three decades. The intensity-based precipitation indices (RX1Day, RX5Day, R95p, R99p, and SDII) showed a significant decrease in extreme intensity events over time, while the count of consecutive dry days (CDD) and consecutive wet days (CWD) indicated a significant decrease in duration at multiple stations. The annual counts of days with precipitation more than or equal to 10 mm (R10), 20 mm (R20), and 25 mm (R25) exhibited a significant decrease in frequency of extreme precipitation events, with the decrease more pronounced in the northern parts of the study domain. The findings of this study indicate a significant decline in the intensity, frequency, and extent of precipitation extremes across the northern highlands of Pakistan over the past 30 years.

Green Synthesis of ZnO and Black TiO2 Materials and Their Application in Photodegradation of Organic Pollutants.

ZnO and black TiO2 have been selected as the most efficient materials for organic pollution abatement due to their increased efficiency when compared to other materials. However, the concept of green chemistry makes it desirable to design green synthesis approaches for their production. In this study, black TiO2 was synthesized using an environmentally safe synthetic technique with glycerol as a reductant. ZnO was prepared by using ionic-liquid-based microwave-assisted extracts of Polygonum minus. To investigate the materials' potential to photodegrade organic pollutants, methylene blue (MB) and phenol were chosen as model organic pollutants. Both materials were found to exhibit spherical morphologies and a mesoporous structure and were efficient absorbers of visible light. ZnO exhibited electron-hole pair recombination lower than that of black TiO2. Black TiO2 was discovered to be an anatase phase, whereas ZnO was found to have a hexagonal wurtzite structure. In contrast to black TiO2, which had a surface area of 239.99 m2/g and a particle size of 28 nm, ZnO had a surface area of 353.11 m2/g and a particle size of 32 nm. With a degradation time of 60 min, ZnO was able to eliminate 97.50% of the 40 mg/L MB. Black TiO2, on the other hand, could reduce 90.0% of the same amount of MB in 60 min. When tested for phenol degradation, ZnO and black TiO2 activities were reduced by nearly 15 and 25%, respectively. A detailed examination of both ZnO and black TiO2 materials revealed that ZnO has more potential and versatility for the degradation of organic pollutants under visible light irradiation.

Dual S-Scheme Heterojunction CdS/TiO2/g-C3N4 Photocatalyst for Hydrogen Production and Dye Degradation Applications.

This study investigated a ternary CdS/TiO2/g-C3N4 heterojunction for degrading synthetic dyes and hydrogen production from aqueous media through visible light-initiated photocatalytic reactions. CdS, TiO2, and g-C3N4 were combined in different mass ratios through a simple hydrothermal method to create CdS/TiO2/g-C3N4 composite photocatalysts. The prepared heterojunction catalysts were investigated by using FTIR, XRD, EDX, SEM, and UV-visible spectroscopy analysis for their crystal structures, functional groups, elemental composition, microtopography, and optical properties. The rhodamine B dye was then degraded by using fully characterized photocatalysts. The maximum dye degradation efficiency of 99.4% was noted in these experiments. The evolution rate of hydrogen from the aqueous solution with the CdS/TiO2/g-C3N4 photocatalyst remained 2910 µmol·h-1·g-1, which is considerably higher than those of g-C3N4, CdS, CdS/g-C3N4, and g-C3N4/TiO2-catalyzed reactions. This study also proposes a photocatalytic activity mechanism for the tested ternary CdS/TiO2/g-C3N4 heterojunctions.