Environmental pollution,energy import,and economic growth: evidence of sustainable growth in South Africa and Nigeria

Environmental Science and Pollution Research - Simultaneous achievement of sustainable development goals (SDGs), especially energy efficiency (SDG 7), economic growth (SDG 8), and pollution...     

Elemental mercury (Hg0) removal from coal syngas using magnetic tea-biochar: Experimental and theoretical insights

Mercury is ranked 3^rd as a global pollutant because of its long persistence in the environment. Approximately 65% of its anthropogenic emission (Hg⁰) to the atmosphere is from coal-thermal power plants. Thus, the Hg⁰ emission control from coal-thermal power plants is inevitable. Therefore, multiple sorbent materials were synthesized using a one-step pyrolysis method to capture the Hg⁰ from simulated coal syngas. Results showed, the Hg⁰ removal performance of the sorbents increased by the citric acid/ultrasonic application. T5CUF_0.3 demonstrated the highest Hg⁰ capturing performance with an adsorption capacity of 106.81 µg/g within 60 min at 200 °C under complex simulated syngas mixture (20% CO, 20% H₂, 10 ppmV HCl, 6% H₂O, and 400 ppmV H₂S). The Hg⁰ removal mechanism was proposed, revealing that the chemisorption governs the Hg⁰ removal process. Besides, the active Hg⁰ removal performance is attributed to the high dispersion of valence Fe₃O₄ and lattice oxygen (α) contents over the T5CUF_0.3 surface. In addition, the temperature programmed desorption (TPD) and XPS analysis confirmed that H₂S/HCl gases generate active sites over the sorbent surface, facilitating high Hg⁰ adsorption from syngas. This work represented a facile and practical pathway for utilizing cheap and eco-friendly tea waste to control the Hg⁰ emission.     

Poly[β-(1→4)-2-amino-2-deoxy-D-glucopyranose] based zero valent nickel nanocomposite for efficient reduction of nitrate in water

Chemical reduction of nitrate using metal nanoparticles has received increasing interest due to over-dependence on groundwater and consequence health hazard of the nitrate ion. One major drawback of this technique is the agglomeration of nanoparticles leading to the formation of large flocs. A low cost biopolymeric material, poly [β-(1 → 4)-2-amino-2-deoxy-D-glucopyranose] (β-PADG) obtained from deacetylated chitin was used as stabilizer to synthesize zero valent nickel (ZVNi) nanoparticles. The β-PADG-ZVNi nanocomposite was characterized using infra red (IR), UV-Vis spectrophotometric techniques and Scanning Electron Microscope (SEM). The morphology of the composite showed that β-PADG stabilized-ZVNi nanoparticles were present as discrete particles. The mean particle size was estimated to be (7.76 ± 2.98) nm and surface area of 87.10 m²/g. The stabilized-ZVNi nanoparticles exhibited markedly greater reactivity for reduction of nitrate in water with 100% conversion within 2 hr contact owing to less agglomeration. Varying the β-PADG-to-ZVNi ratio and the ZVNi-to-nitrate molar ratio generally led to a faster nitrate reduction. About 3.4-fold difference in the specific reaction rate constant suggests that the application of the β-PADG-stabilizer not only increased the specific surface area of the resultant nanoparticles, but also greatly enhanced the surface reactivity of the nanoparticles per unit area.     

Recent developments on gas–solid heterogeneous oxidation removal of elemental mercury from flue gas

Environmental Chemistry Letters - Mercury is a toxic and persistent environmental pollutant which has been recognized as a global threat to human health and our ecosystem because mercury...